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v East Dorset and
The
MND is a neurological condition that
destroys the Motor Neurones and that in turn affects the muscles leaving people
unable to do the everyday things the rest of us take for granted. Walking,
talking and swallowing may become very difficult, yet the mind and senses are
rarely affected. The severity of the
disease varies from person to person, as does the speed of deterioration. There
are a number of variants of the disease.
For more information about the disease visit the main site at
www.mndassociation.org/life_with_mnd/what_is_mnd/index.html . At present there is no cure for this disease but
research continues into the cause of the disease, which someday may result in
treatment that may cure, or at least hold the disease in remission
We liaise with health and social care
professionals such as: Speech Therapists, Occupational Therapists and the
Medical Profession.
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Our Branch holds regular support meetings for people living with MND and their carers. These provide an opportunity to meet with other people living with the disease, and to share experiences and ideas. The 'Flash Movie' above shows group members from November 2003 to May 2008. It should be noted that on each occasion certain members of the group were not present for a variety of reasons. *** The next 'Get - Togethers' are listed in the table below ***
Fundraising and raising awareness are also very important aspects of Branch activities, and we organise several events throughout the year, which are well supported.. KEEP UP THE FIGHT Having MND can cause such awful strife But we must all remember To retain our zest for life! MND is different for each and every one But that does not mean to say We cannot still have fun. If we all support each othe And set our talents free We can still achieve a lot So, Thumbs Up …. Fight MND! Sonje Coldwell Triumphal parade through Moors Valley
Another ambition was achieved thanks to Aunt Audrey and the committee: I always wanted an open top tour through hordes of people pointing and wishing they were in our place. True we did not have the Gold medals and the crowds were toddlers who think any ride is exciting or young mums wishing for a few moments peace but anyone can dream! Our driver and guide Alan again skilfully navigated the bumps and hollows of the woodland and gave us an insight into the thinking and planning of the Forestry Commission. Disappointingly we did not stop to enjoy any of the climbing frames or playgrounds but there is always next time. As we moved smoothly through the crowds Len, as befits his South African background, rode “Shotgun” and Barbara led us in our version of the Royal Wave as we acknowledged the crowds parting like the Red Sea as we passed among them. Gil to my relief came (came out?) in a tasteful pink shirt and artfully engineered last place on the trailer planning I am sure to be first off and first into lunch. Steve Thorpe and Jack Burkitt added a certain gravitas and decorum to the occasion and Doug and Veronica Horton comported themselves well on their first outing with us. The usual crowd of camp followers and porters straggled in our wake valiantly keeping up with us as we ploughed on. Alan cheekily ruined the day of two golfers by parking directly behind them as they drove off. I doubt if they really intended to slice that much and the parting wave they gave us was ambiguous to say the least! The meal was substantial and filling and as always there was much jollity and humour. The weather was clement and we added another chapter to the epic tome “Adventures with Audrey” Mike Hardy ************************************************************************************************************************************ The East Dorset & New
Forest Branch is completely run by
volunteers.
We are always interested in hearing from people who can help with events or
who want to get involved with running the Branch. DONATIONS: If you would like to make a donation to enable us to continue to support those affected by MND, please send cheque payable to "MND Association East Dorset & New Forest Branch" to MND Association, Poole Advice Centre, 54 Lagland Street, Poole, BH15 1QG. All donations are acknowledged. For information about the work of the Association, and up to date information regarding the disease, care and research, please visit the National Office website at www.mndassociation.org. Care Information Service As from the 1st May 2007 the Care Information Service, including the Helpline, will be known as the MND Connect Team with it’s own logo and email address which is as below:
Email address: mndconnect@mndassociation.org If you have any questions regarding this service please contact Heidi Macloud on 01604 611871 
Motor Neurone Disease
Association
"Translations provided by WorldLingo"
Website updated on: Sunday, 09 November 2008
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