Looking for Sickled Patients who live in Canada and Ontario

[Finalybeingheard]

If you are in this support group, please msg me! I am looking to help implement a standard protocol in all ontario hospitals for Sickle Cell patients to help end the systemic racism that we have to face everytime we are hospitalized. And it can be the most subtle form of it, it is still wrong and must not be tolerated or accepted.

Msg me if you agree! I am also going to continue to bring awareness on my podcast, Finding Self with Regena and I'll be doing a live interview on March 31st on thatchannel.com at 3pm discussing my struggle with the disease, late diagnosis and my experience with our broken health system and incompetence doctors. I'm interested to know if this only an Ontario issue or a Country wide problem.

Please let me know your experience.