Can’t regulate body temperature.
Hi. I’m a newbie here and am like probably everyone has been - at my wits end. I need to find a new Dr but don’t know where to start. Problem is - I can’t regulate my body temperature at all. One moment I am hot. Next I am sweating. Next minute I’m shivering cold and totally wet from the sweat. Doesn’t matter if it is day or night. House is at 63, ceiling fan on high, naked in bed with single sheet for cover - I’m sweating- then cold … 10 mins later same thing again. All night long ball day long too. Outside in 33 degree weather and I’m sweating in a long sleeve t shirt. Hair wet from sweat. Can’t get cool. Then all of a sudden I’ll get cold for a little bit and shiver for a while. I’ve had test after test and yesterday I got a diagnosis of hereditary angiogram’s and mast cell activation. That makes no sense based on symptoms although I may have that too I doubt it. It isn’t hormonal and not thyroid related. I’ve searched and searched but can’t find anything similar. Any help is welcomed. Thank you
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Can I ask how much synths and np thyroid you are on? I have Hashimotos and my thyroid needs adjusting. .
I am on 88 mcg of synthroid and 45 mg of np thyroid
My rheumatologist dropped me too. If they can’t figure it out in their tunnel vision they dismiss you in pain. I knew I had PMR, but since only my primary saw me during the attack and she ganpve me prednisone, the rheumatologist tried to wean me off prednisone too fast. He said sero negative arthritis. Because of him I had a major flare.
I test negative for rhemotoid arthritis. Honestly, I don’t think anyone really knows what I have, but I know this is all from the covid first 2 vaccines. I’ve been on prednisone low dose 7 mg for 3 years with ups and downs, can’t get lower than that.
My rheumatologist did ultrasound on my wrist and hands. Being an RN Iam not stupid. He said I had seronegative RA. I told him I can’t have level 3 seronegative RA because the only way to get RA nodules is if you are stage 3 seropositive RA. He got really mad at me. I showed him the documentation on it proving him wrong. Oops he got really mad.
I was taking 100 mg a day for one week. I started seeing things that really weren’t there couldn’t make out certain objects for a while. I would think it was something other than it was. Extremely groggy and very forgetful. Definitely couldn’t function in normal life. I wish gabapentin would work for me.
It's so interesting how medications can affect different folks so differently! Sorry the gaba doesn't work for you.
I'm actually weaning off mine because I was diagnosed with lichen planus (red sore lesions all over my back) which can be a drug reaction to gabapentin. The lesions have been getting worse over the past two years and nothing has worked to make them go away (I've tried many topicals) so I'm biting the bullet and stopping the gaba. I've already noticed my night sweats picking up again, sigh. It's always something.
Ugh, I'm so sorry. Praying the tapering off gets better. Are you planning on Lyrica or something else?