HUNTER SYNDROME FOUNDATION

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The Hunter Syndrome Foundation is a 501(c)3 non-profit corporation with a mission to fund potential therapies that will ultimately find a cure for this disorder. Hunter Syndrome or Mucopolysaccharidosis Type II (MPS II) is a rare genetic disorder that slowly destroys the body's cells. This is a rare condition affecting 1 in 150,000 males. There is currently no cure, and the disease is progressive and life-limiting.

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464296623

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Prosper

Address: 102 E Broadway St. #203, ProsperWeb: Sign in to see organisation websiteICO: 464296623

Hunter Syndrome Foundation Hunter Syndrome Foundation A CURE IS WITHIN REACH. Welcome. The Hunter Syndrome Foundation is a U. S.

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Helen

What innovative fundraising strategies could the Hunter Syndrome Foundation implement to increase awareness and support for families affected by this rare disease?

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Adam

🙏 Grateful for organizations like the Hunter Syndrome Foundation! Together, we can raise awareness and support families affected by this rare disorder. Every share counts!

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Pauline

How can we enhance collaboration between researchers and families impacted by Hunter Syndrome to accelerate the development of effective treatments?

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Patrick

❤️ So inspired by the work the Hunter Syndrome Foundation is doing! Every little bit of awareness helps bring us closer to a cure. Let’s keep fighting for our children!

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Prosper

Organisations from HUNTER SYNDROME FOUNDATION

1. MANE GAIT

Join in Mount Up Ride Tall At ManeGait Therapeutic Horsemanship, children & adults with disabilities.

2. Prosper Ladies Association

The Prosper Ladies Association (PLA) provides opportunities to serve the people and needs of our community.

4. CORNERSTONE ASSISTANCE NETWORK OF NORTH CENTRAL TEXAS

Our mission is to empower local Neighbors in need through relationships and comprehensive services to.

5. NEIGHBORS NOURISHING NEIGHBORS

Neighbors Nourishing Neighbors is a community food pantry, sharing food and personal hygiene product.

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MEF2C FOUNDATION (uk)

MEF2C Foundation is partnering with scientists to fund research into MEF2C-gene related conditions.

THE SOCIETY FOR MUCOPOLYSACCHARIDE DISEASES (uk)

MPS Society UK supports those affected by Mucopolysaccharide, Fabry and related lysosomal diseases.

THE CHILDREN'S RARE DISORDERS FUND LTD (uk)

The Children's Rare Disorders Fund is dedicated to curing childhood rare genetic disorders.

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