Coronavirus Disease 2019 (COVID-19)

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Coronavirus Disease 2019 (COVID-19)
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    Community Voices

    Mast cell after covid vaccine

    Hi I am new and needing to know if anyone has suffered a rash that was ongoing after covid vex,
    Eight days after second vaccine I developed a terrible facial rash that itched and burned.
    The rash was treated with ice and antihistamines and resolved, but returned every time I tried to stop or lower antihistamines.
    Now I have a terrible rash on upper chest!
    I need some hope..please anyone.
    Thank you💓 #mast cell rash after covid vaccine

    1 person is talking about this
    Community Voices

    Shattered

    Today I said my last farewells to my best friend (and “FavoritePerson”) as she and her husband are relocating from MA to GA.
    If that wasn’t hard enough, I got home from that to a phone call from my brother. My dad, who has been in the hospital and rehab after extensive abdominal surgery to repair a failed hernia repair surgery. We really thought he was going to bounce back when he was moved to a better rehab. But he took a turn for the worse - got COVID on top of a raging infection in his abdomen and pneumonia. His body just couldn’t take it. Life support was stopped and he was gone at 11:56am Arizona Time. I live in MA and was already planning to go out there this coming week. I was too late to get one last hug.
    I’m at a total loss as to how to deal with all this grief. #BorderlinePersonalityDisorder #MajorDepressiveDisorder #c -PTSD #Grief

    Community Voices

    Do all teens think like me?

    When i was a 5th grader i used to think all these things in my head, i was a skinny child who could easily make friends and fit into groups. As i grew i didn't knew i would change into an introvert. But i didn't seem to care in 9th grade, i couldn't small talk. Then i found about something called a personality type, i already knew few of my traits so out of curiosity about finding about my true self i started studying my personality type the INTJ (or the INFJ i am not quite sure).
    These past years have been incredibly weird. During the covid lockdown i changed.
    I lost interest in everything tried to study but got bored, listening to music got boring, even watching tv or youtube got boring but i had nothing to do so i just sat watching things on tv everyday for a year.
    I don't know what it was, i thought it was my hormones, or it could be i was depressed. I am never sure and i found out that i over think things(one of the worst traits people can have).
    Now i am here, this year my dad passed away. I cried but i didn't miss him. I have a thinking that people pass away and thats how life works, i had told myself that since 9th grade. I would never do something to my body just to increase my life span, i even started working out to stay healthy(it didn't end well, i stopped when we switched homes and now i just feel nausea and dizziness after working out). But few days back as always i tried talking to someone about my inside personal thing, things i have never shared to anyone cause I don't have friends. Lets keep that aside for the moment, i talked to my mom but as always it failed. I think why couldn't i get a mom who understood and so today i cried after waking up realizing that all my traits have come from my dad and now i don't have anyone to share this to.

    So i am writing here thinking maybe someone will understand.
    I know it is long passage but i just wanna know if there really are people like me, who can understand me.

    17 people are talking about this
    Community Voices

    Temperature Dysregulation : ME and long Covid.

    <p>Temperature Dysregulation : ME and long <a href="https://themighty.com/topic/corona-virus-covid-19/?label=Covid" class="tm-embed-link  tm-autolink health-map" data-id="5e678dcff3e6f44cb2d93fd4" data-name="Covid" title="Covid" target="_blank">Covid</a>.</p>
    Community Voices

    Anyone with MECFS or long covid, is experimenting temperature dysregulation?

    If any is interested to know more about, I would share a post with link to a international site, about MECFS/along covid, where they explain about this and more.

    I don’t like to post information about disorders, unless someone ask them. I don’t like someone feel pushed or such. Since I was diagnosed, I have been searching info about ME, and these people are serious and share a lot of info. About some documental/films too.

    So if yes, please let me know in comments, and I would be pleased to post for you having ME.

    Thanks for reading, wishing a great weekend!

    #MECFS #Fibromyalgia #RA #Depression #Anxiety #Trauma #Loneliness

    9 people are talking about this
    Community Voices

    My Dad used to say he was “collecting smiles” Being an open hearted and kind person isn’t always as easy it sounds! But a smile goes such a long way!

    <p>My Dad used to say he was “collecting smiles” Being an open hearted and kind person isn’t always as easy it sounds! But a smile goes such a long way!<br></p>
    3 people are talking about this
    Community Voices

    Any advice for covid with EDS, POTS, MCAS?

    #COVID19 #PosturalOrthostaticTachycardiaSyndrome #EhlersDanlosSyndrome

    I have hypermobile type EDS, POTS, and suspected MCAS, and i just got diagnosed with Corona for the first time (2x boosted on top of Moderna). My whole body is on fire, my joints are all angry and I've got a gnarly migraine. Any advice or warning signs that i should contact my PCP? I'm temporarily living in a foreign country by myself too so i don't have a lot of my normal coping tools.

    6 people are talking about this
    Matt Sloan

    Delivery Driver Told Me He ‘Wasn’t That Worried’ About My COVID-19

    I’ve finally begun to see the light at the end of a week of hell that has been COVID-19. I finally have a little more energy, able to work at a reasonable pace without feeling exhausted, but I’m still testing positive and the lingering effects of the Omicron variant make me feel like my airways are filled with expanding insulation foam. Meanwhile, my partner’s cough moves ever-deeper into suspected bronchitis (at best) and she sleeps away her days in fatigue. We needed groceries. We left a warning (as we are expected to do), but the first sign of your negligence came when you strolled up to my door, maskless like so many, disregarding the social distancing that’s meant to protect us both. I was courteous, asking if you’d seen the note. You hadn’t — no big deal, I thought, fighting the disbelief that you wouldn’t still be checking for such a thing. So, I told you we were positive for COVID-19 and asked you to take a few steps back for your own protection. “Yeah,” you said. “OK. I’ll step back here. I’m not that worried about it, though.” It was a slap. I’ve grown increasingly impatient with the growing population failing to take proper precautions, but coming off the back of this week of fear… I’d had enough. I told you a little about what I’ve been through. You seemed nonchalant. I wish I could’ve said more, but anxiety held my tongue for fear of the retribution that could’ve followed. After all, I don’t know you; I don’t know what you could be capable of doing to me and mine. So, instead, I’ll tell you here. Have you ever watched the one you love struggle to breathe, barely able to stay conscious, talking about pins and needles rising through her limbs and a shooting pain in her left arm? Have you ever watched such a thing when you’re already haunted by the ghosts of loved ones lost, fearing the next person could be your partner? Have you been told by paramedics to fetch a defibrillator if one is available? Because I have, and I felt so sure, at one point this past week, that I was about to lose the person dearest to me. It all worked out OK, but we were lucky; 6.32 million people weren’t lucky, at the time of writing this article. And sure, you’re probably fit; you’re maybe even vaccinated, but you just don’t know how this virus is going to affect you and yours. This week was harrowing, and that comes from me — the person who has been terrified of catching this virus for over two years, who has been practicing every safeguard and yet still caught it anyway due to the growing complacency of a vast number. I’ve coughed so much I thought my throat would tear. I’ve cried, feeling too weak to cook, eat, stay awake, and take care of my partner. And the funny thing is, I’ve had it reasonably easy. My partner has slept most of every day. Her fatigue has barely lessened. And, while I’m able to work now, she’s still unable to. We’re both afraid of the possibility of long-COVID. What happens then? Are you just not that worried about losing income? Losing loved ones? Losing yourself? As infections spike again in the United Kingdom, and breaking studies suggest that two new Omicron variants are unaffected by antibodies from vaccination and prior infection, I have to wonder what it would take for someone like you to care. For what it’s worth, though, I hope you don’t get it from me. This week wasn’t fun, and instead of making me less afraid of COVID-19 as I hoped it might, it’s actually done the opposite. My fears are fresh and ripe, as they should be for you. COVID-19 is still here, and we haven’t seen the last of it. If someone like me — who is reasonably healthy, vaccinated, wearing a mask, and routinely sanitizing his hands — can catch COVID-19 despite every precaution, what does it mean for the more vulnerable among us? What does it mean for someone like you, who “isn’t that worried” about it?

    Community Voices

    Fear that I'm not really ok...

    I was diagnosed with #POTS 2 1/2 years ago, and have been living with symptoms for at least 7 years. For the first 2 yrs after my diagnosis, I was stuck with a doctor who clearly wasn't putting in much effort to help me, so I saw no improvement at all. I now have a great doctor that I love, and his treatment plan was so encouraging, but I'm currently pretty #discouraged because since January I have had covid and walking pneumonia, therefore I've had a big setback. I'm so tired of feeling bad ALL the time. I have 2 young kids, and I feel like my lack of ability to participate in things with them is wrecking their childhood. I also have always been a big worrier, so even if I've dealt with certain symptoms before, if they are really acting up, I get afraid that the doctors missed something, and I'm gonna die. I just need a community that understands and that can reassure me that my symptoms are normal to my condition. #mentallyexhausted #sotired
    #heartflutterssuck

    Community Voices

    I'm new here!

    Hi, my name is Girlonth3Go. I'm here because I am having many health issues that become far worse COVID and I wonder if my symptoms are actually EDS that have been made worse by COVID infection. My D was Dx with hEDS and I had symptoms as a child. I haven't had any formal Dx but suspect EDS.

    #MightyTogether

    2 people are talking about this