Our ambassadors

Oritsé is best known as the founding member, and one quarter of boy band JLS. Raising awareness of multiple sclerosis is a cause close to his heart, having grown up as a carer himself after his mother was diagnosed with MS when he was just 12 years old.

Promoting a better life for people living with MS has been on Oritsé’s agenda for a long time. As a child, he vowed to his brother that he would become a musician and use the money he earned to fund his brother’s ambition to become a biomedical scientist or a doctor with the aim of treating MS. Incredibly, both brothers have achieved their goals. Oritsé’s successes have seen him attain 2 Brit Awards, 5 MOBO Awards and earn international acclaim, meanwhile, his brother continues to work in his mother’s honour - but the fight against MS goes on. 

Oritsé’s own story and his support of the MS Trust will help to raise vital awareness of just how devastating MS can be on an individual and their family. He is expertly placed to highlight just how important it is that people living with MS receive the specialist support they need and deserve.

Oritsé said of the partnership:
“I’m really excited to be working with the MS Trust to help raise awareness of MS. So many other illnesses get given the spotlight and people don’t understand just how varied and debilitating MS can be".

Oritsé's links
- Twitter(X)  / Instagram / Threads

I am a writer for The Times and a frequent broadcaster on Radio 4 and Times Radio. My connection to multiple sclerosis is that my mother, Edith, had primary progressive MS for 22 years. She was braver than anyone I'll ever know, but it was a long road. I saw firsthand her challenges with kit, with mobility, with care, with stigma, and with pain management. I saw the impact that MS can have on families, too, not just in terms of strain but also in the way it brought us all much closer together. So I couldn't be more delighted to help raise awareness in any way I can.

Hugo's links
- Twitter(X)  / Times / Threads / Instagram

I am a video journalist working for the Guardian. I was diagnosed with relapsing remitting multiple sclerosis in 2010, which mainly affects my mobility. My work tries to help increase disability visibility through his reporting. In 2022 I made 'A sceptic's guide to wellness', a video series for the Guardian which looked at my own experiences with CAM therapies in relation to autoimmune conditions like MS. I am delighted to be on board as an Ambassador.

Richard's links
- Twitter(X)  / Guardian

I have been an MS specialist physiotherapist for almost forty years. I am, first and foremost, a clinician but during that time I have collaborated with the MS Trust, the MS Society, NHS England, the Neurological Alliance and the Neurological Academy to work towards increasing health professionals’ knowledge about MS and creating better services for people with MS, their families and carers. I was a member of the NICE Guideline Committee for MS in 2014 and was also co-chair of Therapists in MS (TiMS) for six years. During that time, I led on developing a comprehensive MS Skills and Knowledge Framework for physiotherapists and occupational therapists. I lecture widely and am involved in MS research projects around the UK. I am passionate about education, improving services for people with MS and especially giving more people access to and retaining specialist therapists. I am honoured to be asked to be an Ambassador for the MS Trust.  

Wendy's links
- Neurology Academy

Hi, I’m Liam Senior, and I’m proud to be an MS Trust Ambassador, as well as a passionate advocate for the MS community. Since being diagnosed with Multiple Sclerosis, I’ve made it my mission to use my experiences to raise awareness, share insights, and support others living with MS. Through my YouTube channel and Instagram, I create content that includes personal stories, tips on managing MS, mental health advice, and interviews with experts. My goal is to build a safe space where people with MS can connect, learn, and feel less alone.

I'm originally from the North West of the UK, but have spent the last 11 years in Teesside in the North East. I am married and have two children, aged 3 and 5. Before MS, I regularly played ice hockey and played numerous musical instruments, both things I am trying to keep my two in with, but having MS makes it difficult. 

I’m committed to empowering others, fostering a sense of community, and bringing hope to everyone affected by MS. By sharing my journey with honesty, humor, and education, I aim to help my audience navigate life with MS, one step at a time

Liam's links
- Instagram / YouTube 

I’m a professional musician and theatre director. I was diagnosed with RRMS in March 2014. I was heading out on my first sold out UK Tour with my band. It took a while for it to sink in with me that I had MS. I knew about it because my Dad also suffers from it. One thing I really try to do is try to make people aware that it isn’t the end of the world once you’ve been diagnosed. Trying to have a positive outlook makes such a difference. It’s a slippery slope to get out of once you go down there. I’m hoping that by being an MS Trust Ambassador I can help people realise that it isn’t a death sentence and that no one is alone in their journey 

Nigel's links
- Instagram / Twitter / Spotify 

I've been an active patient advocate in MS and chronic illness since being diagnosed with relapsing MS in 2008. My diagnosis was a disempowering experience and I didn't want this to be the case for other people.

I started to volunteer with various MS organisations in order to help inform, raise awareness and support the community. This has involved all sorts of things, from writing newsletters, to sitting on steering committees, to speaking in the media. I have been especially active within the Asian community, where MS is not well known or understood.

Now, I work full-time in patient engagement and advocacy, both in MS and in many other health conditions. I work with the NHS, clinicians, pharma companies, digital health companies and others in the UK and all over the world, to better embed the "voice of the patient" into their work. It's become my whole life and has led me to experiencing some amazing things that have enabled me to put MS on the map. One of the most memorable was being chosen to participate in a special edition of Strictly Come Dancing in 2015 on the BBC because of my advocacy work.

I'm delighted to become an Ambassador for the MS Trust and through this role hope to continue to support and raise awareness of the invaluable work it does for the MS community

Trishna's links
- Twitter(X) / Instagram / Facebook

I am an illustrator and a passionate activist for disability rights. My artwork has graced the platforms of organisations like Greenpeace, the UK Parliament and The Guardian, serving as a way to illuminate the often-unseen realities of individuals living with conditions such as MS.

In 2019, my life took an unforeseen turn with a diagnosis of Relapse-Remitting MS, a journey that began after a brain injury sustained in an accident. This diagnosis became a catalyst for myr exploration of illustration and art, a creative outlet I turned to when I was unable to work due to my health.

From my personal experiences with chronic illness, I draw inspiration to uplift and support others navigating similar challenges. Through my unique blend of words and artwork, I offer a message of solidarity and resilience, reminding individuals facing MS and other chronic illnesses that they are not alone.

As an Ambassador for the MS Trust, I hope to bring my distinctive voice and perspective to the forefront, championing the cause with creativity, resilience, and unwavering dedication, and fostering a sense of community and understanding among those impacted by MS.

Ananya's links
- Main Site  / Twitter(X) / Instagram 

I'm a seasoned neurologist with over 14 years of experience in the field of multiple sclerosis. I want to use my knowledge and a pioneering spirit to transform the lives of those living with MS. As the lead for Multiple Sclerosis at CRN South West Peninsula, my research initiatives include the nationally recognised MS Infoflex management tool, the Connect Plus App, and the MS PKB platform. As a consultant neurologist at Torbay and South Devon NHS Foundation Trust, I successfully implemented the Healthy lifestyle MS group clinics, empowering patients to take control of their own health and well-being. My contributions were honoured with the prestigious international MS Brain Health Team award in 2022. I am also the founder and host of the #BeewellwithMS healthcare podcast, where I hope to inspire and educate on a global scale, sharing expert insights and revolutionising the approach to MS management.

Agne's links
- YouTube  / Twitter(X) / Instagram / BeeWellWithMS

I'm Daniel. I was accidentally diagnosed with multiple sclerosis in 2015, and subsequently retrained as a doctor. I'm all about breaking the stigma; spreading awareness and pushing boundaries. Advocating for life with chronic illness. Inspiring. Achieving the unachievable.

Daniel's links
- Instagram / Facebook