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About Us

No family facing a rare disease should have to navigate their journey alone. Somebody To Talk To exists to make that a reality — for every family, regardless of income, location, language, or access to medical professionals.

We serve every person touched by rare disease:

Patients & Families
Rare Disease Caregivers
Parents of Children with DMD
Sickle Cell Community
Amyloidosis Patients
Siblings & Partners
Newly Diagnosed Families
Long-term Caregivers
Bereaved Families
Medical Professionals
Patient Advocates

STTT provides free, professionally-led group sessions covering emotional wellbeing, caregiving skills, parenting strategies, and relationship support. Our sessions are available to every rare disease family — live via Zoom, on-demand, and at no cost.

Psychotherapy is effective but cannot scale to meet the needs of thousands of families impacted by chronic illness. STTT is built to scale — one disease community at a time.

Help us reach every rare disease family

Your support funds free sessions for families who need them most.

Click Here If You'd Like To Help

Somebody To Talk To, Inc. is a CT nonprofit corporation operating through a fiscal sponsorship with Players Philanthropy Fund, a Maryland charitable trust recognized by IRS as a tax-exempt public charity under Section 501(c)(3) of the Internal Revenue Code (Federal Tax ID: 27-6601178). Contributions to Somebody To Talk To are tax-deductible to the fullest extent of the law. The information provided on this website is for educational and informational purposes only and is not intended as medical advice. Always consult with a qualified healthcare provider regarding any medical conditions or treatment options.