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At POGO, we give kids with cancer the support they need–not just during the difficult time around therapy, but for years after when they can face complications from the treatments that saved them. Each year in Ontario, 400 children are diagnosed with cancer and 4,000 families are currently going through active treatment or follow up care. Many of these families are accessing POGO’s financial assistance program for the unexpected costs associated with a childhood cancer diagnosis. While 82% of children survive, many survivors of brain tumours and other cancers may face learning challenges later in life. POGO counsellors work with these young people to help them match their dreams with their abilities and move on to college or university. POGO also maintains an aggressive research agenda. We are asking the types of questions that will benefit these young cancer patients, their families and survivors—in Ontario and around the world—today and well into the future.

Bringing comfort and dignity as life nears its end.

OMF’s mission is to accelerate and enhance scientific research, advocacy, and awareness of ocular melanoma and to provide education and support to patients, their families, and healthcare professionals. For patients and their loved ones, OMF aspires to be the top destination for up-to-date OM-related educational information, a meeting place, and advocacy resource. For doctors and researchers, OMF strives to be the connective tissue, facilitating interdisciplinary cancer research. The goal of OMF is to have there exist accessible and effective treatments for ocular melanoma and, one day, a cure

To improve the quality of life for all LGBTQ+ people in Upstate, South Carolina.

The Cystic Fibrosis Foundation's mission is to find a cure for cystic fibrosis (CF) and to improve the quality of life for people living with the disease. We accomplish this by funding life-saving research and working to provide access to quality care and effective therapies for people with CF. Our work has contributed to doubling the life expectancy for people with CF beyond the age of 18, and increasing the availability of nearly every CF drug through the Foundation's support.

The National Multiple Sclerosis Society's mission is to cure multiple sclerosis while empowering people affected by multiple sclerosis (MS) to live their best lives. The organization pledges to accelerate cures through global leadership, and improve access to personalized, affordable, high-quality MS healthcare. It empowers people affected by MS to solve everyday challenges and strengthens the MS movement through more and deeper connections.

The Knights and Orchids Society (TKO) envisions a future where Transgender, Lesbian, Bisexual, and Gay (TLBG) Black people are empowered to live full and healthy lives free from harm. Our mission is to build the power of TQBLG Black people across the south by providing a spectrum of health and wellness services designed to address the social determinants of health that negatively impact our communities. Since 2019, we have provided 258 clients with services through our primary program Fast, Affirming, Innovative Testing and Healthcare or FAITH.

The Parkinson’s Foundation makes life better for people with Parkinson’s disease by improving care and advancing research toward a cure. In everything we do, we build on the energy, experience and passion of our global Parkinson’s community.

Accelerating CF research to save lives through the power of community. Emily's Entourage raises money and awareness to help find a cure for Cystic Fibrosis (CF) with a focus on nonsense mutations. Nearly 70,000 people worldwide with CF are waiting with bated breath for life-saving breakthroughs. We're mobilizing friends, families, businesses and communities to join Emily's Entourage on our quest for new treatments and a cure.

JDRF's mission is to find a cure for type 1 diabetes and its complications through the support of research. It is also committed to developing new and better treatments that improve the lives of people with type 1 diabetes in the near term and keep them healthy while we advance toward a cure. JDRF’s promise is to progressively remove the impact of T1D from the lives of those living with the disease until it is no longer a threat to them or their families. Formerly known as JDRF International or Juvenile Diabetes Research Foundation

THE MISSION OF THE AMERICAN ASSOCIATION FOR PEDIATRIC OPHTHALMOLOGY AND STRABISMUS (AAPOS) IS TO IDENTIFY AND PROMOTE THE HIGHEST QUALITY MEDICAL AND SURGICAL EYE CARE WORLDWIDE FOR ALL CHILDREN, AND FOR ADULTS WITH EYE MISALIGNMENT.