Dysautonomia Awareness

Spreading awareness of Dysautonomia is extremely important to me. As a patient myself, I have experienced firsthand the lack of knowledge, within the medical field itself, about Dysautonomia. Take POTS (a specific form of Dysautonomia) for example: It takes an average of 5 years to be diagnosed. On top of that 85% of patients have had a medical professional tell them it’s “all in your head”. The damaging isolation that can come from living with dysautonomia should not still exist. This is why education and awareness are crucial. For more information visit: dysautonomiainternational.org To donate go to: curedys.org