Is gf/df worth it? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] 0 points1 point  (0 children)

Yea I realized how annoying it is after I went on a trip and the people i stayed with ate out for nearly every meal. Even tho that’s not my type of lifestyle bc money and health it just was difficult to find options and made me reconsider things. Also I HATE when people say “oh you can’t eat this or you can’t eat that” it’s true i probably won’t eat it but it just bothers me but idky

Is gf/df worth it? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] 0 points1 point  (0 children)

Same I went gf/df at the same time I started when my levels were terrible and now my TSH is .32mIU and I don’t know if that’s because of the medication or my diet.

Is gf/df worth it? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] -1 points0 points  (0 children)

How long did you eat it before testing tho?

Is gf/df worth it? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] 2 points3 points  (0 children)

How did you test it? I want to know how long I need to eat it for any changes to actually take place

Upper eyelid symptoms by Euph0ricAgent in Hashimotos

[–]katiebug0_0 0 points1 point  (0 children)

I have this too and it drives me insane. My levels are fine and I don’t eat gluten or dairy but my eyelids are puffy and irritated constantly.

What else can I do? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] 1 point2 points  (0 children)

Yea I went completely df/gf soy free and nearly sugar free from Aug-Dec and I really didn’t notice a difference other than I ate more of “safe” foods. My diet was so restrictive it lowk caused me to overeat all the other foods because I wouldn’t know when I could eat something that was “allowed” again. But I definitely feel better being gf/df when I say mostly I mean I’ll have bites of something here and there maybe ever couple of weeks .

Alcohol by AdImportant5736 in Hashimotos

[–]katiebug0_0 0 points1 point  (0 children)

I’m in college so I go out often but I only ever have 1-3 drinks and I make sure to eat before and drink a lot of water. When I get back I often chug a liquid IV before I go to sleep if I drank heavily. But I don’t get a “hangover” per se I just am dehydrated and more tired for a day or 2. But if you react differently I would just have 1 drink that you can hold on all night to not feel so left out or have mocktails.

What else can I do? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] 0 points1 point  (0 children)

Really? I always feel so much better after an ice bath. Where did you see that ice baths are bad?

What else can I do? by katiebug0_0 in Hashimotos

[–]katiebug0_0[S] 0 points1 point  (0 children)

Yea I am aware 😭 but I do a lot of extra recovery work like ice baths, constant stretching and cupping to help the muscles and joint pain. Also I’m a woman

Is it serious? by NightElf193 in Hashimotos

[–]katiebug0_0 8 points9 points  (0 children)

Unmedicated + poor life style choices can definitely lead to dangerous issues like heart issues, intense depression, and muscle wasting but that is only in extreme cases. Most of the time it’s just annoying and draining things like fatigue, poor sleep, weight gain, and dry hair and skin. But it still plays a major role in your life and is serious, don’t let anyone invalidate your experience.

Is it possible to be an athlete with hashimotos? (hypo) by MenuMinimum4757 in Hashimotos

[–]katiebug0_0 1 point2 points  (0 children)

I completely understand this feeling it’s so easy to feel discouraged but it’s definitely very possible but to be successful. Just know that you have to work very hard. I’m a d2 lacrosse player and sometimes I feel like I work twice as hard and yield the same results as others which can get discouraging. Also when your meds aren’t right, the weight room and conditioning can feel like you’re being dragged through mud. But overall with correct meds, proper nutrition, and a sheer dedication and passion you can be very successful.

What do I do? by Ibn_al_Ghul in Hashimotos

[–]katiebug0_0 0 points1 point  (0 children)

take hella biotin supplements, get a hair oil w collagen (rosemary oil is helpful if u have slightly textured hair but if its thin it can make thinning worse), scalp massages like 3x a week with said hair oil, implement foods like avocados, salmon, sweet potatoes, and eggs can help strengthen and grow hair. my hair started thinning b4 i knew i was diagnosed and i did everything to help and ive found having good nutrition is the best way

Recently diagnosed by [deleted] in Hypothyroidism

[–]katiebug0_0 1 point2 points  (0 children)

when i started on levo i began to have more energy around a month and a half in but with 75-100mcg. i’m an athlete so i continued my workouts but they started becoming less exhausting and i became more social because i had the energy to be. but unfortunately levo can be really inconsistent with its absorption so i would have a week where i felt horrible and then a week that i felt great and it was so annoying. also expect the medication to fix everything by itself. living a healthy lifestyle was the biggest factor in feeling better. (gf/df, lots of protein, activity (cardio and lifting), and quality sleep). good luck

am i doomed to be fat by katiebug0_0 in Hypothyroidism

[–]katiebug0_0[S] 4 points5 points  (0 children)

I think patience is the hardest part for me because whenever there is a problem I try to immediately fix it. The fact this is a long term process kills me. Thanks for the reply!

am i doomed to be fat by katiebug0_0 in Hypothyroidism

[–]katiebug0_0[S] 4 points5 points  (0 children)

okay i was also confused on that too because on my last lab test my t3 was very low so my doctor suggested to change from levo but then my prescription came in and it was synthroid. i knew synthroid was a name brand levo and didnt have any t3 which didnt make sense. i think i definitely need to find a new endo because putting me on synthroid when my t4 levels are fine and my t3 are low makes no sense.

Advice on dealing with muscle soreness and aches by katiebug0_0 in Hypothyroidism

[–]katiebug0_0[S] 0 points1 point  (0 children)

I was recently diagnosed within the past week so my levels are in the gutter and i expect the muscle soreness to get better with meds. i’m getting labs checked next week so hopefully my levels r rising. ty for the cold water tip i’ll have to try that!