RettSyndromeMA

Official Twitter Page of Rett Syndrome Association of Massachusetts (RSAM)

[RettSyndromeMA @rett_ma]

Rett is Rare-Campaign for Rare Disease Day - https://t.co/b73vEcEt2B

[RettSyndromeMA @rett_ma]

Rett is Rare-Campaign for Rare Disease Day - https://t.co/b73vEcEt2B

[RettSyndromeMA @rett_ma]

Team Rett Marathon 2021 - https://t.co/kvz6SoEj4K

[RettSyndromeMA @rett_ma]

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[RettSyndromeMA @rett_ma]

Maria McTernan Sibling Scholarship https://t.co/NLYieB9HaS

[RettSyndromeMA @rett_ma]

Santa Update Invite! - https://t.co/kLcnkfdxCf

[RettSyndromeMA @rett_ma]

Merry Holidays and Happy Christmas 🎄🕎☃️ Stories with Santa on Christmas Eve! Join us for some holiday stories of the season. Registration link here: https://t.co/hQlY5WWD5f

[RettSyndromeMA @rett_ma]

Exclusive Invite! Stories with Santa - https://t.co/HZeyKtnX3a

[RettSyndromeMA @rett_ma]

Giving Tuesday-the force is with you - https://t.co/80l7gqy9g7

[RettSyndromeMA @rett_ma]

Final Reminder!  RSVP today for Family Check Nov. 18th at 7:30pm.

[RettSyndromeMA @rett_ma]

RSAM BIG NEWS! Monthly Newsletter in your inbox tonight!

[RettSyndromeMA @rett_ma]

This is a test https://t.co/wVx2GDSeOW

[RettSyndromeMA @rett_ma]

We have a New Name! RSAM is Rett Syndrome Angels! #rettsyndromeangels

[RettSyndromeMA @rett_ma]

Boys living with Rett Syndrome #rettsyndrome #boyswithrett #rettangels https://t.co/x0estC2kJ6

[RettSyndromeMA @rett_ma]

Rett Syndrome Awareness Month💜 Thank You Mayor Walsh! https://t.co/achx25jpZx

[RettSyndromeMA @rett_ma]

💜Your Everything Our Everything 💜

[RettSyndromeMA @rett_ma]

Can’t wait to see you! Space is limited to register soon!

[RettSyndromeMA @rett_ma]

Exciting things happening!!

[International Rett Syndrome Foundation @Rettsyndrome]

Did you know clinical trials for Anavex 2-73, Ketamine and Epidiolex are recruiting children and adults with Rett syndrome at sites across the country? A clinical trial for Trofinetide is slated to begin enrolling later this year. Learn more at: https://t.co/jhSnlLyiAu

[International Rett Syndrome Foundation @Rettsyndrome]

On September 10, join Dr. Huda Zoghbi as she provides a research update following the 20th anniversary of the discovery of the MECP2 gene. Sign up for this free webinar today at: https://t.co/Q0H4m2BG5r