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Gocovri
Has anyone tried Gocovri for dyskenesia? I have been taking generic syrup for Amantadine and want to try continuous release Gocovri.
Has anyone tried Gocovri for dyskenesia? I have been taking generic syrup for Amantadine and want to try continuous release Gocovri.
ladya2020
in
Cure Parkinson's
3 years ago
Wearing Off or Dyskinesia
Wearing Off or Dyskinesia Author: Jill Marjama-Lyons, MD and Mary J. Shoman ….possible changes to your medicines…discuss with your doctor. •Use Sinemet CR (controlled release) or Sinemet ER (extended release). •Add a dopamine agonist. •Add a COMT inhibitor to Sinemet (immediate release, CR form
Wearing Off or Dyskinesia Author: Jill Marjama-Lyons, MD and Mary J. Shoman ….possible changes to your medicines…discuss with your doctor. •Use Sinemet CR (controlled release) or Sinemet ER (extended release). •Add a dopamine agonist. •Add a COMT inhibitor to Sinemet (immediate release, CR form
Hidden
in
Cure Parkinson's
3 years ago
Hallucinations
Can anyone give me advice on hallucinations. My partner just started on 100/25 c/l 3 times a day and has been hallucinating intermittently ever since... moreso at night. They aren’t troubling hallucinations so he’s coping fine but I worry that they’ll become more difficult to distinguish from reality
Can anyone give me advice on hallucinations. My partner just started on 100/25 c/l 3 times a day and has been hallucinating intermittently ever since... moreso at night. They aren’t troubling hallucinations so he’s coping fine but I worry that they’ll become more difficult to distinguish from reality
Scrudgie
in
Cure Parkinson's
3 years ago
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Is edema a side effect of RYTARY?
[i]I noticed some edema in my foot and ankles when first trying medications for PD. I tried Sinemet but also tried amantadine and ropinerole. I never knew which medication caused the edema. Now I'm on Rytary alone and edema is back. I wore shorts today and both the neuro and my wife noticed
[i]I noticed some edema in my foot and ankles when first trying medications for PD. I tried Sinemet but also tried amantadine and ropinerole. I never knew which medication caused the edema. Now I'm on Rytary alone and edema is back. I wore shorts today and both the neuro and my wife noticed
kaypeeoh
in
Cure Parkinson's
3 years ago
Should I start pramipexole???
I am on Rasagiline and Amantadine but neither seem to help my tremors. My neurologist wants to add pramipexole to the mix but I read about all the side effects like compulsive behavior and the inability to stop taking it due to serious withdrawal. What do you recommend dear friends?
I am on Rasagiline and Amantadine but neither seem to help my tremors. My neurologist wants to add pramipexole to the mix but I read about all the side effects like compulsive behavior and the inability to stop taking it due to serious withdrawal. What do you recommend dear friends?
Hidden
in
Cure Parkinson's
4 years ago
Neupro - 1st day on...working I think...
So this is interesting. I didn’t take my Sinemet this morning and thank God I didn’t because the constipation I’ve had from it has been so awful and actually gave me an impacted bowel so I did the next best thing and took a lovely suppository and that worked incredible magic needless to say. Sorry for
So this is interesting. I didn’t take my Sinemet this morning and thank God I didn’t because the constipation I’ve had from it has been so awful and actually gave me an impacted bowel so I did the next best thing and took a lovely suppository and that worked incredible magic needless to say. Sorry for
MissRita
in
Cure Parkinson's
4 years ago
PTT FUS in Switzerland - One month later
Not so detailed as Marc, but here is my fellings. After the surgery i was like new. No tremor, no dysknesia, no dystonia, no slowness. Then one week after i had two hard days, like withdraw symptoms, witch i assume it was of cutting meds to fast, especially C/L. I had also a lack of balance on the first
Not so detailed as Marc, but here is my fellings. After the surgery i was like new. No tremor, no dysknesia, no dystonia, no slowness. Then one week after i had two hard days, like withdraw symptoms, witch i assume it was of cutting meds to fast, especially C/L. I had also a lack of balance on the first
Markbit
in
Cure Parkinson's
4 years ago
Exercise poll
Dear Fellow PWPs, How many times per week do you exercise? What do you do, bike, walk, run, swim, weights etc? What level of intensity? My neurologist showed me an article about the theracycle and doing 60-80rpms for 45 minutes three times per week. Doctors said it had the same benefit as PD meds
Dear Fellow PWPs, How many times per week do you exercise? What do you do, bike, walk, run, swim, weights etc? What level of intensity? My neurologist showed me an article about the theracycle and doing 60-80rpms for 45 minutes three times per week. Doctors said it had the same benefit as PD meds
Hidden
in
Cure Parkinson's
4 years ago
Has anyone taken Vinpocetine with Rasagiline and Amantadine?
If you have taken this combination please let me know. I want to add Vinpocetine to my daily supplements but I’m concerned about any interactions with Amantadine and Rasagiline. Thank you my enlightened friends.
If you have taken this combination please let me know. I want to add Vinpocetine to my daily supplements but I’m concerned about any interactions with Amantadine and Rasagiline. Thank you my enlightened friends.
Hidden
in
Cure Parkinson's
4 years ago
Now what?
Three years ago I developed a tremor in my dominant arm. At the same time I developed a Deep Vein Thrombosis in the same arm. Then a 100% obstruction of the LAD coronary branch. The LAD is also known as the widow maker. A stent plus drugs cleared all that up but nothing has helped get rid of
Three years ago I developed a tremor in my dominant arm. At the same time I developed a Deep Vein Thrombosis in the same arm. Then a 100% obstruction of the LAD coronary branch. The LAD is also known as the widow maker. A stent plus drugs cleared all that up but nothing has helped get rid of
kaypeeoh
in
Cure Parkinson's
4 years ago
Artane for Dyskinesia
I have been taking Amantadine but it is not very effective for the severe dyskinesia I have been experiencing every morning. Someone in the forum mentioned Artane. Can you please tell me something about your experience with it?
I have been taking Amantadine but it is not very effective for the severe dyskinesia I have been experiencing every morning. Someone in the forum mentioned Artane. Can you please tell me something about your experience with it?
ladyaudree
in
Cure Parkinson's
4 years ago
Anyone had good results from Amantadine (SYMMETTREL) ?
A anti viral med that is used for PD ?
A anti viral med that is used for PD ?
Vegegardner
in
Cure Parkinson's
4 years ago
Amantadine - first time user - haven’t tried yet
Hello all! Has anyone used this medication at all? Curious about reactions positive and negative. Thanks so much!
Hello all! Has anyone used this medication at all? Curious about reactions positive and negative. Thanks so much!
MissRita
in
Cure Parkinson's
4 years ago
Amantadine sulphate
Amantadine sulphate - I was diagnosed with PD a few months ago (45 yo) and have been on Sifrol, (Mirapex), Azilect and Dekinet (Biperiden)Due to cognitive memory issues my doctor reduced the level of dekinet and it helped. It also slowly led to a regression of tremors and right hand weakness. I am
Amantadine sulphate - I was diagnosed with PD a few months ago (45 yo) and have been on Sifrol, (Mirapex), Azilect and Dekinet (Biperiden)Due to cognitive memory issues my doctor reduced the level of dekinet and it helped. It also slowly led to a regression of tremors and right hand weakness. I am
Yb252
in
Cure Parkinson's
4 years ago
When is it supposes medication have an effect?
By middle of November 2020 I was diagnosed with a “clinical picture suggestive of PSP”, being freezing of gait (FoG) my claim. This is the end of a long road of claims (inbalance, neck pain, radiculopathies, a.s.o.) after being submitted in November 2015 to a ACDF surgery to decompress my spinal cord
By middle of November 2020 I was diagnosed with a “clinical picture suggestive of PSP”, being freezing of gait (FoG) my claim. This is the end of a long road of claims (inbalance, neck pain, radiculopathies, a.s.o.) after being submitted in November 2015 to a ACDF surgery to decompress my spinal cord
BluesHealer
in
PSP Association
4 years ago
Starting Mucuna
reposted You will forgive me if this information has already been disseminated. I am a PWP, diagnosed 2 years ago, after 2 years of misdiagnosis. I currently take Amantadine 3x/day as my only PD med. My neurologist has been "pushing" me to start c/l. I have been reluctant , up until
reposted You will forgive me if this information has already been disseminated. I am a PWP, diagnosed 2 years ago, after 2 years of misdiagnosis. I currently take Amantadine 3x/day as my only PD med. My neurologist has been "pushing" me to start c/l. I have been reluctant , up until
docjleonard55
in
Cure Parkinson's
4 years ago
Starting Mucuna
You will forgive me if this information has already been disseminated. I am a PWP, diagnosed 2 years ago, after 2 years of misdiagnosis. I currently take Amantadine 3x/day as my only PD med. My neurologist has been "pushing" me to start c/l. I have been reluctant , up until now. With worsening tremor
You will forgive me if this information has already been disseminated. I am a PWP, diagnosed 2 years ago, after 2 years of misdiagnosis. I currently take Amantadine 3x/day as my only PD med. My neurologist has been "pushing" me to start c/l. I have been reluctant , up until now. With worsening tremor
docjleonard55
in
Cure Parkinson's
4 years ago
Amantadine and Covid-19
I was doing some research today, because I take amantadine, and wondered if it would be helpful warding off Covid as an antiviral. Found some encouraging news! https://link.springer.com/article/10.1007/s43440-020-00168-1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290190/ One article stated that people
I was doing some research today, because I take amantadine, and wondered if it would be helpful warding off Covid as an antiviral. Found some encouraging news! https://link.springer.com/article/10.1007/s43440-020-00168-1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290190/ One article stated that people
Mezzomom1
in
Cure Parkinson's
4 years ago
Amantadine for fatigue/spasms
There was a post on here recently about Amantadine and I commented on how I took it 4 or so years back. Was one of the first drugs I took for AMN once I'd found a decent neurologist who was open to prescribing anything that wasn't Baclofen or Valium. Amantadine is an antiviral, was effective against
There was a post on here recently about Amantadine and I commented on how I took it 4 or so years back. Was one of the first drugs I took for AMN once I'd found a decent neurologist who was open to prescribing anything that wasn't Baclofen or Valium. Amantadine is an antiviral, was effective against
monkeybus
in
AMN EASIER
4 years ago
Rasagiline and Depression
I have been taking Azilect and then the generic Rasagiline for 12 years after being diagnosed at 34. I also took generic Dopamine Agonists for ten years but had such pronounced OCD behavior that I finally quit cold turkey two years ago. Today I take Rasagiline 1mg, 100mg Amantadine, and CL 25/100. I've
I have been taking Azilect and then the generic Rasagiline for 12 years after being diagnosed at 34. I also took generic Dopamine Agonists for ten years but had such pronounced OCD behavior that I finally quit cold turkey two years ago. Today I take Rasagiline 1mg, 100mg Amantadine, and CL 25/100. I've
jlmerten
in
Cure Parkinson's
4 years ago
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