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Well said Babesbrown.
Maybe PUK should be looking into things that improve daily life and living with the condition, rather than a cure, because I have heard all this for so many years I am almost at the point of cancelling my monthly direct debit to PUK because all the money that is sent from branches and individuals for research is getting us nowhere nearer a cure after decades.
With respect, PUK Admin on here always avoid the main issue and take up the side issue, with a referral to the helpline.
Well I agree with all comments here but the money needed for research is a major obstacle why are humans so stupid , spending trillions on killing machines when so many suffer I have left my brain to science though I only have 10 brain cells now at 66 so by the time Im 76 ill be left with 1 or 2, anyway we live brains to work out ways of defeating parky , also the odds of winning the lotto are 128000000 to 1,so imagine the scenario Im given a cheque for £124 000 000 which I will give £100 000 000 to Parkinsons research and the news comes through that a cure has been found as a result,, the shock stops my heart,,,good old sods law eh
The answer is simple!
Spending trillions on killing machines...massive profits for arms manufacturers.
No cure for Parkinsons....trillions spent on Parkinsons meds....massive profits for drug companies.
No wars...no profits.
Cure for Parkinsons.....no profits....and no huge CEO salary for head of PDUK.
How I wish it wasn't so.
Nnng, I am a thicko at times, I never thought of it like that but you are absolutely correct so we are doomed then, should I go ahead with this painfull toth extraction tooth tooth extraction or let some nutter ( rhymes with bump) extract my life as he annoys the NKs Chinese and Russkie into a showdown, I would rather miss the dentistry , so its armageddon then,, decisions decisions, at least it wiill cure evryones parky.
I'll feedback your thoughts and feelings on this matter to the relevant people in the organisation. If you'd like to discuss the matter of cancelling direct debits and your reasons with someone please let me know, I'll put you in touch.
It must be frustrating for some of you, I can see it. But I'm a moderator of these forums. I'm here to support you or answer your questions when I can. When I cannot and I feel you need to talk to either a Parkinson's nurse or an adviser, I'll remind you that this service is there. That is my job and I try to do it to the best of my ability. I understand that it is not always enough. We want what is best for the community.
Please let me know if you'd like to talk to someone about what's been raised here.
Thank you for your kind concern , I know some of my posts are a bit ranty ,is that a worn ,,, at times silly at others and scared at some developements and then of course there silly which I like, I tend to be silly in the morning from 7 30 until 1 00 1 30 ish then I begin to slide back slowly at first and no noticible by others but inside my head a small war is underway and its no quarter given, I press the boost on Ddopa and that halts pd in its tracks (for a while) but after 1hr or so it starts again and by now im tired, and the fights gone out of me the only thing is distraction,, ie this toplap, or constructive arguments but eventually its bedtime, then a new war starts in my dreams which are so gutwrenchingly awful I cant even write abut them here prostate and viscous back pain and NPS round off the average day for me, as I said thankyou for your kindness in a average day for me I find kind is blind in m mind, ,,,,a little silly still there ??
Kind Regards FED AND GREAT NEW YEAR to you kind young person