The-MS-Fund-logo

Support for People Affected by Multiple Sclerosis

The MS Fund was created to raise funds and awareness to support individuals and families impacted by Multiple Sclerosis.

OUR STORY

About The MS Fund

The MS Fund was created from my own experience of watching my Dad live with Multiple Sclerosis & the challenges he has faced.

He was first diagnosed at the age of 26, the year I was born, but for many years his symptoms were minor and had little, if any impact on daily life.

That changed around the age of 43, when problems with his legs began. Over the years his mobility got worse & by the age of 55, he lost almost all mobility, only being able to turn his head and move his left hand slightly before it tires.

Seeing how this progressed over the years has shown me how deeply MS affects lives, and it’s what drives my commitment to helping others facing the same challenges.


 

OUR MISSION

To make a difference

The aim of The MS Fund is to support people living with MS in any way it can whether that be by raising awareness, helping to fund essential equipment and aids that promote independence and daily living or contributing to MS related causes and research.

Raising awareness
Fundraising
Equipment/aids
Supporting MS research
ABOUT MS

What is Multiple Sclerosis?

MS is a lifelong condition where the immune system attacks the protective coating (myelin) around nerves in the brain and spinal cord, disrupting signals and causing varied symptoms that can come and go.

It’s different for everyone:
symptoms and severity vary widely.

Types of MS:
relapsing‑remitting, secondary progressive, primary progressive.

Common symptoms:
fatigue, numbness/tingling, mobility or balance issues.

Muscle and movement:
stiffness, spasms, weakness or tremor.

Thinking and memory:
“brain fog,” slower processing, concentration dips.

Bladder/bowel changes:
urgency, frequency or constipation.

Sensitivity to heat:
symptoms can temporarily worsen in heat.

Vision problems:
blurred or double vision, pain with eye movement.

Treatment options:
disease‑modifying therapies and symptom management.

Support matters:
physio, occupational therapy, mental health and peer support help people stay independent.

Information here is for awareness only and not a substitute for medical advice. If you’re worried about symptoms, speak to a qualified professional.

Fundraisers

This page is where we celebrate everything your support makes possible. From current campaigns to past events, every donation and every effort helps us move closer to our mission of supporting people living with MS.

Current Fundraiser
Goal Reached 65%

Get Involved

DONATE

Every penny counts

To ensure every penny helps people with MS, please donate by bank transfer or standing order if possible — card payments include processing fees & will come off the total donation amount.

Sort code: 60-40-09
Account number: 42512867
Reference: Donation (If for a specific fundraiser, please put Donation – ‘Fundraiser name’)
JOIN OUR FUNDRAISER

Take part & help us reach our goal.

25 miles till Christmas!

For our first fundraiser & to get in to the Christmas spirit, we will be running 25 miles from December 1st until Christmas Day to try and raise awareness & donations.

Get involved whether that’s joining in the run (or walk) or sharing the message across social media. Get in touch & share your progress!

 

VOLUNTEER

Create your own fundraiser

Want to create your own fundraiser with our support? Get in touch and we’ll help with planning, branding, donation links, and promotion.

  • Share your idea (walk, run, quiz night, coffee morning).
  • Spread the word wherever you can.
  • We’ll help provide guidance, support & share your fundraiser across our channels.
SPREAD THE WORD

Follow & Share

Support our mission by following us and sharing our message.

CONTACT

Contact Us

Questions, ideas, or support requests? We’d love to hear from you.

info@themsfund.co.uk

08000 337 235

The MS Fund