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The mission of the Malan Syndrome Foundation is to improve the lives of individuals and families affected by Malan syndrome in the global community through support, outreach and research.​​ Provide a broad network of support to families affected by Malan syndrome and help advance access to a diagnosis Promote knowledge development, awareness and sharing of information Explore research pathways to treatments and cures, as well as enhance understanding of Malan syndrome and related disorders

Best Day Foundation helps children with special needs build confidence and self-esteem through safe, fun, adventure activities like surfing, bodyboarding, kayaking, outrigger canoeing, SUP, snow-tubing, and more. Please join us in creating special days for kids with Autism, Down Syndrome, Cerebral Palsy, Blindness, Cancer, Spinal Cord Injuries, and other physical and developmental challenges!

Nearly one in two Albertans will develop cancer in their lifetime and nearly one in four will be lost to cancer. At the Alberta Cancer Foundation, we intend to change that. Our promise to our donors is progress in cancer research, prevention, treatment and care. Your dollars make a transformational impact right here at home by advancing Alberta’s leading-edge provincial research strategy and the compassionate work of the Tom Baker Cancer Centre, the Cross Cancer Institute and Alberta’s 15 other cancer centres. Representing nearly 200,000 donors, the Alberta Cancer Foundation is the number one non-governmental source of funding for cancer research and programs. Last year we invested $23.3 million towards our vision of a cancer-free future. We know something can be done about cancer and we're willing to do it. With you by our side, we can continue pushing for accelerated change, progress and above all, results.

The Living Well Foundation is a nonprofit youth/family health and development organization established in 2006 in the state of Missouri. The mission of the Living Well Foundation is to create healthier individuals/families through experiential learning. Our current focus deals with obesity. Camp Jump Start, an award winning and nationally recognized ?best practice? in the treatment of childhood obesity assisted in developing the strategies at the Living Well Village to prevent obesity using a holistic approach. Our philosophy is ?fair does not mean that everyone gets the same treatment---fair is that a person gets what they need?. This opens the doors for education to those with limited means. The Living Well Village wishes to have room for anyone seeking knowledge so that they may take personal responsibility for their own health. Because when ?we know better, we can do better? and then we teach our family. This is how we change the course of health issues in the world today.

We established Getty Owl Foundation to help families and fight Spinal Muscular Atrophy (SMA), the #1 genetic killer of young children. We assist people and families affected by SMA, fundraise to advance SMA research, and raise awareness SMA awareness. There is so much to be done, and our children are counting on us. We hope you continue with us on this journey and support the cause. Together, we will wipe out SMA!

BrightFocus Foundation At BrightFocus, we support research to end Alzheimer's disease, macular degeneration, and glaucoma. We are a nonprofit organization under section 501(c)(3) of the Internal Revenue Code of the United States and are working to save mind and sight. Our Mission BrightFocus drives innovative research worldwide and promotes awareness of Alzheimer’s, macular degeneration, and glaucoma. Our Vision Living free from diseases of mind and sight.

The mission of the Brigance Brigade Foundation is to equip, encourage and empower people living with ALS (Amyotrophic Lateral Sclerosis); they strive to improve the quality of life for them and their families by providing needed equipment, resource guidance and support services, in addition to funding various research initiatives. 90% of our grant funding supports families in the greater Maryland region; our ALS research and education awards are given to organizations with national impact and resources.

Myhre Syndrome Foundation is a patient advocacy organization dedicated to providing hope and improving the lives of those impacted by Myhre syndrome. Myhre is an ultra rare genetic disorder affecting just 200 people in the world. It is progressive and can have life-threatening complications, currently there is no cure. We foster collaboration among all relevant stakeholders to build a strong, global community in order to advance research, as well as support, educate and advocate for those impacted by Myhre syndrome.

Hunter’s Hope Foundation was established to address the acute need for information and research with respect to Krabbe Disease and related Leukodystrophies. In addition, we strive to support and encourage those afflicted and their families as they struggle to endure, adjust and cope with the demands of these fatal illnesses. Accordingly, our mission is four-fold: • To broaden public awareness of Krabbe Disease & other Leukodystrophies thus increasing the probability of early detection &treatment.• To gather and provide current, functional information and service linkages to families of children with Leukodystrophies.• To fund research efforts that will identify new treatments, therapies and ultimately, a cure for Krabbe Disease and other Leukodystrophies.• To establish an alliance of hope that will nourish, affirm and confront the urgent need for medical, financial and emotional support of family members and those afflicted with Leukodystrophies.Among the essential goals, founders Jim and Jill Kelly, seek to inspire an appreciation of all children and express a thankful heart towards God for these precious gifts of life. These bedrock values are categorically and vigilantly expressed throughout all of the Foundation's programs and activities.Hunter's Hope is a not-for-profit with tax-exempt 501c(3) status and is registered as a charitable organization in New York State

The Cystinosis Research Foundation is dedicated to finding better treatments to improve the quality of life for those with cystinosis and to ultimately find a cure for this devastating disease.CRF is committed to finding a cure through an aggressively funded research agenda. CRF issues research grants bi-annually to accelerate the research process and to ensure that there is never a gap in funding new cutting-edge research ideas. We are focused and determined to improve the quality of life for our patients and to find better treatments, including a cure, for our adults and children living with cystinosis

International Eye Foundation is dedicated to helping people see! Since 1961 IEF has taken up the challenge in poor countries around the world, helping to restore sight and prevent blindness. IEF offers strong new strategic directions that focus on making eye clinics financially self sufficient. IEFs achievements include developing eye health services, training ophthalmologists and para-medicals, and fighting vitamin A deficiency, trachoma and river blindness. IEF is now strengthening the management, quality of service, and income generating activities so that eye clinics are less dependent on outside donors and government funds.

TO IMPROVE THE HEALTH OF THE PEOPLE OF WASHINGTON STATE. IN 2014, WHF MADE THE DIFFICULT DECISION TO END ITS PERSONAL HEALTH ADVOCATE PROGRAM AND OTHER ACTIVITIES AND ESSENTIALLY SUSPENDED OPERATIONS AS THE BOARD EVALUATED ITS OPTIONS. IN 2015, THE BOARD CONTINUED TO ASSESS ITS FUTURE OPPORTUNITIES AND ALSO CONCLUDED THAT IT WAS BEST TO ALLOW ANY POSSIBLE PAST CONTINGENT LIABILITIES TO BE IDENTIFIED AND SATISFIED BEFORE PROCEEDING FURTHER. THE FOUNDATION BOARD HAS NOT IDENTIFIED ANY SUCH LIABILITIES BUT HAS DECIDED TO MAINTAIN ITS CURRENT LIMITED APPROACH FOR ANOTHER YEAR OR TWO. ACTIVITY IS CURRENTLY LIMITED TO COMMUNICATING ITS PAST ACHIEVEMENTS AND LEGACY THROUGH ITS WEBSITE WWW.WHF.ORG