Hello,

I’m here to share a story of strength, hope and positivity. Though I’ve recently been diagnosed with multiple sclerosis (MS), I’m approaching this challenge with optimism and a commitment to continue living life to the fullest. MS is an autoimmune condition where the body’s immune system attacks the protective covering of nerve fibers, causing inflammation and damage. It affects the central nervous system, which can lead to a wide range of symptoms such as difficulty with movement, balance, and even speech. MS has presented me with challenges, like struggling to walk for even five minutes unaided, climb stairs, and sometimes gather my thoughts, but I’m determined to face these obstacles and grow stronger each day. My ability to always say the right words or phrases has definitely led to some amusing moments, especially with Kev, who can’t help but laugh when I totally say the wrong words, especially when talking to Alexa or the dogs!

Despite these challenges, I feel incredibly grateful for the strength and resilience I’ve found within myself, and the love and support of my partner, Kev, our beautiful little boy, Arthur and some of our amazing family and friends. Every day, I am becoming stronger, learning how to manage the ups and downs of MS, and finding ways to live my life fully—whether that means taking it one step at a time or laughing through the little struggles.

Recently being diagnosed with MS has taught me the importance of raising awareness about invisible disabilities. It’s not always easy for people to understand what someone with MS or similar conditions goes through, especially since many of the challenges are invisible. I want to help change that by sharing my experience and encouraging understanding and compassion for the unseen battles people face every day.

I’m excited to take part in the MS Walk Manchester on Saturday, 17th May, walking the 10k distance. I chose this event because I get to do it alongside Kev, Arthur, and friends — and because Arthur’s pram is officially my favourite walking aid!

That’s why I’m supporting the MS Society. This organisation has been invaluable to me and countless others. They fund critical research, provide support and resources to people living with MS, and raise awareness about the condition. Their work helps those of us living with MS manage our symptoms, access treatments, and feel part of a community that truly understands our journey.

By supporting the MS Society, you are helping fund research that could one day lead to better treatments and even a cure. You’re also providing vital support to individuals like me, who are working hard every day to live our lives with MS, while striving for a future where MS is better understood and managed.

Thank you so much for taking the time to read my story and for supporting the MS Society. Your kindness will make a real difference and help improve the lives of many people living with MS.

With love and gratitude,

Becca 🧡🎗️