User talk:Cmaestas1970

Hello, I am a mother of a child with Homozygous Acute Intermittant Porphyria (AIP). She is the only known case in the United States with this disease to my knowledge. Homozygous refers to two gene mutations of the HMBS gene vs just one (heterozygous). People with AIP as described in the Acute Intermittant Porphyria wiki page and the general Porphyria page only have one gene mutation. I have not been able to find ANY online published information either on Wikipedia or other similar sources that would describe the Homozygous version of the disease, its symptoms, its treatments, its prognosis, etc with the exception of pubmed. I think its critical for families who have a child with this disease in the future to have access to information about this disease,in Wikipedia and other accessible and widely used places. Before my daughter was diagnosed, we spent 2 years searching through reams of online information to try to figure out what her disease was. Porphyria did NOT come up because the symptoms of Homozygous porphyria vs heterozygous porphyria are DIFFERENT. Had we been able to diagnose her earlier than we did perhaps her outcome could have been better. At the very least we would not have had to drag her around the country to doctors of every possible specialty who were also stumped. My goal in writing this talk page is to see if anyone would be willing to create a page or section regarding Homozygous AIP. I am not a Wikipedia contributor and I am probably not qualified to do it myself (I wouldn't know where to start). But I know just about everything about the disease and I know of the papers that have been published about it (just a few). I could certainly be a consultant to start the page. In other words, I would really like this disease to be known and documented but I really do not know how to get it done. Any help you can provide could ultimately save another child's life in the future, especially as gene therapies become reality in the next many years.

Thank you. Cmaestas1970 (talk) 18:48, 26 August 2016 (UTC)