← Return to Pain from Rare Genetic Metabolic Disorder
DiscussionPain from Rare Genetic Metabolic Disorder
Chronic Pain | Last Active: Nov 5 5:42pm | Replies (3)Comment receiving replies
Replies to "Hello @msclean, Receiving a diagnosis of Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) must have been both a..."
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@JustinMcClanahan I've been doctoring for 9ys with many health problems. Each specialist only looking at the symptoms they handle and sending me on to another specialist for another symptom and test. Never putting everything together because they weren't trained to do so. Our medical world is terribly broken. If Doctors were trained to look at the body as a whole and not have so many specialties and subspecialties, people could get the care they need sooner. Big changes need to happen in the medical training world!
The U of M has been no help. The genetic dr refused to prescribe me anything for the muscle pain. I had to go to Urgent Care for that. I'm the only adult they have seen with this. Still waiting on the Mayo referral. Mount Sinai will take me however they are not sure the treatment they use will work for me. They used medical grade ketones from the UK. MADD presents very very differently for each person. There are hundreds of gene variants of MADD located in different parts of the gene causing different problems for everyone.