thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile
thenerveofmymultiplesclerosis

@thenerveofmyms

ID: 1539525587051626496

calendar_today22-06-2022 08:28:06

480 Tweet

88 Followers

272 Following

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We’re so excited to host an exclusive Cocoa Beans Dialogue for Ghanaian MS warriors this Saturday! 🎉 We can’t wait to connect and support these amazing warriors on their journeys! 💜 #MultipleSclerosis #MSAwareness #Ghana #CocoaBeansDialogue #supportgroup #ghanaianmswarriors

We’re so excited to host an exclusive Cocoa Beans Dialogue for Ghanaian MS warriors this Saturday! 🎉 We can’t wait to connect and support these amazing warriors on their journeys! 💜 #MultipleSclerosis #MSAwareness #Ghana #CocoaBeansDialogue #supportgroup #ghanaianmswarriors
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

She is so encouraging in the group and I love the way she utilised her contacts with a local radio station to raise awareness. Shortly after her interview people started reaching out to her reporting similar MS symptoms that she described so she advised they see a Neuro ASAP

thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

You see Racists will always exist but if the UK is truly serious about tackling it in all institutions in UK society it needs to police it in such a way that racists will be too scared of the consequences.

thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

"reflecting 8 years since my MS diagnosis! 🌟 I'm committed to ensuring Black voices in the MS community are heard and represented. Together, we're building a movement. #BlackMSCommunity #MSAdvocate"

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We’re working hard to support the Black MS community! 🌟 With more initiatives coming soon, we’re creating a welcoming space for those affected by MS from the black community, wherever in the world. Your support is crucial as we push for change and break barriers together. 💪🏾

We’re working hard to support the Black MS community! 🌟 
With more initiatives coming soon, we’re creating a welcoming space for those affected by MS from the black community, wherever in the world. Your support is crucial as we push for change and break barriers together. 💪🏾
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

🌍✨ The Invisible Cover Girls of MS! ✨ Black women, if you’ve ever felt alone or unheard in your MS journey, know that your voice matters! You are powerful and deserve to take up space. Let’s amplify our stories together! #InvisibleCoverGirls #MultipleSclerosisAwareness

🌍✨ The Invisible Cover Girls of MS! ✨
Black women, if you’ve ever felt alone or unheard in your MS journey, know that your voice matters! You are powerful and deserve to take up space. Let’s amplify our stories together!
#InvisibleCoverGirls #MultipleSclerosisAwareness
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

Life of a health advocate when you are fighting your own health battles is wild. One of my autoimmune diseases gives me very dry mouth and throat but with all the speaking jobs I have had I won’t be silenced #msawareness #ms #msfighter #neverstop

thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

8 years with Multiple Sclerosis (MS) today. Living with Relapsing-Remitting MS has its challenges, but it’s also taught me resilience and the importance of community. No known cure yet, but I’m hopeful for the future! Let’s raise awareness together! 💙 #MultipleSclerosis

8 years with Multiple Sclerosis (MS) today. Living with Relapsing-Remitting MS has its challenges, but it’s also taught me resilience and the importance of community. No known cure yet, but I’m hopeful for the future! Let’s raise awareness together! 💙 #MultipleSclerosis
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

🎉 I’m thrilled to announce that I, Natalie Busari, will be speaking at the MS Society's annual Carols by Candlelight event, sponsored by MetLife UK, at Westminster Chapel on Thursday, 12th December. If you’re attending, come and say hi! 🎄✨ #ChristmasCarols #MSSociety

🎉 I’m thrilled to announce that I, Natalie Busari, will be speaking at the MS Society's annual Carols by Candlelight event, sponsored by MetLife UK, at Westminster Chapel on Thursday, 12th December. 
If you’re attending, come and say hi! 🎄✨ 
#ChristmasCarols #MSSociety
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

There are approximately 150,000 people living with multiple sclerosis (MS) in the UK. I need to see ethnicity data because I want to understand the prevalence of MS in black heritage communities. It's a no-brainer for me. Differences in Diagnosis: There may be underdiagnosis or

There are approximately 150,000 people living with multiple sclerosis (MS) in the UK. I need to see ethnicity data because I want to understand the prevalence of MS in black heritage communities. It's a no-brainer for me.

Differences in Diagnosis:
There may be underdiagnosis or
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

We're on easyfundraising which means you can raise free donations for us when you shop online for Christmas! Over 8,000 retailers will make a donation to us on your behalf! Join today here: join.easyfundraising.org.uk/the-nerve-of-m…

thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

🇬🇭🌟 Historic moment in Ghana! The 2024 elections see John Dramani Mahama and Jane Naana Opoku-Agyemang as President and Vice President, showing progress in Africa. Proud of our Ghanaian roots, we support MS, NMOSD, & MOGARD patients. Together, we're stronger. ❤️💪

🇬🇭🌟 Historic moment in Ghana! The 2024 elections see John Dramani Mahama and Jane Naana Opoku-Agyemang as President and Vice President, showing progress in Africa. Proud of our Ghanaian roots, we support MS, NMOSD, & MOGARD patients. Together, we're stronger. ❤️💪
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

"Grateful for 2024! 🎉 Thanks to all who supported The Nerve Of My Multiple Sclerosis CIC. Ready to amplify underrepresented voices even more in 2025. Big thanks to Ocean Outdoor, Queen Mary University, and Media Trust. Here’s to a powerful New Year! 🌟 #MSAdvocacy #Inclusion

"Grateful for 2024! 🎉 Thanks to all who supported The Nerve Of My Multiple Sclerosis CIC. Ready to amplify underrepresented voices even more in 2025. Big thanks to Ocean Outdoor, Queen Mary University, and Media Trust. Here’s to a powerful New Year! 🌟 #MSAdvocacy #Inclusion
NHS Race & Health Observatory (@nhs_rho) 's Twitter Profile Photo

Today, we announce a new partnership with NHS England to improve diversity in patient access to genomic medicine in the NHS. Find out more about this here: nhsrho.org/news/partnersh… #NHSGenomics2024

Today, we announce a new partnership with <a href="/NHSEngland/">NHS England</a> to improve diversity in patient access to genomic medicine in the NHS. Find out more about this here:

nhsrho.org/news/partnersh…

#NHSGenomics2024
thenerveofmymultiplesclerosis (@thenerveofmyms) 's Twitter Profile Photo

🌟 Quick update! Our virtual winter forum is now set for 4th Jan 2025, 3-5pm GMT. Join us to hear our 2025 plans and connect with our incredible community supporting those with chronic neurological conditions. #MultipleSclerosis #ChronicIllness ❤️

Keir Starmer (@keir_starmer) 's Twitter Profile Photo

We're going further and faster to build the homes and infrastructure Britain desperately needs. Creating jobs across the country, making the dream of homeownership a reality, and delivering economic growth in every region. That's my Plan for Change in action.