Search Nonprofits

WE WORK TO FILL IN THE GAPS NEEDED TO CREATE REAL CHANGE AND BUILD A MORE INCLUSIVE FUTURE FOR THOSE WITH DISABILITIES. WE PROVIDE PRACTICAL FAMILY SUPPORT, FUND SMA RESEARCH, AND ARE BUILDING THE FIRST INCLUSIVE PLAYGROUND IN SANTA BARBARA.

We are starting a research department at Monroe Carell Jr Childrens Hospital at Vanderbilt for Duchenne Muscular Dystrophy.  We are raising money to fund research for Duchenne Muscular Dystrophy. We have 2 sons that were diagnosed in 2009 with this horrible disease.  We are searching for a cure for this disease which is 100% fatal by early 20's and crippling by age 12.

TO RAISE MONEY FOR CHILDREN AND THEIR FAMILIES AFFECTED BE LEUKODYSTROPHIES

NPF’s mission: “to drive efforts to cure psoriatic disease and improve the lives of those affected.”

Our mission is to convene passionate, collaborative partners to help build bold, data-driven systems and solutions that promote healthy communities for all.

Lakeridge Health invests in equipment to pinpoint and treat health problems quickly and accurately to meet the healthcare needs of Durham Region families. Our medical professionals deliver the quality health care our families have come to expect by using the latest technology. Lakeridge Health is always in need of new equipment and depends entirely on community support to get it. Not many people know that the Provincial Government covers only operating costs of hospitals but does not fund the purchase of equipment. This is why donations from the community are so important. By investing in new technology used in patient care, your contributions go a long way in helping our families, neighbours and friends continue to get the best healthcare possible. High priority programs include: •Kidney and Diabetes Care •Surgery •Emergency and Critical Care •Clinical Support Services

Cure JM's mission is to find a cure and better treatments for Juvenile Myositis and improve the lives of families affected by JM.

To improve the quality of life of those affected by PCD and to develop the means to find a cure.

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.

We seek to assure that terminally ill patients can live their final days to the fullest

To enhance the lives of people with HADDS through research, education, support and advocacy. ​

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