hashimoto

With Fibromyalgia, Hashimoto’s, Depression, Anxiety and 4 back surgeries, I found out yesterday that I have to have another surgery and it’s a doozy. My kyphosis scoliosis went from 10 to 40 degrees in a year, and 13 more degrees in 4 months. I live in constant chronic pain, which my medications no longer provide much help. My neurosurgeon told me my spine is basically collapsing on itself. My muscles and tendons are not doing their job supporting it and my only hope to not live in so much pain is to have a scoliosis surgery, where rods and screws will be put in my thoracic area. 3-5 day hospital stay and doc says I will hate him for the first 6 months. I am in my early 50’s, and scared to do it but also scared to have it progress even more.
Anyone else out there have this surgery? I’m nervous as hell. #kyphosis scoliosis #Fibromyalgia #hashimoto #Depression #Anxiety #Mixed connective tissue disease

Hi, my name is Chris. I've been diagnosed with

#MightyTogether #Anxiety #Depression #Migraine #hashimoto Disease. I am struggling with this diagnosis. My most recent TSH level was 34.18!!!! The doctor has told me this is one of the highest levels she has ever seen. I am a married momma with 5 children, four of them are under the age of 8 and range from 16 to 3. I am tired all of the time and my back always is tense and sore. I've been told I am lazy, unproductive, and overweight. I've been told that I don't care enough about myself or my family. I suffer with debilitating depression, anxiety, and panic attacks. I drift through life feeling like im in a fog 95% of the time and I cannot describe how I feel.

Good afternoon fellow Mighty’s! I am diagnosed with Fibromyalgia, Hashimoto’s, Arthritis, Psoriasis, and failed back surgery syndrome.
I have a question- does anyone else experience arm weakness and pain at night? This is a new symptom for me. UGH will it ever stop? Some doctors say Fibromyalgia does not get worse with age, I call bull#%¥+
on that! #Fibromyalgia #hashimoto ’s #chronic pain

I am a new member with a few rare diseases and mental health conditions due to an entire life filled with trauma. I’m hoping to find others like me so I don’t feel so alone in this daily fight to stay alive. #MightyTogether #ComplexRegionalPainSyndrome #Agoraphobia #EmptySellaSyndrome #hashimoto #Anxiety #PTSD #OccipitalNeuralgia #longhaulcovid

I'm having mixed emotions with hubby and his kids/their family.
We have been married for a number of years and still have problems with boundaries with kids.
I'm feeling trapped frustrated and angry. I've been told I'm the problem with relationships and reason for son writing his dad off by his daughter.
Now, we are retired and watching great grandkids 3 x a week. I'm wanting to travel with him, take classes and get out more.
We had issues with grandkids and the demands getting too much and when we set a limit, it ended up a nightmare.
I guess I just needed to vent , but I'm feeling like I need to run,,,,#Depression #Diabetes #hashimoto #EatingDisorders

I have just recently started my autoimmune journey, and I have for the most part been taking everything into stride. I'm really relieved that all of my symptoms have an actual cause behind them, and have been trying to make better lifestyle choices to push the antibodies into remission and minimize symptoms. Even so, I still get flare ups and it's so frustrating. I can't concentrate at work, can't enjoy little things, and I feel like no one in my life can understand me right now. I had to hold in the tears just now at work. If anyone else is going through something similar, I feel for you. I am here too. You are not alone.
#CheckInWithMe #hashimoto 's #autoimmune #hashimotos #Hypothyroidism #ChronicIllness

So is this it for me? I have a Masters Degree.  I taught for 10 years in public schools before this damn autoimmune crap.  I started my own Family Child care business for 12.0.0.5 years .  I was the care giver for my grandma for 9 of those 12 years,  My grandmother passed away in Nov. She was 98 Her health started to decline in June of last year. Coincidently, I loss more than half of my child care clients as well as more than half of my income at that time.  I was diagnosed with Lupus in September.  I have been anxiety ridden, stressed and all the rest since then   Right now, I need income I am applying to jobs, Looking for work at home jobs because my vehicles transmission went out and also because I let some family stay here and I honestly don't know if I feel comfortable leaving them here all day if I go to work.  I know  sounds dumb but she has a baby and is bipolar and has no where else to go.   I interviewed for a work at home job yesterday and I DID NOT get it,  I feel like CRAP,  I really suck at interviews.  I just knew I had this job.  This disease makes me NOT think clearly so I know my answers did not flow.  I really needed that job.  I went thru so much to prepare.  What the hell am I going to do?? These bills are piling up