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Our mission is to provide information on accessible and equitable treatment options for every child affected by TUBB4A-related leukodystrophy, regardless of their geographical location or socioeconomic status. We are committed to relentlessly pursuing research, collaboration, and advocacy to ensure that no child's journey is defined by limitations, but rather by possibilities for a healthier and brighter future.

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."

We need your help today so that Grandview Children's Centre can provide critical therapy services for children and youth with special needs in Durham Region. We believe that Ours Kids deserve the opportunity to access the critical therapy services they need. The support of our community is vital to make this possible. Grandview serves over 4,300 children and youth, but nearly one thousand are still on a wait list.

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 prevent the pain and trauma of burn injuries to children, and to heal, and to give children who suffered severe burns the opportunity to reach their full potential, physically, psychologically, and sociallly.

VBF provides support and informational resources for individuals affected by vascular birthmarks and their caregivers, and sponsors conferences, clinics, education, and relevant research.

1) To provide the LATEST MEDICAL / RESEARCH information and EDUCATION so that they may make wise medical decisions and continue their independence despite their vision. Provide information and research data to the medical and research community so that they may join in our fight against blindness. The AFI International Aniridia Medical Registry and Gene Bank is the main project of our research. 2) To SUPPORT the low vision / blind people born with aniridia and their families who struggle emotionally and financially due to having aniridia. To assist them in accomplishing their dreams and remain independent, self sufficient and a productive member of society. 3) To help fund RESEARCH especially the AFI created program which collects DNA samples, comphrehensive medical questionaires, and clinical photographs to add knowledge to physicians and advance research. Our international faculty of AFI Medical Advisory and Scientific Boards assist us with this program. We also help fund research and patient care services as funds allow and look forward to raising funds to expand our efforts to stop this genetic condition from continuing into future generations.. 4) To further PUBLIC AWARENESS about all the conditions that make up aniridia, and the misconceptions of people who are blind or low vision,

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.

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.