This is going to sound terribly heartless, but I have very little sympathy for the chronically ill or disabled.
Let me explain…
My mother-in-law was diagnosed with MS when she was pregnant with her first child (my husband). Over the next few years, it was clarified into being of the Chronic Progressive type (Always there, always gets worse). She was given a 10-15 year life expectancy, and told that having more children would be a great strain on her body. She and my father-in-law had always planned on having three children. It was their plan, they wanted three kids. So, seeing as she’s the most stubborn person I’ve ever met, she went ahead and had two more kids. They WERE a great strain on her body. She went to physical or occupational therapy (depending on what insurance was covering this year) a couple times a week, kept up with cutting-edge research, pushed her doctor to get her enrolled in experimental treatments, and basically did everything she could to fight.
Since I’ve known her (going on 11 years now), she was already a couple years past that original 10-15 year life expectancy thing. She’s a fully-certified quadriplegic (which doesn’t mean she can’t move her arms at all, it’s just very difficult - she can feed herself about half the time), has some serious mobility issues, and the MS (and medications) has caused her to have some foggy memories and thought processes sometimes. However, she still makes it a point to get out of the house several times a week, to call friends and relatives (constantly!), to keep up with the news and her favorite TV shows, and basically live life as “normally” as possible. That’s not to say she’s happy all the time - she goes through pretty normal ups and downs related to her illness, and she once confided in my husband that she’s occasionally considered suicide because she hates being a burden on the family, but decided against it (She’s a very devout Catholic, so for her to admit that means she was pretty serious), and she’s gotten pretty frustrated a couple times in restaurants when she’s having trouble gripping a fork or whatever.
But, despite all that, she keeps going out, and trying to live life to its fullest. She went on a cruise in the Carribian last year, and is now saving up for an Alaskan one. She delights in meddling in her children’s lives, and has a large social network.
So, where the lack of sympathy comes in is when I see my friends talk about their relatives who have medical problems that “prevent” them from doing things, like going out to the store or the theater. If my mother-in-law can manage these things, you have to be seriously bad off not to, and most of these people aren’t, they’re just whiney. It drives me up a wall to see people who are wallowing in their illnesses, and letting that define what they can and can’t do with their lives. I mean, yes, be realistic, you’re probably not going to be doing marathons when you’re wheel-chair bound, but if you’re not controlling your pain well enough to join your family for a dinner out or a movie, then you’re not doing it right, and I don’t have much sympathy for you.
I know that makes me sound a little heartless, but I’ve seen someone who, perhaps not overcame, but dealt with significant restrictions on what her body could do. And instead of feeling sorry for herself, she just kept on keepin’ on, mostly through the gallons of stubbornness and spite that replaced her blood years ago.