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    Feeling Alone #CysticAdenomyosis #Adenomyosis

    Every time I’m laid here in crippling agony, tears streaming down my face, I just want someone to say “I know how you feel”. However with Cystic Adenomyosis I’ve yet to find anyone else with this ugly disease that can say that. I feel alone, in pain and wishing someone else could say those words. Then I realise I’m wishing this ugly disease on someone else, which I’d never dream of. I can’t win.. #CysticAdenomyosis #Adenomyosis

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    Period Pains

    Have you ever just wanted to yell at your uterus because your period hasn’t started yet but you keep getting period pains? #Endometriosis #PolycysticOvarySyndrome #Adenomyosis

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    Ovary Removal

    Had my right ovary removed yesterday! While I’m still in a ton of post op pain, I’m not feeling the constant pain I’ve felt for the past 4 years. My doctor also checked for endometriosis and hasn’t seen any new growth, and of course my uterus still shows signs of adenomyosis. #PolycysticOvarySyndrome #Endometriosis #Adenomyosis #Surgery #ovary #ovaryremoval


    I'm new here!

    Hi, my name is JJ5718. I'm here because I want to learn more about self care and living my best best life despite!

    #MightyTogether #rhuematoidarthritis #Endometriosis #ic #interstital cystitis #Adenomyosis #Fibromyalgia #ChronicPain


    Feeling down and depresses

    I am feeling somewhat down and depressed plus anxious. I joined The Mighty a few days ago and I'm just now feeling more comfortable telling my story. In 2006 i was diagnosed with Leukocytoclastic vasculitis. I had purpura all over both legs and it was very painful. It took a few months but I recovered and was relatively healthy for several years. Then as soon as I hit 40 it was like my health fell off a cliff. I was extremely tired all the time, depressed, and had night sweats. My doctor repeatedly checked my hormone and thyroid levels but they kept coming back "normal". Then I went to an ENT to get my ears cleaned. During the exam he felt my throat and said my thyroid was enlarged. I had an ultrasound and my thyroid levels checked, again. Finally I was out of range and I started synthroid. I noticed over the next few months my symptoms got worse and my neck was getting bigger. I had another ultrasound and talked my doctor into increasing my dose. The ultrasound showed I had nodules on my thyroid so he sent me to a pathologist who I well known around me for only testing the thyroid. I had a fine needle biopsy which came back benign. However, he said he could tell by looking at my thyroid I had hashimotos and sent a note to my doctor to test my TPO. It came back way, way out of range at over 800. My doctor said I had hashimotos in the past. By this point though I had been doing my own research and new that wasn't correct. Plus I went to an endocrinologist who was concerned I not only had hashimotos but graves disease too given how large my thyroid was. The graves test came back inconclusive. Meanwhile, I was on a hormone rollercoaster plus I developed shingles. I wound up in the hospital a few times and was taken seriously once till shift change where the new doctor brushed me off and sent me home. My primary care doctor was not happy the hospital brushed me off because I had chest pain. I saw a cardiologist a few times, was taken off synthroid then back on because my thyroid levels were all over the place, then after about 6 months everything calmed down and I was stable. I ended up changing primary care doctors since I couldn't get the old doctor to believe I had hashimotos plus he wouldn't check my iron levels. The new doctor checked my iron at my first appointment and found my ferritin level was very low but never tried to figure out why. Fast forward a couple of years and I start having severe pelvic pain. After seeing 6 doctors in the span of 2 months I finally get diagnosed with adenomyosis and fibroids. Nothing was helping with the pain and I had a total hysterectomy only keeping my ovaries. I woke up from surgery and the pain I had been in daily for several months was gone. Then about 7 months later the thyroid pathologist told me my thyroid was getting so enlarged I should see a surgeon about getting it removed. The same week I severely sprained my ankle and lost my insurance. Two months later with new insurance and still dealing with the sprained ankle I went to a pain management specialist and he sent me the physical therapy. By this point it was December so the holidays interfered with starting therapy and my Achilles tendon quit working and I was on crutches. Meanwhile, I couldn't work because I worked in catering and had a heck of a time getting on disability. I ended up having to quit my 2nd job because I just couldn't walk and be on my feet as long as that job required. Over the next 6 months I faithfully went to therapy and doctor appointments. I wound up in a walking cast at one point, sprained my ankle again, and had the big toe on the same foot sprained after someone walked right into me and stepped very hard on my foot. This caused me to go on workers compensation because it happened at work. Meanwhile at the same time my landlord decided he didn't want to renew my lease so I had to fight him in court and look for a new apartment. Oh and my insurance decided I had enough physical therapy so they cut me off. This brings us to January 2020. My whole family got sick in January with what we now know was covid, we didn't then. While I was still recovering we moved. I was able to return the physical therapy for a brief period till lockdown in March. I had a few virtual appointments then I was discharged about a month later. In September I went to a new endocrinologist and she looked at my records, ordered a new ultrasound. She confirmed my thyroid was way to large to even figure out what was thyroid tissue and what was nodules. She sent me to a surgeon who immediately scheduled me for surgery for a total thyroidectomy. I recovered from that, my anxiety spiraled way out of control and my husband took me to the emergency room one day. That got me into the counseling and with a psychiatrist right away and I'm on medication. With my anxiety getting under control of course something else had to start. In October I started having what I think are vasculitis flares. I tell my doctor who prescribed gabapentin and also started me on a statin due to high cholesterol because genetics. I am allergic to dairy, have gluten intolerance and overall already eat fairly healthy. So I started both new medications and immediately break out in hives over Thanksgiving. I stop both new medications and the hives don't go away. So after 2 rounds of prednisone they finally go away. The doctor wanted to wait a few months before trying anything new again. Meanwhile, the pain my legs gets worse but mostly tolerable. Then one day in February I'm doing normal housework and halfway through the day I am in so much pain I can't walk. I'm laid up in bed for a week. I make an appointment with a rheumatologist who I saw last week. He was really thorough, nice, and clearly explained his thoughts. He doesn't think it's the vasculitis flaring up and runs A LOT of tests, 12 vials of blood and a cup of urine. He briefly mentioned fibromyalgia. When I Google fibromyalgia I do check a lot of boxes for it. He said expected all the test results to come back negative but they didn't. I did what I know you're not suppose to do but I Googled the test results that came back out of range and the only things I can speculate is maybe I do have fibromyalgia, the vasculitis is flaring, and I may have a mild case of a hereditary blood disorder that is in my family, my dad had it and several cousins have it. It's spherocytosis. The only reason I speculate on the fibromyalgia is the soles on my feet really hurt and that does not go with vasculitis. I'm currently learning that I can't push myself or I over do it and wind up in a lot of pain. My feet constantly throb. I am starting to pace myself. I see the rheumatologist the first week of May to go over the test results. So that's my story, sorry it's long.

    #Anxiety #hashimotos #Hypothyroid #Adenomyosis #Hysterectomy #HighCholesterol #Undiagnosed #Fibromyalgia #LeukocytoclasticVasculitis #ChronicPain #MultipleDisabilities #Spherocytosis #ChronicPain


    Post Surgery

    I’ve still been in a lot of pain. My surgeon said if physical therapy doesn’t work that we’ll start having a conversation around a hysterectomy. He also wants me to try IV Ketamine treatments concurrently with physical therapy. My surgeon thinks I might have adenomyosis as well and the only cure for that is a hysterectomy. I’m so frustrated and sad. I thought the excision surgery would help me but it didn’t. #Endometriosis #Adenomyosis #ExcisionSurgery #Chronicpelvicpain


    Post-Endometriosis Surgery

    I had excision surgery for Endometriosis 111 days ago. I still experience intense pain during my period. I also suffer from chronic pelvic pain. I have physical therapy scheduled for the end of December. The surgeon suspects I have Adenomyosis as well. If physical therapy doesn’t work we’re talking about a hysterectomy because hormonal treatment makes me worse. I’m frustrated and I feel so alone in all of this. #Endometriosis #Chronicpelvicpain #ExcisionSurgery #Adenomyosis



    I am disabled and chronically ill. My boyfriend is nondisabled. We've been together almost five months now, and he's a wonderful man. I get nervous that one day he's going to get sick of me and all my health issues. Does anyone have an tips to cope with and work through that anxiety and fear? #neisvoid #MyastheniaGravis #Fibromyalgia #Endometriosis #Adenomyosis #Disability

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    Treating yourself on hard days

    I’ve been struggling with #Endometriosis and #Adenomyosis pain and fatigue and got some bummer test results back today. So, here’s how I treated myself at target while I waited for my meds to be filled:
    1) I got myself some new gel pens! I’m starting to bullet journal and hoping to track #Migraine and endo symptoms in them. I think it helps with my #Anxiety as well. I’m a terrible artist though!
    2) I got some fun hair clips and eyebrow makeup! I have no idea how to do eyebrows, but it’ll be fun to try.
    3) I got some period underwear (never tried before but hoping to get some bleeding relief!) and bubble bath. I can’t wait to soak.
    4) Bought myself Starbucks on the way out! Nothing cheers me up like Starbucks.

    So, even though I got some bummer results today, and I feel far from my best, today wasn’t all bad. I’m working on finding silver linings on the hard days. What do you do to cheer yourself up when things get hard? #MightyTogether

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    Hoping for answers soon #Endometriosis

    I’ve been having issues with my women’s health for many years now. All women on both sides of my family have a history of fibroids and endometriosis. All of the women in my family have had a hysterectomy and went into early menopause because of it. Yet it’s taken me more than ten years to be heard by doctors. I have a specialist appointment in June and I’m hoping that I’ll get some answers.

    Endometriosis affects 1 in 10 women, yet it can take an upwards of 10 years to be diagnosed. Endometriosis isn’t just a bad period, and pelvic pain isn’t normal.

    It might be the end of Endometriosis Awareness month but that doesn’t mean we don’t keep fighting for advocacy and fighting for our doctors to listen to us. Sending love to all Endo warriors out there and all others who are trying to find answers about their women’s health, keep fighting.

    (Artwork done by myself on IPad Pro)

    (Pic ID - shot of Amelia’s stomach and pelvic area with a striped shirt on and black pants. With a drawing over the top of a uterus)

    #EndometriosisAwarenessMonth #ChronicFatigue #WomensHealth #Disability #Hysterectomy #PolycysticOvarySyndrome #Adenomyosis #Infertility #InterstitialCystitis