Top Tweets for #worldmsaday
Join us and participants around the world as we mark World MSA Day today. Let's raise awareness for Multiple System Atrophy and honor the patients and all those affected by this disease.
#WorldMSADay #MSA #MultipleSystemAtrophy
For too long, #multiplesystematrophy (MSA) has lived in the shadows. On #WorldMSADay, we rise above the noise to fund vital #support & #research. Your gift makes an immediate difference. Donate: https://t.co/w1tpiiHIDe.
Never heard of #MSA? Learn more: https://t.co/SsVme97lQl
#WorldMSADay is just one week away!
Your #support funds critical initiatives like our #advocacy efforts, #MSA #research progress, 31 #MSACentersofExcellence, and so much more.
Be a part of the #impact:
#Donate: https://t.co/tY5OaOMYfO
Reminder: https://t.co/pHWzYecOh5
Today on #WorldMSADay, we raise awareness for those impacted by multiple system atrophy. Thank you to everyone supporting our Path to a Cure 5K, whether in Dallas, Chicago, or virtually! Every contribution brings us closer to a future without MSA. Donate: https://t.co/wIYjMCIvDo
Today is #WorldMSADay, a time to raise awareness about #MSA, a neurodegenerative disorder often misdiagnosed as Parkinsonβs disease. Eye movement monitoring could offer hope for better diagnosis and care. Let's work towards improved outcomes for MSA patients!
Today is #WorldMSADay A day to raise awareness of multiple system atrophy. We want everyone to know about the support available to those affected by MSA and our work towards a world free of MSA.
Share this post to raise awareness of MSA and to help ensure no one faces MSA alone.
Today is #WorldMSADay A day to raise awareness of multiple system atrophy. We want everyone to know about the support available to those affected by MSA and our work towards a world free of MSA.
Share this post to raise awareness of MSA and to help ensure no one faces MSA alone.
today is Oct 3rd, which is also #WorldMSADay. MSA is a rare, degenerative disease similar to Parkinsons except it effects ALL systems. There is currently no cure, and no known cause. While it is only found in about 5/100,000 people, that is 5 too many. (est. 50,000 people effected in the US)
I would never wish the pain of watching the people you love lose their independence. But if this ever happens to you or your loved ones I hope you have hope. I hope you have options. I hope you have resources. I hope you have doctors who are familiar w/ this disease. And all that begins w/ awareness.
In web3 we value rarity. but in the real world, rare diseases don't get enough attention. Tell the people you love that you love them <3
&& as always ty to everyone who donated to @MSACoalition earlier this year + supported the OE I did with my dad. Updates on that soon π
On #WorldMSADay #AskBio joins advocacy groups like the @MSACoalition to shine a light on #multiplesystematrophy as we continue to investigate potential #genetherapy treatment opportunities. Click the 'learn more' link to watch their educational video.
Today is World MSA Day! Join us in spreading the word about Multiple System Atrophy and making a difference.
Click here to learn more about MSA: https://t.co/PzmkjkUZxU
Click here to donate: https://t.co/2QOpPK6l7s
#multiplesystematrophy #msaawareness #WorldMSADay
Together with Theravance Biopharma, we pay tribute to the MSA community on World MSA Day!
#defeatmsa #kickmsa #theravance #WorldMSADay
For our final post of #WorldMSADay we wanted to share this video created by our member Kenneth outlining his experience with MSA and the Trust - https://t.co/MVpGWFDwot (1/2)
Happy #WorldMSADay! Today we celebrate the incredible strength & resilience of those living with MSA, the unwavering care & love provided by caregivers & the critical contributions of individuals who participate in clinical trials. Your collective strength inspires us every day.
Today is #WorldMSADay - a day to raise awareness of multiple system atrophy worldwide & collaborate with other organisations like @MSACoalition towards a world free of MSA.
Please share this post to raise awareness of MSA and to help ensure no one has to face MSA alone. #Share
Today is World MSA Day! Join us in spreading the word about Multiple System Atrophy and making a difference.
Click here to learn more about MSA: https://t.co/PzmkjkUZxU
Click here to donate: https://t.co/2QOpPK6l7s
#multiplesystematrophy #msaawareness #WorldMSADay
In honour of #WorldMSADay our CEO Karen Walker refelcts on what has happened at the Trust since the last World MSA Day.
Read Karen's blog here - https://t.co/UaKY4qGkbz #ShareRepost
Today is #WorldMSADay - a day to raise awareness of multiple system atrophy worldwide & collaborate with other organisations like @MSACoalition towards a world free of MSA.
Please share this post to raise awareness of MSA and to help ensure no one has to face MSA alone. #Share
Our @UHP_NHS colleagues can find out more about MSA by checking out our display board on Level 10 #WorldMSADay
Tomorrow is #WorldMSADay so we wanted to remind people that membership of the MSA Trust is open to anybody, regardless of where in the world you are living.
Find out what we can offer our international members by visiting our page for Non UK Residents - https://t.co/hyZcBdaigb
In the lead up to #WorldMSADay on the 3rd of October we will be posting about work we have done & ways you can get involved. Today we wanted to share some of the results from our most recent MSA Needs Survey #ShareRepost
Today is #WorldMSADay - I miss my Mom every day. With a much disrespect as I can muster, fuck this disease.
My mom passed 3 years ago from this horrific, rare disease. We need a cure. ππΌ
Miss you every day, Mom. She was my BFF. πππ
#FuckMSA #WorldMSADay
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