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We are an organization created by parents of children diagnosed with rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene. Our vision is to find effective treatments and a cure for SCN2A related disorders. Our mission is to improve the lives of those affected by SCN2A related disorders through research, public awareness, family support and patient advocacy. We are a registered 501(c)(3) organization.

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

To promote; Research. Education, and Advocacy regarding Lyme and other Tick borne disorders.

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.

To advocate for and fund research directed towards a cure or treatment options for patients with Sanfilippo syndrome.

End Well is dedicated to the belief that all people should experience the end of life in a way that matches their values and goals. When faced with issues of mortality, we often suffer needlessly for a variety of reasons, from cultural and clinical to matters of access. End Well brings together a multidisciplinary community that unites design, technology, health, policy and activist initiative to transform how the world thinks about caregiving, grief, illness and the end of life experience with the ultimate goal of creating a future where ending well becomes a measure of living well.

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."

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

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.

To provide the space and support where nonprofits succeed at helping children and families.

Cutting-edge medicine and advocacy, regardless of ability to pay. It is through this mission we are striving to reach 30 countries and save over 100,000 lives. Some see it as an impossible goal. We see it as a necessary one. AHF pledges to fight this disease no matter whom it afflicts, or where it is found. We will not rest until AIDS is eradicated from the globe.