MS Society

Why I’m fundraising for MS Society

Charlie Bright

Charlie Bright

My Story

In 2022, at the age of 43, my sister in law Catherine was diagnosed with Multiple Sclerosis (MS). 

MS is an unpredictable disease that impacts the brain, spinal cord and optic nerves which make up the central nervous system and controls everything we do.   

The exact cause is unknown, but we do know that something triggers the immune system to attack the central nervous system in the body.  The resulting damage to myelin, (the protective layer insultating wire-like nerve fibers in our bodies) disrupts signals to and from the brain.  

The interruption of communication signals can cause unpredictable symptoms such as numbness, tingling, mood changes, memory problems, pain, fatigue, blindness and/or paralysis.   Everyone's experience with MS is different and these losses may be temporary or longer lasting.   

MS is most commonly diagnosed in people in their 20's, 30's and 40's although can develop at any age.   Its about 2 to 3 times more common in women than men and is one of the most common causes of disability in younger adults.  There is currently no cure for MS.   

Inspired by Catherine's courage and determination in the face of her diagnosis, I will be running the London marathon in April 2024 to raise money for MS Society.  They are a charity focused on funding world-leading research to find a cure and provide information, services and support so everyone can live well with MS. 

Any donation, however small is hugely appreciated.  Thank you so much in advance for your support!

MS Society

Raising for:

MS Society
51%

Funded

  • Target
    £10K
  • Raised so far
    £5,095
  • Number of donors
    138

My Story

In 2022, at the age of 43, my sister in law Catherine was diagnosed with Multiple Sclerosis (MS). 

MS is an unpredictable disease that impacts the brain, spinal cord and optic nerves which make up the central nervous system and controls everything we do.   

The exact cause is unknown, but we do know that something triggers the immune system to attack the central nervous system in the body.  The resulting damage to myelin, (the protective layer insultating wire-like nerve fibers in our bodies) disrupts signals to and from the brain.  

The interruption of communication signals can cause unpredictable symptoms such as numbness, tingling, mood changes, memory problems, pain, fatigue, blindness and/or paralysis.   Everyone's experience with MS is different and these losses may be temporary or longer lasting.   

MS is most commonly diagnosed in people in their 20's, 30's and 40's although can develop at any age.   Its about 2 to 3 times more common in women than men and is one of the most common causes of disability in younger adults.  There is currently no cure for MS.   

Inspired by Catherine's courage and determination in the face of her diagnosis, I will be running the London marathon in April 2024 to raise money for MS Society.  They are a charity focused on funding world-leading research to find a cure and provide information, services and support so everyone can live well with MS. 

Any donation, however small is hugely appreciated.  Thank you so much in advance for your support!