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C.F.S.R. Foundation, Inc. | Caffarelli Family Study Research Foundation

The Caffarelli Family Study Research Foundation, Inc. (C.F.S.R.) is a non-profit organization founded by our family whose members live with scapuloperoneal muscular dystrophy (SPMD.) C.F.S.R. is dedicated to educate the public and raise awareness of SPMD and is committed to promote research and investigation in identification of the gene, the cause and correction of the defected gene.

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CONTACTS AT CFSR.ORG

CFSR Foundation

Patty Colasurdo

112 M●●●●●ee Rd

Tom●●●ver , NJ, 08753

US

1.73●●●●1858
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CFSR Foundation

Patty Colasurdo

112 M●●●●●ee Rd

Tom●●●ver , NJ, 08753

US

1.73●●●●1858
rp●●●●●●●●●@verizon.net

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C.F.S.R. Foundation, Inc. | Caffarelli Family Study Research Foundation | cfsr.org Reviews
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The Caffarelli Family Study Research Foundation, Inc. (C.F.S.R.) is a non-profit organization founded by our family whose members live with scapuloperoneal muscular dystrophy (SPMD.) C.F.S.R. is dedicated to educate the public and raise awareness of SPMD and is committed to promote research and investigation in identification of the gene, the cause and correction of the defected gene.
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C.F.S.R. Foundation, Inc. | Caffarelli Family Study Research Foundation | cfsr.org Reviews

https://cfsr.org

The Caffarelli Family Study Research Foundation, Inc. (C.F.S.R.) is a non-profit organization founded by our family whose members live with scapuloperoneal muscular dystrophy (SPMD.) C.F.S.R. is dedicated to educate the public and raise awareness of SPMD and is committed to promote research and investigation in identification of the gene, the cause and correction of the defected gene.

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We Dedicate Our Mission to Our Loved Ones | C.F.S.R. Foundation, Inc.

http://www.cfsr.org/inMemory

We Dedicate Our Mission to Our Loved Ones. Love, your Grandchildren". Victor Salvatore Babe Chillemi, Jr. The name says it all, Babe . He was our babe, a man who loved life, his country and his family. As Daddy’s progression of the disease got worse, our family became more adamant in seeking answers to the hard questions of why, how and when? On November 28, 1989 at 8:05 pm, Heaven gained a new angel and C.F.S.R. was born. Daddy, there is not a day that goes by without me missing and thinking about you&#...

2

C.F.S.R. Links | C.F.S.R. Foundation, Inc.

http://www.cfsr.org/links

Help C.F.S.R. Find a Cure. CFSR Newsletter - Issue #41 April 2014. CFSR Newsletter - Issue #40 April 2013. CFSR Foundation in the News. Tri-Town News - June 12, 2008. Tri-Town News - September 22, 2005. Tri-Town News - September 18, 2003. Contact C.F.S.R. Support C.F.S.R. Contact C.F.S.R. Support C.F.S.R. To educate the public and raise awareness about scapuloperoneal muscular dystrophy. Provide funding for research which would isolate the gene or genes responsible for causing the neuromuscular disease.

3

Support C.F.S.R. | C.F.S.R. Foundation, Inc.

http://www.cfsr.org/donations

Help C.F.S.R. Find a Cure. Support C.F.S.R. Any financial contributions may be sent to:. CFSR Foundation, Inc. Toms River, NJ 08753. The Caffarelli Family Study Research Foundation, Inc, is recognized as tax-exempt under section 501(c)(3) of the Internal Revenue Code. EIN: 22-3557181. As such, all donations are fully tax deductible. All proceeds will go towards C.F.S.R. research. Donations can also be made through PAYPAL using the button below. Contact C.F.S.R. Support C.F.S.R. Contact C.F.S.R.

4

Executive Board | C.F.S.R. Foundation, Inc.

http://www.cfsr.org/board

Help C.F.S.R. Find a Cure. Patricia M. Colasurdo. Susan B. Chillemi. Denise C. Lance. Contact C.F.S.R. Support C.F.S.R. Contact C.F.S.R. Support C.F.S.R. To educate the public and raise awareness about scapuloperoneal muscular dystrophy. Provide funding for research which would isolate the gene or genes responsible for causing the neuromuscular disease. To further fund research which would correct the defect in the gene.

5

Understanding Scapuloperoneal Muscular Dystrophy | C.F.S.R. Foundation, Inc.

http://www.cfsr.org/spmd

Help C.F.S.R. Find a Cure. Understanding Scapuloperoneal Muscular Dystrophy. Scapuloperoneal muscular dystrophy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Scapuloperoneal muscular dystrophy, or a subtype of Scapuloperoneal muscular dystrophy, affects less than 200,000 people in the US population. Contact C.F.S.R. Support C.F.S.R. Contact C.F.S.R. Support C.F.S.R.

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Links | Heartfelt Wellness

http://www.heartfeltwellness.com/links

Skip to main content. The Hahnemann Clinic for Heilkunst. The international center for the practice of medical Heilkunst. Provides a comprehensive, integrated treatment based on safe, non-toxic remedies. Holistic therapy method created by Ute Arnold. Caffarelli Family Study Research Foundation. CFSR is dedicated to educate the public and raise awareness of SPMD. Transforms communities by providing a safe space for a physical and spiritual growth and fully integrated personal development.

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