Blogs

Latest blogs

How counselling skills and mindfulness helped after my MS diagnosis

24 Oct 2017 | Noor Jawad
Noor Remembering the world is a beautiful place may sound like a cliché – but I also think it’s something we don’t do often enough. How often do we really notice what’s around us, the colour of the pavement we’re walking on or the sounds as we cross the road? I only realised the benefit of noticing all the small happenings in my world after I was diagnosed with MS three years ago. Struggling with...

4 tips for autumn half term family fun

20 Oct 2017 | hmaunder
Autumn leaves Looking for autumn half term activities to do with your children? Read on! Four mums and dads living with MS share some great ideas for indoor and outdoor fun. Chloe and her kids get creative in the kitchen...

Under the microscope: the immune system after HSCT

20 Oct 2017 | Katie Roberts
Image credit: Chris McMurran, University of Cambridge Haematopoietic stem cell transplantation (HSCT) is an intense chemotherapy treatment for MS. It aims to stop the damage MS causes by wiping out and then regrowing your immune system, using your stem cells. >> Read more about HSCT The big question is – what actually happens after the stem cells are put back? We take a closer look. The rebuild After HSCT, haematopoietic stem...

Buy your MS Society Christmas cards

19 Oct 2017 | Hannah Paull
Photo shows Christmas card featuring kittens in stockings Buy our MS Society Christmas cards and help us stop MS. Our cards are now available online and in Cards for Good Causes shops around the UK. We have everything from fun, playful styles to more traditional Christmas scenes. Every year Cards for Good Causes sells charity Christmas cards at 300 pop-up shops all over...

MS Active Together: how I got back in the saddle

17 Oct 2017 | Rachael McIntyre
Rachael on a cycling trip Ever since I was little, I’ve always loved to cycle. I remember getting my first ‘grown up’ bike when I was 10 for Christmas. I loved that green bike! When I graduated from university, I bought myself a road bike and did some bike touring on Orkney and in Sutherland. Cycling was something I loved to do. So, as you can imagine, when I had a bad relapse and it affected my ability to...

6 weeks of action for MS

16 Oct 2017 | Babs Guthrie
Too many people affected by MS across the UK are having to fight for the treatments, care, and financial support they need. Now, more than ever - we need to speak up together. Right now there's a lot of talk about Brexit, but we need to make sure people with MS aren’t forgotten. We’ve come together over six weeks, to take action on key issues to stand up for people living with MS across the UK...

‘The financial assessment was really stressful’

13 Oct 2017 | Babs Guthrie
Photo of Edith in her wheelchair sitting at a kitchen table looking to camera Edith is 30, she was diagnosed with relapsing MS aged 16. She works full-time and receives social care for everyday essential needs. But getting the care she needs wasn't easy. “My MS started worsening about five years ago. I moved back in with my parents and they became my full time carers, helping me...

'I want a say in my care'

13 Oct 2017 | Babs Guthrie
Pam is 50, lives in Liverpool and has primary progressive MS. “Five years ago I had an operation and was sent home with a care package. I have had a care package ever since. I have two carers each morning and evening now. Carers are coming later and later I work four days a week in an accounts department for a hotel. The carers used to be very good about coming on time in the mornings...

‘I just struggled alone’

13 Oct 2017 | Babs Guthrie
Photo of David in his garden looking directly to camera David  was diagnosed with MS in 1996. He used to have a good social care package, but had to contribute a lot more after being financially reassessed in 2010. He put a stop to his care because of the stress caused by the financial burden.  “I remember being discharged from hospital and a social worker visiting me the...

‘My husband is at breaking point’

13 Oct 2017 | Babs Guthrie
Angela is 35 and lives with her husband and two daughters. She is a mother of two who was diagnosed with RRMS in 2015. This is her story. “Day to day the biggest challenge is my energy levels, which are very low. I’m mobile but I fall from time to time. I really need support with the domestic tasks, like laundry and cleaning. I don't have the energy to fight for...

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