The MS Society, 60 Year Anniversary. ~ Living La Vida Lola

The MS Society, 60 Year Anniversary.

If you have been reading my posts you will know that I am hoping to raise money Multiple Sclerosis. MS is a disease my father has had since he was 39, that’s 34 years ago, it’s a given that I would raise money for MS.

I am working with the MS Society to raise funds and awareness in what is their 60th Anniversary year. To follow is a little more about the disease.

MS takes many forms in the way it attacks the body and can progress at different rates. I will talk more about this later as it something I have lived with all my life with my father being diagnosed when I was 6 years old. For now here is a brief overview.

About Multiple Sclerosis (source MS Society)

  • Multiple sclerosis (MS) is a condition of the central nervous system
  • In MS, the coating around nerve fibres (called myelin) is damaged, causing a range of symptoms
  • Around 100,000 people in the UK have MS. It’s normally diagnosed in people between the ages of 20 and 40, and affects almost twice as many women as men
  • Once diagnosed, MS stays with you for life, but treatments and specialists can help you to manage the symptoms
  • We don’t know the cause and we haven’t yet found a cure, but research is progressing fast

This link is a copy of my MS Permission to Fundraise letter for anyone who wishes to validate.

Please Share to Help Us Grow!
Related Posts
No related posts for this content

About the Author

Thank you for visiting. I am first and foremost, a single mum to a beautiful daughter. ​The other hat I wear is an author who loves to travel and learn, inspiring others along the way. As a parent, I am driven to inspire my daughter through the world around us. I am very aware that life is short and I don't want to find myself looking at Lola at 16, thinking "wow, where did the time go!"

Leave a Reply 0 comments