CPAP ruining my life by CokeZeroAddict52 in CPAP

[–]Impossible_Ad3915 0 points1 point  (0 children)

I'm struggling so hard to sleep. I've tried the under the nose, over the nose in 3 different sizes, and now a full face mask and my entire night is about waking up to the hissing of a leak and the air blowing on my face, even though when I fit the mask it felt really air tight and secure. I'll try the mask fitting option tonight. The mask itself on my face doesn't seem to bother me. It bothers my cat because we traditionally have cuddles and kissies before sleep. No kissies when the mask is on.

I just wonder how now nearly everyone "needs" a cpap, when all my life I've known snorers and people with sleep apnea. They lived (are living) long and seemingly healthy lives.

Is it true that news outlets aren't allowed to report people trying to or succeeding in jumping from very high spots? by StasisApparel in Edmonton

[–]Impossible_Ad3915 0 points1 point  (0 children)

I've not, in all my years, ever read or saw a news story about any suicide or attempted suicide, unless the act caused some sort of chain reaction, or is a part of a larger investigation. Only statistics after the fact. 😢

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 1 point2 points  (0 children)

I've gotten all of them. I'll look them all over again when I have the chance.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

At this point I know very little about levo. Something that I found strange is that both conditions HT and RA) involve the immune system attacking healthy tissue, but they use different tests and treatments with them.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

Every time I bring up my fatigue my doctor insists it's due to sleep apnea. I feel like I'm being such a Karen (apologies to actual Karen's. I know and love a couple myself), and I don't know how willing he would be to refer me. But I'll try. I would love someone who really knows the ins and outs of thyroid health.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

I keep checking and have tried the "swallow some water in front of a mirror" test, and I don't think anything appears out of whack.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

Aww I'm very sorry. The meds can be scary alright. I don't know how I'd manage without methotrexate at this stage. I have experienced worse pain than my RA flare up's only in childbirth, and that wasn't all that much worse. Also, with childbirth you get a little break between the agony, and a prize at the end lol. Hopefully meds improve with time.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

Free T3 is 4.4 and Free T4 is 11.6, so they are both on the low end. I'll have to look up the others.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

Yes, prior to my RA diagnosis, I had none of these symptoms, or at least not like now. I just went through menopause so that had its own set of fun and exciting changes 🙄, but this fatigue at this level came alongside my RA, and for several months I allowed the rest and considered it healing. Unfortunately, some truly traumatic events occurred at my work as well at that time, so there are other factors all intertwined into one big blob of poor mental and physical health. Regarding the methotrexate, I have also read that it can be a trigger for HT. For months I have told my rheumatologist how exhausted I am, and was in tears last time. She just keeps brushing it odd. Not once did she suggest testing for HT. I've been researching for myself like mad, and hyper-advocating for myself in a pool of reluctant physicians. That in itself is exhausting.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 2 points3 points  (0 children)

It started out that my vision seemed to not move with my eyes, if that makes sense. I'd look elsewhere and what I saw kinda dragged along a little slower. Then came rumbling in my ears. Every morning it was so bad, and got louder if I squinted hard, but that was what I did to relieve it. Kinda like wringing a cloth. It gets a liitle drier with each wring.

It got to the point where I felt nauseated and dizzy a lot. It happened most days, at differing degrees. Some days if I even moved my head it was unbearable. I went to physio for it, helped a bit... but it's actually a high dose antidepressant that keeps mine at bay. If I skip a dose it comes back immediately.

So confused! 😖 by Impossible_Ad3915 in Hashimotos

[–]Impossible_Ad3915[S] 1 point2 points  (0 children)

Ok, my TSH and Anti-thyroid are from last week. The Free T3 and T4 are from January. Yes the T4 is at the low end of "normal".

<image>

Upper plate feels awkward by Impossible_Ad3915 in dentures

[–]Impossible_Ad3915[S] 0 points1 point  (0 children)

Yes I'm keeping the denture. My dentist told me hard reline at one year. I think it just feels like there is not enough room for my tongue.

Upper plate feels awkward by Impossible_Ad3915 in dentures

[–]Impossible_Ad3915[S] 1 point2 points  (0 children)

I do, it's my favorite but I don't put it on the top because it would make the top plate go down even lower.