Experiences with

Azatadine

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

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

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.

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

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?

A anti viral med that is used for PD ?

Hello all! Has anyone used this medication at all? Curious about reactions positive and negative. Thanks so much!

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

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

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

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

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

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

Has anyone else heard of Amantadine for ADHD? Or used it?

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 had my appointment with my new neurologist today, she is very nice and took her time with me She gave me a very thought exam, more than my other movement specialist did (she my third one but I believe she's a keeper ) she lowered my neupo patch decreased cl which was just change due to rotary not being

My "PD" is modulated by: Norepinehrine loss in CNS. Amantadine helps. Dysautonomia (ANS pathologies). Eg, elevated norepinephrine in periphery. Midface hypoplasia (eg, severe malocclusion, high arched palate). Also, I've come to believe: distorted development of my insular cortices and interconnected

Hello to All, Has anyone taken the drug Amantadine, brand name Symmetrel, to treat MS fatigue? I’ve been on it for a few days but unfortunately I had a pretty bad adverse reaction today and I will have to stop taking it. I’m interested to know if you had any side effects while on it or withdrawal issues

I’ve been on Amantadine for about 6 weeks and have felt worse than ever. Symptoms were worst I’ve ever had. Dry. Mouth, very dry eyes to the point of not being able to see. Starting seeing images all over my house, bad dreams. D/C per MDS, but.nothing to replace. Has anyone else had these issues?

"Amantadine is an antiviral medicine that blocks the actions of viruses in your body. Amantadine is used to treat or prevent influenza A in adults and children. Amantadine may not be effective during every flu season because certain strains of the virus may be resistant to this medicine. Amantadine