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Founded in 2004 to provide the Deaf equal access to mainstream products, services and amenities through Sign Language TV, media, music and film.

To nurture and empower women in their personal and professional walks in life: supporting their transformation through counseling and education.

The mission of the organization is to enable individuals with sickle cell anemia to live lives to the extent possible unhampered and uncompromised by their sickle cell conditions, while increasing knowledge and understanding of sickle cell disease as a health problem through professional standards of administration, health care, public relations and fundraising.

KHF helps children with hemophilia and similar bleeding disorders.

Picking Me advocates mMental health awareness and acceptance for Body Focused Repetitive Behaviors- such as Dermatillomania aka Skin Picking Disorder- for sufferers, supporters, and educational communities alike, encouraging individuals to take control back from the OCD related disorder by sharing why they are #PickingMe over their BFRB.

We support artists who raise awareness about dementia and who inspire creativity in people with dementia and Alzheimer’s Disease.

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Our mission is to mobilize a community for patient support and advocacy, as well as drive and support impactful research that translates into advances for patients with migraine and other disabling diseases that cause severe head pain. Our core beliefs guide everything we do, from the research we promote to our efforts to build a supportive, welcoming community for all people living with migraine. Advocacy and education is the only way we will increase awareness and recognition of migraine for the disabling disease it truly is.

EDUCATION/SUPPORTING RESEARCH & FAMILIES AFFECTED BY KAWASAKI DISEASE IN KIDS.

Jack’s Corner is a nonprofit organization dedicated to improving the quality of life and finding a cure for children with SPG50 through the acceleration of gene therapy treatments, funding of research, and raising awareness of the disease.SPG50 is an ultra-rare neurodegenerative disease that affects children. The disease causes spasticity that starts in chldren's legs, slowly taking away their ability to walk. The spasticity then takes away their ability to use their hands, and ultimately, their mental capacity.

EASING ANXIETY, FEARS AND STRUGGLES

Our mission is to improve quality of life for people suffering from dry eye disease and ocular surface pain disorders.Our articles of incorporation describe our purpose as follows: "The purpose of the Corporation is to help alleviate the suffering of people with dry eye diseases by (i) educating patients and their loved ones about the diseases and their treatments, (ii) providing patients with information and tools to advocate for their needs effectively, (iii) educating the medical community about advances in dry eye assessment and care, (iv) raising public awareness of dry eye disease risk factors, and (v) encouraging and supporting scientific research that focuses on the priorities of dry eye disease patients."