I did a DNA test for my PD dad back in February (around the time he had worsening dementia) and got the results back recently. There's a section on neurotransmitters, ie dopamine, norepinephrine etc and shows he has risks with Parkinsons.
Not sure how accurate these tests are, obviously no idea what risk genes are even tuned up (or down) was just wondering if anyone has done the same. It's quite interesting to see things like he possibly has converted dopamine to norepinephrine too rapidly all his life, or that MAO is already possibly tuned down, or that like a lot of PWP he has a risk of low methionine.
Makes me wonder if some people aren't just right for standard medication, as he isn't doing well at all on dopamine.
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Dee1980
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They link my PD with being of Ashkenazi Jewish decent
Re: ur dad not responding to dopamine ... it's my understanding that if a patient doesn't respond to the Meds, the perhaps PD is not the correct diagnosis
They've doubled his dopamine dose. I'm not sure what we're meant to be looking for with a response. He's still bent over, dizzy, unstable, hand tremour and bladder issues. I'm worried it'll crash his serotonin and we'll be dealing with depression too.
Yeah I did wonder if it was just a low dose and not taking up the slack. He was diagnosed about ten years ago I think, though the hand tremour started after he had a stent in 2005. I think the Kemadrin (anticholinergic) helped a fair bit with stiffness and tremour, he's definitely worse physically off it. No idea if the pramipexole and rasagaline are doing anything.
I guess we'll have to wait and see if he picks up.
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