great read about the experience of pain - LUPUS UK

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great read about the experience of pain

katidid profile image
6 Replies

A dear friend sent me this article from a woman who suffer autoimmune issues and writes for the New Yorker. Some of the things, especially about what it's like to experience pain as the sufferer vs supporter, I thought was sooooo true. Insightful and comforting in a way.

newyorker.com/magazine/2013...

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katidid profile image
katidid
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Barnclown profile image
Barnclown

🌟🌟🌟🌟🌟😆 great post & great article!

When it first was published in 2013, my USA family read this article and finally began to understand a bit more about my life with infant onset lupus (I was 60 in 2013 😉). This is a really good article for any friends & family & colleagues who just don't "get" what you're up against day in & day out + on & on & on....

🍀🍀🍀🍀 coco

soootired profile image
soootired

Thanks for the link I really enjoyed reading the article. 😊

Her description of life with an autoimmune illness is so accurate.

The author makes a good point about not becoming overly obsessed with the disease - I feel I'm on a constant tightrope trying to balance not becoming totally, as she puts it, narcissistic when I'm asked how I am, but at the same time being honest.

pixiewixie profile image
pixiewixie

This is indeed a great read & somehow leaving a feeling of connectedness with the author. I feel that this is often how I live 'what will be, will be', or 'what is it now?' As you say Coco the on & on & on factor. It is also that enduring painfulness to it, or the itchiness, or the despair of the lost personality, but yet the acceptance that this is in fact now your life & 'this is as good as it gets & sometimes it is ok!' To Progress: Peace & Love Pixiewixie xxx

webar4780 profile image
webar4780

Loved reading that article. Thank you for sharing.

I do wonder if most of us also get to that point, of putting up and shutting up, outside of this community. I know I have.

If I wanted to stay married and keep my friends, I needed an alternative outlet. Fortunately, we are able to be accepted just as we are here. Good and not so good days we come together and feel amongst 'knowing' friends.

Friends here, provide reassurance that life is not over; just different, when diagnosed with autoimmune disease. They help us reduce visits to medics and to take better care of ourselves.

I loved the self depreciating sense of humour in the New Yorker article. Very necessary survival technique in autoimmune life!

Bebe76 profile image
Bebe76

Great article. Thanks for sharing this!

Penelope-Mary profile image
Penelope-Mary

Thank you for that link, terrific read....we are all rather brave souls I feel. You expect the article to conclude with a definitive dx and a satisfying treatment regime...but as we all know, that's 80% is what we have left just to be.

Hugs 🤗 and strength to carry on everyone.

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