@lenadunham we are the only charity in the world providing financial grants to #EDS and #Hypermobility patients in the U.K. to help with early diagnosis, treatment & management. We would love to connect with you to see if you’d help support our mission!
https://t.co/tcwRcfIojj
We are OPEN for Financial Support Grant Applications for U.K. #EhlersDanlosSyndrome patients! Deadline 31st July 2021 for online applications. Visit https://t.co/8YK2cPKrIg
🎉FIRST AMBASSADOR ANNOUNCEMENT🎉
Mind Body EDS™ has announced the appointment of young award-winning film-maker, musician and EDS sufferer, Ashleigh Harley @ashleighharley to be its first Ambassador as the charity… https://t.co/oLLwHdVKMG
Mind Body EDS charity Founder, Laura Sylvester, was kindly invited to be interviewed on the @wellrestorer Wellness Podcast by Fisiwe Muvirimi.
“She shares her life-changing experience of living with Ehlers-Danlos… https://t.co/LFxbtrhyiC
The documentary movie ‘The Dark Horse’ is searching for EDS sufferers to have the chance to feature in the film!
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Fellow EDS sufferer and director @ashleighharley is holding an online virtual concert to take place… https://t.co/9o5ouRKXyo
🔴 #REDS4VEDS DAY 2020🔴
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Today, we show our support by wearing red to help spread awareness of Vascular Ehlers-Danlos syndrome (vEDS). Get involved by doing the same and share it on social media to raise awareness… https://t.co/UPZRlys0OY
🔴 #REDS4VEDS DAY 2020 🔴
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Today, we show our support by wearing red to help spread awareness of Vascular Ehlers-Danlos syndrome (vEDS). Get involved by doing the same and share it on social media to raise awareness… https://t.co/NpkAHQH3az
Thank you @vmvndvlynn for this week’s #myedsdiagnosis feature story. Together, we can help make our invisible, visible.
Spread the hope, the love, and the awareness #zebrawarrior#ehlersdanlossyndrome… https://t.co/To8ZhStn9G
Thank you adiepohlman for this week’s #myedsdiagnosis feature story. We appreciate you being able to share your story to help raise awareness about EDS. Together, united, we can help make our invisible,… https://t.co/qpu1HtYuiC
Thank you flyingthroughit for this week’s #myedsdiagnosis feature story. Your story is one we hear too often but together we'll raise awareness, achieve earlier diagnosis and support EDS patients manage… https://t.co/TQ1BJTq7VJ
🌟HAPPY NEW YEAR🌟
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When it comes to New Year Resolutions with those living with a chronic illness, it can be a tricky time. Seeing those who are more able-bodied planning extremely ambitious new year goals can be… https://t.co/oZODAbS82i
🎄CHRISTMAS CAROL #fundraiser Thank you to all the volunteers who came and sung carols in the Farnham to help raise money for our #charity
We’re happy to announce we raised a total of £355.30! We are so grateful for the generous donations. Merry Christmas 💙
Want to volunteer for Mind Body EDS? We have opportunities to get involved in fundraising or helping out one of our charity events. If you want to find out more about the opportunities available please contact… https://t.co/XeLE5p8sdh
Thank you nanipelekai84 for this week’s #myedsdiagnosis feature story. Greater awareness and education around EDS will help give patients more control over this chronic illness.
Spread the hope, the love, and the… https://t.co/ZZVBIYeSR0
Thank you masteringthedisaster for this week’s #myedsdiagnosis feature story. Mind Body EDS aims to provide relief and resolution through financial grants to patients and supporting medical research. We no longer… https://t.co/vbL08cVq89
🌟#BlackFriday 29th November 🌟 @amazonsmile donates 0.5% of the net purchase price (excluding VAT, returns, and shipping fees) from your purchases to your charity of choice. Support Mind Body EDS here: https://t.co/6wGoygqMeS