Change in diagnosis?

My visit with the movement specialist this week was interesting. She is questioning if I have been miss-diagnosed. She is suspect that I might actually have PSP (Progressive Supranuclear palsy) so she wants to follow me more closely and not have the nurse practitioner do one of my appointments each year. PSP is a Parkinsonism and much rarer than Parkinson’s. The reason she is thinking thus is; the fact that I don’t see any significant improvement from taking carbo/levo/dopa. and my being so unbalanced and frequency of falling. I have trouble keeping my eyes open and am hyper sensitive to bright lights. I have prism lens in my glasses., ad I have trouble with blurry vision.. But she also says my eyes move too well and if I have it I have a really light case, because the life expectancy is ten years , and I’m doing way too well… She considers when my legs were so weak that I needed help to get out of a tree in 2015 is where they start counting when I acquired the condition.

I told her I am taking a nutritional supplement that I believe is helping me.

How to Manage Parkinson’s Naturally

 I found this article to be well written, useful and informative.

(I will put any additional comments that I add into parinthise and italics)

By Dr. Kate Henry, N.D.

There have been many advances in medicine that allow people with Parkinson’s to maximize their health, happiness, and well-being. In this article, we’ll cover some of the basics about Parkinson’s Disease (PD), including what it is, how to manage it, and some natural methods for improving outcomes.

What Is Parkinson’s Disease?

Parkinson’s Disease (PD) is a neurodegenerative disorder that affects roughly 1% of the world’s population. PD impacts the whole body, including the musculoskeletal system (fine and gross motor control), autonomic and nervous system, digestive system, mood, cognition, and more. Symptoms of PD are typically grouped into categories called “motor” and “non-motor” symptoms.

In the past few decades, our understanding of PD has progressed from one that was defined by a lack of dopaminergic neurons in the substantia nigra of the brain and tremor to a more complete understanding of PD as a whole-body disorder which begins decades before we can see changes in central nervous system tissue. PD also involves multiple neurotransmitters (not just dopamine), and highly progressive forms of PD are linked with chronic inflammation, cell damage, protein glycation, high blood sugar, lack of activity, poor dietary choices, and more.

While this might feel overwhelming to hear, it means that there are tons of evidence-based, natural, lifestyle-based changes you can make to decrease your risk of Parkinson’s and to potentially decrease your symptoms if you already have it. Remember, health happens the 364 days you spend outside of the doctor’s office each year. Your choices at the dinner table, in the gym, and in your home affect your health and you can use them to improve many disorders, including Parkinson’s disease. Let’s talk about the variety of exciting, easy interventions that are proven to improve outcomes in PD. 

Pharmaceuticals Are A Mainstay of Parkinson’s Disease—Here’s Why

You might be wondering, “Why is Dr. Kate’s number one ‘natural’ recommendation to take and optimize pharmaceutical medications?” Simply put, it’s because if you don’t have enough dopamine in your brain, you can’t do any of the other lifestyle changes I’ll be asking you to do later in this article. Pharmaceuticals are a mainstay of Parkinson’s disease treatment because they help to replace missing dopamine that your brain desperately needs to stay motivated and to keep moving.

Dopamine’s Role in the Brain and Body

Dopamine is the reward neurotransmitter that helps us feel motivated to do things like get outside, cook healthy meals, and exercise. It also helps us coordinate movement. When people with Parkinson’s don’t have enough dopamine, they can get symptoms like depression, apathy, fatigue, tremor, and poor balance. They can even experience freezing—a phenomenon in Parkinson’s disease where people feel stuck or unable to move.

It’s not hard to imagine how the symptom list above would make it difficult—if not impossible—to go out for a run, take medications consistently, or want to go to the grocery store to look for ingredients for a new plant-based recipe (other natural interventions that are proven to reduce progression in Parkinson’s). These symptoms can even make it hard to take supplements or eat healthy foods since a lack of dopamine can cause difficulties with swallowing. For that reason, we need to make sure dopamine levels are optimized first before we try other natural treatment options in PD.

Dopaminergic drugs and in particular Levodopa (also known as Sinemet, Rytary, Carbidopa-Levodopa, or Duopa), are the closest things to our own body’s dopamine that we can make in a lab. They work. I’ve seen people with Parkinson’s who couldn’t stand up, take a step, or smile become completely transformed within hours of taking their first dose of Levodopa. In my opinion and the opinions of most neurologists, PD specialists, and PD patients, dopaminergic drugs are effective medications. They just have to be taken the right way and with the right nutrients to make them work for you.

How to Use Optimize Parkinson’s Disease Medications With Nutrition

There are a number of ways to optimize your response to oral medications for Parkinson’s disease. One of the first is to make sure that you’re digesting and absorbing those medications adequately. For PD medications, in particular, there are several nutritional considerations you must factor in when designing a medication plan that works for you.

1. Take PD medications with small snacks, not meals

Dopaminergic medications need to be taken away from high-fat, high-protein meals because amino acids and peptides compete for absorption across the blood-brain barrier, and high-volume meals can dilute stomach acid and delay the absorption of medication into the bloodstream. If you eat a big steak with your dopamine meds, they won’t be absorbed as well as if you ate them with a lower-protein snack like an apple.

Because of the need to avoid combining protein with dopaminergic medications, people with Parkinson’s have to be very careful to make sure they still get enough total protein in the day and that they optimize their nutrition. Protein is important because it helps our bodies heal, repair tissues, and balance blood sugar, among many other things. It pays to work with a naturopathic doctor, registered dietitian, or nutritionist who can help you develop a plan that works for you to still optimize your nutrition while you increase your ability to absorb medications. Some of my strategies for PD patients involve an adjusted feeding schedule, protein shakes between meals, small and frequent snacks throughout the day, and collagen powders in drinks that my clients don’t take with meds.

2. Take B vitamins when taking dopaminergic meds

Additionally, the human body also requires cofactors like vitamin B6cholinezinc, and vitamin B12 to metabolize and use dopaminergic pharmaceuticals. A deficiency in these vitamins and minerals can impair your ability to respond to dopaminergic medications effectively and without side effects.

Many people are surprised to learn that deficiencies in B6 and B12 are quite common. Roughly 10% of the U.S. population is deficient in B6, and 2% is deficient in B12. Because the top food sources of B vitamins tend to also be protein sources like beans and meat, people with Parkinson’s may actually be at a higher risk of these deficiencies if they’ve been attempting an unsupervised low-protein diet.

Consider taking a B complex or multivitamin that contains at least 100% RDA of B vitamins and zinc to make sure you’ve got enough of these nutrients to allow dopaminergic drugs to work their magic! If you have trouble swallowing, sublingual B12 or a liquid multivitamin may be the best option for you. Studies have shown that repleting levels of B12 and folate can help to minimize adverse reactions to L-Dopa-containing medications and protect nerve and cardiovascular tissue long-term.

3. Drink enough water and electrolytes to avoid orthostatic hypotension

One of the most common side effects of dopaminergic medications is orthostatic hypotension. Symptoms of orthostatic hypotension including feeling dizzy when you stand up, feeling fatigued due to low blood pressure, and frequent brain fog. Orthostatic hypotension also increases the chances of falling while walking. To help to reduce the chances of experiencing orthostatic hypotension when taking dopaminergic medication, make sure to drink enough fluids like water, decaffeinated teas, and low-sugar sports drinks, consume adequate electrolytes, and to consume enough protein. These factors combined help to ensure your best chances of maintaining normal blood pressure.

A Word about Natural Dopamine Replacement

Clients often ask me if they can use mucuna pruriens to help treat their PD instead of dopaminergic pharmaceuticals like Levodopa. The answer is that it depends.

Mucuna is a plant that contains significant amounts of L-Dopa. Some studies suggest that it can be as effective as Levodopa for controlling motor symptoms in PD and that it can have fewer side effects. These studies have mainly been conducted in remote areas where access to pharmaceutical medications is limited.

Currently, mucuna is not available as a prescription. This means that it is not subject to the same purity and safety regulations as pharmaceutical drugs are in the U.S. Taking it means that you’re accepting the risk that it might be contaminated or that it may contain more or less of a product that is on the label. It also isn’t covered by insurance, so the cost of taking mucuna daily is often prohibitive for many of my clients when compared to the cost of Levodopa.

If you’re willing to accept these risks and drawbacks, then mucuna could be a good herbal medicine for you to include in your PD treatment program. You have to work closely with a doctor (ideally one like a naturopathic doctor who’s also trained in herbal medicine) to determine and continually adjust your ideal dose of it.

It’s worth noting here that many other medications can be used to help manage Parkinson’s symptoms. This article is a good starting point for learning how to use lifestyle to optimize dopaminergic pharmaceuticals, but if you have more questions, schedule an appointment with a neurologist who specializes in PD and ask them what might work best for your body. 

Movement: The Mainstay of Natural Treatment for PD

Now that you’ve got enough dopamine in your system, your next best bet is to get moving! Exercise is one of the most effective interventions for Parkinson’s symptoms—second only to dopaminergic medication.

You should always work with a physical therapist to determine which exercises are safe for you depending on your symptoms and abilities. But the key takeaway from this section should be that regular exercise improves overall outcomes, quality of life, and nearly all symptoms of Parkinson’s disease.

Whether it’s balance, fall risk, depression, energy, strength, speed of movement, or sleep, there’s at least one study proving that exercise can help improve it in Parkinson’s. It sounds simple, but it’s profound.

Some of the most studied forms of exercise for improving PD symptoms include:

  • Strength training
  • Balance training
  • Dance, including tango and foxtrot
  • Yoga
  • Running
  • Boxing

How to Use Movement as Medicine in PD

Movement is mostly free. It’s available to all of us, and it really works to improve symptoms of PD. But getting regular movement can feel tricky if you’re already someone who has a hard time with balance, strength, or motivation.

This is why you need good movement specialists on your team. Whether it’s a physical therapist, personal trainer, chiropractor,  coach, or fitness instructor, create a community of folks who can help you determine how to move safely in a way that you love so you can stay active with PD in the long term.

This is also why we talked about medications first in this section. Medications can help you to minimize motor symptoms and maximize your ability to get moving so that you can begin to practice a program that will eventually build strength, flexibility, and balance.

Additionally, because apathy and depression are often symptoms of PD, it can be hard to motivate yourself to exercise. Get friends and join a boxing group, hiking club, or pilates class. Agree to walk dogs for a local shelter, or volunteer to take younger relatives to a park. Whatever it takes to keep you accountable for moving, build it into your schedule so that your other symptoms don’t derail your movement progress. If you don’t have a community locally, find one online.

Finally, it’s worth reiterating that moving safely is the foundation for any exercise program that works long-term. Get a medical professional (physical therapist, orthopedic doctor, etc.) on board to help you determine how you can move in a way that’s best for your body, and then make a commitment to do it each day.

Dietary Changes for Parkinson’s Disease Management

In general, a diet that is adequate in vitamins, minerals, low-glycemic fiber, complete proteins, and water is more beneficial for PD and other neurodegenerative diseases than one that is high in inflammatory oils, processed sugars, and excess calories. This is because protecting nerve fibers and cell membranes is critical for keeping folks with PD healthy, and to do this we have to:

  • Provide our cells with what they need to work correctly (vitamins and minerals)
  • Reduce the food ingredients that cause cellular damage via inflammation, toxicity, and impaired cell signaling (inflammatory oils, processed sugars, and excess calories).

Plant foods (fruits, vegetables, tubers, nuts, seeds, legumes) and moderate amounts of animal protein are the most beneficial foods for people with Parkinson’s to eat because they accomplish both of these goals.

Some people use diets like the Mediterranean diet, DASH diet, Wahls diet, Whole 30 diet, or other specific diets as a shorthand way of describing the diet outlined above. In general, though, a whole foods diet that includes many fruits and vegetables is the best for someone with PD.

One fascinating study, in particular, has established that the following foods seem to be associated with a dose-dependent decrease in PD symptoms long-term. (Put differently, the more of these foods you eat, the better you feel when you have Parkinson’s).

The same study suggested that sodas, canned foods, and fried foods, as well as processed sources of dairy, seem to be linked with faster rates of Parkinson’s progression (i.e. worse outcomes) long-term.

I typically advise my patients to focus on adding more of the foods in the list above to their diets, rather than restricting their diets. Simply including two servings of fruits or vegetables at each meal, adding more trail mix and nut or seed-based snacks throughout their day, and eating omega-3 rich fish like salmon several times per week can help you get there.

If you need more specific advice, consider working with a naturopathic doctor or nutrition professional to help you create a plan that’s customized for you. If you have trouble swallowing, work with an OT and your neurologist to develop a plan to help you eat the healthiest foods in a safe way for you.

Low-Glycemic Diets Improve Symptoms in PD

Managing blood sugar is vitally important for people with neurodegenerative disorders like PD. This is because hyperglycemia and diabetes are risk factors for mitochondrial dysfunction, impaired blood flow and oxygen delivery to organs including the brain, reduced brain volume, and more. All of these effects make the symptoms of PD worse.

Any dietary plan should include low-glycemic foods like fiber-rich fruits, vegetables, grains, legumes, and protein sources. If you have high blood sugar, ask your doctor and nutrition practitioner to help you get it under control.

Supplements for Parkinson’s Disease Management

Many people with Parkinson’s take supplements as part of their health routines. In a study of supplement habits in people with PD, the following supplements appear to be associated with a decreased rate of progression of PD symptoms. 

CoQ10 is an important antioxidant that helps our cells make energy. Because mitochondrial dysfunction and impaired cellular energy metabolism are implicated in the development of Parkinson’s disease, it makes sense to ensure that you are—at the very least—not deficient. One of the ways to do this is to supplement regularly with an over-the-counter CoQ10 supplement. In animal studies, CoQ10 supplementation has even been shown to halt or reverse the progression of Parkinsonian symptoms.

5MTHF stands for 5-methyl-tetrahydrafolate. It’s a methylated form of folate that’s thought to be more bioavailable than folic acid. Many people with PD take this as a part of the protocol recommended at the beginning of this article to maximize the effectiveness (and reduce side effects) of some Parkinson’s medications.

Turmericresveratrol, and quercetin are thought to protect cell membrane health mostly via their antioxidant capabilities. Antioxidants quench free radicals that would normally damage the fatty lining of every single cell in our bodies. By doing this, they protect cell membrane health and preserve the ability of our cells to manufacture energy and signal to each other appropriately. 

Multivitamins also contain many minerals and vitamins that are antioxidants. Additionally, they can be part of a good holistic plan to prevent nutrient deficiencies, which helps any human feel healthier and maximize their chances of good health. These supplements are safe for most people, but you should always ask your health provider before adding them to your routine.

There are many reasons to feel empowered and hopeful about your ability to manage and thrive with Parkinson’s disease. I hope this article gives you a good start!

Difficulty of Swallowing in Parkinson’s

I have only a couple suggestions for readers other than what is written in this article….. I find I don’t choke near as often, if I use a straw when I drink, It was explained to me, that the sucking gives my throat the message that food is on the way, giving my muscles time to react. and when taking medication, besides using a straw, it helps to Ad something like LuminAloe in almond milk… or applesauce to help get the capsules or tablets to go down without sticking.

. Written by: Sarah Winfrey

“Parkinson’s disease can cause a person to have difficulty chewing and swallowing. This can have many effects on their health and quality of life. They can develop dry mouth, dehydration, or malnutrition. They can also aspirate (inhale) food, liquid, or saliva into their windpipe, which can be frightening. As one My ParkinsonsTeam member shared, “I recently started choking on my own spit, and for the first time ever, I got really scared because I couldn’t get any air.”

Difficulty swallowing (dysphagia) can be a challenging symtom of Parkinson’s. The good news is that it can be treated. Here’s what you need to know about this symptom, including why it happens and how it can be managed.”

How Do People Experience Difficulty Swallowing With Parkinson’s?

“Many people diagnosed with Parkinson’s experience difficulties swallowing at some point while living with the condition. Dysphagia can occur at any point over the course of the disease, even during the early stages. As one member wrote, “I have trouble swallowing now. This is new to me — it’s only been a problem over this last week. It makes it hard to swallow my meds.”

“Having trouble swallowing can cause many other problems, depending on why a person struggles to swallow and how severe their dysphagia is. Many people find that they drool or can’t keep food and drinks in their mouths. Others find themselves sputtering, choking, or dealing with a sore throat during or after meals. Some may not even realize there is a problem until they start without trying.”

“Some people with dysphagia start to avoid certain foodrs or drink fewer liquids when swallowing becomes difficult. Over long periods of time, this can lead to other problems. As one member observed, “My husband has had the same swallowing problems and was losing way too much weight.”

Why Does Parkinson’s Cause Difficulty Swallowing?

“Swallowing involves the coordination of many complex muscle movements in the mouth and neck. Changes that lead to problems with swallowing can occur anywhere along the upper digestive tract, from the mouth to the esophagus.”

“In Parkinson’s, swallowing difficulties can be caused by the loss of dopamine neurons in different parts of the brain.  If they are lost in the substantia nigra region in the midbrain, the problem is considered a motor symptom. However, losing dopamine neurons in the lower brain stem or the cortex can cause issues with coordination. This is considered a non-motor difficulty because the problem is with the coordination itself and not with the way the muscles are functioning.”

The Risks Associated With Difficulty Swallowing

“Many risks are associated with swallowing problems.  Unintended weight loss is common, as having problems swallowing may make a person less inclined to eat. Long-term dysphagia can also deprive a person of nutrients, leading to malnutrition.”

“Aspiration pneumonia is another potential problem. When swallowing is difficult, people can end up inhaling liquid, food particles, or saliva in their lungs. Since the lungs cannot get rid of these substances easily, an infection can develop. Sometimes, these infections can lead to significant illnesses like aspiration pneumonia.”

Manage Swallowing Problems With Parkinson’s

“You can do many things to manage swallowing problems associated with Parkinson’s. As the Parkinson’s Foundation notes, first step to treating dysphagia is telling your neurologist about the problem. They can refer you to a specialist, known as a speech-language pathologist (SLP), for treatment.”

“The SLP will begin by asking you about the swallowing difficulties you’ve been experiencing. They will evaluate your symptoms and medical history. In most cases, they will order a video X-ray or an endoscopy to see how your swallowing muscles are functioning as you eat and drink.”

“After identifying the cause of your swallowing problems, the SLP will recommend one or more approaches to help you start swallowing and drinking as normally as possible. Some interventions may work for some people. You may have to try several before you find one that improves your swallowing.”

Treat Parkinson’s With Medication

“Managing dysphagia often begins with treating the underlying cause. In swallowing problems caused by Parkinson’s, this can mean treating Parkinson’s with medication.”

“Many medications are available for people diagnosed with Parkinson’s. For example, levodopa helps ease stiff muscles and slow movements. As with most drugs, you might experience some side effects while taking levodopa. These can include constipation, dizziness, insomnia, and anxiety. If you experience any of these side effects while taking levodopa, let your health care provider know right away.”

“Finding the best drug treatment for your Parksinson’s your swallowing function. Swallowing problems dont go away for everyone taking Parkinson’s medication, but there’s a good chance that you will see at least some improvement.”

Get a Swallow Test

“Some doctors, clinicians, and SLPs can administer a swallowing test or perform a swallowing study. These tests, as well as symptom questionnaires, can help indicate whether you are having problems swallowing and pinpoint where the dysfunction is occurring. After these procedures, doctors and speech specialists can target a person’s treatments so that they address the unique problems contributing to their dysphagia.”

“Some MyParkinsonsTeam members recommend these tests to anyone who struggles with swallowing. One member told another, “Please ask your doctor to order a barium swallow test to determine why you have difficulty swallowing.”

“Another explained, “Your doctor may do a ‘swallow test’ on you, even if you’ve already had one, to see if things are worsening.”

Work With a Speech-Language Pathologist

“Certain types of speech and language interventions may help improve your swallowing. Lee Silverman Voice Treatment (LSVT)is one type of treatment that seems to help people diagnosed with Parkinson’s swallow better. This approach helps you isolate certain muscles in the swallowing process and learn to strengthen or better control them while eating or drinking. Think of it as muscle strength training for swallowing.”

“Some of our members have had great success with this treatment. One shared their experience: “I finally found a great speech therapist in my area who is well-trained in LSVT. I’ve worked with her for two years. She has me 80 percent to 90 percent better. It works, but it does take discipline doing daily exercises and not giving up!”

Change How You Eat and Drink

“There are a number of changes that you can make to how you eat and drink that may make swallowing easier. These include:

  • Taking small sips of drinks and small bites of food
  • Changing the thickness or texture of the foods you eat
  • Eating and drinking when your medication is most effective, rather than right after you take it or when it wears off
  • Sitting up as straight as possible when drinking and eating
  • Reducing distractions, like conversations, during mealtimes
  • Making sure you swallow saliva regularly to control excess saliva or drooling
  • Focusing on keeping your mouth closed while eating and drinking.”

Stages of Parkinsons…

to answer a quesstion a sister asked me, because her husband has recently been diagnnosed…..what to expect?? Written by : Kelly Crumrin

There are five commonly recognized stages of Parkinson’s. Neurologists stage Parkinson’s based on the way the condition typically progresses. However, symptoms of Parkinson’s vary by the type of parkinsonism and between individuals. An individual with Parkinson’s will not necessarily experience all or even most symptoms and may not experience them at the same stage in which others experience them. Parkinson’s is a progressive disease, which means that symptoms worsen gradually over time, new symptoms appear, and disability accumulates.

Assessing the stage of Parkinson’s helps anticipate disabilities and plan accordingly for care.

The Five Stages of Parkinson’s

The stages of Parkinson’s are based on the Hoehn and Yahr scale introduced in 1967. The Hoehn and Yahr staging system focuses on disability caused by motor symptoms such as bradykinesia (slowed movements), tremor, and loss of balance. Some neurologists also use a newer scale called the Unified Parkinson’s Disease Rating Scale (UPDRS). The UPDRS scale takes into account changes in mood, cognitive function such as thinking and remembering, and social behavior.

Stage 1

Motor symptoms occur on one side of the body only. There is minimal or no disability.

Stage 2

Motor symptoms worsen and begin to affect both sides of the body. There may be difficulty walking and changes in posture, facial expression, and voice. Daily activities become harder and take longer.

Stage 3

In the middle stage of Parkinson’s, loss of balance becomes apparent and falls are more common. Motor symptoms make it difficult to eat, dress, and perform self-care, but the person is still capable of living alone.

Stage 4

At stage 4, a person is no longer able to live alone. Disability is severe, and the person requires help with many daily tasks. They may or may not be able to stand and walk without assistance. Many people begin using walkers at this stage.

Stage 5

During stage 5, the person cannot rise from a chair or bed without help. Motor symptoms include stumbling and freezing. They may lose the ability to stand or walk, and a wheelchair becomes necessary. Assistance is required around the clock for all activities. Some people begin to experience psychotic symptoms such as hallucinations or delusions.

Another View of Parkinson’s Progression

A newer theory of Parkinson’s progression called Braak’s hypothesis suggests that Parkinson’s may begin years before motor symptoms develop. According to Braak’s hypothesis, loss of smell and digestive symptoms such as constipation are the earliest signs of Parkinson’s, showing up many years before motor issues. While these early symptoms do not show up on an official Parkinson’s stage yet, many researchers are working on ways to identify and treat Parkinson’s earlier, even before stage 1.

Wounded

I put LuminAloe right on a wound I received on Tuesday sealing it in with a large bandage. The injury was about 1 1/2 inch long and at lesast 1/2 inch wide with the skin peeled back. I took the bandage off today, wiped off the ecess LuminAloe revealing a slightly scarred arm. Even the skin I expected to appear dead…. is sealed down and looking healthy… no oozing or weeping I am leaving the bandage off. and it is just Thursday… 2nd day after I fell.. I would have expected a much longer time to have my arm restored… befor I had access to LuminAloe!!

A Balanncing Act

Freezing & Fall Prevention

I have had too many falls of late.I have begun to be more proactive, spending ten minutes a day on a vibrarionalplate nd doing 100 squats and 100 knee lifts. And I HAve3 gone to several sessions with PHysical Therapists. They released me today, after I demonstrated a great improvemet in my balance. John and I both feel like it was very helpful.

Then, As I was reading a newsletter ‘Villoages PD Support Groups’ compiled by Rose Lang, wife of a husband with Parkinsons, I ran across a link that I Found very insightful. So I have posted it here. He talks about things the care give3r can do to assist. And quotes statistics like a person with Parkinsons is twice as likely to fall, than a healthy person. And he does a great job of explaining why. I encoutrage all of my followers to set aside time to listen to it.

Sue

pressure points

The statistics are pretty high, with PwP and shoulder,neck and back pain, In response to their comments on their suffering, I posted the following suggestion:

I had the blessing of a chiropracter who showed my husband pressure points on my back wwhich apear to break the cycle of spasms, thus pain.  Just have your care partner gently brush their hand across your shulders and down your back.. If there is a hint of pain, have them press hard on the spot… it may cause extreme pain, but oh, the relief once your cargiver lets up…  .Good Luck,
Sue

What if?

I have read about Blepharospasm, and it sounds very much like what I have going on.   My left eyelid is frequently closed and my vision seems to get worse as each day progresses, till in the evening I am resorting to using a magnifying glass to read, I suppose this is at least in part to the fact that I do not think to put wetting solution in my eyes. I do not notice any twitching in my eyelids untill I lay down to sleep. But I saw this post in a Parkinsons Conversation .

“Have you been to an ophthalmologist or just your PCP or optometrist?  As in all things Parkinson’s it is important to see the right doc. An ophthalmologist will do a Schirmer test to diagnose the problem. If he prescribes Restasis, it works in about 75% of cases. It is used twice a day, whereas conventional wetting eye drops might be needed 20 to 50 times a day. It is worth trying. My optometrist, who prescribes it now, uses a Canadian mail order pharmacy at about 1/10 the cost.”

I just thought I’d share it as a “what if?”

My Testimonial about LuminAloe

I received my diagnosis on March 30, 2019

I was told I had lost Dopamine in my brain, — When I met a motion specialist Her first comment was.”Yes, I can see that you have the loss of Dopamine”  I asked her how she could tell?    Her reply: Your Hands are hanging limp at your sides, You have a facial mask * flat expression on face* , and you have a very soft voice.                                     

6 MONTHS LATER…i STARTED  A BLOG..I have included the dates of various noticed   improvements

May 2021 – I acquired New Eden ( the precursor to LuminAloe )                                              6 weeks later I noticed my arms were swinging again.

November 2021 – I heard Dr. McDaniels (one of the creators of New Eden) say that   they had “documented that a previously badly scarred heart lost all of the scarring.“  I thought: “If that will work on varicose veins, I can document that. “ so I took a photo of my leg.

Jan 2022 – I transitioned from New Eden to the frequency activated more comprehensive nutrition, LuminAloe.

Feb 2022 – I met with my Primary Caregiver for him to  review the results of my lab work.  I told him upfront that, “I have been consuming a  product with more comprehensive nutrition.”  As he looked at the report, his first comment was “Wow, your Cholesterol levels look great! That cholesterol medication I’ve had you on must have really kicked in!”  To which I replied, “Or it might be the LuminAloe supplement I told you I have been taking, because you have had me on that medicine for at least two years.”  After he had reviewed the rest of the report, he said, “I’d like to know more about the product. If it can do that for you, maybe some of my other patients can benefit from it, too.

September 2022 the Movement specialist/neurology doctor told me I was doing so well, she didn’t need to see me for a year.

??  noticed new hair growth   …which required me to shave my legs again,… (Not so cool), but happy to see new hair on my forehead filling in where I had noticed I was getting a widow’s peak.

4/13/23 Thay say we should write down how we are feeling when we begin to use the LuminAloe, because we may not recognize as we are improving because the normalizing of health takes place over time.  A friend who suffers from the same motor malfunctions as I do asked me… “ARE your legs= stiff? Mine hurt and feel so heavy,, they feel like I’m dragging cement.” I told her,  “That sounds awful, but No, I don’t”       

As I was pondering her stiffness during the week, it dawned on me that I had been stiff. I had felt so stiff in 2021, I had resorted to using a toilet seat riser, to make sitting down easier, and stop falling onto the commode. Then In October 2021 My daughters gave me a bidet to help me avoid UTI’s and I had to remove the six inch lift. At that point in time, it was difficult to sit gracefully. Due to stiffness, it was more like I would fall in. So, gradually, without noticing, the stiffness had been resolved.

When I revealed to her, that I had been stiff in October of 2021, she purchased some LuminAloe.  A couple months later she was having surgery. to have a ligement in her footor leg reattached    When I saw her a number of months later, I asked her if she was still  experiencing  stiffness in her legs?   She seemed  surprised, as she thought about it saying, “I hadn’t  thought about it… but NO the stiffness is all gone!”   She and her husband continue to consume LuminAloe.

8 months after took the first photo of my leg, I was very impressed when in July of 2023

NOVEMBER of 2022

                                                                                                                July of 2023

My question is….if it can do that for my leg, what other good things are happening in my cardiovascular system.

July 2023 … Yesterday, John took me to visit the Neurologist at the Fixel campus at the University in Gainsville, Fl.  Well they scheduled me for 2 months short of a year, and I’ve been consuming LuminAloe and continue to recognize additional improvements. While there, they had me visit with Physical and Occupational Therapists.  When they tested my grip, they reported that I was stronger than I was a year ago. And when they timed how fast I can walk, my speed was reportedly faster as well. I told them about an exercise I’ve added to help with balance… And they encouraged me to keep following the same protocol,… that my balance had also improved.

August / Sept 2023… Late in August, I developed a very uncomfortable rash in the fold of my skin. I unsuccessfully treated it for three days with a traditional natural therapy. Then I recalled Reg reported he applied dry LuminAloe directly in his mouth after he had oral surgery, and pain was so well controlled, he forgot to mention he had even had the procedure when he was presenting at our meeting that evening. So the next question was how to keep the LuminAloe, on long enough to benefit me.. I decided to use a facial cream along the crease of the skin fold and then sprinkle the LuminAloe along the crease and rub it in, Ahhh, instant relief! When I woke up and went to shower it off, the rash was nearly gone. I noticed yellow staining on my clothing, so I took a clean old sock and placed it along the fold, to protect my clothing. After another night, of treating the rash with LuminAloe, all tenderness was gone.