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Spoonie Love - Chronic Illness and Disability Paintings

by Madhox Posted 2nd Oct 2016 at 11:06 PM - Updated 3rd Oct 2016 at 1:51 AM by Madhox : fixed misspelling, because grammar is important
 
33 Comments / Replies (Who?) - 7 Feedback Posts, 25 Thanks Posts
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Test Subject
THANKS POST
#26 Old 1st Jun 2017 at 6:40 AM
As someone that struggles with chronic illnesses myself these are amazing! Ty!!
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#27 Old 11th Nov 2017 at 2:51 PM
What a wonderful job! Finally someone who thinks about spoonies! Thank you so much!
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#28 Old 24th Nov 2017 at 12:18 AM
Thank you for this! I have an "invisible" chronic illness too and these will help brighten my simming time.
Test Subject
#29 Old 24th Nov 2017 at 5:23 AM
Quote: Originally posted by ladybarefeet
How neat, I at first didnt believe my eyes! I have HOTS which is Hyperadrenergic Postural Orthostatic Tachycardia Syndrome (and I have Lupus too). On my down days, I take the laptop to my bed and build in Sims all day and shut the world out Its a good way to zone out. Great to see us have some goodies in here.


I have hyperadrenergic POTS, as well..My doctor treating pots says we are very unique because only 20% have it that have POTS..

Life is short, but so am I
Test Subject
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#30 Old 15th Jun 2018 at 6:27 AM
You're giving us far more than EA ever would with these!!! Thank you so much, it feels great to be seen ♥
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#31 Old 1st Aug 2018 at 7:32 AM
I will use these a lot in my builds! Thank you!
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#32 Old 9th Oct 2018 at 1:01 AM
Thank you....I live with Lupus so i really appreciate these :)
Test Subject
#33 Old 4th Mar 2019 at 4:48 AM
Hi there! I really love these designs and wish to use it in the game, however, they're not showing up in the Paintings and Posters. I have inserted the file into the Mods folder and searched custom content, yet they still don't appear. Does this CC need to be updated? Thanks a lot!
Test Subject
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#34 Old 14th Mar 2021 at 10:57 PM
My sister has what we believe to be dysautonomia, so I'm glad to see some visibility! We've been having trouble getting a diagnosis (we've been trying for a few years now), but all her doctors have agreed that dysautonomia is likely.

When her symptoms first started getting real bad, I taught her about spoon theory, so she could more accurately describe how she's feeling (and also so she could see that there are lots of others who share in her challenges).
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