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Replies to "Hi Paula, welcome to Connect. I searched the members of Connect. @billjan posted about tumid Lupus..."
Sorry about your illness I have auto immune PBS I just caught a Macy's home sale I got one of the chilling pillows on a great sale they had the cooling jell mattress top for a king bed for 120.00 normally 799.00 keep an eye for their sales my pillow was 20.00 from 120.00 keeps my neck cool at night if I find them on sale again will try to reach you I need the mattress cover for sure nothing worse than being hot while attempting to sleep, God Bless and prayers to you and your illness hope Drs can make you comfortable? Deena
Does the heat feel like it's coming from your skin or more from deep inside of you?
More like deep inside and you can actually feel the heat coming off me especially when a fan blows on it
Do you also have issues with sweating, facial flushing, body aches, or anything else? And if you don't mind, what medications are you taking and for how long?
I actually use a chillow pillow every night. They are my saving grace when I sleep. Since it keeps my head and neck cool I think it helps regulate the temp of the rest of my body. I have not seen the cooling gel mattress covers but will keep an eye out for them. Thank you for the info
I had the hot-deep-inside-of-my-torso issues that you are explaining for years. I didn't wear a coat for a decade, and I live in western NY. I also wore my hair up for years because if the back of my neck was covered, I would become incredibly more hot. The heat issue was in addition to a slew of other, snowballing issues. I started going to Mayo a year ago, and in November, I asked them to evaluate me for drug hypersensitivity. Eventually, I was referred to Mayo Pharmacogenomics in the Center for Individualized Medicine. They ran tests on me, and it turns to that I have a bunch of polymorphisms in my Cytochrome P450 liver enzyme system. We all have a bunch of different enzymes, and these are how the body metabolizes most of the medications we take. Polymorphisms that we are born with can make these enzymes perform too slowly or too quickly. Most of my polymorphisms make me metabolize meds too slowly, and getting hot was one of my symptoms. With that said, even if you don't have polymorphisms, many medications inhibit these enzymes from working properly as well, which makes your enzymes slow down even more, and the longer you are on an inhibitory enzyme that your body needs to metabolize a medication that you are taking, or the more medications that you take that also inhibit, the worse and worse you will feel.
After ceasing P450-metabolized medications, my body slowly detoxed, and my symptoms, including this one, completely disappeared.
Sorry it took so long for me to answer but I do have facial flushing but not sweating unless I am doing something physical. Actually when I sweat for a long time continually I feel better. It's like getting the heat released from my body but usually it only works when I'm cleaning house which takes me 2-3 hours and I am drenched in sweat when I get done but I feel normal for a while. I take plaquenil and gabapentin which is something my dermatologist wanted to try to see if it would help and it does some.I have been taking medication for a year
This is how I would be, too. Absolutely drenched with sweat after activities that normally wouldn't do that to me. And the more medications that were added to my regimen and the longer I was on them, the worse my symptoms got. If symptoms persist or worsen, please consider this testing.
Just saw your post. I am trying to find a doctor that can treat me so I don't have answers. Although I too have the same problem. I have red splotches on my arms that never go away and will fade to a almost unseeable, but then I when I go in the sun they will begin to get a brighter red. Depending on how much time and how often I am in the sun depends on how much they slightly raise and turn brighter red. And as for the heat, I too have problems and usually at night after dinnertime. I will get so hot that I have to spray myself down with cold water and turn my ac down low and leave it that way until I cool off. I can't say it freezes my skin, but I am very uncomfortable when air blows directly on my skin.
I have the symptoms that come with this condition which are photosensitivity and red spotches from exposure to direct sunlight and fluorescent light but mine seems to be extreme. I am constantly hot but my biggest issue is during the evenings when seem to start burning from the inside out. Terrible heat comes from my body from my neck down and if use a fan it freezes the top layer of my skin but I'm still hot so now I'm both got and cold and terribly miserable. This has my Dr stumped too.