Hashimoto's Encephalitis

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Hashimoto's Encephalitis
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    Not sure ho to deal with my mean cousin saying how out of shape I am and look at her she could run circles around me and she’s ten years older then me

    She was very overweight even 2-3 years ago so to make fun of my weight talking about how in shape she is is cruel and hurtful who can offer me support and love and advice? She really hurt my feelings I didn’t ask for a pandemic to make me gain weight nor did I ask for being out of shape it’s a very personal thing I have challenges she does not have such as pcos fibromyalgia and scoliosis and siatica. So to make me feel bad for my pulling my back out yesterday from having to lift a heavy Amazon box by myself I don’t have a boyfriend or husband to help me. What can I do to help myself? #PolycysticOvarySyndrome #Fibromyaliga #FibromyalgiaDiagnosis #Fibromyalgia #PinchedNerve #Bipolar2Disorder #BorderlinePersonalityDisorder #BorderlineStigma #PTSD #CPTSD #CPTSDinrelationships #MyalgicEncephalomyelitis #pcosfighter #Aspergers #AspergersSyndrome #Anxiety #ADHD #Exercise #Yoga #BingeEatingDisorder #Art #Depression #Photography #ArtTherapy #Sports #frisbee #Walking #Love #Hugs #Faith #god #CatholicChurch #Church #Support #SupportGroups #Music #Chatting #Chatspace #Disability #Spoonie #FlareUps #flare #BipolarDisorder #BipolarDepression #MightyFeatures #MightyBookClub #MightyQuestions #TheMightyTakeaway #MyMightyMonth #TheMighty #52SmallThings #52smalltasks #CheckInWithMe #Upallnight #Selflove #Disabled #TheSecret #TheBible #goodthoughtsyourway #Positivity #sad #lonely #ObsessiveCompulsiveDisorder #oa #HashimotosEncephalitis #MyalgicEncephalomyelitis #goals #Hope #DBT #Dbtskills

    Question

    LDN questions

    My doc recommended I try LDN low dose naltrexone as my next avenue for #HashimotosThyroiditis #Fibromyalgia #PolycysticOvarySyndrome
    #ChronicEpsteinBarrVirus. We are also investigating if my symptoms are due to  #HashimotosEncephalitis. I'd love to chat with some of you who may use it. My questions are:
    How long have you been taking LDN?
    How long did it take for you to begin feeling some relief or change happening?
    Have you experienced any side effects or changes overall due to the LDN?
    Any suggestions/additional input you'd give someone starting it?

    Thank you for your input!

    Post


    The mask is what you don’t know
    It’s what I don’t show
    It’s the pain everyday that I don’t “woah”
    Cause woe is not me
    Nah I’m a pro

    Breathe in
    Go with the flow
    One step at a time
    Nah, you don’t know
    One rhyme at a time
    I’m good though

    Shavasana
    It’s my new pose
    Cause I can’t “flow”
    So i Let go
    Of that sorrow
    Hold tight for that rainbow
    Bite tight on that pillow

    Authenticity becomes a burden
    My mask, my warden
    What you don’t know won’t kill you
    It might kill me but it’s uncertain
    Nothing to see here, pull the curtain

    You don’t want want to know cause you hurtin?
    You can’t say nothing cause of disservice?
    To me or to you?
    Don’t know what to say?
    Say what, no don’t.
    Quick change the subject, we need a diversion

    My coercion is not inadvertent
    This version of me is what I’ve determined,
    This assertion of me no doubt a costly exertion,
    A necessary front
    My warrior shadow
    I’m still in here just through these windows

    #MightyPoets

    #HashimotosEncephalitis #Encephalitis #EhlersDanlosSyndrome #Syringomyelia