MagicMeerkat wrote:
She keeps saying it's a "spectrum" and you don't have to have every single symptom. She's adamant I have it because I was a "floppy baby" and now "failed to thrive" (the first time I have ever heard of that about myself). I told her the major symptom and the main thing about it is the excessive appetite an inability to feel full. But no, you don't need all the symptoms apparently. She will only let me have a DNA test from 23 & Me, not one from a doctor and I don't particularly trust 23andMe. She did not even know what prader willi was until she saw a CSI episode about it. (She's gotten lots of things wrong because her first exposure to them was a CSI episode and thinks that's how all those people are in real life). She used to look at the local foster kid website as if she were looking at puppies on Craigslist and some of them had prader Willi. As we were watching Gibson and Co remove content from the man's stomach, my mom said, "Oh, that is what some of those foster kids have." She did not start saying I have it until recently and it's making me self-conscious about eating.
She's full of crap.
She won't let you take a chromosome test even though it could prove her right if she is so convinced. (Prador willi is a known partial deletion on the 15th chromosome)
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Diagnosed autistic level 2, ODD, anxiety, dyspraxic, essential tremors, depression (Doubted), CAPD, hyper mobility syndrome
Suspected; PTSD (Treated, as my counselor did notice), possible PCOS, PMDD, Learning disabilities (Sure of it, unknown what they are), possibly something wrong with immune system (Sick about as much as I'm not) Possible EDS- hyper mobility type (Will be getting tested, suggested by doctor) dysautonomia