#thyroid symptoms and cure

[pdmhospital13]

Thyroid plays a vital role in your health. Learn about thyroid function, disorders, and management tips for optimal wellness.

[diabetes-health-corner]

Can BP, Thyroid, etc. Be Reversed

Rising urbanization and the unhealthy diets, and sedentary lifestyles that go with it have enabled this unrecognized, rising pandemic of non-communicable chronic diseases. When the insulin produced in the body is unable to function as required, glucose builds up in the blood and, left untreated, leads to a host of problems like diabetes, hypertension, high cholesterol, PCOD/S, and more.

Read more to know how to reverse it: https://www.freedomfromdiabetes.org/blog/post/can-bp-thyroid-etc-be-reversed-like-diabetes-can/2889

[sharath21]

Thyroid Specialist Doctor in Hyderabad, Kukatpally | MicrocareENT

[arogyamcentre]

[wellextol]

Your Thyroid, Your Metabolism: How a 30-Second Technique Can Change Your Life After 35

[kailash-hospital-greater-noida]

Dr. Ashish Saini, Consultant Endocrinologist at Kailash Hospital in Greater Noida, is committed to unraveling the nuances of thyroid disorders specifically in male patients.

[kailashdeepakhospital]

In this article, we shed light on male-specific thyroid symptoms, the avenues for treatment, and the importance of seeking expert care.

[myfitnessteacher]

Thyroid Cure | Cure Thyroid Problem Permanently in 4 Steps(100% Guaranteed)

Hyper and Hypo thyroidism are two most common endocrine disorders that originate as a result of malfunctioning of the thyroid gland, when this butterfly shaped gland in your neck doesn’t work at its peak efficiency it causes an overall imbalance this results in the form of fatigue sudden increase or decrease in weight hair, fall bulging eye's mood swings, depression, menstrual disorders and even infertility, no doubt thyroid malfunction is a serious disorder. Read more

[cripplecharacters]

Sorry to bother you,

Your blog is wonderful! Since it's one of the most dialogue/explanation oriented, i wondered if i may please come to you with a more general doubt. i'm sincerely confused... Why is "curing" disability bad per se?

So far, the arguments (on Tumblr) seem to be,

i. Consent.

ii. Generalisation. ("Everyone will want this same thing".)

iii. The undercurrent ideology holding disability as a flaw to be "cured" (including the use of the term "cure").

On which we all agree, they're implicitly bad no matter if it's disability or a haircut. Very well.

But.

What of magical healing per se is inherently bad? Because being given a choice implies that for every given person agreeing, there are going to be others who won't. So we should still write our fantastical society around them, that's not in any way in question.

But these, the possibility of magical treatment and the non-necessity of the same, are not mutually exclusive. You don't have to "take one before the other", they can very well coexist.

Last question (i promise), is seeking treatment for oneself bad?

Like, if there came up a quest to get the glittering flower blooming once a millennia guarded by the Evil Dragon of Evil and capable of magically taking away OCD and PTSD, sign me up! Or if there's a spell to resuscitate my thyroid or an alchemical pill that solves ADHD's executive dysfunction. i mean, that's kind of what my medications should do if they weren't so costly and inaccessible, and that would be a one-time thing too.

Autism's doing alright, i'd keep everything, thanks.

Disclaimer, i'm obviously not advocating for eugenetics (as this term has been often used and misused in these discussions, better to precise).

All these conditions in one way or another define me and effect my life in a pervasive, quotidian way, or/and on a more existential scale. Not always in bad ways -my life is not a tragedy, and this i wish to make clear. i'm not saying that a "magic cure" should come before a change in society to accommodate disability. What i'm advocating for is their coexistence, as a choice -not evil per se, but nocive if inserted in a context of ableism, negation of individual consent, and, indeed, choice.

Or at least that was what i was arguing for until a few months ago. Now however, seeing as the collective opinion is one of strong rejection for these ideas, i believe there must be some important fallacies in my reasoning, and i wish, before everything else, to correct them. To understand.

Sorry for the monologue, but, may you help me?

Thank you for your time and for your kindness,

Anonymous Sloth.

Thank you for your ask! The reason curing disability is bad in media is because the disabilities cured often cannot be cured in real life. People with incurable disabilities already have so little representation, taking away the characters they see themselves in with an impossible cure is incredibly disheartening. I live with multiple incurable physical conditions, and I’ve accepted that I’ll live with them for the rest of my life. Day to day I already deal with people saying how much better my life would be if I didn’t have these conditions I had no choice in getting, I don’t want to see that in my stories! If someone has my conditions I don’t want the author to get rid of them with magic, I want to see that character going on cool adventures and being badass! Sure a magical cure might be nice, but that’s never going to happen. I’m going to be living in this body for the rest of my life, and I want to see stories where people like me get to live their lives with their conditions!

Disabled people should be allowed to see themselves in sci-fi and fantasy stories! People who can’t be cured, who can only have their symptoms managed, who have to be on medication/assistive devices the rest of their lives and who don’t want to be cured should be allowed to see themselves in media without the constant reminder that most able bodied people think their lives would be so much better is they would simply stop being disabled.

Additionally, even conditions that do have cures or ways to manage them aren’t realistically portrayed. There are never any symptoms, side effects or rehabilitation, it’s always portrayed as a magical cure that completely gets rid of the disability. This rarely happens in real life, and I don’t think it’s wrong for someone who shares a condition with a character to want to see that condition accurately portrayed.

It’s perfectly fine for a disabled person in media to want to seek treatment, plenty of disabled people in the real world also have to fight to get treatment (though the fighting is usually against insurance and doctors, not dragons and wizards). But like I said above, it should be at least somewhat realistic. The world is already over saturated with stories of people getting magical cures that make everything better forever, but what about cures with long lasting or permanent side effect? What about healing that requires extensive physical therapy? Or someone who needs to take potions for the rest of their lives to manage their condition? These realities should also be portrayed. Sure maybe some people want to see an escapist fantasy where their conditions could get cured, but not everyone wants that and it’s almost entirely done by abled authors who fathom why anyone would want to see a disabled person who isn’t trying to ‘overcome’ their disability.

We’ve also reblogged this post & answered this ask that deal with similar topics if you want to check them out.

I hope this helps! Have a nice day,

Mod Rot

-

Everything Mod Rot said.

Basically, it's like giving us representation and then taking it away. Readers with that disability are going to read that book and relate to that character. Having a character like you in a work can be so important. But then the character is magically cured of an incurable condition, and now they're completely abled. Good for them. But the reader is still disabled. The reader will still always be disabled.

Disabled representation is already so rare. It's not really nice to take away what little we have.

- Mod Aaron

Echoing what everyone else has said, I want to add an extra thing:

If there was a wealth of disabled characters in media, represented with respect and nuance and care and all that, some stories involving disability being cured wouldn’t feel out of place, because there would already be so much to see that it would be an interesting departure and not posed as the only option for a happy ending.

And if you’re writing something about curing a disability that you have because that’s your experience and it’s what you want, that would make sense as well.

But since so many representations of disability in media have the underlying message that the only way to truly be happy or worthy or whatever with a disability is to have it cured, to have the least amount of signs of disabilities ever, then adding more of the same to that can be not just frustrating but harmful.

An “overcoming” of disability, a “making invisible” of a visible disability, or a cure for a disability are not the only stories worth telling about disabled people—because they are also not the only lives worth living for disabled people.

— mod sparrow

[balkanradfem]

Health news!

So, I've been having neck pain, that turned into head pain, for a year and a half now, and while I've had some more comfort since the center of pain was switched to my head, I've still been unable to walk, run, dance, jump, or use any tools like a hammer or a hoe. My right arm became functional again, but my left arm hurts from even holding a cup of tea. I had a neck MRI, and then a brain MRI, and there was no visible cause of pain, so I had a talk with my doctor, and she decided to test my blood for low vitamin D and low B12, and to check my thyroid function.

It turned out my thyroid is fine, but I had low b12, and critically low Vitamin D. She explained to me I need to get b12 shots every month, and that this could be the cause of the pain. When I came in, the doctor seemed overjoyed we finally found something concrete that is wrong with me, that we could treat, while I was wildly skeptical because I've been looking up symptoms of the deficiencies. While I had every symptom for vitamin D deficiency, I had none for b12, and only one article suggested there could be muscle pain as a result of it. Seems like feeble proof.

I have not been ignorant of my poor diet and living habits, I knew I had low vitamin D, and had supplemented it over the winter months, but apparently the store-bought dose I was taking was not enough. I did suspect a b12 deficiency as well, and was starting to take some B vitamins recently, but then read somewhere that they're dangerous to randomly take so I stopped. So what I'm saying is I knew I was sorta deficient, didn't think it was a big deal, I thought I was fixing it, I wasn't, my supplements didn't affect my pain or health. I got prescribed some powerful Vitamin D supplement, and got a b12 shot.

I have to say though, the nurse who was giving me the shot was acting ridiculous, first she was saying it to me like I'm a child, and I'm an adult, so I said 'I like shots, this won't be a problem'. She was not impressed. When she put the needle in me, I commented on how I can barely feel it, because I love acting cool in front of women with my high pain tolerance, but then she said 'When people tense their muscles it can get real bad and the needle can get stuck inside of them'. She said that while the needle was in me! I said 'I don't think I should be hearing this right now' and struggled to stay relaxed, and then she quickly pulled it out and it was fine. Maybe she just hated my positive attitude about getting the shot and needed me to be more apprehensive and afraid, which I don't feel is an attitude a medical professional should have?? Anyway. The shot was free for me so I love that.

The doctor told me 'you're going to feel much better next few months', super confidently, but I am still skeptical, I mean I wish I did feel better, and I'm relieved that something at least is getting attempted, and maybe a healthy dose of vitamin D will help with mental health, so okay, that would be an improvement. I doubt it will cure my head hurting while I walk though. Maybe I just don't understand deficiencies.

[pseudowho]

Hello Haitch! Hope you are doing well.

Last year during summer, I was diagnosed with PCOS (i had gotten it checked because i hadnt had my period in like 3 months) and since i was just 17, the doctor asked me to maintain a proper lifestyle and see till November and said that if it wasnt fixed by then, i had to do a checkup again. But i'd gotten my period by august so i never reached out again.

but this year (im 18 now), the last time id gotten my period was in april so it's been 6 months now. im gonna go to the doctor again later this month. but here's the thing— last year, i went to a gyno abroad because women's healthcare isnt the best in my country. but this year, its not possible for me to go abroad right now so im gonna have to work with a gyno from here.

now i have a feeling that theyll put me on pills and while i agree thats the easy way to fix this, im worried itll mess things up for the long run. the lifestyle the first gyno asked me to follow is a little difficult for me to get into since she'd asked me to exercise plenty and im a full time alevel student and it gets hard for me to maintain a proper routine like that. i also struggle with binge eating which i've heard comes with having pcos (im not sure if this is true tho).

so in one hand, i feel like it's easier to just start taking pills but then again it has so many side effects i don't know what to do right now.

Lots to unpack here.

CW/TW: PCOS, medical discussion, endocrine disorders, diabetes, hypothyroidism, weight management, medication management

Firstly, PCOS is often diagnosed based on vague criteria; lots of doctors flippantly diagnose it based on a volume of loose criteria. If you have an increasing number of these criteria, then yes, the chances are you have PCOS. However, it's often erroneously diagnosed without proper diagnostic procedures such as scans, bloods, and a full review of your longer term health history.

That being said, being on the pill doesn't 'cure' PCOS, it can simply manage the symptom of irregular periods. There's flimsy evidence on the pill's ability to manage/prevent weight gain and the development of other disorders that are associated with PCOS.

While weight loss is often harder for women with PCOS, especially if you have associated conditions such as an under active thyroid, it's not impossible.

Your lifetime chances of developing Diabetes are significantly higher with PCOS, and this chance goes up again if you struggle with increased body weight. PCOS and appetite changes like binge eating have been associated with each other, too.

So you'll only know if managing your weight and eating habits make a difference with your PCOS, when you've actually tried them to the absolute best of your ability. If you are at an increased ideal weight, losing weight can be very effective to manage and reduce the symptoms of PCOS.

Of the many, many thousands of women I've looked after, I'm sorry to say that those with PCOS who are very pro-active with managing their weight, perhaps taking medications as advised by their doctor (the pill and Metformin are the most common ones I see), and exercising regularly, are those who have the highest chance of being 'healthy' (though I do not use the term 'healthy' lightly).

Ultimately, PCOS is one of those things that just happens and isn't your fault. I also have an endocrine disorder that makes it very easy for me to gain weight and very difficult for me to lose it, so I absolutely understand the situation yours in right now.

But, what do you do with this information? Do you say, "I am X, Y and Z because of my PCOS" and leave it at that? Or do you say "I suffer with X, Y and Z because of my PCOS, so I make life choices to reduce the impact of my PCOS by 1, 2 and 3".

So my advice is this: PCOS may be the hand you've been dealt, but your lifestyle choices can massively improve the chances of you reducing its impact on your long-term health. I'm not blaming you, or acting like healthy eating, exercise and medication decisions are easy; they are not. Please recall I'm in a similar boat, and I'm not one to blame women for their complex health conditions.

I could talk all day about PCOS but this is my best attempt to summarise it for you.

It's really hard making tough life choices to manage the hand you've been dealt. I fully understand. I've gotten better at it as I've gotten older. @mrhaitch makes similar big decisions, because he has two diabetic parents and one diabetic siblings, so he takes care of his health to a brilliant degree, to try to give himself the best chance of not developing diabetes himself.

☝️ me being your hype man

Love,

-- Haitch xxx

[diabetes-health-corner]

Thyroid: Causes, Symptoms, and Treatment

TSH tells the thyroid what needs to be done to get the body back to normal. As long as these hormones are released in the correct quantity, your metabolism will function with no hitch. But if this goes out of whack—as it sometimes does, it leads to hyper- or hypothyroidism.

Read more to know the causes and symptoms of Thyroid: https://www.freedomfromdiabetes.org/blog/post/thyroid-causes-symptoms-and-treatment/2876

[sharath21]

Thyroid Specialist Doctor in Hyderabad, Kukatpally | MicrocareENT

[astrogirlythings]

My PCOS journey:

Vulnerabilities and all.

The biggest problem with new age women's health issues is that even many women fail to empathize with them. How can we expect men to empathize with women's health?

When I talk about women's health I don't mean "PERIODS" or "PTSD Post pregnancy" or "MENOPAUSE".. There are so many health issues that are not being talked about enough (at least from where I'm from 😒). Starting with a few - PCOS, PCOD, Thyroid, Hormonal imbalance and other lifestyle diseases. Not to mention that they have no cure and the only solution we have is to manage it and its symptoms.

While fighting with its symptoms.. one of the biggest things that helped me overcome my PCOS and Hormonal imbalance is some much needed moral support. Of course strength training, diet, 8 hours of sleep, managing stress and having a positive mind too.. but being surrounded by those who make an effort to understand ur health is a blessing.

I suffered excessive hair loss and weight gain and as a woman I've been constantly reminded that those "Assets" (Head full of hair and a slim figure) are the only things that add value to me and my existence.. and it's messed up how even the most educated are unaware about women's health.

Truth be told, I've spent years of my life picking up my pieces and reconstructing myself emotionally, mentally and physically. The sleepless nights I had were consumed by me obsessing about my body, its image and how it was perceived by everyone around me. The world has successfully convinced me that I am nothing without this so called "Perfect body". I lost many opportunities because of my negative body image. Deep down I knew that I am smart, creative, funny, kind and I am also known to be a good friend. But people succeeded in making me feel less than what I am.

As I write this, I want to convey that you are not alone. I believe that I am not the only one feeling this way.

Being surrounded by people who truly make an effort to understand ur health and ur erratic mood swings (because of ur health) is a huge blessing.. God knows that I want that in my life. Everyone wants to feel empathised and if u don't have someone that empathises with ur health.. I hope my empathy towards women's health helped u.

I am now 27 years old and I have finally succeeded in managing my PCOS symptoms (Physical and mental symptoms) after struggling with them for the past 9 years. Yup.. I lost most of my 20s to PCOS and I am cautiously optimistic that the struggle is over now. And even if it comes back.. at least I know how to deal with it.

[wellextol]

Your Thyroid, Your Metabolism: How a 30-Second Technique Can Change Your Life After 35