My wife suffers from PD. Interested in any ways of alleviateing dyskinesia via. Medication or DBS
New to the forum: My wife suffers from PD... - Cure Parkinson's
New to the forum
What type of dyskinesia? what medications do you take? A little information helps.
It’s my wife that is the sufferer. She is on Sinemet, ropinerole and razagaline. The medication is losing its effectiveness and she is experiencing restless leg syndrome and dyskinesia (involuntary movement). She was diagnosed 10 years ago. We have an appointment with her Parkinsons nurse who over the years has “tweaked” her medication dosage but we are worried and frightened that she might have reached the stage where she has to choose between Bradykesia and Dyskinesia. We are also interested in people’s experiences of DBS if her condition worsens further.
Have she ever taken vitamins, type b1 or group b in general?
No she hasn’t, will her nurse be able to advise as to which ones to use
Reference for the high-dose vitamin B-1 protocol:
High-dose vitamin B-1 has helped many here.
Generally speaking, most healthcare providers are not knowledgeable regarding this protocol.
MRIgFUS in Switzerland solved both for me.
And it cost Markbit?
Dont forget apomorph can work well too thtc.
Agree with Mark bit. I have zero dyskinesia and no and offs anymore. My bradykinesis is 80% less. A trial is starting for PTT by FUS in the US in April (the surgery we both had).
My father is being considered for DBS, after reading your experience I would like him to see if he qualifies for the PTT, thoughts on experience/ability for the trial affecting outcome over the team in Switzerland?
Team in Switzerland is always going to be better than someone with no experience. Plus they are awesome!
Thank you! Do you know time frame now, I see that you had your second side done not that long ago, thought you might know. He is 81, do you think age would disqualify him? We just came from his neurologist and she ok'd him for dbs but now we have this info...If I start checking into it do I just contact the clinic in Switzerland?
I had FUS in Switzerland and My dyskinesia is totally gone.
Excuse my ignorance but what is FUS?
Hi...what kind of dyskinesia did you have again?
Levodopa induced dyskinesia. Are there other types with Parkinson’s?
Sorry... I meant peak dose versus wearing off/diphasic
If you end up considering Dr. Costantini's high dose thiamine/vitamin B1 protocol, here is a link to all of the information which Dr. C left with the forum while he was able :
healthunlocked.com/parkinso...
Quite a few members on this forum use B1 and have reported good results. Good luck!
Art
After having Parkinson’s for 10 years, I had DBS surgery and it stopped the dyskinesia. There are other benefits too.
Can you explain the other benefits please
I do not have tremors any more and I don’t experience “freezing” either. I take much less medication. DBS surgery was great for me.
Is she sleeping ok or somewhat fitfully?
Sleeping is ok at present. Seeing her PD nurse Thursday to see id we can “tweak” the timing and dosage of ther medication
Hi thfc. I have been able to overcome most of my Pd symptoms. I have been Pd-Medication-free since 2002 I took Pd medication for 10 years. It is too much to tell you on this website, If you email me at johnpepper@telkomsa.net I well send you everything including videos at no cost. It is the only way I am aware of to reverse Parkinson's symptoms.