Grazie a tutti. I will try tell by myself my question.
Now I want know if anybody use fenilalaninaDLPA of Vitabasix and has any positive results for sintoms of P.D.
Grazie a tutti. I will try tell by myself my question.
Now I want know if anybody use fenilalaninaDLPA of Vitabasix and has any positive results for sintoms of P.D.
I haven't tried fenilalaninaDLPA of Vitabasix, but I believe in one of your other posts you were looking for alternatives to medicine for Parkinson's. I do non-contact boxing, which is helping to slow the progression. I'm sure it works similar to what John Pepper talks about with his walking. I started with Rock Steady Boxing (RSB) (a non-profit gym strictly for Parkinson's patients) a little over 7 years ago, almost from the beginning of when Rock Steady started and it has helped slow the progression and has also been a wonderful "support group" type thing because it's someplace I can go & not have to worry about what someone else thinks because everyone there has Parkinson's. Because the program is helping so many people, they are trying to reach out to the world and RSB now has many affiliates in the USA, as well as, one in Canada, Australia, and Italy. Your husband may want to check this out if it's close to you. Here is the information I copied for Italy from our website which is rocksteadyboxing.org
Rock Steady Boxing Como Lake (Italy) Address: via Bressanella 22030 Longone al Segrino Mobile +39 3487252279 Visit our Facebook page! facebook.com/RSBComoLakeItaly
Address: 22030 Longone al Segrino
Hope this helps.
Hi, laglag
I thank you very mutch, because I didn't know this boxing, but RSB isn't near my city.
You are very gentile (polite?). now my husband tries a little north walking, exercises for postura total body and therapy for to do anything of difficult ( es. to go to sleep on the bed ...)
I hope well for him , and hope the doc neurologo gives him few levodopa or change med , because in these latest times he has some allucinations (?) sorry for my english