u/KatanaAmerica

Phone triggered dyshidrotic eczema?

Phone triggered dyshidrotic eczema?

Really weird situation.

Last Monday, I was goofing around on my iPhone when I started to get tingles on my fingers and tiny pink areas. When I looked, I could see little bumps forming before my eyes. I’ve seen something like them before in a milder version after I pet my roommate’s cat with wet hands, but this was much different. ( I don’t do that anymore and it’s been fine.) Ever since, I’ve been getting weird tingles in my fingers when I touch any part of my phone for any period of time and bumps have been popping up left, right, and center on them, too. Currently typing this with a stylus, and that helps, but wtf??

I tried cleaning it and going without my phone case to see if that was the issue, but it felt more “electric” when I did that, even with touchscreen gloves. This has never happened to me before with this phone and case, which I have had for several years. I tested out other iPhones of a similar generation, and the sensation was lesser, but I believe still present.

I think this is dyshidrotic eczema, but i don’t get why a phone case, iphone, or screen protector would randomly cause this after years of use. Critically, the bumps would appear on areas of fingers that weren’t actually touching the phone at all, ie outer knuckle of middle finger pad that is currently touching the phone screen. Anyone else experience something similar?

u/KatanaAmerica — 4 days ago

Low everything but still have HH?

Hi,
I just visited the hematologist a few days ago and got my labs done. Originally I was sent to her because my iron was 300 ug/DL, but now it seems to be 27? Ferritin and hematrocrit are also low. For context, I have had a 3 month long period that thankfully stopped. (Yes, bleeding for 3 months straight.)

I think she ran the HH gene test just to see, and it looks like she mentioned that I did have it, but it was high when I was bleeding, and now low that it has stopped. 2 weeks before we saw 300, my levels were 67, so a little low, but not suuuuper low like now. Is this even possible???

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u/KatanaAmerica — 6 days ago
▲ 2 r/zoloft

No appetite after stopping Zoloft??

I took 25 mg of Zoloft for about 6 days in a row before stopping Sunday morning because it was aggravating my burning mouth syndrome (probably caused by Cymbalta— long story). That’s all well and good, but I have had LESS appetite after stopping, to the point where I forgot to eat dinner tonight, which is very unlike me. I’ve had this in conjunction with a weird finger rash/sensitivity thing, again, after stopping. Definitely still have the weird dreams, too.

Has this ever happened to anyone else? Is this normal? I hate that all of the meds I’ve tried have had such weird effects on me.

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u/KatanaAmerica — 10 days ago

I took this med for a couple of months and had to stop because it was making my mouth unbearably raw and sensitive. It’s gotten a little better after I stopped earlier this year, but anything sharp like a tortilla chip or literally spicier than black pepper tears it up. (Jalapeño tastes like ghost pepper now!!!) That was not the case before I started this med.

I spoke to an ENT about it and some other mouth stuff and he told me that some people experience burning mouth syndrome whilst on this drug. I have never heard of this as a side effect. Has this happened to anyone else? Did it ever get better for you?

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u/KatanaAmerica — 22 days ago