Does anyone have Parkinsonism Atypical MSA? If so how are you coping. What meds are you taking, are any of them helpful.

Does anyone have Parkinsonism Atypical MSA? If so how are you coping. What meds are you taking, are any of them helpful.

Has anyone got any of the above and how are they coping. Are you able to get about easily, has your memory been affected. Has anyone found any of the above drugs working or can recommend any others.
I am taking clonazapan, madopar, movical,solifenacin, amitriptiline, fludrocortisone,

A MyParkinsonsTeam Member said:

i was diagnosed with atypical parkinson since 2012, first they thought i had the vascular varint, but about 6-8 monthsd ago my bslance , freezing and my stffness progressed rapidly that my neurologist change my dignosis to multiple systems atrophy. the medication i take now is 1 1/2 tablets of Ldopa/carbidopa 100 mg 4x a day,. with vey little or no effect. How am i coping? Struggling but still kicking.

posted over 3 years ago
A MyParkinsonsTeam Member said:

I am taking madopar with levodopa and benserazide for the park inside of it.

posted over 3 years ago
A MyParkinsonsTeam Member said:

My husband took rasalgilene with no effect. Another neurologist put him on amantadine. I feel his tremors are worse, and he now has accidents with tableware and drinking glasses. He also seems to be sleeping more.

posted 9 months ago
A MyParkinsonsTeam Member said:

I will have to do some checking on the madopar. Never heard of it b4.

posted over 3 years ago
A MyParkinsonsTeam Member said:

oops, getting late, parkinson side

posted over 3 years ago
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