Discover and read the best of Twitter Threads about #Hashimotos

Most recents (4)

When I first began to experience neck & shoulder pain in 2015 and the inability to digest food, I switched my 2016 insurance plan to a barely affordable PPO, determined to find out what was ailing me. Here's a diagnostic thread for #InvisibleIllnesses. - @jenna_payne
Like most people who thought they were healthy (more on that tomorrow?), we've been told that if you feel sick you go to the doctor and they can fix you unless it's something like cancer or Alzheimer's. I was in for a rude awakening....
CW: diet, eating disorder?
This scene from my medical revenge HYSTERIA is more or less lifted from real life. This was my first appointment after starving myself at 1200 calories/day and gaining 40 pounds in 2/3 years. The problem was NOT my diet.
Read 91 tweets
Greetings! I'll be your disabled hostess for this week. I am grappling with #AnkylosingSpondylitis, #Hashimotos, #EhlersDanlos, and some yet to be discovered issues. I write, direct, and produce films and am figuring out how to do that while disabled. - @jenna_payne A wall of money with the writing $300 MILLION. In front of tMe with dark hair pulled up in a messy bun lying on a white
The above pictures are from my wedding & after the last biggish live action short film I directed.

In 2015 & 2016, I felt an increasing amount of pain & began to struggle to digest food. In late 2016, it began to rain inside our apartment. Six months later my spine caught fire.
I worked my last film production job - a career I both loved b/c there's nothing like it & hated b/c the hours & stress were brutal - in the spring of 2017. Between that & the eventual Aspergillus that was discovered in my apt (& a blood test), I have been disabled ever since.
Read 8 tweets
[Your opinion needed]
I have learned how to manage my #Lupus and #Hashimotos naturally. For nearly 2 years, I've shared a thread about this (see attached). Now I'm ready to unpack this and add how I am keeping my symptoms in remission. /1 #newblog
I'm finally ready to write my #blog series:

"Everything I use to maintain my health and keep my #autoimmune symptoms in remission."

Do you also seek ways to take back control and possibly improve your own diagnosis?

Then please answer my short POLL⬇️

#lupus #hashimotos /2
Please ANSWER #POLL⬇️

Managing #autoimmune conditions is tough. Even though I had many healthy habits, I still had to change the way I was living to enjoy improvements. That said:

What do you want to improve to experience better health right now?

#lupus #hashimotos #blogger
Read 3 tweets
.@SarahbaxterSTM's argues that #fibromyalgia, #mecfs, #lupus, #depression, self-harming and #anorexia are caused by female ambition and fragility.

What's c. 1880 is new again.

thetimes.co.uk/article/kirsty…
This is just so silly. In the 19th century, there was a panic in the medical profession (and among social commentators) about women becoming ill with neurological and "nervous" conditions because they were overworking their brains/nerves, which were naturally weaker than men's.
This “fact” was used to bolster the argument in favor of stopping women's formal education after age 16 and most certainly not letting them enroll in university.
Read 26 tweets

Related hashtags

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3.00/month or $30.00/year) and get exclusive features!

Become Premium

Too expensive? Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal Become our Patreon

Thank you for your support!