Helen was diagnosed with Primary Progressive MS in 1997 when she was 37 years old. Being ineligible for any Disease Modifying Treatment (DMT) within the UK National Health Service, she began to explore holistic approaches to managing her condition. She discovered OMS in 2008 and has followed the programme ever since.
Helen lives in Conwy, a small, medieval town in North Wales. In 2017, she took medical retirement from the University of Manchester where she was a Professor in the Department of Art History and Cultural Practice. As an Emerita Professor, Helen continues to research and teach doctoral students. She also spends time hand-weaving and learning Welsh, the language of her ancestors. Helen has never taken medication for her MS and is committed to living well through active self-care.
Questions covered:
- Can you please tell us a bit about yourself, where you’re from, what you do, family, etc.
- Let’s understand a little bit about your MS journey – when were you diagnosed and how did you initially handle it?
- When did you discover OMS and why did you decide to follow the program?
- You’re a member of the OMS community with PPMS – can you shed some light on what PPMS is and what life is like with that specific type of MS?
- How does the OMS program fit into the realities of someone with PPMS?
- What are the biggest obstacles to someone with PPMS adopting the program?
- How do you personally suggest dealing with these obstacles?
- In your own experience with both PPMS and OMS, how do you measure progress?
- If you could articulate one specific outcome that five ago, looking forward, you can say you really wanted to achieve and which you’ve now really nailed through adopting OMS, what would that be and why?
- As someone with PPMS, what can you share with others that have PPMS that motivates or inspires you?
Useful links:
Follow Helen on Instagram
Learn more about Feldenkrais in the UK and globally
Coming up next:
On our final Coffee Break installment for 2020, travel to the UK to meet Alexandra Storey and hear how she’s helping do her part to ensure OMS has a successful outing on Giving Tuesday, all on Living Well with MS Coffee Break #12, which premieres on Monday, November 30, just one day before Giving Tuesday. And to our friends and community members in North America, Happy Thanksgiving!
Listen next

S5E35 Webinar highlights: Guide to the Overcoming MS Diet with Gillian Robertson and Ashley Madden


S5E33 Oils and Fats with industrial chemist Mike Newton
Add comment
I so appreciate Helen you mentioning the fact of how MS is portrayed on OMS. I do feel a bit excluded by it as well!
Hi Helen, you are the first person to describe something similar to my experience with PPMS - since 2009! Thank you thank you. I tried the Instagram contact but apparently you are no longer there? I'm in your time zone, near Lisbon, Portugal.
Please log in or sign up to comment.
Sign up or log in to leave comments
Already have account? Log In