Lupus Spouses


© Karyn Moran Holton
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If there's one thing that I can think of that would be worse than having to deal with lupus, it would have to be watching my husband deal with it. Don't get me wrong -- he's an amazingly strong individual, mentally, physically and spiritually. He is probably more "qualified" than I am to deal with the physical symptoms, the mental stress and the self-doubt that accompanies any chronic illness.

But I would give up half my soul if I thought it would help him avoid it entirely.

I've said this before, but it bears repeating: It's difficult enough to be ill yourself, but it's immeasurably harder to watch a loved one battle an illness. I can only imagine how it feels to stand helplessly by while someone you love suffers through severe fatigue, crippling joint pain, sleepless nights, and mouth sores that leave them unable to eat. To spend endless nights in the hospital, just watching them breathe. To grit your teeth in pain (real and sympathetic) as your loved one grips your hand like a vise because the nurses have to make a fifth attempt at starting an IV.

It takes incredible character, strength, selflessness and an endless capacity for love to manage these things. How else (aside from Divine Intervention and Celestial Visitors) can you explain someone who loves a lupie? Talk about high maintenance? Lupies really win the prize in that category! Ivana Trump is easier to take care of!

Think about it: Lupus patients can be incredibly selfish. We are needy, demanding, short-tempered and cranky. We don't get enough sleep, we're in pain all the time and we have no patience for other people's problems. We can be whiny, self-centered, insensitive and distant. We lose our hair, get deforming facial rashes, gain weight from steroids, swell up from water retention and kidney failure and get nasal sores. When we're not burning up with fever, we have icy cold hands and feet from circulatory problems. (Makes you just want to cuddle right up with us, doesn't it?)

We need constant reassurance and affirmation, because we're always having some sort of emotional crisis. We feel useless because we can't work. We're tired of juggling meds, having tests and seeing doctors without any change in our symptoms. We feel ugly and unlovable because of physical symptoms, medication side effects or "just because"! We feel irresponsible because we have children and grandchildren that we can't play with or participate in activities with. We get angry because of our limitations. We become incensed because no one understands us and that @#$% neighbor made another insensitive remark about lazy housewives and we know that she was talking about us!

This Is True Love!
High Maintenance, Indeed!
The Lupus Spouse: Everything To Everyone!
   

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Here's the follow-up discussion on this article: View all related messages

7.   Nov 17, 2001 8:20 AM
In response to message posted by eddiez:

Hi Eddie,

I'm so sorry to hear about your g/f's lupus. It must seem very strange and scary f ...


-- posted by scottishgirl


6.   Nov 13, 2001 2:25 PM
hello, i am writing to find out all that i can about lupus. what i can do to help when my girlfriend is active. she doesn't know i am doing this. we have only been dating for three months & this is th ...

-- posted by eddiez


5.   Aug 16, 2001 6:45 AM
In response to message posted by MaryfromNH:

Hi Mary,

I'm sorry about the delay in my reply to your requests, but my wolf has made my ...


-- posted by scottishgirl


4.   Jul 19, 2001 8:55 PM
Hello Karyn,

My name is Mary Anderson. I have sent you at least 3 letters requesting permission to print your wonderful article in the NH Lupus Foundation Newsletter. Perhaps my letters never reach ...


-- posted by MaryfromNH


3.   May 10, 2001 8:55 AM
In response to message posted by micklady:

Hi everone have been off the com for a few days but did enjoy your article karyn.,and would li ...


-- posted by zula





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