Ehlers-Danlos Syndrome Research Foundation

We strive to promote evidence-based Neuromuscular and Musculoskeletal medicine for Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorder.

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

We hope you enjoy this sneak peek!

Wishing you a Dazzling New Year!

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

Coming this winter is a new resource for the EDS Community, the EDSRF Medical MasterClass series! In these webinar sessions we will bring the EDS Experts to you! Each webinar will end with a live Q&A section.

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

In this video, join P.R.I.S.M. Spine & Joint physicians, Dr. Alissa Zingman, MD MPH and Dr. Sara Cohen Solomon, MD as they discuss the difference between school and workplace regulations. They will talk about which types of accommodations are most prevalent in their EDS patients

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

#EDS #hEDS #HSD #hypermobile #EDSRF #EDSresearch #EDSneedsfunding #dazzle #dazzling #dazzleseason #Donate #EDSresearch #NewYearsEve2023 #medicalresearch #EhlersDanlos #EhlersDanlosSyndrome #EhlersDanlosSyndromeResearchFoundation #2023Giving #endofyear #2024goals #zebrastrong

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

Best Wishes for a Dazzling New Year from the Ehlers-Danlos Syndrome Research Foundation!

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

The link to donate is in our bio above!

We still have funds available for our $75K anonymous match, please help us reach our goal. Together we can ALL make a difference for EDS! Thank you to everyone who has already donated.

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

Together we can ALL make a difference for EDS! Thank you to everyone who has already donated.

Best Wishes for a Dazzling New Year!

#EDS #hEDS #HSD #hypermobile #EDSRF #EDSresearch #dazzle #Donate #EDSresearch #medicalresearch #EhlersDanlos #2023Giving #zebrastrong #rare

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

As 2023 draws to a close, dazzle us with an end-of-year donation! EDS research is underfunded. Your support will help make a difference. Finish the year strong and fund critically needed EDS research! Your donation today will push us towards our end-of-year goal!

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

Click the link to donate: https://t.co/gd4b4NtRSk

We still have funds available for our $75K anonymous match, please help us reach our goal. In 2024, we intend to fund even more innovate and creative minds ready to become the next generation of top EDS researchers.

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

#EDS #HSD #hEDS #EDSRF #EDSresearch #Dazzling #Dazzle #EhlersDanlosSyndrome #HolidaySeason #Celebrate

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

Warmest wishes for a Dazzling Holiday Season from the Ehlers-Danlos Syndrome Research Foundation! As we embrace the holiday season, we ask you to pause to acknowledge the added challenges people with Ehlers-Danlos Syndrome (EDS) may encounter during this time.

[Ehlers-Danlos Syndrome Research Foundation @ehlersresearch]

Please consider an End-of-Year contribution to help support EDS Research. We have a $75K Match from an anonymous donor, help us meet our goal this year!

https://t.co/Mc4xHc01ft

Thank you for being a part of our dazzling community!