Quote:
Originally Posted by Blackfeather
I am in rapid decline both physically and mentally. My dystonia is unbearable now, a product of Parkinson's. I gave it my best effort but can barely function now. Can't use the keyboard any to peck out words anymore. If I can endure I will check in when I can. Either way good luck with this illness. I love you all
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Blackfeather,
Your post concerns me.
Ive had PD a long time and would like to help you but need to know some facts that have come from a neurologist who treats P.D.
Have you been given a firm diagnosis of M.S.A.?
Are you taking any anti parkinson meds e.g. levodopa?
if so how many mgs and how often?
Dystonia is in my opinion the most uncomfortable and distressing of all the symptoms that P.D. presents with.
I no longer have it and am happy to help but I must let you know I follow evidence based and peer reviewed studies for my treatment.
You having had P.D. for what 5-6yrs by now you should have some sort of drug regime that some of us here can help you out with.
Best wishes.