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Post by oneladyff on Aug 28, 2015 1:33:17 GMT -5
Hi I am new to this site I am a physician and scientist working on fructose and hereditary fructose intolerance I am also collaborating with Dr Tolan in Boston We are trying to develop a safe drug or possibly nutraceutical to help patients with hFI that has been officially diagnosed One thing we need to know more about is the natural history-- how common does liver disease occur-- how often one gets severe reactions like nausea or hypoglycemia Would people be interested in completing a questionnaire and are you aware of there is an official registry? I would love to help reverse this disease Richard johnson Richard.johnson@ucdenver.edu R
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Post by colormist on Aug 28, 2015 7:38:03 GMT -5
Yes! I'm interested in completing the questionnaire!
I knew there was some kind of official group on the Boston Lab website, but I wasn't aware of an official registry.
Very excited to hear about this!
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Post by Tammy on Aug 28, 2015 8:41:59 GMT -5
Count me in for questionnaire
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Post by Tammy on Aug 28, 2015 8:44:01 GMT -5
Count me in for the questionnaire. My daughter is registered on Dr Tulans site.
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