Thank you for this footage. I shared with the Navajo nation here in Northeast Arizona USA. I am considering I’m starting Parkinson’s advocacy with my tribe. Again, thank you and help you’re well.
I am in Maine in the USA - THANKS for this video. I was diagnosed almost a year ago but had symptoms for probably 3 years. It helps to see others and what they are doing about their PD, even if short & sweet. GOD BLESS.
Parkinson's can gate crash the most intimate of relationships . It's neither party's preference but drooling, bowel movement history, garbled stories delivered in a low, monotonous tone , and more are not the foreplay pleasures enjoyed by both of us in the pandemic era but maybe the vaccines Rollout will mitigate the worst effects here also. In the meantime , show Helen that there are many ways to skin the pussy ( deliberate play on words!!).... we are after all trying to alternate foreplayism now that I know that Helen and I are both in dread of giving in to Helenitis. We need help from lots of stakeholders but most especially from ourselves!
Hi Shane, you are doing a good job advocating research for Parkinson's disease on behalf of your mother. However, I have researched my own diseases and found the cause and cures and methods of preventing them in 350 million other patients but nobody in the media, e.g. the House of Wellness, ever interviews me, so others, who did nothing, take the credit. Perhaps you might like to watch my RU-vid video to learn why I don't publish my discoveries and treatments for other illnesses now, and maybe contact me for a talk. See my RU-vid videos about this here . . . ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-mxlIc7TKX0c.html and see a video about my interview with Sir Mark Oliphant in the 1980's here ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-hL07jv0jllk.html Max Banfield, Banfield Research
