Become an Advocate for the International FOP Association

While you may think that you are just one person, and your voice is too small to be heard, every effort makes a difference! In fact, it is essential that you write to your elected officials. That's how grass-roots lobbying has its largest impact. The greater number of people who write and call their representatives, the more influence we have in order to make a difference in the lives of those with FOP.

Remember: FOP is serious. If the discovery of the FOP gene is found it will benefit FOP patients world-wide and also will have great implications for millions of patients who suffer from more common bone ailments, such as arthritis, osteoporosis, hip replacements, post-amputation treatment, fracture treatment, certain spinal cord injuries and some heart valve disorders.

For those who suffer from FOP, it is a painful metamorphosis into progressive immobility and a lifelong obstacle to physical freedom.

We matter!

PLEASE HELP the children and adults living in bodies encased in bones. They have the same dreams, aspirations and goals as other people but unfortunately face each day with greater struggle.

We need your suppport!


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The International FOP Association does not provide medical advice. The material contained in this web site is provided for informational purposes only. It should not be used for diagnostic or treatment purposes. Please consult your physician before acting on this or any other medical information.
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International FOP Association · PO Box 196217 · Winter Springs, FL 32719-6217
407-365-4194 · E-mail
together@ifopa.org