Carla Callaghan

This year for MS Week we got loud for MS specialist nurses, and the fantastic work they do across Scotland to support people with MS.

An MS specialist nurse explains what her work involves and how she supports people with MS to live well.

I have been an MS specialist nurse for three years. Before me, there was no MS nurse service in this area of Scotland, so I've had the opportunity to create a service that best fits the needs of this remote and rural MS population.

Zoe was just 16 when she was diagnosed with relapsing remitting MS. In part two of her blog series, she talks about the journey to finally reaching a diagnosis.

Aaron Solowoniuk, drummer for Canadian band Billy Talent has been living with MS for over 15 years. He speaks about diet, exercise and his aims to drum again following a relapse.

Zoe is an 18-year-old student who is writing a blog series on what it was like to be diagnosed with MS at 16 when she was about to sit her exams.

There is a real opportunity to change the disability benefits system and create something new which has dignity and respect at its core.

Former marine Paul Kerr writes about his shock MS diagnosis and how a positive outlook has helped him grab every opportunity.

In his first ever blog, Scott discusses taking part in Tough Mudder not long after being diagnosed with multiple sclerosis.

Colin Barclay gives some advice on training for walking events after taking part in the Aberdeen Kilt Walk where he raised over £1100.

Hannah Lithgow talks about taking part in her first triathlon and how she and her mum have raised over £4,000 through various events.

Gail Sutherland says her first Loch Ness Marathon 10K was ‘nerve-racking’ but considering her MS had meant Gail needed to use a wheelchair, we think she’s nothing short of an inspiration!

Mum-of-three Jenny Potter writes about living with Primary Progressive MS (PPMS), her family and how she'd like to find a job again.

My name is Derek McCambley, and I was diagnosed with relapsing remitting MS in 2005.