Going back 3 years from now, i had no idea what the next few months would involve, i had no idea, that i would lose all function of my limbs, that my skin would feel like it was crawling with beasties, that electric shocks would fire all over my body, and that life would never be the same again.

After 3 weeks in hospital, months of numerous appointments with physio to walk again, with occupational nurse to help mentally , and MS nurse to help emotionally, i get through life independently again. I couldn't do it without the help of my amazing 11 year old daughter, who has had to grow up quickly and makes up my tablets every morning. She is my motivation xx

 I still recieve on going monthly infusions to help keep relapses at bay, but this disease wont go away. Infact it will only get worse unless we raise as much as we can to help find new ways of treatment, or even a cure.

The thoughtful sister that i am arranged a skydive for my brother's birthday. The look on his face was not impressed..haha, so bribed him by saying ill do it with him and we'll raise money together for MS.

He's definitely excited and motivated now that it's for a great cause, and im hoping we raise as much as possible to contribute towards the amazing work being done already.

I hate asking for help in general, and to ask for money, well...no one likes that, but if everyone we know even donated £1, it would be very much appreciated. It can be done anonymously or you can leave a wee message. 

Please donate, and please also share.

Love, faith and hope.. Siobhan and Michael xx

The MS Trust could not continue their work without the support of donors like yourself. Thanks to you, they can continue to provide trustworthy information for everyone affected by MS and have a dedicated enquiry team who are a friendly voice at the end of a phone call or email. They are also able to continue to train MS specialist nurses and fund them in areas where they are needed most. Thank you for making a real difference for people living with MS today.