CREATING CONNECTIONS, DRIVING RESEARCH, INSPIRING HOPE

for Hypothalamic-Pituitary Brain Tumor Survivors

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Working to Improve the Quality of Life for Rare Brain Tumor Survivors

The Raymond A. Wood Foundation is a parent and patient-led, rare disease patient advocacy organization.

Our mission is to empower survivors of craniopharyngioma and hypothalamic-pituitary brain tumors with an improved quality of life by providing access to education, technology, and evolving treatments.

Learn More About Us

Darren, craniopharyngioma patient

Raymond A Wood Foundation Impact

Support Our Work in Advocating for Survivors of Hypothalamic- Pituitary Brain Tumor Patients & Caregivers. Your donation helps us to continue what we do.

$

1.8

M

Raised since 2017

$

350

K

Allocated to Research

$

575

K

Direct Support to Patients
Help Us Make An Impact

Patient & Family Resources

We can all use some help. Discover our range of resources we provide to those Newly Diagnosed, Survivor Resources or Caregivers.

For Newly Diagnosed

Get support for the early days of diagnosis and treatment.

For Survivors

Find out about support groups and current research.

For Caregivers

Get connected to research, education and support.

Learn more about conditions caused by craniopharyngioma and hypothalamic-pituitary brain tumors.

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