A podcast for people affected by MS (Multiple Sclerosis) ...
MS stories, MS news, and coming to know you’re not the only one.
Whether you're newly diagnosed with MS, a fully-fledged person with disabilities or want to find out more about this chronic, neurological illness, this show's for you.
Hear from experts, influencers and patients.
The show is created by Bron Webster - she’s been living with MS for over 25 years.
This podcast is home of the MS ACTION TAKERS (R) . You can take action by being an MS Action Taker (R).
We’d love you to get in touch. Ask questions, comment about the episode, tell us what you want to hear by emailing at this address - hello@multiplesuccess.co.uk
The best way to spread the word about MS and the show is by rating and reviewing the podcast - it seems to increase the visibility.
May 27, 2020
This is the 2nd part to this interview.
Holly is a young person with Primary Progressive MS. Her diagnosis story is one of frustration.
She was aged 24 at her eventual diagnosis but she had to go to her Doctor 3 times and kept being told ‘there’s nothing wrong with you’.
Prof. Giovannoni from St. Barts in London...
May 26, 2020
Holly is a young person with Primary Progressive MS. Her diagnosis story is one of frustration.
She was aged 24 at her eventual diagnosis but she had to go to her Doctor 3 times and kept being told ‘there’s nothing wrong with you’. Using some great advice from her Personal Trainer, Holly was eventually sent by her...
May 20, 2020
The 2nd part of Rachael's story. Having just received a diagnosis of Primary Progressive MS (PPMS) - Rachael, now aged 53, answers the question “How is life with Primary Progressive MS?”After coming to terms with losing her job, stopping swimming and struggling to watch live Rugby League.
You can find Rachael...
May 19, 2020
Initially diagnosed with PPMS in 2018 - now aged 53 - Rachael Tomlinson is an MS force to be reckoned with.
Initially had a mini-stroke diagnosis in 2013 and went on to be diagnosed with benign MS in 2013 but never told. Used to have stressful job involving lots of travelling and hours. Fatigue was a massive problem -...
May 13, 2020
In this 2nd instalment of Grant's diagnosis story He reflects on the disease progression by remembering his stages of requiring walking aids.
A big advocate pf maintaining a positive outlook and having a reason to get up Grant remembers starting to use aids (sticks/wheelchair) before he actually needed to. This helped...