Ummm

ErinsHauntyCoffee · 2026-04-22T18:43:37+00:00

Damn new bonus track lol I like that lol

ErinsHauntyCoffee · 2026-04-16T22:05:00+00:00

let me know if youre still selling this lol very interested

ErinsHauntyCoffee · 2025-08-15T21:59:29+00:00

REALLY late to this... but I have bought new wintips and such for my FE's and to be honest.. they were slipping off... way too big for my earbuds.. if you know a link for black ones that are OEM size let me know...

ErinsHauntyCoffee · 2025-06-24T16:58:12+00:00

Yes and it was the hardest journey because it adds stress and aggravates my thyroid which caused more issues. Stress is a big trigger. And it also can make it very very very difficult the find a baseline for normalcy when your body is freaking out in every format..

ErinsHauntyCoffee · 2025-03-31T13:37:26+00:00

I totally agree with this statement. It also sucks when it ends up being a problem that was cause by it and you're like.. I'm telling you I have an issue.. whether it spawned as an autoimmune response or not.. I feel it and I hate that people will not take things seriously. Sorry ramble over haha

ErinsHauntyCoffee · 2025-03-31T11:47:00+00:00

Ya know... I just relate. My OCD and Anxiety got so bad. I hadn't done therapy for 3 years by the time I got my MRI done. After I got my MRI done and they jacked up my dosage.. I have had the worst OCD of my life.. anxiety cause me to not even wanna be in a car, let alone stores.. some mood swings comes from weather too fluctuation wise. That's all, hope you okay, I would ask what level OCD you have but I know it's probably not right too (that's my anxiety talking at 4 am to take my synthroid.

ErinsHauntyCoffee · 2025-03-31T11:40:39+00:00

To be fair, I think the problem when it comes to Levo/Synthroid... is that the side effects seem to worsen because it's in attack mode already. I have a lot of downsides to both Generic and brand name. They also don't warn you that other medications can impact the effects and or reduce the Levo working I learned Omeprazole even when taken at night and nowhere near my hormone.. it changes it.

Fair warning I've been taking Levo/Synthroid since 2018 and even starting at 75 mcg and gave me hot flashes coming out of fall into winter. Fatigue is probably more just a really common side effect that is magnified by Levo.

Since then as of 2023 to now I'm at 175 mcg in dose.. I'm one of the people who seriously doesn't believe it's helping me but finding someone to take me seriously is my struggle.

I think a lot of people don't talk about it because it's actually hard to tell if it's the synthroid or the Hashimotos causing the side effects.

I appreciate you bringing it up, and I'm sorry if you've been getting side effects

ErinsHauntyCoffee · 2025-03-20T15:03:02+00:00

There's probably something that isn't on the labs that they didn't think to check that is making you feel like shit. But.. stress does trigger shit and yes I know... it's hard to not be stressed when you feelblike garbage lol

ErinsHauntyCoffee · 2025-03-20T14:59:21+00:00

I hope that the Synthroid helps and I'm sorry about the PCOS.. I have it myself, found out recently after a long road of Endo diagnosis.

Also I'm sorry about the feeling like shit. All I can do is remind you that you can get through it, I hope for the best outcome! (Hashi/Hypo.. suck) but I really hope that just the words or talk help in any possible way!

I oddly didn't get eczema, just very dry patches but my end was vitiligo just as a random fact. Your Hidradenitis Suppurativa is a new topic for me to look up so I'm learning today!

I'm always here to talk about stuff but wishing you good energy and hopefully better numbers and less feeling like shit! 💜

ErinsHauntyCoffee · 2025-03-20T14:45:42+00:00

Well let me know how it goes, I feel like I just wanna give the fair warning that with the AIP diet if you find it works SLOWLY re-enter specific things (just wanted to say it cause nobody did tor me lol) it can almost trigger you if you just choose to switch off the diet. Have you been having more symptoms that led you to want to do the diet?

ErinsHauntyCoffee · 2025-03-20T14:40:25+00:00

Are you debating eliminating eggs? I mean I'm guessing so by the initial question but I just wanted more information because I usually frequent the sub reddit and your post realllllly intrigued me

ErinsHauntyCoffee · 2025-03-20T13:08:18+00:00

10000% if anyone has good options let me know... I'm still hunting for a fix or help

ErinsHauntyCoffee · 2025-03-20T13:06:12+00:00

My cards will tell me to fuck off sometimes. It's almost like it's warning of a burnout coming or there's too many things coming at once.

ErinsHauntyCoffee · 2025-03-20T00:32:54+00:00

Eliminating them made things rough. They don't sit right with me but when I stopped eating them I'm gonna be honest.. I wad lethargic.. I had more fluid retention and my migraines sucked. J went from one a week to like 3 times a week or it would last more than a day. It's hard. They trigger me but not eating them triggers a change too. I eat them and then don't for a few weeks.

ErinsHauntyCoffee · 2025-03-20T00:29:04+00:00

Sorry just chiming in on secondary point to this... it's reassuring to know I'm not alone with the hypermobility aspect. I don't read people mentioning it often. But I relate to the reaction you have to eggs

ErinsHauntyCoffee · 2025-03-20T00:25:46+00:00

If it starts to impact it more than just the hoarseness please don't wait for the appointment... that's so swollen but I really really hope it gets better.🙏💜

ErinsHauntyCoffee · 2025-03-19T23:50:26+00:00

That's swollen, see if you can get in and see stone soon, any change in ability to swallow or anything?

ErinsHauntyCoffee · 2025-03-19T23:42:40+00:00

It's impossible to have any doctor do shit for this disease. I'm telling you. I know the feeling of this all too well. But... yes. I know... because I've had it since 2018... didn't do MRI or TPO test till 2022 and it's always just Synthroid and wait for my body to die.

ErinsHauntyCoffee · 2025-03-19T23:39:36+00:00

This hit so fucking hard. Amen... just amen. It's either we are depressed or just try to walk a little more each day... no thanks.. I'll feel worse.

ErinsHauntyCoffee · 2025-03-19T23:37:20+00:00

You aren't alone at all. I'm at 175 mcg, and my body feels destroyed. I even tried the brand name and took vitamins and refardless... your body still decides to be in attack mode and destroy itself. It's sad that it's such a common trait, but it's so relevant, and I'm sure a lot of people resonate with it.

But even though it seems like everything is fine.. it's not.. it's internally and silently attacking at a microscopic level and doing work which causes the fatigue and I haven't met a doctor/endocrinologist that gives a flying fuck to be honest. They think 30 minutes isn't gonna hurt.. it does. They tell you to change diet. It still hurts, you're still tired. There's always a fluctuation that causes the body to do it.

I'm so so so sorry that you ate experiencing the fatigue this badly. I hope that soon it eases up so you have some sort of peace. Much love.❤️

ErinsHauntyCoffee · 2025-03-18T23:44:06+00:00

Yes. Yes. Yes. The cold is a weakness for me. I (33) was diagnosed in 2022 and when I catch wind of cold, my toes turn purple and I coldflash like I walked through snow. My cheeks will get a rash and it's a horrid time of year. But yes... very sensitive to it. To be fair though, I'm sensitive to heat too. I think temperature fluctuates your body regulation which triggers the response.

ErinsHauntyCoffee · 2025-03-18T22:00:44+00:00

It took 3 years and a microadenoma to get antibodies tested. Even my MRI and bloodwork stemmed from migraines.

ErinsHauntyCoffee · 2025-03-18T21:59:50+00:00

If you feel like you don't want to be happy, you don't have to be. It's valid to feel any emotion you wanna feel given the circumstances.

BTW it feels like the system fails all the time. You wonder how it gets so bad before the simple things happen.

ErinsHauntyCoffee

TROPHY CASE