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Not all forgetfulness is created equal. Find out how to differentiate between normal memory lapses and signs that it’s time for a memory screening.
By Aqualane Research – Naples, Florida
Have you ever walked into a room and completely forgotten why you went there? Or how about searching for your keys for what feels like the hundredth time, wondering if this level of forgetfulness is really normal? Memory lapses can be both frustrating and concerning. When is forgetfulness simply an everyday occurrence, and when is it a sign of something more serious? These are questions that many people ask themselves or worry about silently.
In this article, we’ll demystify the difference between normal forgetfulness and more concerning signs of memory decline. You’ll learn how to distinguish occasional absent-mindedness from early indicators of something that may warrant medical attention, such as mild cognitive impairment or dementia. We’ll also explore practical steps you can take to preserve and improve your brain health—and how you can take advantage of our free memory screening at Aqualane Research in Naples, Florida if you suspect that your forgetfulness might be more than just a “senior moment.”
By the end, you’ll have a clearer perspective on forgetfulness vs memory loss, the signs of memory decline, and when to seek help or additional evaluation. Armed with this knowledge, you’ll be better prepared to navigate future memory issues—either for yourself or a loved one—with confidence, empathy, and understanding.
We all forget things from time to time. Whether it’s misplacing your phone, struggling to remember someone’s name, or finding a half-finished cup of coffee in the microwave, everyday forgetfulness is a common part of the human experience. But why does it happen, and how can you differentiate it from something more serious?
Modern life is full of distractions: emails, text messages, social media notifications, and the general hustle and bustle of daily tasks. In many cases, “forgetfulness” could just be the result of cognitive overload—trying to manage too many tasks at once. In these scenarios, your brain is simply filtering out non-essential information to keep up with the barrage of stimuli.
For example, you might forget where you placed your sunglasses because you were simultaneously thinking about your grocery list, your child’s soccer practice schedule, and an upcoming work deadline. This type of forgetfulness often resolves itself when you slow down and focus more carefully on your tasks.
As we grow older, certain changes in the brain can lead to slower information processing. This doesn’t automatically signal a serious memory disorder; sometimes it’s just a natural part of aging. Many individuals experience a degree of “tip-of-the-tongue syndrome,” where you momentarily can’t recall a word or a name you know well, only to remember it a short time later.
In normal age-related forgetfulness, your recall abilities might slow down a bit, but you’re still generally able to function independently. It won’t drastically interfere with your daily routines, though you might need more time to complete tasks than before.
Another sign that your forgetfulness may be within the realm of normal is the frequency of these lapses. Occasional forgetfulness—such as missing a dinner appointment once in a while or walking into a room and pausing to remember your purpose—typically isn’t cause for alarm. It becomes concerning when these lapses grow persistent, more frequent, and begin to disrupt your daily life or relationships.
Take note if your friends and family start commenting on your memory issues more often, or if you find yourself routinely forgetting events, tasks, or conversations in a way that feels uncharacteristic.
Sometimes, what appears to be a simple case of forgetfulness can be an early warning sign of cognitive decline. Understanding these indicators can help you recognize potential problems sooner rather than later, allowing you or your loved one to seek help before symptoms escalate.
One key difference between normal forgetfulness and more concerning memory issues is the inability to remember recent events or details of conversations. Maybe you had a chat with a neighbor this morning about an upcoming community event, but by afternoon, you have no recollection of that conversation whatsoever. If this kind of short-term memory loss happens frequently, it could be a red flag.
We all have off days when we feel scatterbrained. However, if you or someone you know frequently struggles with tasks that used to be second nature—like preparing a favorite recipe, balancing a checkbook, or navigating a routine driving route—it might be time to consider a more formal evaluation. These tasks rely on procedural memory (knowing “how” to do something), so noticeable declines in this area can be particularly telling.
It’s one thing to lose your keys in a cluttered house; it’s another to find them in the freezer or tucked away in a random drawer. Placing objects in illogical locations can be a telltale sign of memory issues that extend beyond normal forgetfulness. If you notice this type of behavior happening with increasing frequency, pay close attention to any other cognitive or behavioral changes.
Early-stage cognitive decline can sometimes show up in the way a person communicates. You might notice that you or a loved one struggles to find the right words during conversations or frequently stops midsentence. Alternatively, the words used might be noticeably vague, incorrect, or repetitive, suggesting a struggle to retrieve appropriate vocabulary.
Memory issues aren’t just about forgetting details or tasks; they can also affect mood and personality. Someone experiencing cognitive decline may become more anxious, irritable, or withdrawn, especially if they’re aware that their memory lapses are happening more often. Conversely, they might become unusually passive or lose interest in hobbies and social activities they once enjoyed.
For many people, subtle changes in problem-solving ability or judgment happen in tandem with early memory issues. You might find it harder to follow a detailed plan (like a new medication schedule or home repair instructions) or notice increased difficulty in making decisions about finances and other important matters.
Before jumping to conclusions, it’s important to note that memory loss or cognitive decline can stem from multiple causes—and not all of them are permanent or progressive. Understanding these causes can provide valuable context and reduce unnecessary worry.
MCI is a stage that exists between normal age-related forgetfulness and more advanced conditions like Alzheimer’s disease. People with MCI have more memory or cognitive problems than would be expected for their age, but these issues may not be severe enough to interfere significantly with daily life. However, MCI can progress to dementia if left unchecked, which is why early detection and intervention are crucial.
Dementia is an umbrella term describing a range of conditions characterized by cognitive decline that’s serious enough to impact daily functioning. Alzheimer’s disease is the most common form of dementia, accounting for up to 70% of cases, but vascular dementia, Lewy body dementia, and frontotemporal dementia are also possibilities. Identifying the early symptoms of these conditions can be life-changing, as new treatments and interventions may slow disease progression.
Mental health issues can significantly impact cognitive function. Prolonged stress, anxiety, or depression often lead to difficulty concentrating and remembering details, creating a cycle that further exacerbates mental strain. In such cases, addressing the underlying emotional or psychological concern can substantially improve memory.
Chronic lack of sleep is a common yet often overlooked cause of memory problems. During sleep, your brain consolidates new information and repairs neural pathways. If you’re not getting enough quality sleep, this vital process can be disrupted, leading to short-term forgetfulness that may mimic early dementia.
Certain vitamin and mineral deficiencies—especially in vitamins B12, B1, and D—can cause cognitive issues. A well-balanced diet and, in some cases, supplements can make a difference in restoring normal brain function. These cases highlight the importance of a thorough medical evaluation before concluding that dementia or another progressive condition is the cause of memory loss.
Medical conditions such as thyroid disorders, kidney or liver problems, and even some infections can interfere with cognition. Often, treating or managing the underlying condition can alleviate or reverse memory issues. This possibility underscores why a comprehensive assessment is essential for anyone experiencing persistent memory problems.
One of the most pressing questions is, How do you know when forgetfulness is severe enough to warrant professional help? While everyone’s situation is unique, there are some general guidelines.
If you’re experiencing forgetfulness multiple times a day in a manner that disrupts your normal routine—missing crucial appointments, repeating the same questions to loved ones, or feeling disoriented in familiar places—this frequency may indicate a more serious problem. Listen to feedback from family and friends, as they’re often the first to notice significant changes.
Are memory issues making it hard for you or a loved one to maintain personal hygiene, manage finances, or drive safely? If these core activities of daily living are becoming stressful or hazardous, it’s a strong sign that professional intervention is necessary.
In many cases, individuals have a gut feeling that their forgetfulness is beyond the norm. This intuitive sense of unease can be an important guide. If you sense something is off, it often helps to consult a healthcare professional for a proper evaluation—even if it’s just to rule out more serious conditions.
Routine check-ups with a primary care physician might reveal risk factors (like high blood pressure or elevated cholesterol) that increase the likelihood of cognitive decline. If your physician suggests further screening due to these risk factors or because of noticeable memory lapses, following through promptly is a wise step.
If you’re concerned about your memory or that of a loved one, you might feel apprehensive about seeking help. Fear of a possible diagnosis can be overwhelming. However, early detection of memory-related conditions often brings tangible benefits.
The earlier you catch conditions like MCI or dementia, the more opportunities you have for medical intervention. Certain medications can help slow progression or manage symptoms more effectively when administered during the early stages. Additionally, support services like occupational therapy, cognitive training, and nutritional counseling are more beneficial when started sooner.
Knowing you have a condition that affects memory can push you to plan for the future. This can include legal and financial planning, discussions about living arrangements, and conversations about care preferences should the condition progress. While these are never easy conversations, having them earlier allows for clearer communication and more thoughtful decisions.
The process of wondering and worrying—Is this normal forgetfulness, or is something seriously wrong?—can be a significant source of stress. Getting a professional opinion, even if it reveals concerning news, can be liberating. It removes the weight of uncertainty and places you in a position to take proactive steps.
Early detection also means early access to support groups, counseling, and other community resources. Whether you’re dealing with mild cognitive impairment or the early stages of dementia, tapping into a network of professionals and peers can lighten the emotional load and equip you with coping strategies.
While not all causes of cognitive decline are preventable, there’s growing evidence that lifestyle choices can significantly impact the health of your brain. Here are some strategies you can incorporate into your daily routine—whether or not you’re currently experiencing signs of memory issues.
Regular exercise benefits not just your heart, but your brain as well. Activities that get your heart pumping—like walking, swimming, or dancing—improve circulation and help protect the blood vessels that supply your brain. Aim for at least 150 minutes of moderate exercise or 75 minutes of vigorous exercise per week, in alignment with most national health guidelines.
Crossword puzzles, reading challenging books, learning a new language, or taking up a musical instrument all help keep your brain engaged. These mental workouts promote neuroplasticity, the ability of the brain to form and reorganize synaptic connections. The more you “exercise” your brain, the more resilient it can become to age-related changes.
Isolation and loneliness can accelerate memory decline. Regular interaction with friends, family, and community groups can help keep your mind sharp. Whether it’s joining a book club, attending local events in Naples, Florida, or even having weekly game nights with neighbors, social stimulation plays a vital role in mental wellness.
Sleep is not a luxury; it’s a necessity for optimal cognitive function. Aim for seven to nine hours of quality sleep each night. Poor or insufficient sleep can impair your ability to form and retain memories. If you’re having trouble sleeping, consult a healthcare professional who can help you identify underlying issues such as sleep apnea, restless leg syndrome, or chronic stress.
Consider following eating plans like the Mediterranean or DASH diets, rich in fruits, vegetables, whole grains, lean proteins (especially fish), and healthy fats like olive oil. Research consistently shows a relationship between these diets and lower rates of cognitive decline. Reducing processed foods, sugars, and saturated fats also helps maintain a healthy weight and supports heart health, both of which contribute to better brain function.
If you have conditions like hypertension, diabetes, or high cholesterol, managing them effectively is crucial for protecting brain health. These conditions can reduce blood flow to the brain, increasing the risk of vascular dementia and other forms of cognitive impairment. Keep on top of your prescribed medications, and maintain regular check-ins with your healthcare provider.
Chronic stress affects your ability to concentrate, recall information, and maintain emotional balance. Practicing mindfulness, meditation, or relaxation techniques can help. For some, regular therapy sessions can be transformative in learning to cope with stress and anxiety that might otherwise compromise brain health.
If you’ve reached this point and find yourself asking, “Is it time to get checked?”, a free memory screening is an excellent first step. At Aqualane Research in Naples, Florida, we offer free memory screenings to help you clarify what you’re experiencing—whether it’s normal forgetfulness or early signs of a more significant issue.
Memory screenings typically involve brief tests of your cognitive functions, such as recalling words, following instructions, and problem-solving tasks. These tests are noninvasive, can be completed in under an hour, and provide immediate feedback. You don’t need to prepare extensively, and you can continue with your day once the screening is over.
If the screening suggests that your memory lapses are within normal ranges, you’ll gain peace of mind and can focus on preventive measures. Should the screening reveal potential issues, you’ll be directed toward further evaluations or referred to a specialist who can pinpoint the cause of your symptoms and outline a plan of action.
One common reason people delay seeking help is cost. By making these screenings free, Aqualane Research removes one of the most significant hurdles that prevent individuals from addressing memory concerns. Access to early detection shouldn’t be a privilege; it should be readily available to anyone who needs it.
By encouraging community members to take advantage of free memory screenings, we collectively reduce the stigma around cognitive decline. The more people who understand the difference between normal forgetfulness and serious memory loss, the more compassionate and supportive our community becomes.
If you’re ready to learn more about recognizing memory issues or want to confirm if your experiences are within the realm of normal aging, scheduling a screening is easy. Simply visit our Memory Screening Landing Page to learn how our process works and to book an appointment. Our team is dedicated to ensuring that you feel comfortable and informed every step of the way.
When is forgetfulness a sign of memory issues?
Forgetfulness becomes concerning when it’s frequent, persistent, and interferes with daily functioning. Missing occasional appointments is likely normal; however, repeatedly forgetting recent events or consistently misplacing items in odd locations may suggest a deeper issue.
How to tell if memory decline is normal?
Ask yourself whether your forgetfulness is mild or occasional, or if it disrupts important daily tasks. If you’re able to complete daily activities without significant difficulty and generally remember essential details, it’s probably normal. If in doubt, consider a free memory screening for an expert perspective.
What are the early signs of memory loss?
Early signs may include difficulty recalling recent events, struggling with familiar tasks, language challenges, mood changes, and placing items in unusual locations. If you notice these symptoms happening more frequently, consult a healthcare professional.
Is memory screening a formal diagnosis?
No. A memory screening is a preliminary assessment that evaluates aspects of your cognitive function. Should the results suggest concerns, further evaluation by a specialist (neurologist or geriatrician) will help determine a formal diagnosis.
Who should get a memory screening?
Primarily older adults or those noticing consistent cognitive changes. However, younger individuals with a family history of dementia or certain risk factors may also benefit from periodic screenings to establish a cognitive baseline.
What if the screening shows potential problems?
If we detect red flags, we’ll refer you for further testing or specialist evaluation. Early detection can significantly improve treatment outcomes, and we’ll guide you toward the resources you need.
How can I improve my memory?
Lifestyle factors like a balanced diet, regular exercise, sufficient sleep, social engagement, and mental stimulation can help. If you’re concerned, a screening can identify early issues, allowing you to make targeted changes under professional guidance.
(Note: Names are fictional, but scenarios reflect common experiences.)
These scenarios demonstrate how diverse forgetfulness can appear. Some are benign and tied to daily stress, while others signal a deeper concern. Recognizing the difference is the key first step in protecting your long-term well-being.
There’s no shame in experiencing memory lapses. Everyone, from busy parents to retirees, has moments of forgetfulness. However, there’s a big difference between occasionally misplacing your keys and consistently forgetting critical information, conversations, or daily tasks. By adopting a proactive approach, you empower yourself with knowledge, enabling you to catch potential problems early and manage them effectively.
It’s all too common for individuals to avoid addressing memory concerns out of fear. However, adopting an attitude of curiosity rather than dread can make the process less intimidating. Viewing a memory screening as you would a routine physical check-up reframes it into a responsible act of self-care.
Family members and close friends can be your biggest allies in identifying shifts in memory and behavior. An open conversation can ease worries, break down stigmas, and encourage early intervention. If your loved ones have expressed concerns, listening openly and consulting a professional can strengthen relationships and improve peace of mind.
Scientists and medical professionals continually make strides in understanding memory decline. From new medications to novel behavioral therapies, staying informed can help you find cutting-edge solutions if you or a loved one is diagnosed with a cognitive condition.
At Aqualane Research, located in the heart of Naples, Florida, we’re dedicated to helping individuals navigate the often-confusing realm of forgetfulness vs memory loss. We believe in the power of education, early detection, and compassionate care.
Our free memory screening program reflects our commitment to the community: by removing financial barriers, we encourage anyone with concerns about their memory to find answers without delay. Our team of experts provides a respectful, welcoming environment, ensuring that each person feels heard and supported throughout the process.
Memory is deeply tied to who we are—our stories, our relationships, our ability to live independently. It’s only natural to feel concerned when forgetfulness moves from a minor annoyance to a potential warning sign of cognitive decline. Yet, the good news is that many forms of forgetfulness fall under the category of normal human experience, and even in cases where memory lapses signal something more serious, early detection can make an extraordinary difference in treatment outcomes and quality of life.
If you find that you’re continually questioning whether your forgetfulness is normal—or if you’re noticing signs of memory decline in a loved one—don’t wait. Take advantage of the resources available. Schedule a free screening, speak openly with your family and healthcare team, and explore lifestyle changes that may bolster your cognitive health.
At Aqualane Research, we’re committed to demystifying the difference between routine forgetfulness and more significant memory concerns. We invite you to reach out for a free memory screening and let us guide you toward a clearer understanding of your cognitive health. After all, knowledge is the first—and most critical—step in ensuring you can continue to cherish your memories and maintain a fulfilling, independent life.
Ready to Take the Next Step?
Visit our Memory Screening Landing Page to learn more about the process and schedule a free screening. Whether you’re seeking peace of mind or early intervention, our caring professionals at Aqualane Research are here to help you embrace a brighter, more confident future.
Preventing Setbacks, Falls & Avoidable Hospital Readmissions: Helping Someone With Parkinsons Stay Safely at Home Part 4 of the PennDYNAMIC Care at Home Parkinsons Recovery & Wellness Series For a person living with Parkinsons disease, returning home after a hospital or rehabilitation stay can feel like a major victory. But families often have another concern: How do we keep Mom or Dad from going back to the hospital? This is an especially important question for someone with Parkinsons. Changes in mobility, balance, medications, nutrition, hydration, cognition and the ability to manage everyday activities can make an already complex condition even more challenging after a health setback. A fall, missed medication, poor nutrition, increasing weakness or an unnoticed change in condition can disrupt recovery and potentially lead to another emergency room visit or hospitalization. At PennDYNAMIC Care at Home, our post-hospital and post-rehabilitation approach is designed to help bridge the transition home, support continued recovery and help families recognize concerns before they become bigger problems. The goal is not simply to get someone home. The goal is to help them stay safely at home. --------------------------------------------------------------------------------The Revolving Door Families Want to Avoid Hospitalization can be particularly difficult for an older adult with Parkinsons. A person may return home weaker than before, less steady on their feet or with changes to their medications and daily routine. They may also be receiving instructions from several healthcare professionals. There may be follow-up appointments to schedule. Therapy recommendations to continue. New medications to understand. Dietary instructions to follow. Mobility equipment to use. Symptoms to monitor. Families are often expected to coordinate all of this while simultaneously helping their loved one adjust to being home. It can be overwhelming. This is where structured, coordinated support can make a meaningful difference. -------------------------------------------------------------------------------- PennDYNAMIC's LifeCARE Pathway is built around proactive, evolving care, while DYNAMIC NeuroWELL at Home provides specialty support for individuals with neurological conditions such as Parkinsons. Together, these approaches help families focus on an important objective: Protect the recovery and reduce preventable setbacks. -------------------------------------------------------------------------------- 1. Make Fall Prevention a Daily Priority Falls can be a significant concern for people with Parkinsons because the disease can affect balance, walking and movement. After a hospitalization or rehabilitation stay, weakness and reduced confidence can add to the risk. Fall prevention begins with understanding how the person functions in the actual home environment. Are pathways clear? Is there adequate lighting? Are there loose rugs or clutter? Does the person have difficulty getting to the bathroom? Are recommended mobility devices within reach? Is the individual trying to move too quickly when getting up? Does the person require assistance with transfers or walking? A caregiver can help maintain a safer environment and provide the level of mobility assistance identified in the client's care plan. But fall prevention should not mean eliminating movement. As we discussed in Part 3, unnecessary inactivity can contribute to further loss of function. The goal is: Safe movementnot no movement. -------------------------------------------------------------------------------- 2. Pay Attention to Changes in Function Families sometimes assume that every new difficulty is simply another symptom of Parkinsons. But a noticeable change from someone's usual level of function deserves attention. Perhaps Dad suddenly needs much more assistance getting out of his chair. Mom is walking differently than she did several days ago. A normally engaged client is suddenly sleeping most of the day. Someone who was eating independently is now struggling at meals. The caregiver does not diagnose the cause. Instead, the caregiver can play an important role by observing, documenting and communicating changes to the family and appropriate healthcare professionals. Knowing someone's normal routine makes it easier to recognize when something is different. That is one of the advantages of consistent care at home. 3. Support Medication Adherence Parkinsons medication routines can be important to a person's daily functioning. After a hospitalization, medications may have been added, discontinued or changed. Families should make sure they understand the discharge medication instructions and direct medication questions to the appropriate physician, pharmacist or other healthcare professional. PennDYNAMIC caregivers can provide medication reminders consistent with the client's care plan. They can also observe whether the person is having difficulty following established routines and communicate concerns appropriately. For complex clients, medication support is not about independently changing medications or making clinical decisions. It is about helping the established plan work in everyday life. -------------------------------------------------------------------------------- 4. Don't Overlook Nutrition and Hydration Eating and drinking may seem unrelated to preventing hospitalization, but they are important components of overall health and recovery. Someone returning from a hospital or rehabilitation facility may have a reduced appetite, fatigue or difficulty managing meals independently. Parkinsons may create additional challenges around mealtimes. PennDYNAMIC caregivers can support meal preparation, hydration and established dietary recommendations. Just as importantly, caregivers can pay attention to changes. Is the person eating significantly less? Are meals being skipped? Is drinking becoming more difficult? Has something changed about the person's ability to manage meals? Concerns can then be communicated to the family and appropriate healthcare professional. 5. Keep the Person Moving Safely Following a hospitalization, it can be tempting to encourage someone to take it easy for an extended period. Rest may certainly be necessary. But when healthcare and rehabilitation professionals have recommended movement, exercises or daily activities, consistency matters. PennDYNAMIC caregivers can help clients follow established recommendations from physical therapists, occupational therapists and other members of the rehabilitation team. That might mean helping the person safely participate in everyday activities or supporting completion of exercises that have been prescribed or recommended by the appropriate professional. -------------------------------------------------------------------------------- We do not replace rehabilitation. We help reinforce the recovery plan at home. The objective is to help protect the progress already made while supporting continued function. 6. Make Follow-Up Care Part of the Recovery Plan Discharge from the hospital does not mean medical care is finished. There may be follow-up appointments with a primary care physician, neurologist or other specialists. There may be therapy appointments. There may be changes in the care plan based on how the individual is progressing at home. For families already balancing careers, children and other responsibilities, coordinating all these moving pieces can become difficult. This is why care navigation and progress monitoring are important components of the PennDYNAMIC approach. The goal is greater continuity between what healthcare professionals recommend and what actually happens at home. -------------------------------------------------------------------------------- 7. Watch the Caregiver Too There is another potential crisis families sometimes overlook: Caregiver exhaustion. A spouse may be trying to provide around-the-clock assistance. An adult daughter may be working all day and then spending evenings managing medications, meals and personal care. A son living out of town may be trying to coordinate everything by telephone. Families can continue like this until something happens. The spouse becomes exhausted. The adult child misses too much work. Someone gets injured trying to transfer the person. Or the family reaches a point where it simply cannot continue. Professional caregiving is not only about supporting the person with Parkinsons. It can also provide critical support to the family system. A family that has appropriate help may be better positioned to make thoughtful decisions instead of waiting until exhaustion creates the next crisis. -------------------------------------------------------------------------------- Create a Parkinsons Stay-at-Home Plan Families can make their care plan more proactive by asking several questions: What usually causes problems for our loved one? What changes should we watch for? Who should be contacted when we notice a change? Are medications and follow-up appointments organized? Is the home environment as safe as possible? Are rehabilitation recommendations being followed? Is our loved one eating and drinking adequately? Is the family caregiver becoming overwhelmed? Do we have enough help at home? These questions move the family from reacting to problems toward anticipating them. -------------------------------------------------------------------------------- Know What Is Normal for Your Loved One One of the most useful things families and caregivers can understand is the person's baseline. What does a normal day look like? How does Mom usually walk? How much assistance does Dad normally need getting dressed? How much does he typically eat? How alert and conversational is she? What activities can the person normally complete? Once you understand the person's usual pattern, changes can become easier to recognize. A good care plan should therefore be dynamic. As needs change, support may need to change too. That principle is central to PennDYNAMIC's LifeCARE Pathway. -------------------------------------------------------------------------------- How DYNAMIC NeuroWELL at Home Supports Parkinsons Families PennDYNAMIC's DYNAMIC NeuroWELL at Home was created to provide coordinated, disease-informed support for people living with Parkinsons and other neurological conditions. Depending upon the individual's needs and established care plan, support may include: Personalized, disease-informed in-home caregivingFunctional fitness, movement and restorative supportMedication adherence and chronic symptom observationNutrition and mealtime supportNeurocognitive stimulation and memory supportEmotional well-being and family educationCare navigation and progress monitoringCommunication and collaboration with the healthcare team For families, this means having support that looks beyond individual caregiving tasks. The focus is on the whole person and the many factors that can influence the ability to remain safely at home. -------------------------------------------------------------------------------- The Best Hospital Readmission Is the One That May Be Prevented Not every hospitalization canor shouldbe prevented. Parkinsons is a complex condition, and medical emergencies sometimes occur despite excellent care. Home care should never replace necessary medical attention. But families can take proactive steps to reduce preventable setbacks. Support safe movement. Follow the established medication plan. Encourage adequate nutrition and hydration. Continue rehabilitation recommendations. Attend follow-up appointments. Watch for meaningful changes. Communicate concerns. And make sure the family has enough support. These actions may seem simple individually. Together, they create something powerful: A safer and more coordinated environment for recovery. -------------------------------------------------------------------------------- Home Should Be More Than the Place Someone Returns To For a person living with Parkinsons, home represents familiarity. Routine. Family. Memories. Dignity. Independence. And often, the place where the person most wants to remain. At PennDYNAMIC Care at Home, our goal is to help families protect that possibility. Through personalized care, proactive communication, disease-informed support and coordination with the individual's healthcare team, we help make home a place where recovery can continue and quality of life remains the priority. Because getting someone home is only the first step. Helping them stay safer, stronger and supported at home is the next. -------------------------------------------------------------------------------- Love Is Not Enough When You Are Dealing With Parkinsons Disease When someone you love is living with Parkinsons, you may find yourself constantly wondering whether you are doing enough, watching closely for the next fall or worrying about another trip to the hospital. You do not have to carry all of that responsibility alone. The right support can help your loved one remain safer at home while giving your family greater confidence and peace of mind. When someone you love is challenged with Parkinsons and you need assistance, please call PennDYNAMIC Care at Home at 610-467-7827. We would be honored to listen to your concerns, learn about your loved one's needs and discuss how PennDYNAMIC Care at Home may be able to support your family. PennDYNAMIC Care at Home Personalized. Coordinated. Expert-Led Care at Home. www.DynamicCareAtHome.com
Rebuilding Strength, Mobility & Independence: Helping Someone With Parkinsons Function Better at Home Part 3 of the PennDYNAMIC Care at Home Parkinsons Recovery & Wellness Series For someone living with Parkinsons disease, independence is often lost gradually. Walking becomes slower. Getting out of a chair requires more effort. Dressing takes longer. Fear of falling may cause someone to move less. After a hospitalization or rehabilitation stay, these challenges can become even more noticeable. But needing assistance does not mean a person should stop participating in life. At PennDYNAMIC Care at Home, we believe one of the most important goals of Parkinsons care is helping each person function at the highest level safely possible. That means looking beyond what someone cannot do and asking a more powerful question: What can this person still doand how can we help them keep doing it? For families, that shift can change the entire approach to care. Parkinsons Can Create a Cycle of Declining Function Parkinsons can affect movement, balance, coordination and the ability to initiate movement. As everyday activities become more difficult, people naturally begin doing less. Then a difficult cycle can develop: Movement becomes harder the person moves less strength and confidence may decline everyday activities become harder even more assistance is needed. ---------------------------------------------------------------------------------------A hospitalization can accelerate this process. Someone who was previously walking through the house independently may return home needing assistance. Someone who dressed independently may suddenly need help. A person who enjoyed going outside may become afraid of falling and begin spending most of the day sitting. Families understandably want to protect their loved one. But protection should not automatically mean inactivity. The goal is to create the right balance between safety, assistance and continued participation. The Goal Is Not to Do Everything for the Person When someone struggles with an activity, our instinct is often to take over. It is faster to button the shirt. It is easier to bring the meal to the recliner. It may feel safer to tell Dad to sit down while someone else does everything for him. Sometimes complete assistance is necessary. But when an individual can safely participate, doing everything for that person may remove valuable opportunities to move, think, make choices and maintain abilities. At PennDYNAMIC Care at Home, assistance can be approached differently. Instead of automatically asking: What can the caregiver do for the client? We can also ask: What can the caregiver help the client continue doing? That is the foundation of function-focused care. --------------------------------------------------------------------------------------- Everyday Activities Can Support Function Maintaining function does not happen only during formal rehabilitation. It happens throughout the day. Consider how many movements are involved in an ordinary morning: Getting out of bed. Standing. Walking to the bathroom. Washing your face. Brushing your teeth. Getting dressed. Walking to the kitchen. Sitting down for breakfast. Using utensils. Carrying on a conversation. Each activity involves some combination of movement, balance, coordination, cognition and endurance. For a person with Parkinsons, maintaining participation in appropriate everyday activities can be meaningful. The caregiver's role is not to turn the home into a rehabilitation facility. Instead, it is to support the individual's established care plan and help create an environment where safe participation can continue. --------------------------------------------------------------------------------------- 1. Support Safe Movement Movement is an important part of living well with Parkinsons. Depending on the person's condition and recommendations from healthcare and rehabilitation professionals, this may include walking, prescribed exercises, transfers and participation in daily activities. A trained caregiver can help by providing appropriate assistance, helping maintain a safe environment and encouraging the person to follow established mobility recommendations. The key word is safe. Caregivers should not independently create rehabilitation programs or ask clients to perform activities outside their professional care plan. Physical therapists and other rehabilitation professionals determine appropriate therapeutic interventions. PennDYNAMIC caregivers can then help support those recommendations in everyday life. 2. Help Rebuild Confidence After a Fall or Hospitalization Physical weakness is only part of the challenge. Sometimes the bigger obstacle is fear. A person who has fallen may become afraid to walk. Someone who struggled during a hospitalization may no longer trust their body. A spouse who witnessed a serious fall may become so concerned that they discourage almost all independent movement. --------------------------------------------------------------------------------------- That fear is understandable.On the other hand, fear can lead to inactivity, and inactivity can further limit participation in daily life. A supportive caregiver can provide reassurance, appropriate assistance and encouragement while following established safety recommendations. Small successes matter. Walking safely to the kitchen. Participating in dressing. Sitting outside. Completing recommended exercises. Joining the family for dinner. Each accomplishment can help restore something Parkinsons often threatens: Confidence. 3. Make Personal Care Part of Maintaining Independence Bathing, dressing, grooming and toileting are sometimes described simply as personal care. But these activities represent much more. They are part of a person's identity, routine and independence. Instead of automatically completing the entire activity for someone, care can be adjusted to the person's abilities. Perhaps Mom can wash her face but needs assistance getting into the shower. Perhaps Dad can select his clothes and put on his shirt but needs assistance with buttons or shoes. Perhaps the individual can walk to the bathroom with appropriate assistance instead of routinely relying on more restrictive alternatives. The appropriate level of assistance will differ from person to person. The principle remains: Provide the help that is needed while preserving the abilities that remain. --------------------------------------------------------------------------------------- 4. Reinforce the Rehabilitation Plan at Home Physical, occupational and speech therapy can play important roles in Parkinsons care. But therapy sessions represent only a portion of the person's week. The rest of life happens at home. When therapists provide specific recommendations for mobility, positioning, exercises, assistive devices or daily activities, families may struggle to consistently incorporate them into the day. Professional caregiving can help provide that consistency. PennDYNAMIC Care at Home can work alongside the client's healthcare and rehabilitation professionals, helping families carry established recommendations into everyday routines. That distinction is important. We do not replace rehabilitation. We help support its continuity at home. 5. Pay Attention to Nutrition and Hydration Maintaining function requires adequate nutrition and hydration. After hospitalization or rehabilitation, some individuals may return home with poor appetite, fatigue or changes in eating patterns. Parkinsons can create additional challenges around mealtimes. Caregivers can assist with meal preparation, hydration and following dietary or mealtime recommendations established by the individual's healthcare team. They can also observe and communicate meaningful changes. Is Mom suddenly eating much less? Is Dad struggling with something that previously was not difficult? Has there been a significant change in appetite or ability to manage meals? Changes should be communicated to the family and appropriate healthcare professional rather than simply becoming part of the new normal. --------------------------------------------------------------------------------------- 6. Create Opportunities for Cognitive and Social Engagement Function is not only physical. Parkinsons can affect emotional, cognitive and social well-being as well. When mobility becomes difficult, people may gradually stop participating in activities they once enjoyed. They may go out less. See friends less. Talk less. Participate less. Life can slowly become centered around illness. PennDYNAMIC's DYNAMIC NeuroWELL at Home approach recognizes that neurological wellness involves the physical, cognitive, emotional and functional dimensions of a person's life. Meaningful engagement might include conversation, music, family interaction, hobbies, appropriate outings or other activities that are meaningful to the individual. The goal is not simply to keep someone occupied. It is to help the person remain connected to life. 7. Measure Progress by Function, Not Just by Diagnosis Parkinsons is progressive, but families can still establish meaningful functional goals. Instead of focusing exclusively on the disease, consider asking: What does a good day look like for this person? For one person, success may mean walking safely to breakfast. For another, it may mean continuing to shower and dress with minimal assistance. For someone recovering from hospitalization, success may mean gradually returning to a previous routine. For someone with advanced Parkinsons, success may mean maintaining comfort, dignity, engagement and the abilities that remain. The goal should be individualized. --------------------------------------------------------------------------------------- PennDYNAMIC's LifeCARE Pathway is designed to provide structured, proactive and evolving care that can change as the client's needs change. Look for the Small Wins Recovery and functional improvement do not always happen dramatically. Sometimes progress looks small. Dad needed less assistance standing today. Mom walked a little farther. He participated in dressing. She finished her meal. He completed the activities recommended by his therapist. She was confident enough to sit outside again. He joined the family at the dinner table. These accomplishments matter. For someone living with a complex neurological condition, small improvements can represent meaningful steps toward greater function and quality of life. Notice them. Encourage them. Build upon them. The PennDYNAMIC NeuroWELL Approach PennDYNAMIC's DYNAMIC NeuroWELL at Home was developed to provide specialty support for individuals living with neurological conditions, including Parkinsons disease. --------------------------------------------------------------------------------------- Our approach recognizes that successful care may involve more than assistance with bathing, dressing and meals. Depending on the individual's needs and established professional care plan, support may include: Personalized and disease-informed in-home caregivingFunctional fitness, movement and restorative supportNeurocognitive stimulation and memory supportMedication adherence and chronic symptom observationEmotional well-being and family educationCare navigation and progress monitoring The goal is coordinated, individualized support delivered in the place where the person lives. Home. From Taking Care of Someone to Helping Them Live Well There is an important difference between keeping someone alive and helping someone live. People living with Parkinsons still have preferences. They have routines. They have relationships. They have abilities. They have goals. They have things they enjoy. And they have a desire to maintain control over their lives for as long as possible. Good Parkinsons care recognizes the disease without allowing the disease to become the person's entire identity. --------------------------------------------------------------------------------------- At PennDYNAMIC Care at Home, we believe care should help protect what matters: Function. Independence. Safety. Confidence. Dignity. Connection. Quality of life. When Someone You Love Is Challenged by Parkinsons Life Can Be Challenging. Watching someone you love lose strength or independence can be difficult, particularly after a hospitalization, rehabilitation stay, fall or change in health. But your family does not have to manage those challenges alone. With the right support, home can become a place where your loved one is encouraged to keep moving, keep participating, maintain important routines and live as fully and independently as possible. When someone you love is challenged with Parkinsons and you need assistance, please call PennDYNAMIC Care at Home at 610-467-7827. We would be honored to listen to your concerns, learn about your loved one's needs and discuss how PennDYNAMIC Care at Home may be able to support your family. PennDYNAMIC Care at Home Personalized. Coordinated. Expert-Led Care at Home. www.DynamicCareAtHome.com
Coming Home After the Hospital or Rehab: Why the First Weeks Are Critical for Someone With Parkinsons Part 2 of the PennDYNAMIC Care at Home Parkinsons Recovery & Wellness Series For a family caring for someone with Parkinsons disease, hearing the words Your loved one is ready to go home can bring tremendous relief. The hospitalization is over. Rehabilitation has helped. Everyone is looking forward to returning to familiar surroundings and normal routines. But for someone living with Parkinsons, discharge is not the end of recovery. In many cases, it is the beginning of one of the most important phases of recovery. The first days and weeks at home can determine whether a person continues to regain strength and functionor begins to lose some of the progress made during rehabilitation. At PennDYNAMIC Care at Home, our goal is to help families bridge that critical gap between hospital or rehabilitation care and successful recovery at home. Why Coming Home Can Be Harder Than Families Expect Hospitals and rehabilitation facilities are structured environments. Meals arrive on schedule. Medications are administered. Staff members are available to assist with walking, bathing, toileting and transfers. Therapists provide structured rehabilitation. Someone is watching for changes in the patient's condition. Then the person comes home. Suddenly, much of that structure disappears. A spouse or adult child may find themselves responsible for medications, meals, personal care, mobility, exercises, appointments and safetyoften with little preparation for the complexity of the role. For someone with Parkinsons, this transition can be even more challenging.------------------------------------------------------------------------------ The person may still be weak from the illness that caused the hospitalization. Parkinsons symptoms may make movement slower and more difficult. Balance may be impaired. Medication routines may have changed. The individual may be afraid of falling. The family may quickly realize: Mom is homebut she isn't back to where she was before. That is precisely when a well-organized recovery plan becomes important. The Goal Should Be More Than Keeping Someone Safe Safety is essential. But the goal after hospitalization or rehabilitation should not be limited to preventing falls and helping someone complete basic activities. Families should also ask: How can we help our loved one regain as much function as possible? PennDYNAMIC Care at Home's post-hospital and post-rehab recovery approach focuses on helping clients transition home while supporting the goals established by their medical and rehabilitation professionals. That may mean helping the person safely get out of bed, walk to the bathroom, dress, eat meals, maintain hydration, follow medication routines and participate in prescribed activities. These may appear to be ordinary activities. For someone recovering from a hospitalization while living with Parkinsons, however, ordinary activities can become part of an extraordinary recovery. 1. Protect the Progress Made in Rehabilitation One of the greatest concerns after discharge is losing the gains made during rehabilitation. A person may have worked with physical, occupational or speech therapists to improve walking, transfers, balance, strength, communication or the ability to perform everyday activities. But progress requires continuity. ------------------------------------------------------------------------------ Once the person returns home, the routines and recommendations established by the rehabilitation team need to become part of everyday life. PennDYNAMIC caregivers can help reinforce the established plan by encouraging clients to participate in appropriate daily activities and follow the instructions provided by their healthcare and rehabilitation professionals. The caregiver does not replace the therapist. Instead, caregiving helps create the supportive environment in which the rehabilitation plan can continue between professional visits. 2. Encourage Movement and Function With Parkinsons, movement can become difficult. After hospitalization, it may become even harder. Because families are understandably concerned about falls, they may begin doing everything for their loved one. But when it is safe and consistent with the person's care plan, participation matters. If Dad can safely help dress himself, let him participate. If Mom can walk to the dining room with appropriate assistance rather than having every meal brought to her chair, that movement may be meaningful. If rehabilitation professionals have provided exercises or mobility recommendations, help create a routine that makes it easier to follow them. At PennDYNAMIC Care at Home, our DYNAMIC NeuroWELL at Home approach emphasizes functional fitness, movement and restorative support as part of caring for individuals with neurological conditions such as Parkinsons. The objective is not to push someone beyond what is safe. It is to help preserve and support the abilities they still have. ------------------------------------------------------------------------------ 3. Pay Close Attention to Medications Medication routines can be particularly important for someone with Parkinsons. After hospitalization, families should understand the discharge medication instructions and know whether anything has changed. Questions should be clarified with the appropriate healthcare professional. A home caregiver can provide medication reminders and help support adherence to the established medication plan. Caregivers may also be in a valuable position to observe changes in how the individual is functioning throughout the day and communicate concerns to the family or appropriate healthcare professionals. The goal is continuity, observation and communication. 4. Rebuild Strength Through Everyday Life Recovery does not happen only during a therapy appointment. Much of recovery happens during ordinary life. Getting out of bed. Walking to the bathroom. Getting dressed. Sitting upright for meals. Participating in grooming. Moving around the home. Engaging in conversation. Completing recommended activities. Eating nutritious meals. Drinking enough fluids. These seemingly small activities can help create structure and encourage continued participation in daily life. ------------------------------------------------------------------------------ The PennDYNAMIC philosophy is not simply to ask: What can we do for this person? We also ask: What can we safely help this person continue doing for themselves? That distinction can be especially important for preserving dignity, confidence and independence. 5. Nutrition and Hydration Matter Recovery requires energy. Someone who has recently returned from the hospital or rehabilitation facility may have a reduced appetite, fatigue or difficulty managing meals independently. Parkinsons can add additional challenges. Families should follow the nutritional, swallowing and dietary recommendations provided by the individual's healthcare team. Caregivers can help with meal preparation, hydration and mealtime routines while observing for changes that should be reported. Good nutrition is not simply about providing food. It is about helping create the conditions the body needs for recovery and continued function. 6. Watch for Changes Before They Become Crises One advantage of having consistent support at home is having someone who becomes familiar with the person's normal routines and abilities. A caregiver may notice that the client suddenly needs more assistance getting out of a chair. They may notice a change in appetite. Perhaps the individual is sleeping significantly more, appears more confused, is having greater difficulty walking or is no longer participating in activities that were manageable several days earlier. Caregivers do not diagnose these changes. But they can observe, document and communicate. Early communication gives families and healthcare professionals an opportunity to determine whether additional evaluation is needed. This is one way coordinated home care can help support the broader goal of reducing avoidable setbacks and readmissions. ------------------------------------------------------------------------------ 7. Create a Coordinated Recovery Team Families should not have to manage complex Parkinsons recovery alone. A successful transition home may involve several professionals: PhysiciansNeurologistsPhysical therapistsOccupational therapistsSpeech-language pathologistsHome health cliniciansIn-home caregiversFamily members Each may have a different role. The challenge is making sure the different pieces of the plan come together in the place where the individual spends most of the day: Home. PennDYNAMIC Care at Home emphasizes proactive communication and collaboration with healthcare providers. For medically complex clients and those recovering after hospitalization or rehabilitation, that coordination can be especially valuable. ------------------------------------------------------------------------------ A Simple Question Families Should Ask Every Week After someone with Parkinsons comes home, families can ask: Is my loved one getting stronger, staying the same or becoming weaker? Look beyond the diagnosis. Can Dad get out of his chair more easily than he could last week? Is Mom walking farther? Is she participating more in dressing? Is he eating better? Is she becoming more confident moving around the house? Are medications and appointments staying organized? Is the family caregiver becoming less overwhelmedor more overwhelmed? Small changes can tell an important story. The objective is to recognize those changes early and adjust the care plan when appropriate. ------------------------------------------------------------------------------ The PennDYNAMIC LifeCARE Pathway: Bringing Structure Home PennDYNAMIC Care at Home's LifeCARE Pathway provides a structured, proactive and evolving approach to care. For individuals with Parkinsons and other neurological conditions, DYNAMIC NeuroWELL at Home adds disease-informed support centered around physical, cognitive, emotional and functional wellness. Depending upon the individual's needs and professional care plan, support can include: Personalized, disease-informed in-home caregivingFunctional fitness, movement and restorative supportMedication adherence and chronic symptom observationNutritional and mealtime supportCognitive and emotional engagementFamily education and communicationCare navigation and progress monitoring PennDYNAMIC Care at Home is not intended to replace physicians, therapists or skilled home health professionals. Our role is to help connect the pieces of the recovery plan to everyday life at home. ------------------------------------------------------------------------------ Recovery Has to Continue Between Therapy Visits A therapist may see someone several times during the week. A physician may see the person periodically. But the individual lives the rest of life at home. That is where meals happen. That is where medications are taken. That is where falls may occur. That is where exercises mayor may notget done. That is where families begin to notice whether their loved one is getting stronger or weaker. And that is where confidence and independence must gradually be rebuilt. For someone with Parkinsons, the hours between professional healthcare visits matter. With the right support, those hours can become opportunities to reinforce recovery rather than simply wait for the next appointment. ------------------------------------------------------------------------------ Coming Home Should Be the Beginning of the Next Chapter A successful discharge should mean more than getting someone through the front door. It should begin with a plan for what happens next. What does recovery look like? What abilities are we trying to restore or preserve? How will we support safe movement? Who will help with meals and medications? Who is watching for changes? How will the family know whether the person is progressing? And who will help coordinate the many moving pieces? At PennDYNAMIC Care at Home, we believe the best home care has purpose. For someone recovering from a hospitalization or rehabilitation stay while living with Parkinsons, that purpose is clear: Protect the progress. Rebuild function. Support independence. Reduce setbacks. Help the person live as well as possible at home. Because getting home is an important milestone. Getting better at home is the next goal. When Someone You Love Is Challenged by Parkinsons Watching someone you love struggle with Parkinsonsespecially following a hospitalization or rehabilitation staycan be difficult for the entire family. You do not have to navigate the transition home alone. When someone you love is challenged by Parkinsons and your family needs assistance, please call PennDYNAMIC Care at Home at 610-467-7827. We would be honored to learn about your loved one, understand what your family is facing, and discuss how the right support at home may help. PennDYNAMIC Care at Home: Personalized. Coordinated. Expert-Led Care at Home.
HistoryWith a combined 50+ years of clinical research, Dr. Justiz, Dr. Baker, and Kelly Calistri founded Aqualane Clinical Research in 2022. Since 2005, Dr. Justiz and Dr. Baker have been conducting studies together as Principal Investigators for their private practice. With a shared vision for a larger research institute, Kelly, a long-time consultant to the doctors, joined them in forming Aqualane Clinical Research.Message FromOur FoundersAt Aqualane, we always put our patients first.We promise to educate each potential participant and their family members on all options available to them and to support them in their decision-making process. Striving to make clinical trials a practical healthcare option, we provide a comfortable, caring and compassionate environment.Our founders are passionate about their contributions to the advancement of medicine and to the opportunities they provide to people searching for new treatment options. With expertise and experience in research and the central nervous system, you can trust our team of neurologists and researchers to provide the best possible opportunity for you or your loved one.OurTeamDr. William A. Justiz, MDMedical Director, Principal InvestigatorDr. William Justiz completed his undergraduate degree at Northwestern University before receiving his medical degree from the University of Miami School of Medicine. He is board certified in neurology and is a certified physician investigator through the Association of Clinical Research Professionals.With over 20 years of research experience and specialization in degenerative diseases of the nervous system, he has been in continuous practice in Naples, Florida since 1999. He is a founding member of the clinical research program that has grown into Aqualane Clinical Research.Community outreach and service is one of the core values of Dr. Justiz and Aqualane Clinical Research. Dr. Justiz demonstrates this with his 23-year commitment to providing low-cost or free services to epilepsy patients through Epilepsy Services of Southwest Florida. In addition, he has delivered a free educational lecture series every month on all Alzheimer's topics since 2015 through the Alzheimer's Support network.Kelly E. Calistri, B.A.Chief Operating Officer, Site DirectorKelly is a native Floridian, born and raised in Central Florida. Shortly before graduating from The University of Tennessee, Knoxville, with a degree in Psychology, she was introduced to the research industry. Almost immediately, she knew this would be her career path.While working at a privately owned clinical research site in Atlanta, she gained experience in several areas, including patient intake, research coordinator, regulatory, and cognitive rater. Working for years across many therapeutic areas, her passion for research grew. With this experience, Kelly received promotions into management roles. Her responsibilities included conducting training, oversight of a staff of 50 people, managing Phase I studies in a unit with 40 beds, and being responsible for business development by attending industry meetings to represent her site. Before opening Aqualane Clinical Research in 2022, she used her expertise and experience to build two startup research sites. Building a team of experts who excel in their field is among her strongest qualities. Her passion for people and the advancement of medicine drives her daily to continue learning. Kelly has seen how new medications can change the lives of people around her.In her free time, you can find Kelly and her husband, who are high school sweethearts, at local baseball fields cheering on their two sons. They are a close family who loves to travel and spend time together. Kelly also loves reading business and personal development books.Dr. Matthew J. Baker, MDPrincipal InvestigatorDr. Baker is a board-certified neurologist practicing for over 20 years. He has been a Principal Investigator in numerous clinical trials, many of which have resulted in regulatory approval of novel therapeutics across the spectrum of neurologic disease, both here and abroad. His primary areas of interest include Neuroimmunology, migraine, and the Neurobehavioral manifestations of disease. Dr. Baker is a nationally recognized educator and lecturer. He enjoys teaching colleagues, medical residents and patients on such topics as Multiple Sclerosis and Myasthenia Gravis. In his spare time, he loves riding roller coasters with this family and playing with his two dogs.Micaela M. Acres, RN, BSNInfusion NurseJacqueline E. BradyCommunity Outreach Coordinator/ ReceptionMatthew B. Cagney, B.S.Clinical Research CoordinatorElena Capron, B.S.Regulatory Coordinator / Social Media CoordinatorBrittany N. Cordero, B.S.Office Manager / Human ResourcesJessica M. DEntremont, RN, MPH, BSNInfusion NurseDarious T. Davis, M.A.Head of Business DevelopmentLaura Gold, B.S.Finance CoordinatorKarma L. Hamilton, M.S.Lead RaterBethany J.M. Henchesmoore, MBAClinical Research CoordinatorJennifer Jimenez-Perez, RN, BSNInfusion NurseCarmen L. Ojeda, M.S.Quality Assurance / Quality ControlMichelle A. O'Neill, M.S.RaterMayve SantosResearch PharmacistAlexandria L. SmithClinical Research Coordinator
HistoryWith a combined 50+ years of clinical research, Dr. Justiz, Dr. Baker, and Kelly Calistri founded Aqualane Clinical Research in 2022. Since 2005, Dr. Justiz and Dr. Baker have been conducting studies together as Principal Investigators for their private practice. With a shared vision for a larger research institute, Kelly, a long-time consultant to the doctors, joined them in forming Aqualane Clinical Research.Message FromOur FoundersAt Aqualane, we always put our patients first.We promise to educate each potential participant and their family members on all options available to them and to support them in their decision-making process. Striving to make clinical trials a practical healthcare option, we provide a comfortable, caring and compassionate environment.Our founders are passionate about their contributions to the advancement of medicine and to the opportunities they provide to people searching for new treatment options. With expertise and experience in research and the central nervous system, you can trust our team of neurologists and researchers to provide the best possible opportunity for you or your loved one.OurTeamDr. William A. Justiz, MDMedical Director, Principal InvestigatorDr. William Justiz completed his undergraduate degree at Northwestern University before receiving his medical degree from the University of Miami School of Medicine. He is board certified in neurology and is a certified physician investigator through the Association of Clinical Research Professionals.With over 20 years of research experience and specialization in degenerative diseases of the nervous system, he has been in continuous practice in Naples, Florida since 1999. He is a founding member of the clinical research program that has grown into Aqualane Clinical Research.Community outreach and service is one of the core values of Dr. Justiz and Aqualane Clinical Research. Dr. Justiz demonstrates this with his 23-year commitment to providing low-cost or free services to epilepsy patients through Epilepsy Services of Southwest Florida. In addition, he has delivered a free educational lecture series every month on all Alzheimer's topics since 2015 through the Alzheimer's Support network.Kelly E. Calistri, B.A.Chief Operating Officer, Site DirectorKelly is a native Floridian, born and raised in Central Florida. Shortly before graduating from The University of Tennessee, Knoxville, with a degree in Psychology, she was introduced to the research industry. Almost immediately, she knew this would be her career path.While working at a privately owned clinical research site in Atlanta, she gained experience in several areas, including patient intake, research coordinator, regulatory, and cognitive rater. Working for years across many therapeutic areas, her passion for research grew. With this experience, Kelly received promotions into management roles. Her responsibilities included conducting training, oversight of a staff of 50 people, managing Phase I studies in a unit with 40 beds, and being responsible for business development by attending industry meetings to represent her site. Before opening Aqualane Clinical Research in 2022, she used her expertise and experience to build two startup research sites. Building a team of experts who excel in their field is among her strongest qualities. Her passion for people and the advancement of medicine drives her daily to continue learning. Kelly has seen how new medications can change the lives of people around her.In her free time, you can find Kelly and her husband, who are high school sweethearts, at local baseball fields cheering on their two sons. They are a close family who loves to travel and spend time together. Kelly also loves reading business and personal development books.Dr. Matthew J. Baker, MDPrincipal InvestigatorDr. Baker is a board-certified neurologist practicing for over 20 years. He has been a Principal Investigator in numerous clinical trials, many of which have resulted in regulatory approval of novel therapeutics across the spectrum of neurologic disease, both here and abroad. His primary areas of interest include Neuroimmunology, migraine, and the Neurobehavioral manifestations of disease. Dr. Baker is a nationally recognized educator and lecturer. He enjoys teaching colleagues, medical residents and patients on such topics as Multiple Sclerosis and Myasthenia Gravis. In his spare time, he loves riding roller coasters with this family and playing with his two dogs.Micaela M. Acres, RN, BSNInfusion NurseJacqueline E. BradyCommunity Outreach Coordinator/ ReceptionMatthew B. Cagney, B.S.Clinical Research CoordinatorElena Capron, B.S.Regulatory Coordinator / Social Media CoordinatorBrittany N. Cordero, B.S.Office Manager / Human ResourcesJessica M. DEntremont, RN, MPH, BSNInfusion NurseDarious T. Davis, M.A.Head of Business DevelopmentLaura Gold, B.S.Finance CoordinatorKarma L. Hamilton, M.S.Lead RaterBethany J.M. Henchesmoore, MBAClinical Research CoordinatorJennifer Jimenez-Perez, RN, BSNInfusion NurseCarmen L. Ojeda, M.S.Quality Assurance / Quality ControlMichelle A. O'Neill, M.S.RaterMayve SantosResearch PharmacistAlexandria L. SmithClinical Research Coordinator
HistoryWith a combined 50+ years of clinical research, Dr. Justiz, Dr. Baker, and Kelly Calistri founded Aqualane Clinical Research in 2022. Since 2005, Dr. Justiz and Dr. Baker have been conducting studies together as Principal Investigators for their private practice. With a shared vision for a larger research institute, Kelly, a long-time consultant to the doctors, joined them in forming Aqualane Clinical Research.Message FromOur FoundersAt Aqualane, we always put our patients first.We promise to educate each potential participant and their family members on all options available to them and to support them in their decision-making process. Striving to make clinical trials a practical healthcare option, we provide a comfortable, caring and compassionate environment.Our founders are passionate about their contributions to the advancement of medicine and to the opportunities they provide to people searching for new treatment options. With expertise and experience in research and the central nervous system, you can trust our team of neurologists and researchers to provide the best possible opportunity for you or your loved one.OurTeamDr. William A. Justiz, MDMedical Director, Principal InvestigatorDr. William Justiz completed his undergraduate degree at Northwestern University before receiving his medical degree from the University of Miami School of Medicine. He is board certified in neurology and is a certified physician investigator through the Association of Clinical Research Professionals.With over 20 years of research experience and specialization in degenerative diseases of the nervous system, he has been in continuous practice in Naples, Florida since 1999. He is a founding member of the clinical research program that has grown into Aqualane Clinical Research.Community outreach and service is one of the core values of Dr. Justiz and Aqualane Clinical Research. Dr. Justiz demonstrates this with his 23-year commitment to providing low-cost or free services to epilepsy patients through Epilepsy Services of Southwest Florida. In addition, he has delivered a free educational lecture series every month on all Alzheimer's topics since 2015 through the Alzheimer's Support network.Kelly E. Calistri, B.A.Chief Operating Officer, Site DirectorKelly is a native Floridian, born and raised in Central Florida. Shortly before graduating from The University of Tennessee, Knoxville, with a degree in Psychology, she was introduced to the research industry. Almost immediately, she knew this would be her career path.While working at a privately owned clinical research site in Atlanta, she gained experience in several areas, including patient intake, research coordinator, regulatory, and cognitive rater. Working for years across many therapeutic areas, her passion for research grew. With this experience, Kelly received promotions into management roles. Her responsibilities included conducting training, oversight of a staff of 50 people, managing Phase I studies in a unit with 40 beds, and being responsible for business development by attending industry meetings to represent her site. Before opening Aqualane Clinical Research in 2022, she used her expertise and experience to build two startup research sites. Building a team of experts who excel in their field is among her strongest qualities. Her passion for people and the advancement of medicine drives her daily to continue learning. Kelly has seen how new medications can change the lives of people around her.In her free time, you can find Kelly and her husband, who are high school sweethearts, at local baseball fields cheering on their two sons. They are a close family who loves to travel and spend time together. Kelly also loves reading business and personal development books.Dr. Matthew J. Baker, MDPrincipal InvestigatorDr. Baker is a board-certified neurologist practicing for over 20 years. He has been a Principal Investigator in numerous clinical trials, many of which have resulted in regulatory approval of novel therapeutics across the spectrum of neurologic disease, both here and abroad. His primary areas of interest include Neuroimmunology, migraine, and the Neurobehavioral manifestations of disease. Dr. Baker is a nationally recognized educator and lecturer. He enjoys teaching colleagues, medical residents and patients on such topics as Multiple Sclerosis and Myasthenia Gravis. In his spare time, he loves riding roller coasters with this family and playing with his two dogs.Micaela M. Acres, RN, BSNInfusion NurseJacqueline E. BradyCommunity Outreach Coordinator/ ReceptionMatthew B. Cagney, B.S.Clinical Research CoordinatorElena Capron, B.S.Regulatory Coordinator / Social Media CoordinatorBrittany N. Cordero, B.S.Office Manager / Human ResourcesJessica M. DEntremont, RN, MPH, BSNInfusion NurseDarious T. Davis, M.A.Head of Business DevelopmentLaura Gold, B.S.Finance CoordinatorKarma L. Hamilton, M.S.Lead RaterBethany J.M. Henchesmoore, MBAClinical Research CoordinatorJennifer Jimenez-Perez, RN, BSNInfusion NurseCarmen L. Ojeda, M.S.Quality Assurance / Quality ControlMichelle A. O'Neill, M.S.RaterMayve SantosResearch PharmacistAlexandria L. SmithClinical Research Coordinator