Any one got any tips on DYSKINKESIA. as i... - Cure Parkinson's
Any one got any tips on DYSKINKESIA. as in hell at moment
My husband saw his consultant yesterday and he suggested evenIng out his
Current medication regime taking less amount in mgs and take more often.
Going to give it a try will let u know if it works x
Dyskinesia: Go on line and Google a request for info, is the best tip I can comeup with as I never heard of this condition before.
You might ask your Dr.about Amantadine Hydroxide genera name in Australia of Symetrel
I have been taking it for a number of years and it helps control the symptoms. is also DBS which if you are eligible is the best known alleviation for this condition...
Good luck
thank-you
I do! For me, I have had pd for 14 years...still living lifers full! Dyskenisa for me has been trial and error....I have found with sinemet as needed...1/2 dose 1/4 dose whole dose mix it up as needed...pray for treatment!
I know what you are going through. Mine was terrible until I reduced the strength of my Sinemet. Now that the disease has progressed, my doctor keeps me on as low dose of Stalivo and Mirapex as possible and up to now I haven't had any more dyskenesia. .But I don't know what will happen as the disease progresses and I require higher strengths. It seems to be a trade off - experience the worsening PD symptoms which for me are mainly gait difficulty - or improve my gait and suffer the dyskenisia. I'm hoping that regular exercise will keep me able to walk without increasing the strength of my meds but I really don't know how well that will work. I'd appreciate hearing from others about this.
Hi Export
My tip for you is Amantadine (Symmetrel) which I take as a preventative against dyskinesia (That is what I believe and given the power of the mind...) and have taken 100Mg twice a day for about 5 years (before I started Sinemet Plus) and now take them with my first two doses of Sinemet Plus. I also take Azilect -2MG - with my first dose. I have been diagnosed for nearly 11 years (in June) and don't have dyskinesia
Thank-you All of you