Calling on the Sickle Cell Community and its Supporters.
We need your help to ensure the passage of the NYS Sickle Cell Treatment Act of 2018. Please take a moment out of your day to call your Assembly and Senate representative to ask them to support this legislation and the budget allocation to fund treatment centers throughout New York State.
Follow these links to find your Assembly and Senate representatives.
Most importantly, we need everyone to call Governor Cuomo to support the Sickle Cell Treatment Act by signing the bill and making sure that the funding is made available in the State’s budget.
#SeptemberisSickleCellAwarenessMonth @1ViralVoice @FallingAngelsVoice #HaveAHeartforSickleCell #SaveLives #NYS #Assembly #AliciaHyndman #KimberlyJean-Pierre #RichardNGottfried #Senate #ShellyMayer #KempHannon @UNTOLDStoryMedia
The Sickle Cell Thalassemia Patients Network is a Brooklyn-based charity serving individuals living with inherited blood disorders, and their families. Follow SCTPN on Twitter & IG @SCTPN FB @SCDThalPatientsNetwork Like Page @SCTPNWalk @UNTOLDStoryMEDIA