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FAMILIES AND 8P HEROES 18 AND ABOVE

Families and 8p Heroes 18 and Above

When: Wednesday, March 9th, 2022 – 7:30 pm EST

Caregivers to adult 8p heroes, this one is for you! A chance to communicate and collaborate about your journey as a caregiver/parent to an adult 8p hero. Rose-Anne Partridge, 8p mother, patient leadership board member, wellness professional and special needs advocate will help lead this discussion.

Please register in advance for this meeting:

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Project 8p Foundation is a registered 501(c)(3) charitable organization with EIN 83-2545342. All contributions are deemed tax-deductible

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The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.
  • Lead with knowledge from patients. Currently, there is no cure for 8p disorders, nor is there a standard course of treatment.

The Project 8p Foundation (Project 8p) was created in 2018 to:

  • Raise transformative funding for pioneering scientific research into treatments for a complex, rare disease involving 250+ affected genes on the short arm of the 8 th chromosome (8p). Rearrangements of these genes causes significant abnormalities to the entire neurological system, thus all organs and functions of the body– with variance in cognitive functions, gross motor skills, social development and other challenges during infancy, and throughout life;
  • Empower a unified community of 8p patients and their families so they can have meaningful lives today; and
  • Accelerate future treatments, not only for 8p, but potentially for other chromosome-wide diseases as well.