Tell the FDA

The FDA meeting is coming up on February 7, 2014 in Silver Springs, MD. Sickle cell advocates, patients, families, and members of the health care industry will all be in attendance. Even if you cannot come, your participation is necessary. It is time to use your voice. Tell the FDA how you are impacted by sickle cell disease, and what treatments, and outcomes that would be most beneficial in the future.

We have a unique portal for sharing this information with the FDA, directly on the Sickle Cell Warrior’s website. You can choose the level of privacy you want, and how much information you would like shared with the FDA, and other researchers, and scientists. This is a chance for sickle cell warriors to get involved in shifting the policy and mindset of rule makers, and will serve us in the coming years. Get involved today.

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