#hashimoto's disease
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“I don’t let me disability stop me”
Good for you. Some people can’t just push through, and we’re still worthy.
#me/cfs#myalgic encephalomyelitis#epilepsy#long covid#pots#seizures#autoimmine disease#hashimoto's disease#actually disabled#disability#chronic illness#disabled
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Only three hours in on my sleep tonight and I wake up in a cold sweat and my muscles are cramping and sending shooting pain everywhere.
Just one night. Id like one night of REM sleep.
#disabilities#disabled#disability rights#disability#fibromyalgia#chronic illness#chronic pain#chronic fatigue#hashimoto's disease#hashimotos thyroiditis#autoimmune disease#personal
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Mia Castro, a model with Hashimoto’s Disease, Hypermobile Ehlers-Danlos Syndrome (hEDS), and Tarsal Coalition.
#mia castro#photography#model#modeling#disability#disabled models#fashion#hashimoto's disease#hypermobile ehlers danlos#ehlers danlos syndrome#heds#eds#tarsal coalition#autoimmune disorders#congenital disorders
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Dietry aspects that help you if you suffer from thyroid issues, specifically hashimoto's disease:
Avoid gluten. It sucks, yeah, but every source i found so far agrees on this. People with thyroid issues are more likely to be straight up gluten intolerant! If that isn't the case, you absolutely don't need to cut gluten out of your life. However, you should try to reduce the intake regardless. But not to worry! You can find brands that have pasta, bread mixes, pizza dough, even little snacks as gluten free! Alternatives are also always rice or corn for a lot of things. If you like to snack on crunchy things like cookies i can really recommend rice waffles. They even come with chocolate and other flavors a lot of the time. And as for the bread mixes don't worry, at least the german brand i get has the lowest effort kinda stuff. As in, put water, stirr, form on tray, oven, done (and i found one that is SO delicious to me even!)
Avoid pork. Also got this one from multiple sources. Like with gluten, it can be a problem if you're out a lot, BUT there is usually plenty of other meat. My go to is chicken or turkey. Beef is great too, but naturally it's more expensive than chicken etc. You don't need to cut out stuff like salami either because these days there's a lot of alternatives to pork in those regards
Veggies, veggies, veggies! I mean, who doesn't this apply to?! Vegetables are great and have so many vitamins. I try to eat a salad a day and have some veggies in my lunch. There is so many different vegetables, there's sure to be SOMETHING for you! In my salad for example i put grated carrots even though i don't like them apart from that. I also put apple to make it more sweet and delicious! (Note: for salad you should put some oil, otherwise your body can't absorb the nutrients that well. I love pumpkin sees oil bc i'm picky and don't like olive oil. But there's more you might like too!) Potatoes count as well for your vitamins. Put anything with some meat or in a stew or with rice, it doesn't really matter how you make them
Fruit is less helpful than veggies, but it's still great! Especially berries, apples, oranges, peaches, plums and more are helpful. That's because they have less sugar that for example pineapple, banana, grapes, or mango
Seeds and nuts. They can help you as well. I usually put sunflower seeds in my salad, but you can also put something in cereal or yoghurt or your lunch! They're nice and crunchy and can be great additions to some food
Less (cow) milk. Milk is fineee, but you shouldn't overdo it. Especialy with things with a lot of fat, like cream
Most fish. Most fish is great, salmon and tuna for example. In general, fish is really healthy. I don't like it but i know many do! So definitely keep eating it! :)
Eggs. Eggs are always good, get your protein! Many lovely ways to make eggs. Just make sure you don't always eat them with too much fat, so be careful with your fried or scrambled egg
Those are things i was told by a doctor or things i found from different sources on the internet. Some is obvious like you should just so in general get protein and vegebtables!
But for example, i've had hashimoto's disease for over six years now and only THIS YEAR i was told by a doctor that i should avoid gluten
So i wanted to make a little post for me and for others to have a quick check list regarding one's diet with thyroid issues! If you know/think of anything else, please share! It'll be much appreciated!
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Small vent, because recently I learned that I have Hashimoto's disease and that does explain a lot since it can cause a lot of different problems, but one of them is lack of libido.
I've identified as an asexual since I've been 14 years old, and over the years I've come to terms with it and became comfortable, even happy, by identifying as ace. I like not having any sexual attractions- but what if it's caused by this illness? It's not that I would feel like an impostor in ace community, but what if I'll get my treatment, and suddenly I'll just feel the attraction, because it wasn't there for the lack of my libido? I would have to accept that the label I was comfortable, that I grew up with, is suddenly not me? I'm suddenly really scared of the treatment even though I really want it, because I feel horrible in my body and this will help to change it, but yeah. I also have my concerns
Submitted May 4, 2023
#asexual#ace#aspec#acespec#hashimoto's disease#hashimoto's#Hashimoto's thyroiditis#impostor syndrome
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IRL Stuff, Woo
Anybody have low-effort/low-spoon recipes for an anti-inflammatory diet? Shoot me your faves if you're so inclined, please!
I'm pretty adventurous but hate doing cleanup after cooking, so particularly looking for things that are quick and easy but still taste like something.
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can never be comfortable in this body. emotionally, physically, or mentally.
#my post#mental health#afab problems#adhd inattentive#rejection sensitive dysphoria#anxiety#depression#monthly#hashimoto's disease#audhd#chronic fatigue#dysphoria#stress#social anxiety#adhd spiraling#anxiety spiraling#executive dysfunction#mental illness#chronic headaches#pain empathy#physical empath#ocd#pda#persistent drive for autonomy#pathological demand avoidance#task paralysis#procrastinator#choice paralysis#co dependency#isolation
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Life update feel free to scroll. Short version: just glad for the distraction this place provides
In 19 days I can see a new doctor. My body is a total wreck and we know what's wrong. We know it's not my thyroid. We know it's my PCOS. We have tried everything my one doctor (endocrinology and reproductive specialist) can think of and her response was just "when do you see your new ob/gyn?" The latest medication has made me so sick and I am preparing myself for the thought of surgery.
My horse's body is a wreck. He is still being treated for EPM, but we found out he's positive for Lyme's disease, so we need to treat that too. He is also lame like he has an abscess in his hoof, so I'm trying to soak his foot enough to encourage it to blow and resolve. Despite my health issues, I would feel so much better if my horse were better. It's kind of like we're both run down.
I am so zoned out and so tired. I have bursts where I can get things done, but they are harder and harder to come by. I've been going through a series of job interviews and projects, hoping to get a better job and a lot of my energy has gone into that, but I finish a video interview, close the laptop, and am ready to crawl into bed. Tomorrow I turn 38. I'm glad that whole doomsday prophecy thing was wrong. Even if I'm kind of out of it, I love you guys and your posts that I see. Even if I can't always interact like I'd like.
#about me#ignore me#medical stuff#health stuff#medication#pcos#hashimoto's disease#obgyn#epm#lyme's disease#fatigue#new job maybe#failed doomsday prophecy mention#i'm glad for the good stuff don't get me wrong#i just also need to sleep for years
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Me at random points throughout the day:
Why does my knee/hand/back/etc feel Like That
Oh right, the undiagnosed probably-Hashimoto's mystery illness
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i lied, it's a fuck around (attempt task) and find out (instant health decline) kind of day
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One moment you’re soaring on the wings of creativity, deeply invested in a scene, and the next, your body is like, Nope, we’re crying now—
—over a commercial, or because that one chord progression in a song felt too powerful. Chronic hormonal sensitivity can feel like you’re walking on eggshells with your own body, never quite knowing what each day will bring. It’s not just the mood swings; it’s the physical toll. You might be deep into editing or brainstorming, but a sudden hot flash or muscle ache pulls you out of focus. You lose time just managing the physical symptoms.
That unpredictability can disrupt the delicate balance between creativity and productivity. Writing requires a certain level of emotional engagement, but when you’re extra sensitive to emotional triggers, you might find yourself overwhelmed by your own stories. A scene that’s meant to be joyful might hit you harder than expected, or a conflict between characters could amplify your own stress.
Then there’s the mental fog that sometimes comes with hormonal fluctuations. You want to work on that intricate plot twist or complex character development, but your brain feels like it’s swimming in molasses. All of it combines to create this tricky dance between your body, your emotions, and the very stories you’re trying to tell.
But here’s the thing: when you manage to harness those heightened emotions, it can bring a richness to your writing that might not have been there otherwise.
We often talk about hormones in terms of balance, but the truth is, they’re never static. They’re in constant flux, shifting in response to everything from stress to sleep. So when we talk about ‘hormonal balance,’ it’s not really about perfect stillness—because that doesn’t exist—it’s more about finding a sense of stability amid the chaos. And for those of us whose bodies seem allergic to their own fluctuations, that idea of balance can feel like chasing a mirage, always just out of reach.
#pmdd#pme#on writing#writer problems#thyroid problems#chronic condition#writer stuff#hashimoto's disease#writers life
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I wish I didn’t have my illness, but I will not hide it to make healthy people feel more comfortable.
#long covid#chronic illness#epilepsy#me/cfs#myalgic encephalomyelitis#pots#potsawareness#autoimmune#hashimoto's disease#disabled#disability#seizures#chronically ill
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I think the main reason I haven't been able to write is I'm really anxious about two things of news this week.
One: whether long term disability finally fucking approves me.
Two: whether my work will accommodate part time work.
I am more optimistic about the first one because my illnesses *shouldn't* be pre-existing conditions but who the fuck knows what they'll deny you for these days.
The second one I'm very unoptimistic about. I have asked multiple other workplaces this same question when I inevitably burn out or am disabled mentally or physically in some way. For those other jobs it was always, "that would put an undue hardship on the business" and so they can't accomodate.
(not like I've been on fucking leave for multiple months and they definitely didn't put a "hardship" on the business but I digress)
I am hoping, that since this is a state job, they are more lenient but, I am not optimistic.
If I am not able to go back to work part time, then I will have to be "let go" by the state due to disability and forced to claim unemployment until I can find something 20 hours a week that pays enough and is remote or a desk job.
I will not let them guilt me into working more and hurting myself for capitalism. I have never had the goal to "climb the ladder" or get rich. I just want to survive.
My partner has suggested reaching out to a pro bono lawyer if they deny my accomodation request. But I am so tired. All the time. Especially about this.
#invisible disability#disabled#chronic disease#chronic pain#chronic illness#spoonie#chronic fatigue#chronically ill#chronic migraine#fibromyalgia#hashimoto's disease#Hashimoto's thyroiditis#autoimmune disease#disabilities#disability#rant#disability rant
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I was diagnosed with Hashimoto's when I was six. I had a fairly large thyroid nodule removed the same year. My thyroid function was monitored until I was about... 10? 11? And then stopped. I strongly suspect this was because my mom's private insurance wouldn't pay for the testing. I didn't get ANY treatment for hypothyroid until I was twenty. Complete thyroidectomy at 22.
Seeing people who are diagnosed with Hashimoto's in their 30s, their 40s, and they talk about how debilitating it is is just like.... I've had what you have all my life. This thing that destroyed your hobbies and job and life.
Have I EVER known what normal feels like?
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I got sent an article on Liam Gallagher talking about hashimoto's thyroiditis and the effect it has on his life. I think it's great he's talking about it, since people don't know much about the symptoms and I've read it is more common in women, so men might not be as aware and be less likely to seek treatment because it's less likely. But less likely does not mean impossible.
Hashimoto's is when your autoimmune system produces thyroid antibodies which disrupt thyroid function and make it underactive. The symptoms are broad and varied. Cold extremities is common, fatigue, brittle hair, goiter, dry scaly skin, it also causes swelling of the joints resulting in pain, abdominal swelling, facial swelling, slow heartrate.... and more. It can be hard to even suspect one illness might behind them and seek treatment.
The Mirror article in question
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#hypothyroidism#hashimoto's disease#hypothyroid symptoms#thyroid#thyroid problems#thyroid awareness month
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