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Summary of Legitimate Stem Cell Therapy.
I recently received an email from Summit for Stem Cell Foundation which contained a great summary of legitimate stem cell research to combat Parkinson's Disease throughout the world. Here it is: Roger Barker, United Kingdom. (2018 – ongoing.) Fetal tissue transplants for Parkinson’s disease.
I recently received an email from Summit for Stem Cell Foundation which contained a great summary of legitimate stem cell research to combat Parkinson's Disease throughout the world. Here it is: Roger Barker, United Kingdom. (2018 – ongoing.) Fetal tissue transplants for Parkinson’s disease.
jimcaster
in
Cure Parkinson's
4 years ago
PD treatment using one’s own skin cells to produce More dopamine in the brain.
https://www.statnews.com/2020/05/12/medical-first-parkinsons-brain-cell-transplant-stem-cells The results will be published Wednesday in a medicinal journal. Doesn’t look to promising.
https://www.statnews.com/2020/05/12/medical-first-parkinsons-brain-cell-transplant-stem-cells The results will be published Wednesday in a medicinal journal. Doesn’t look to promising.
Cons10s
in
Cure Parkinson's
4 years ago
What are the downsides of NOT taking dopamine drugs?
Wondering if I should keep holding off on taking dopamine therapy. I've been avoiding taking it since my diagnosis a year ago due to an overall dislike of pharmaceuticals in general and in hopes of avoiding the side effects. Just watched a talk by Dr. Laurie Mischley (link below, at minute 26) where
Wondering if I should keep holding off on taking dopamine therapy. I've been avoiding taking it since my diagnosis a year ago due to an overall dislike of pharmaceuticals in general and in hopes of avoiding the side effects. Just watched a talk by Dr. Laurie Mischley (link below, at minute 26) where
lbrussell
in
Cure Parkinson's
4 years ago
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Too much of a good thing
The publication twenty years ago describing excessive therapeutic drug dosing in some Parkinson's disease patients foreshadowed behaviours now well recognised. The recognition and description of a behavioural syndrome in a group of patients with Parkinson’s disease (PD) who take dopamine replacement
The publication twenty years ago describing excessive therapeutic drug dosing in some Parkinson's disease patients foreshadowed behaviours now well recognised. The recognition and description of a behavioural syndrome in a group of patients with Parkinson’s disease (PD) who take dopamine replacement
Farooqji
in
Cure Parkinson's
4 years ago
Stem Cell Success in Massachusetts
This was not a double blind test, so placebo effect cannot be ruled out, BUT two years after therapy, there's considerable reason for cautious optimism. "Two years after the surgeries, the patient has had no adverse events and reports improvements in daily function. Standardized examinations of motor
This was not a double blind test, so placebo effect cannot be ruled out, BUT two years after therapy, there's considerable reason for cautious optimism. "Two years after the surgeries, the patient has had no adverse events and reports improvements in daily function. Standardized examinations of motor
jimcaster
in
Cure Parkinson's
4 years ago
Excess sugars profoundly impacts your kidney health
Your nutrition influences metabolic waste output. What is best limited to enhance kidney health? Let’s talk sugars/fast carbs 1st: boiled/gummy sweets; concentrated fruit juice; ultra processed foods e.g shop cakes/pastries/some breads; fizzy pop; commercial ice-cream/lollies. And you know its not just
Your nutrition influences metabolic waste output. What is best limited to enhance kidney health? Let’s talk sugars/fast carbs 1st: boiled/gummy sweets; concentrated fruit juice; ultra processed foods e.g shop cakes/pastries/some breads; fizzy pop; commercial ice-cream/lollies. And you know its not just
WhollyAligned
Administrator
in
Nutrition and Yoga for Health
4 years ago
Might PD pharmaceuticals restore my athletic performance?
Hello. This week marks 1 year since my official PD diagnosis, although I had symptoms for a few years prior. I knew what was coming as my mother has battled PD for over 20 years. One thing that has bothered me is my slower speeds at both bicycling and walking. I have been a bicyclist for over 30 years
Hello. This week marks 1 year since my official PD diagnosis, although I had symptoms for a few years prior. I knew what was coming as my mother has battled PD for over 20 years. One thing that has bothered me is my slower speeds at both bicycling and walking. I have been a bicyclist for over 30 years
lbrussell
in
Cure Parkinson's
4 years ago
Parkinson’s: Autoimmune attack may start years before diagnosis
A new study adds an evidence reinforces the Auto- Immune attack to nerve cells which then develops PD . " Years before motor symptoms arise, other symptoms of Parkinson’s can appear, including a reduced sense of smell, constipation, mood changes, and REM sleep behavior disorder, which involves physically
A new study adds an evidence reinforces the Auto- Immune attack to nerve cells which then develops PD . " Years before motor symptoms arise, other symptoms of Parkinson’s can appear, including a reduced sense of smell, constipation, mood changes, and REM sleep behavior disorder, which involves physically
Abdiqani
in
Cure Parkinson's
4 years ago
Exercise
Hello, i got a question about exercise. I am a sprinter and always enjoyed it. I know the main trial for slowing brain disease was 30 min high intense max HR, on a treadmill. How do they know hitt workouts are not the same or better at protecting the brain. Have the done more trials on exercising?
Hello, i got a question about exercise. I am a sprinter and always enjoyed it. I know the main trial for slowing brain disease was 30 min high intense max HR, on a treadmill. How do they know hitt workouts are not the same or better at protecting the brain. Have the done more trials on exercising?
Girth10
in
Cure Parkinson's
4 years ago
Xarasho
I am Suffering from severe RLS and I’ve tried everything from vitamins to CBT OIL, 5 HTP Hydroxytry.. , nothing works, the only thing helps is the agnostic dopamine drugs which is for Parkinson disease, it has really bad side effects , please someone help me and be. genuine!!!
I am Suffering from severe RLS and I’ve tried everything from vitamins to CBT OIL, 5 HTP Hydroxytry.. , nothing works, the only thing helps is the agnostic dopamine drugs which is for Parkinson disease, it has really bad side effects , please someone help me and be. genuine!!!
Xarasho
in
Restless Legs Syndrome
4 years ago
Insomnia - Ropinorole & Pramipexole the same?
Hi, I have RLS which is under control with Ropinorole, however I think it's also causing me insomnia which I've been prescribed Gabapentin, which seems to help. I wanted to know though if Pramipexole (which I was using years ago) also causes insomnia? I know they are both dopamine antagonists but maybe
Hi, I have RLS which is under control with Ropinorole, however I think it's also causing me insomnia which I've been prescribed Gabapentin, which seems to help. I wanted to know though if Pramipexole (which I was using years ago) also causes insomnia? I know they are both dopamine antagonists but maybe
silkusmaximus
in
Restless Legs Syndrome
4 years ago
Dopamine,
Look for foods to increase dopamine !
Look for foods to increase dopamine !
gerrerd
in
Anxiety and Depression Support
4 years ago
My experience with Buprenorphine
I'm very thankful for Shumbah for introducing the knowledge of this drug that has helped her. I got in touch with Dr Brooks from New York that helped her. After a phone conversation, he agreed to give me a small prescription of 6 tablets of Buprenorphine 2mg. I was to cut in half to 1 mg and take
I'm very thankful for Shumbah for introducing the knowledge of this drug that has helped her. I got in touch with Dr Brooks from New York that helped her. After a phone conversation, he agreed to give me a small prescription of 6 tablets of Buprenorphine 2mg. I was to cut in half to 1 mg and take
Smuu
in
Restless Legs Syndrome
4 years ago
Could my FND actually be dopamine deficiency?
My neurologist has just diagnosed me as FND and has suggested psychotherapy. However, I feel certain my symptoms are dopamine deficiency related. E.G - motor difficulties - extreme leg stiffness, hypertonia, hyperreflexia, falling over, aching legs, PLMD in sleep. All starting 12 months ago. I feel
My neurologist has just diagnosed me as FND and has suggested psychotherapy. However, I feel certain my symptoms are dopamine deficiency related. E.G - motor difficulties - extreme leg stiffness, hypertonia, hyperreflexia, falling over, aching legs, PLMD in sleep. All starting 12 months ago. I feel
Numina
in
Functional Neurological Disorder - FND Hope
4 years ago
Mucuna beans
Is there any research on what causes PSP. Is it lack of dopamine ? Can Mucuna beans help ?
Is there any research on what causes PSP. Is it lack of dopamine ? Can Mucuna beans help ?
pthalo
in
PSP Association
4 years ago
Dopamine through the night
Hi all. I was wondering if any of you take stuff during the night. I never thought it was something I’d consider as I presumed I’d save it for daytime, but I reflected recently that maybe a) it might help with sleep and b) it meant less of an uphill journey for the first drugs in the morning. Your thoughts
Hi all. I was wondering if any of you take stuff during the night. I never thought it was something I’d consider as I presumed I’d save it for daytime, but I reflected recently that maybe a) it might help with sleep and b) it meant less of an uphill journey for the first drugs in the morning. Your thoughts
jeeves19
in
Cure Parkinson's
4 years ago
Flomax & COVID-19 Survival
Tamsulosin [Flomax]
"is a medication used to treat symptomatic benign prostatic hyperplasia (BPH) and chronic prostatitis and to help with the passage of kidney stones." [1] "Tamsulosin is a selective
α1 receptor
[2] antagonist that has preferential selectivity for the α1A receptor in
Tamsulosin [Flomax]
"is a medication used to treat symptomatic benign prostatic hyperplasia (BPH) and chronic prostatitis and to help with the passage of kidney stones." [1] "Tamsulosin is a selective
α1 receptor
[2] antagonist that has preferential selectivity for the α1A receptor in
pjoshea13
in
Advanced Prostate Cancer
4 years ago
🌈May be helpful to someone
During this period of lock down when it’s difficult to get RLS help & advice from your GP I feel it may be worth while to share my own experience. If it helps one person it will be worth it! I have been treated with RLS drugs for at least 10 years & have been through most of them including the various
During this period of lock down when it’s difficult to get RLS help & advice from your GP I feel it may be worth while to share my own experience. If it helps one person it will be worth it! I have been treated with RLS drugs for at least 10 years & have been through most of them including the various
Annieapple
in
Restless Legs Syndrome
4 years ago
EMAIL from Professor Richard P Allen John Hopkins
Dear Mrs Howard I was sad hearing about your travails getting treatment for RLS. Yes buprenorphine is one of the opioids used for refractory RLS with reasonably good results. It tends to get used after methadone is tried, but it is very effective in many patients. We have long term experience
Dear Mrs Howard I was sad hearing about your travails getting treatment for RLS. Yes buprenorphine is one of the opioids used for refractory RLS with reasonably good results. It tends to get used after methadone is tried, but it is very effective in many patients. We have long term experience
Shumbah
in
Restless Legs Syndrome
4 years ago
LDN causing Dystonia or neck jerking?
A neurologist recently thought that I had a motor tic in the back of my neck that keeps me jerking my head forward. After readingn some research I think maybe I have some form of dystonia. I seem to jerk it very hard to the point in the middle of the day it's just hurting and I do it every day. Anyways
A neurologist recently thought that I had a motor tic in the back of my neck that keeps me jerking my head forward. After readingn some research I think maybe I have some form of dystonia. I seem to jerk it very hard to the point in the middle of the day it's just hurting and I do it every day. Anyways
jbicondoa
in
Thyroid UK
4 years ago
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