NotAllDisabilityIsVisible

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    Not All Disability is Visible

    ♥️🧡💛💚💙💜
    Warning Long Message. Please take time to read. Thank you
    I wish more people understood...
    What she has is not a cold or the flu. She will never get better. A nap won't help. She is not lazy but she is tired to the point of a lethargic state. She's on meds to try to make it easier to thrive and merely survive. Many people say that she's faking it or that she just needs to push through it. Well sometimes she can push through the pain and live her life, but there are days where she can't walk without having to hold on to something. Her joints hurt. Her body hurts. Her mood varies, and she is sad a lot. She tries to control her mood swings and intermittent bouts of depression. She takes her meds daily, and more vitamins than you could fathom, to help keep her up but most days nothing works.

    She has an autoimmune disease.🦄

    I'm watching those of you who will take the time to read this all the way to the end.

    🌺To see who reads and who shares without reading please, in honor of someone who is fighting MS, Chronic Lyme Disease, Dermatomyositis, Lupus, Graves Disease, Scleroderma, Ulcerative Colitis, Fibromyalgia, Sjogren's syndrome, Crohn's, Sarcoidosis, Osteoarthritis, Rheumatoid Arthritis, Celiac, Hashimotos Thyroiditis, PBC, CIDP, Aplastic Anemia, Psoriasis, Psoriatic Arthritis, Takayasu's Arthritis or any other autoimmune disease...🌺

    Copy and paste this to your wall, do not share.

    Write "Done" in the comments after you have done so.

    Do this as a sign of your love and support for everyone you know fighting this battle.
    Many of my friends and family are struggling with autoimmune disorders!!! 🌈

    #NotAllDisabilityIsVisible
    #WeAreAllFightingABattleYouCantSee
    #Bekind

    1 comment
    Post

    Not All Disability is Visible

    Warning Long Message. Please take time to read. Thank you
    I wish more people understood...
    What she has is not a cold or the flu. She will never get better. A nap won't help. She is not lazy but she is tired to the point of a lethargic state. She's on meds to try to make it easier to thrive and merely survive. Many people say that she's faking it or that she just needs to push through it. Well sometimes she can push through the pain and live her life, but there are days where she can't walk without having to hold on to something. Her joints hurt. Her body hurts. Her mood varies, and she is sad a lot. She tries to control her mood swings and intermittent bouts of depression. She takes her meds daily, and more vitamins than you could fathom, to help keep her up but most days nothing works.

    She has an autoimmune disease.

    I'm watching those of you who will take the time to read this all the way to the end.

    To see who reads and who shares without reading please, in honor of someone who is fighting MS, Chronic Lyme Disease, Dermatomyositis, Lupus, Graves Disease, Scleroderma, Ulcerative Colitis, Fibromyalgia, Sjogren's syndrome, Crohn's, Sarcoidosis, Osteoarthritis, Rheumatoid Arthritis, Celiac, Hashimotos Thyroiditis, PBC, CIDP, Aplastic Anemia, Psoriasis, Psoriatic Arthritis, Takayasu's Arthritis or any other autoimmune disease...

    Copy and paste this to your wall, do not share.

    Write "Done" in the comments after you have done so.

    Do this as a sign of your love and support for everyone you know fighting this battle.
    Many of my friends and family are struggling with autoimmune disorders!!! ❤

    #NotAllDisabilityIsVisible
    #WeAreAllFightingABattleYouCan ’tSee
    #Bekind

    3 comments