Scheuermanns Disease Fund

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Scheuermann's Disease Fund - Raising Global Awareness for this Spinal Deformity The Scheuermann’s Disease Fund was created to improve the public's awareness and recognition of this spinal deformity, work towards improving early detection in adolescents, and to work with the medical community to better understand the long-term secondary effects Scheuermann's can cause.

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475066738

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MCMURRAY

Address: PO BOX 972, MCMURRAYWeb: Sign in to see organisation websiteFacebook: sdfundRevenue: 48454ICO: 475066738

Scheuermanns Disease Fund Scheuermanns Disease Fund Care Packages for Patient Advocacy CBS KDKAPittsburgh Reporter Jessica Guay interview What is Scheuermanns Disease. Why is Scheuermanns a Rare Disease. Help us Gather Data for SD Research Please watch Living with Scheuermanns Disease Find a Doctor for Treating Scheuermanns in ourInternational Doctor Database Social Media Support Groups for People Affected by Scheuermanns Disease Doug Strott Founder Volunteer Case 213cv01245DSC Document 44 . .

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Margaret

2. How can we enhance collaboration between researchers, healthcare providers, and patients to improve outcomes for those affected by Scheuermann's Disease?

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Deborah

Thank you for all the incredible work you do to raise awareness about Scheuermann's Disease! Together, we can help those affected by this condition find the support they need. 💙

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Sharon

I just watched the interview with Jessica Guay, and it opened my eyes to the challenges of living with Scheuermann's Disease. Let's spread the word and advocate for better understanding and treatment options! 🌍✨

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Brian

1. What are some effective strategies for raising awareness about Scheuermann's Disease in communities that may not have heard of it?

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Scheuermanns Disease Fund

Wishing everyone a wonderful Independence Day.

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