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hope1

Form Letter/Physician & Foundation Database

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I would like to see form letters that can be printed or electronically sent to a members physician explaining what hppd is and how best to treat it. The vast majority of medical practitioners don't know of hppd at all. This cold cut down the amount of doctors seen, aid in disgnosis and prevent the dispensation of medication that could do more harm.

A section should also be dedicated to researchers and foundations that are doing work applicable to this condition and perhaps entice them to take notice as their research might be applicable to alleviate our suffering.

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