Hasan

Hasan hi people i was diagnosed with rr ms 2 years ago have raised so much money for ms so far, please continue helping to raise money by sponsoring me for a run in december a few pounds or whatever you may have, i thank all of you http://www.justgiving.com/Hasan-Ozkoc

Stella

Stella hello to everyone!!i am stella from Greece and i am really happy to be a member of this group:-) i was diagnosed with M.S 10 years ago and i have to say this..the only way to defeat M.S is to...1.BE HAPPY 2.STAY CALM AND 3.THINK POSITIVE!!!!!!!!YOU ONLY HAVE TO LOOK AT THE BRIGHT SIDE OF LIFE!!!!!!!

Tracey Hirst

Tracey Hirst Hi guys was diagnosed with R R MS nearly 6 years ago but try to stay positive. Have set myself a really big challenge by running or at least trying to run the LONDON MARATHON next April for the society if anyone would like to help me raise my sponsorhip I would be very grateful for any donations. All you need to do is go to www.justgiving.com/tracey-hirst thanks every penny helps xx

Ryan S Ward

Ryan S Ward Hey Everyone!!! Become a Fan, invite your friends, and JOIN THE FIGHT!!!Thanks for the Support!!!! One Mission. One Fight. Cure MS!!! www.facebook.com/MSRightNow

G.g. Bella

G.g. Bella Stay positive it's hard don't give in. GG Bella

Yesterday at 8:24am · Report
Katie Peach
Katie Peach
Well i will certainly agree with that... :)
Yesterday at 4:39pm
Hasan

Hasan http://www.justgiving.com/Hasan-Ozkoc Please please donate anything you may have to the MS Charity for the greenwich 5km run thank you

MS Society UK
New research has investigated the possibility that teenage obesity may be linked with an increased risk of multiple sclerosis (MS) in women. View: http://www.mssociety.org.uk/news_events/news/press_releases/obesity.html
Pat Blalock
Pat Blalock
I was stick thin as teenager...and have never been fat...
17 hours ago
Pat Blalock
Pat Blalock
PS...I don't say this as 'anti fat' comment! God knows there's enough obsession with 'being thin' in society...
17 hours ago
Matt Brooks

Matt Brooks
Hi everyone,
I am 30 and in Kent. I am part of the organising team for YUMS based in Kent (Young United by MS). We cover the whole of Kent and organise information and social events including pub meets across the county for young people up to the age of 40. We have around 80 members and offer support to all those affect...ed by MS. Our experiences and reasons for setting up was that old question when we arrived at a branch meeting or at a therapy centre 'Who are you here with?' We wanted something a bit different, aimed at young people, organised by young people...if anyone wants to get in touch for more information about what we do feel free to message me, visit our web page, join our group on facebook or all three!

Cheers,
Matt.

www.yums-ms.co.uk
Read More

Benjamin

Benjamin Hi there, im a 24 year old Immunology PhD student and my mum has had PPMS for the past 5 years. Unfortunately she is now completely paralysed and has 24hr care at home. If any young people from york / yorkshire who have been affected by MS fancy an informal meeting / chat then get in touch. Im hoping to set up a fairly regular event. Thanks. Ben

Shoshana Witcomb

Shoshana Witcomb Hey, I'm organising a pub afternoon in Brighton on Sat 14th November for local Young People with MS - check out the MS Society Young People Chat Forum for details! http://www.mssociety.org.uk/applications/discussion/view.rm?post_id=226

Wendy Taslioglu Was Lewis

Wendy Taslioglu Was Lewis
I am a Fibromyalgia sufferer and have been for 4 years. 2 years ago I was unable to walk and could do very little for myself. I had some intolerance testing in March of last year and the results came back with intolerances to Gluten, Wheat, Dairy and Yeast. After cutting out these my health has improved greatly. Also I... started having holistic therapies which has made me more flexible and comfortable. I also know many MS sufferers who have benifited from the same treatments. Due to this I set up a business organising Mind Body and Spirit Events and I have my next at Derby University on the 14th & 15th Nov. There are loads of stands with health related products and therapists who can give you advice on how to manage your pain with holistic treatments. If you would like to come along then please take a look at www.whitelightevents.co.uk for more information.Read More

November 4 at 11:23am · Report
Katie Peach
Katie Peach
Hi Wendy, your mind body spirit events sound great, would like to live nearer so i could come along. Im a qualified homeopath and run a small business, the remedies are a great help in symptom management. x
November 4 at 11:28am
Alice Ward

Alice Ward i dnt no y u av to b a fan coz im no fan if ne1 wants my ms they can av it. it goin for free

November 4 at 10:15am · Report
Matt Brooks
Matt Brooks
Hi Alice, I agree with your status....i was a member on the fb page and it told me I had to become a fan, it seemed a bit of a contradiction.....definately not a fan of it in the slightest but would just say that having got involved with MS based projects has made such a difference to my outlook on life and hit home the important things in life.
Sun at 12:27pm
Lotte

Lotte Does anyone know when we will hear what is happening with oral Cladribine or where I can keep track of its progress? Thanks!

MS Society UK

MS Society UK Stuck for ideas for Christmas presents? Our online shop is now open and taking orders. Do your Christmas shopping from home and support MS!

Source: www.mssshop.co.uk
Dylan
Dylan
Jacueline i too am in the position of whether to get the swine flu jab i not confident with it as no one no,s wat effects this could have esp.with people suffering from M.S do you not think that 2 flu jabs this yr alone is enough!!!!!!
Sat at 4:52pm
Carol Winterbottom

Carol Winterbottom Hi all, I'm very new to all this,I've been referred to a Neurologist with possible MS. Can anyone tell me what to expect. I've been on the website but thought it might help to get a first hand account. Thanks,Carol.

November 3 at 8:03am · Report
Graham Johnston
Graham Johnston
Get in touch with an MS therapy centre.I was diagnosed 3 years ago and the doctors didn't really tell me much. Where the MSTC Lothian have been brilliant with me and telling me things I need to know. And meeting other people with MS has made it feel like less of a lonely illness. Which it had been for me until this year.
Sun at 1:10am