Experiences with

Azatadine

I have Parkinsons and I have been using Ropinirole also known as Requip for about 13 years. It is an Agonist , that helps the effects of Levadopa last longer. I also have been using Amantadine for the same thing but its effectiveness may have worn off. I was doing OK and then the company GlaxoSmithKline

Has anyone tried this med? Dr added to carbo-levodopa for HwP..

ok, I’ve been called out on being missing. Life is good. Busy as always. Saw my neuro two weeks ago. He had me increase my baclofen to help with pain in my legs. The good news is it’s helping a ton!! The bad news is it’s increased my fatigue a ton too. So I’m getting back on amantadine tomorrow to

Here's an interesting article on some of the less common medications for RLS. It may be of interest to members who have exhausted all other medication options. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983500/ Keywords: clonidine, dipyridamole, perampanel, amantadine, ketamine, carbamazepine,

I have taken this portion of the the report from the article elaborating the results of double blind trial in 1999. "Patient 133 (video segments 17–19) developed parkinsonism at age 42 in 1986. His major problems were wearing-off episodes as well as levodopa-induced dyskinesias, particularly of the

has anyone used Augmentin and seen improved symptoms? I took amantadine and Augmentin and walked better.

In addition to stalevo 100mg 6 times a day and resagaline. I have for the past two weeks been taking Amantadine 100mg once each morning with the intention to increase it to twice a day from next week. However I have noticed that ive been waking up after a few hours sleep every night and finding it hard

Hi all, My mother 57 years old is on C/L Controlled Release tablet (Syndopa 125mg CR) thrice a day with the dosage split as 1/2-1/4-1/4-1/2 , (i.e 62.5mg-31.25mg-31.35mg-62.5mg). Her afternoon dose is split as 1/2 again and hence the 1/4th -1/4th. She also takes Ropinirole 1mg and MAO-B Inhibitor

I have intense itching on my back and stomach and toes an hour after taking amantadine and mucuna. I don’t know if it is an allergy. I also have significant Lipoatrophy which seems to be exacerbated with the amantadine and sinamer and mucuna… does this happen to anyone else? What do you recommend I

Here is a partial list of medication, supplements for other therapies used in Parkinsons What do you believe are the most beneficial/essential to treating Parkinsons and/or mitochondrial damage Which way should I go? Most bang for your bucks Carbadopa/Levadopa  L-5-hydroxytryptophan (5-HTP) Actylcholine

has anyone taking amantadine experienced lLipo atrophy? All of my fat has disappeared, and my buttocks is flaccid. I read that early antiretrovirals could caus Lipo atrophy, and I wonder if amantadine could be doing the same.

I am taking 2 tablets 25-100 C/L 4x per day and 1 tablet of 50-200 at bedtime. Back in August of this year doctor put me on amantadine starting with 2.5 ml. I was supposed to eventually get to 10 ml, but I never got past 7.5 because of the nausea. It seemed to help a little but I still continued to have

Does anyone suffer with stomach pains and or diarrhea when taking meds on an empty stomach? I take amantadine and sinemet and selegine?? Thanks

I was diagnosed with PD 6 years ago. I'm currently taking 6 Stalevo 100mg each day at 6am, 8am, 10am, 1pm, 4pm, and 6pm. I also take Resageline 1mg.Over the last 18 months I have seen an increase in Dyskinesia, mainly later in the day and usually worse as the meds wear off. My Neurologist suggests

Weight loss and amantadine I have lost all my fat I am Taking only amantadine. Has anyone else experienced this?

I have been shuffling my feet lately when I am walking, however otherwise I am doing fine. I have had PD since 2005. I take 3 tablets of carbo / levodopa, 25 - 100mg, 3 - 4 times a day, I never take C/L after 5pm and I take Amantadine., 3pm, 5pm &7pm which controls the dyskinesia. I get plenty of exercise

About 6 months ago, my dyskinesia started getting worse, and I noticed I was starting to get a lot of neck pain. I went to a neuro PT who said she thought my neck pain and stiffness were being driven by my dyskinesia and that I needed to reduce the dyskinesia before we could improve my neck. So I tried

Hey! My friend was diagnosed with PD ten years ago at the age of 30. They are not taking levodopa because of the severe hallucinations it causes. I was looking for alternatives to traditional treatment approach and found the HDT therapy. I'm currently reading "Parkinson's and the B1 therapy" by Daphne

I would like to discuss with anyone else who has my symptoms and is taking my medication. Carbidopa and Levodopa and Amantadine

I was diagnosed with PD a few months ago although I had a hand tremor on the right side for one and half years ago. My hand tremor gets better during mid week usually Wednesday and Thursday, and gets worse after that. I don't take any regular medication as C/L and Amantadine didn't work for me. So I