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Maria smiling at London Pride

Proud to be marching in Pride in London

On Saturday 1 July, we’ll be marching with our community in the Pride London parade to show our support.

We’re excited to be marching in Pride in London for the third time this year. We’ll be joined by our community and colleagues as well as other neurological charities. 

Our registration for the event is now full, thanks to everyone who signed up!

Black Pride 2023

We'll also be at this year's Black Pride event, taking place in Queen Elizabeth Olympic Park on Sunday 20 August 2023.

There's no parade to join at this event. But you can follow us on our Instagram and Twitter page to find out where we'll be.

Our commitment to equality 

We support Pride month because equity is at the heart of our mission to be there for everyone affected by MS.

Pride month is a celebration of how far LGBTQIA+ rights have come. But it’s also a time to look at the challenges LGBTQIA+ communities face right now. And the LGBTQIA+ MS community is no different.

Read more in our blog on health inequalities

Taking part in Pride is one of the things we do to make sure we're here for everyone with MS. You can read more in our EDI strategy.

What does LGBTQIA+ stand for?

LGBTQIA+ is an evolving acronym that stands for lesbian, gay, bisexual, transgender, intersex, queer or questioning and asexual. The + represents other terms (like non-binary and pansexual) that people use to describe their experiences of their gender or sexuality.

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Proud Pride

JJ reflects on what pride means to her. During Pride month and every day.

Woman with curly hair holding a mug stands in front of her garden fence with an orange rainbow behind her

Share your story

Just like MS, every MS story is unique.

We'd love to hear about your MS stories, from diagnosis to how you told loved ones and employers. Maybe you have found an interesting way to manage your symptoms or want to tell us about the challenges you have faced?

We're always on the look out for stories about life with MS to share with the community. So get in touch.

Share your MS story with this form