Devoted to supporting and advancing comprehensive care of patients and families living with sickle cell disease.

The New England Sickle Cell Consortium is a regional cooperative group of New England stakeholders devoted to the education, research, advocacy, support.

Sickle Cell Disease’s Impact:

100,000

Americans affected
by SCD

1 of 16,300

1 out of every 16,300 Hispanic-American births

1 of 365

1 out of every 365 Black or African-American births

3,000

Active sickle sell patients in the New England area

We Work With

Patients and
Families

Caregivers
and Nurses

Schools and
Communities

We’re changing how the world approaches sickle cell disease.


Together, we aim to build a future where every person affected by sickle cell disease in New England can access comprehensive support, leading to improved quality of life and a stronger, more connected community.

Associated Member Organizations:

Upcoming Events

Join us and register for this year’s Annual Sickle Cell Disease Symposium.


“I was born a warrior, a man born with the fight within him, Sickled at birth, but not chiseled to death. I was born a warrior, Born to fight for my every breath, Born to fight to become a victorian, Born to live a war within me.”

— Edonusem H.A.Y. Pomeyie, 15, NESCC Patient

Find Sickle Cell Disease Support:

 

Patient

“Everything The NESCC have been doing for the Sickle Cell community, has been more than encouraging”

Patient

“By the end, I felt blessed to have a team of doctors committed to a safe and healthy delivery for both me and Nathaniel. ”