I suffer from the same condition as you and would like to thank you for sharing your emotions and ways to cope with it. Good luck and keep up this amazingly positive attitude! I've learned from you! Actually I'm giving a thought to set up some kind of blog myself. Gracias Clyde!! Rafa, Spain.
Because I've had familial tremors since I was a tiny child, I was told that I'm 4 times more likely to be diagnosed with Parkinson's disease later in life than any average person would be. Is that true? Another question: would any of the medications Clyde is taking help me-and more importantly, my father-whose entire body is affected by severe tremors? I don't know if I will ever have to fight this particular battle, but either way, I'm thankful for people like Michael J. Fox and Clyde Campbell. I admire them so much! Without people like them fighting hard for a cure, it may never happen. No one is more determined than people whose lives depend on it. THANK YOU! 💜
Hi Clyde. I Olso have parkinsons for the last 5years l have been on a plant based diet and l fill so much better try it for at least 6month no. Meat no dairy no eggs hope U fill better.
My adopted mother was diagnosed in 2017. She too is ALL plant based, but takes in collegen, she is SO MUCH better eating this way. Sending my best to you from Asheville, N.C.
THANKS for such a powerful and personal presentation! It was so informational and inspiring. As a person who was diagnosed with "probable" Parkinson over five years ago, it meant much! Prayerful for you, friend with the Aussie accent! Your family around you are your most wonderful support! Have you made a video of this? Making it available for an affordable amount?
My dad has it too. Other than Parkinson's, there are two other similar diseases called Huntington's disease and Wilson's disease. These two are fatal, meanwhile, with Parkinson's you can slow the progression and it is something you can live with. Every day more research is being done on Parkinson's and the brain as a whole, so we are making progress in medicine. He isn't a lost cause. It won't be easy all the time, but don't lose hope and just do your best to live in the present and enjoy your time with him. Here's the link to a video that's really helped me: ruclips.net/video/Hs-vPqfsO0Q/видео.html
What an amazing man. I wish him and his family the absolute best.
I suffer from the same condition as you and would like to thank you for sharing your emotions and ways to cope with it. Good luck and keep up this amazingly positive attitude! I've learned from you! Actually I'm giving a thought to set up some kind of blog myself.
Gracias Clyde!!
Rafa, Spain.
Wishing Clyde and all the a Parkinson suffers to find a cure soon 🙏🙏🙏
Because I've had familial tremors since I was a tiny child, I was told that I'm 4 times more likely to be diagnosed with Parkinson's disease later in life than any average person would be. Is that true? Another question: would any of the medications Clyde is taking help me-and more importantly, my father-whose entire body is affected by severe tremors?
I don't know if I will ever have to fight this particular battle, but either way, I'm thankful for people like Michael J. Fox and Clyde Campbell. I admire them so much! Without people like them fighting hard for a cure, it may never happen. No one is more determined than people whose lives depend on it. THANK YOU! 💜
Have a look at the M3~Travel device from www.maxwellmagneticmeds.co.za Will make a great difference in your life.
A remarkable man with a positive attitude, truly an inspiration! 👏👏👏👏
Hi Clyde. I Olso have parkinsons for the last 5years l have been on a plant based diet and l fill so much better try it for at least 6month no. Meat no dairy no eggs hope U fill better.
My adopted mother was diagnosed in 2017. She too is ALL plant based, but takes in collegen, she is SO MUCH better eating this way. Sending my best to you from Asheville, N.C.
THANKS for such a powerful and personal presentation! It was so informational and inspiring. As a person who was diagnosed with "probable" Parkinson over five years ago, it meant much! Prayerful for you, friend with the Aussie accent! Your family around you are your most wonderful support! Have you made a video of this? Making it available for an affordable amount?
Thanks very much for the inspiration ....
Thanks for posting!
Beautiful life lesson!
Wow, sending you well wishes and amazing results!
You are an inspiration!!
Nice pad. Best of luck to him.
if you have money anything is possible, but ppl without might not have a chance
At least you’re able to walk around
A wonderful video and so very inspirational .. Hope we can have follow ups * Sharing this video .
My brother was diagnostic with Parkinson and I am afreid to loose him
My dad has it too. Other than Parkinson's, there are two other similar diseases called Huntington's disease and Wilson's disease. These two are fatal, meanwhile, with Parkinson's you can slow the progression and it is something you can live with. Every day more research is being done on Parkinson's and the brain as a whole, so we are making progress in medicine. He isn't a lost cause. It won't be easy all the time, but don't lose hope and just do your best to live in the present and enjoy your time with him. Here's the link to a video that's really helped me: ruclips.net/video/Hs-vPqfsO0Q/видео.html
Hi, I have Parkinson’s and it was so bad that I have to get the DBS have you ever considered the surgery?
Hi, how did the DBS work for you? Much improvement? My father has severe Parkinon's and unfortunately his DBS surgery didnt really help him too much
sorry, did not mean to post so many copies
Don't feel like you are a lot cause I have two people in my family that has Parkinson.
Me too 4 years yes so did I yes it does yes it's a shock oh yeah what cure you are the exactly as me my is left
Hi Clyde, hope you are doing well, look into GLYINE
Parkinson'
......
sorry, did not mean to post so many copies
sorry, did not mean to post so many copies