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Re: [Relapsing Polychondritis] post from a new member

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My mom was diagnosed RP two month ago in China, it was a shock to all

the families. now, she is taking a medicine program similar with the

one for breast cancer, one of her doc is testing the traditional

Chinese herbal medicine on RP.

I am trying to find out what nutritional diet supply would be better

for her. Someone said that the McDougall vegetarian program is good

for RP patients, does anyone have experience with that?

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