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Raising funds for multiple Sclerosis |
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We had a nice E-mail today off a Tania Morrison, a high school English teacher from Green Mountain School, Vermont, U.S.A.
My name is Tania and I am a High School English teacher. Currently, my students are writing research papers on various health conditions. Some of them have chosen to write their papers on multiple sclerosis. In their research, they came across your page ( http://www.jays.org.uk/links/Links.html ) and found it to be very helpful. Thank you for maintaining a great resource! In their research, they also found this informative, well-organized article on multiple sclerosis ( http://www.worldmedassist.com/a-medical-guide-to-multiple-sclerosis/ ) and they would like to suggest it to you to add to your page as an additional resource because they feel it would be helpful and of interest to the visitors of your page. Also, if you do find the article to be useful and decide to add it, they will be awarded extra credit for researching and finding a good resource on the Internet (a little extra credit opportunity I give them). It would be very encouraging for them to see their suggestion being used on your page because they have been putting a lot of time and effort into this research project. Thank you for your time and consideration. I hope to hear back from you soon so I can give my students a verdict : ) Kindest Regards, Tania Morrison
It`s nice to know we are being of help in more ways than one. I like the Schools ethos as well. Check them out click here: I have added thier suggestion to the links page. Burns night malt whisky tasting.
Another great night of sampling malts, the favourite was the Talisker. More details in past events.
Ainsley Harriot is this years face of `Cake Break`
If you have any unwanted present that we could use on our tombola or for raffle prizes, then J.A.Y.s would be very grateful for them, and we promise not to tell !
Article in todays paper
The MS Society has released a new exercise DVD for people with multiple sclerosis (MS) presented by former Olympic champion Sally Gunnell OBE. The exercise programme contains a range of simple, gentle exercises and stretches that can help people with varying levels of disability strengthen their muscles and feel fitter. A warm up is followed by a range of exercises – including squats, pelvic tilts, lunges and shoulder rotations – all demonstrated by Sally and people living with MS. For most of the exercises, there is an alternative option for people who have difficulties with mobility or balance or who are exercising in a seated position. And it`s free.
YAHOO! We have had a bit of trouble with our Yahoo search engine of late. So please use our Yahoo search engine as much as you can because it generates money for JAYs. You cannot just do random searches, you have to click on a result for JAYs to benefit. We get about 5p a click, it does` nt sound a lot but think how many searches you do a week, it soon adds up.
Transport For those people who have problems getting about, Worcestershire transport partnership has a booklet giving details of various schemes throughout the county. Most of the schemes rely on volunteers to deliver the service and there could be one for you. For instance there is the Upton shuttle, Teme hopper-Tenbury wells, Suckley community cars, Redditch dial-a-ride, Worcester wheels, Evesham community cars and lots more. To get the booklet or further information, contact: Community transport partnership project officer, C/O Worcester volunteer centre, 33 The Tything, Worcester, WR1 1JL Tel: 01905 24741 E-mail: enquiries@wvc.org.uk |
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Glad to be back but now for a busy next month with tombolas!
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Went to collect the shaker tin from the Wine Cabin last Thursday and was informed that it had gone missing. The manager in the shop made some inquiries for us and apparentley a woman went into the shop with false ID and stole the shaker.
We have informed the police and they will make some inquires.
It`s a sad world we live in.
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WANTED
Anything we can use on a tombola. Only new stuff or in very good condition. Sorry to be particular but we want to attract the punters.
If you help us and our cause please drop us a line E-mail
We have four tombolas we are doing at the moment, so we need more items.
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Great news
JAYs have been chosen as the charity at this years CAMRA`s beer festival. We had a great time the last time we did it and are looking forward to this year.
Bromsgrove rugby club,
Finstall Park, Finstall, Bromsgrove, Worcestershire, B60 3DH
30th June, 1st & 2nd July
More details in events. Hope to see you there.
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The M.S Society is running it`s cake break fundraiser again this year.
A yummy way to raise funds for M.S on Friday 20th May.
Click on the picture to register with the Society and get your info pack.
It`s easy to do, just bake a few cakes and invite a some friends round or take them to work to sell.
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We have applied today to be the Bromsgrove beer festival charity.
We had a great time at the last festival, made some new friends and made some money for M.S, so fingers crossed we will be chosen again.
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Collected £21.83 from the shaker at Cofton Nursery.
Thanks to everyone who put in.
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Research.
Scientists at the university of Cambridge found a way of reversing damage to myelin using stem cells. This work was funded be the MS Society.
They have now commited £2 million over five years to fund the second stage.
The first stage found a drug that could potentially repair myelin, in stage two they`ll :
~ test this treatment
~ trial it for safety
~ Build on recent advances in myelin repair research.
Work starts in April and will finish in 2016.
The M.S. Society has raised over £28 million in 2010. Of every £1 spent, they spend 84p directly on beating M.S.
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The M.S Society has now become a charitable company on 1st February 2011. They have a limited company number and a new registered charity number.
The legally registered name is now Multiple Sclerrosis Society, no longer called The Multiple Sclerosis Society of Great Britain and Northern Ireland. They will still use MS Society, and national versions will remain in use ( such as MS Society Scotland )
The society took the opportunity to make things simpler and thought it did not reflect how they operate in all four nations.
Being a limited company and a charitable company meant they had to become a new entity and also have new charity numbers.
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Great, I`ve sold another two sets of Beer pump clips on E-bay, so a bit more money for our cause.
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Jackie likes to do a bit of knitting, she has knitted different squares, sewed them together to make a couple of cushions.
She sent the idea off to Take a Break magazine and they published a photo of the cushions.
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A lady called Sonya saw this article and wrote to Jackie a letter last week asking if she would do a few squares as she is having a charity knit for the local hospital. The hospital looked after her grandson when he had Spinal Muscular Althrophy.

The squares Jackie knitted and sent off to Sonia.
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I`ve put a new game in the games section.
Test your geography.
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Great, we`ve sold five sets of beer pump clips and a resin drum major on E-bay.
We made £22.81
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Another button installed `What is MS?`
We had a Guestbook message left by Darren, who said he had a friend with MS and he had learnt a bit more about the disease after looking on here.
I thought I would put a brief explantation of what Multiple Sclerosis is on here and a link to the societys web-pages for anyone else wanting a bit more information.
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A nice lady was talking to Jackie & Yvonne at the Christmas tombola saying that she was moving house soon. They asked for anything that she didn`t want to take to her new house for our tombola or a boot sale.
I have been today to collect various items and back on Monday for a few more, so a big thank you to Lynn and Richard for their kind donations.
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You may have noticed that I`ve added two new buttons to the list on the left.
To try and make the front page less messy I have now added a archive button to put all the old stuff and I`ll try and keep this more interesting.
Also a JAYs photo button, if you see JAYs anywhere, take a pic and sent it to me and I`ll put it on that page giving you the credit, just for a bit of fun.
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A new website that may be of intrest to you. I will put it in the links as well.
Anyone interested in the world of CCSVI ( Chronic Cerebrospinal Venous Insufficiency) from Surgeons, Doctors, Consultants to patients with MS, ME Chronic Fatigue etc; are all welcome
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Collected the shaker before it closed for a refurb, thanks to everyone who put in.
£55.20
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Burns night Malt tasting
A great night with almost a full house. details in past events.
· An estimated 2,500,000 people in the world have multiple sclerosis - including 100,000 in the UK - it is more common in countries further away from the equator
· MS is the most common potentially disabling disease of the central nervous system affecting young adults in the Western world
· Every week around 50 people in the UK are diagnosed with MS
· Diagnosis is usually between 20 and 40 years of age - rarely under 12 or over 55
· Three women have MS for every two men
· Prognosis is uncertain - ranging from benign through 'coming and going' to severely disabling
· Common symptoms include pain, deadening fatigue, problems with sight, mobility and co-ordination
· MS is not hereditary - but there is a slightly higher chance of getting it if a relative has it - and it is not contagious
· There is no cure for MS but there are now drugs which can modify its course for some people and many symptoms can be successfully treated or managed
· MRI (magnetic resonance imaging) is giving neurologists better understanding of MS, helping diagnosis and research into treatments
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