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

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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!

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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

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