Sickle Cell Patient Rights To Life
Donation protected
The life span of Sickle Cell Chronic Pain Patients has plummeted from 45 years of age down to 30 years old. Join the American Pain Institute (API) and the World Sickle Cell Federation’s (WSCF) fight against bigotry and discrimination against patients suffering and dying from complications of Sickle Cell Pain Crisis and the Mistreatment of Chronic Pain Patients.
Join and support our upcoming “America's In Pain! - MARCH ON WASHINGTON - Silent No More!” march on Washington DC and Congressional Briefing to be held at the U.S. Capitol, Wednesdays, April 25, 2018, 12:00 noon to 2:00 pm
Support Sickle Cell Chronic Pain Patients “right to life” and humane treatment. We are seeking to raise 100,000 dollars to cover the cost for setting-up the rallies and traveling fees incurred by the volunteers and speakers. Chronic Pain Patients with Sickle Cell are being denied life-saving hospital and ER treatments due to Government overreach and unlawful persecution of doctors and other healtcare providers.
My name is Billy and I am from Los Angeles California. I am a healthcare medical advocate and I have seen numerous patients with Chronic Sickle Cell Pain denied mandatory treatment subjecting them to early death and excruciating pain. I am a huge supporter of all peoples' rights to fair treatment and that’s why I support the American Pain Institute (API) and the World Sickle Cell Federation (WSCF).
Help spread the word!
2018 PAIN PATIENT ADVOCACY WEEK
April 23rd thru the 30th
Click here to see all the events
Join and support our upcoming “America's In Pain! - MARCH ON WASHINGTON - Silent No More!” march on Washington DC and Congressional Briefing to be held at the U.S. Capitol, Wednesdays, April 25, 2018, 12:00 noon to 2:00 pm
Support Sickle Cell Chronic Pain Patients “right to life” and humane treatment. We are seeking to raise 100,000 dollars to cover the cost for setting-up the rallies and traveling fees incurred by the volunteers and speakers. Chronic Pain Patients with Sickle Cell are being denied life-saving hospital and ER treatments due to Government overreach and unlawful persecution of doctors and other healtcare providers.
My name is Billy and I am from Los Angeles California. I am a healthcare medical advocate and I have seen numerous patients with Chronic Sickle Cell Pain denied mandatory treatment subjecting them to early death and excruciating pain. I am a huge supporter of all peoples' rights to fair treatment and that’s why I support the American Pain Institute (API) and the World Sickle Cell Federation (WSCF).
Help spread the word!
2018 PAIN PATIENT ADVOCACY WEEK
April 23rd thru the 30th
Click here to see all the events
Organizer and beneficiary
Billy Earley
Organizer
Corona, CA
Ronald Doc Myers
Beneficiary
