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Re: Invisible Illness

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What's even worse is when you are accused of being a Hypochodriac. That

hurts more than the pain you mail feel already. Many people who do not

suffer from such illnesses really have no understanding until they have been

there themselves.

Alane

rheumatic Invisible Illness

> Don't be fooled by the invisible

>

> For most of us, " You look so good, " is a compliment. But to a disabled

> person with no visible signs of disability - no wheelchair, no

> deformity -such a comment can be interpreted to mean, " I don't see

> anything wrong with you. "

>

> Isn't that also a compliment? To a person whose life is severely

> limited by extreme fatigue, dizziness, weakness, pain or cognitive

> impairment, such well-meaning statements can add to the frustration of

> coping with the disability. Educating family and friends - and

> strangers - about an invisible medical condition is often an added

> burden.

>

> To read the entire article click here:

> http://www.thereporter.com/editorials/ci_2862629

>

>

>

>

>

> To unsubscribe, email: rheumatic-unsubscribeegroups

>

>

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Well, this is strange! Clicked " reply " to digest and now the digest has

disappeared---not in new mail, or in old mail, so can't find the original

subject line!!! I know it was regarding invisible illness though.

" They are probably just groping around trying to find some way of signaling

to you that they are still there, and sending food is a common one. "

And maybe, if there's family in the home, a way to help with your caretaking

responsibilities?

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  • 2 years later...

i agree i have a heart condition which people can see the scares and i

have a perment bluish tinge of my lips adn fingers they can see and

people are always commenting my hands are cold and do it feel well.

but i also have PPMS which will cause me to limp but on my good days i

don't so people think i am faking the limp to get attention and i also

suffer from ADHD/ bi-polar and that makes me want to do more and mind

races and get the things done and i get mad at myself when i cannot or

if i procrastinate. if i wore a brace then people would see that i had

a back problem and if i were in my wheelchair permentaly and unable to

walk even short distances then people would understand but they don't

and i wouldn't do that is why i don't always use my w/c or my cane or

even wear my back support and that is why i do over due it and push

myself till i am close to the high pain level and breaking point. but

is that of part of having a chronic illness where when my husband has

a cold he enjoys being babied and fussed over? where me on the other

hand i don't like it i get mad at myself having to get help from

others and when i cannot do it myself and know the other day i could

have or if someone without the illness would be able to do it or have

the stenama to do it. later k

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