Re: Parkinson's Disease Society new local group
Good luck again... and let me know if I can help in any way: Yes I would say there is a great need for a support group, I personally don't have time to attened all meetings and so on: however I am more than happy to help in other ways.... I have books and so on, and maybe I could do some kind of fact sheet or something. pm me:
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Re: Parkinson's Disease Society new local group
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Hopefully the Observer are doing an article about Wendy Dwyer retiring as a County Councillor, and her helping to start this new group for Hyndburn and the Ribble Valley. |
Re: Parkinson's Disease Society new local group
I'd like to thank Taggy and Magpie for the kind book donation.
Hopefully this could be the start of a small lending library, where people can borrow books and hopefully glean useful information. I know when I was first diagnosed I knew very little about Parkinson's, and was only given a small leaflet, which was quite brutal in it's style, and left me more in the dark than ever. Knowledge is power, and I'll try to make sure as many people as possible have access to that knowledge. Thanks ever so much...and it was great to meet you both too.:) |
Re: Parkinson's Disease Society new local group
Your most welcome Garinda, it was lovely to meet you too. I dont know if you've read todays Telegraph or not, i've just looked at it now as i've got in the house, and theres a large article about a Clinical Research Study on Page 23, for which they are now enrolling. This looks very interesting, it says participants will receive:
Monitoring of their health as it relates to the clinical study Ongoing study-related medical care by Parkinson's disease medical staff. Investigational medication at no cost. There are certain criteria to qualify, which are mentioned in the article, and this and more info is available at:- Parkinson's Disease Study Might be well worth a look! Best Regards - Taggy |
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I spent part of last week taking part in a research programme for Dr.Leroi, to see how Parkinson's may make some people obsessive, and prone to gambling. Happily I've no desire to start online gambling, and as for being obsessive? Never.:D |
Re: Parkinson's Disease Society new local group
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Best Regards - Taggy |
Re: Parkinson's Disease Society new local group
Just a reminder to those members of Accy Web who've told me they are coming, or bringing someone, that the next meeting of the Hyndburn and Ribble Valley P.D.S. is tomorrow, Saturday 7th March, 11.30 am - 1.30 pm. in the Supper Room (1st floor but lift access) at Accrington Town Hall, and there'll be an informal Jacob's Join lunch.
I look forward to seeing you tomorrow.:) |
Re: Parkinson's Disease Society new local group
On behalf of the Hyndburn and Ribble Valley Parkinson's Disease Group I'd like to thank Hyndburn Borough Council, who have very kindly granted us £250.00 to help with the start up costs involved with running this support group for anyone who's been touched by Parkinson's.
Until we are able to raise more of our own funds this will enable us to run the group and not charge people for attending, which I feel is very important, as many people are living on a tight budget because of the illness. It also means we'll be able to let more people know we are there if they need any help or support from the PDS. My personal thanks to Cllr. Britcliffe, who alerted me to the fact that some help may be available if I applied to the council. The next full meeting is on Saturday 2nd May, in the Supper Room, Accrington Town Hall, 11.30am - 1.30pm. There is wheelchair access via the lift. For anyone who might be in the Ribble Valley there's also a meet and greet at the Rose & Crown, Castle Street, Clitheroe, on April 22nd, 7 - 9pm. A warm welcome will be extended to everyone at both events. |
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Re: Parkinson's Disease Society new local group
Apparently it's Parkinsons Awareness week next. There's an article in the Telegraph which makes you realise how you never know whats round the corner.
Good article G :) Former high-flyer, 44, tells of Parkinson's disease battle (From Lancashire Telegraph) |
Re: Parkinson's Disease Society new local group
Wowee .... :mosher: Good promotion for your group, and a small insight into your thoughts and courageous attitude to your condition .. love ya' to bits x
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Re: Parkinson's Disease Society new local group
The national Parkinson's Disease Society were looking for a few differing people to talk about their lives, so I volunteered, and have done a few interviews recently.
Camilla Sutcliffe, the health editor at the Lancashire Telegraph, was kind enough to let me mention the group, in exchange for me prattling on about my life, as part of an article she wrote for Parkinson's awareness week, which starts next Monday. Apparently there'll be a photograph to go with the article in the paper. There's one the photographer took of me looking wistfully out of a window, and another of me hanging from a branch, in which I look Oriental, and not unlike a Sumo wrestler. I hope they chose wistful, rather than me hanging from a tree.:eek::D |
Re: Parkinson's Disease Society new local group
Great write up G well done you for speaking so frankly about things:)
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Thank you. The headline's a bit cringe making, and not how I'd describe myself. She did a good job of making sense of me rambling on. Perhaps I did say about the wheelchair, but that's not what I meant. I was trying to stress the positive, and that I don't dwell on the future possibilities that may arise, and instead hope the medical research comes up with a cure, not only for PD but for other degenerative illnesses too. |
Re: Parkinson's Disease Society new local group
when we talked about this earlier gary you mentioned they took a few pictures of you in various poses and said how you hoped they wouldnt use the one of you looking like you were hanging off a tree
sorry mate but the picture got leaked :D http://img5.travelblog.org/Photos/48...angatang-0.jpg |
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