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Old 07-01-2006, 04:28 AM   #1
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Fibro Is Killing My Ability to Hav A Relationship

I hurt almost everyday. I find it hard to have a relationship with anyone. I meet women that are interested in going to dinner or drinks and I feel so lousy most of the time...I just can't go. I find that I become irritaed if I spend to much time with someone which I attribute to my Fibro. I feel like a prisoner because all I do is sit home all the time because I just don't feel well enough to do much of anything. It is hard to get someone to understand why you don't want to go out or have to cancel plans. Making plans in advance is out because who knows how bad a flare up you might get a week from now. I wish there was a dating site for people with Fbro because unless you have it, there is no way a normal person can know or be sympathetic to what people with Fibro are going thru.

 
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Old 07-01-2006, 08:16 AM   #2
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Re: Fibro Is Killing My Ability to Hav A Relationship

"I hear you brother!".....had to give up dating and everything else due to this blasted FM. Somewhere along the line I lost all my desire to have a relationship mainly because they take a lot of work and I have to save what energy I have for my life sustaining job. What I mean by taking a lot of work is trying to hide the fact that I feel like you know what 99% the time, not wanting to dress up to go out, taking short trips to anywhere, being in anything else but my pjs and floppy shoes at home. Having him see me taking meds all the time, tossing and turning in my sleep (if you want to call it that). A couple of other problems that I have but I'm to embarrassed to reveal. It was kinda of hard at first but over time it is something I'm just getting use to, becoming apathetic I guess is what you could call it. I'm trying hard to pay attention to my needs for a change instead of every one else's. Not that I'm sitting around feeling sorry for myself all the time, things like laying around when I need to, staying in pjs when I want to, laying in a hot bath as long as I want to when I want to, stuff like that. But I have to admit it does get kind of lonely at times. I don't discuss the my FM with family or friends because they just don't understand it. But I've become accustomed to that as well. So, I understand your pain and concerns, but focus on yourself, doing things that will make you happy for a while. You deserve it!

 
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Old 07-02-2006, 06:31 AM   #3
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This post touched me today..

I understand how you are feeling. With this being a holiday weekend..my husband has 5 days off of work..we are living in a new home in a new state..and he has looked forward to this weekend..in part because his brother came to visit on his way to his vacation....and because we finally would have time to sight see in our area. Well, my fibro has kicked up full force...the pain is waking me up...I am low on energy...and am pushing myself to spend some time with him in the pool we just put in ( mostly for me to be able to get some exercise in). I have lived with this for several years..and he generally has adapted to me and the illness pretty well . But I KNOW he is disappointed on this particular weekend.....

But, I am feeling a lot like you seem to be. I don't have the energy to care about it. It takes all the energy I have to make it thru the day so I can get to my bed at night. I don't have energy to meet new people...I don't have energy to see sights...or to clean the house..or to decorate...or to play a game. It is one of those stretches for me that I feel like all I can do is watch tv...I cannot concentrate enough to read..or play a game. I force myself to plan and cook at least part of dinner..and do clean up ( that can take a couple hours as I have to sit so much between tasks!) I do that because it makes me feel like I have some value in my home!

Thank goodness I do have times where I am better than this...but it seems that flares last longer these days...and it takes less to put me into one. I am TRYING to improve the quality of life by eating well....and having some gentle exercise in my day...but so far there is no miraculous change...and it is taking a toll on my usual positive attitude...
This seems to be similar to where you are right now?

Anyway..I type this to let you know...I understand...and to say, try not to give up hope. One of the things I hang on to is the fact that for many sufferers of the DD, there does come a point where it improves...and although it may not leave altogether....there is a lessening of symptoms...and a time where more "normalcy of life" returns.
I hang on to that hope!

I think that even though there are a myriad of ways you can try to feel better...being a guinea pig for treatments is also very depressing for me. So I have chosen a minimal path of healthy habits..and pain meds to help me manage the worst of the pain. Then , when I am NOT in a flare....I try to stay a positive person..and do my best to enjoy those people that are already in my life.

I wish for you a more hopeful attitude about your life...and a way to find joy in your days!

 
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Old 07-04-2006, 12:30 AM   #4
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Re: Fibro Is Killing My Ability to Hav A Relationship

boy, do I relay to this thread. Let me start by saying this : Had I known three and a half or is it 4 years (?) ago that I was going to have this condition, I would have never pursued a permanent relationship, ever. I feel that I need to have a 100 % CONTROL over my life, this is what these past few years taught me. And being with somebody else, it's not so easy to do that, no matter how easy or understanding the other person is (and nobody can be THAT understanding). I feel very frustrated within myself and lately very resentful over many many people and situations. I hate having somebody witnessing my flare ups. I learnt from the beginning of this thing, when I was freaking out going from doc to doc without knowing what the heck was going on with me, that my personal pain is MY personal pain and nobody else's. I just cannot make plans and I absolutely resent others making plans for me. It's not good for me. I cannot go out as I used to, I cannot travel as I used to, I cannot do anything like I used to anymore. Two weeks ago I went to the island of Myconos (for 5 days only), (i live in Greece) and I came back absolutely shattered from fatigue, believe it or not. Because fibro is not pain only, it's big time fatigue ! I would have preferred staying home, alone, for that matter. Now I'm leaving again on the 12th of July for 10 WHOLE DAYS and I am dreading it from now. And I told my partner, and he knows very well mind you, that 10 days is a lot for me. Staying outdoors, in the sun (or rather tryng to hide from it), in the wind, in a hotel where the mattress bothers me, is a killer for me. But my friend, he needs those 10 days, so you see ? there goes the control. He will not sit and think: ok let me make it 7 days. Plus you cannot drive another person down the gutter with you just because you are not well, all the time, or most of it. I would advise you to have a "controlled" relationship with someone who doesn't need to stick to you all the time, whereby you will be the master of the situation. If my partner didn't travel for his business, which is quite a lot, I would have gone crasy. Now after 4 years, I need to make my own decisions, I cannot take crap from anybody anymore. And yet I used to big time ! I always try to keep a positive attitude within myself, I accept and deal with my condition, but then when you think you have things under control, somebody else comes and changes your plans for you. For Christ's sake, do you all really think that normal people could ever understand what it feels like to have chronic pain and fatigue ? When I was trying to get a diagnosis running from one doctor to the other it so happened that my partner's mother and sister were staying in Greece (they live abroad) with us for 50 whole days !!! they looked and acted towards me as if I was some kind of nut or something. If I had the same brain I have today back then, I would have kicked them out of my house believe me. Today, I don't want anybody staying in my house anymore and witnessing me not being well, although most of the time, mind you, I pretend I'm fine ! I cannot handle stress at all. I need my energy for my daily work. I don't know how I could possibly explain all the above to a new person in my life, really. I think that those of us who already had a relationship/marriage or whatever when the fibro started are better off than someone who has yet to find somebody and deal with the outings, dinners, drinks, explanations, etc. Good luck to you and protect yourself. I have come to the conclusion that I, even with my lousy fibro, am far more worth than many other people i know. I hope you will find somebody who will appreciate you and give you the space you will need when you'll be less fine. good luck

 
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Old 07-04-2006, 12:52 AM   #5
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Re: Fibro Is Killing My Ability to Hav A Relationship

Hi rstarre, I am so sorry you are going thru this. I can only imagine what being lonely and trying to date in todays world with this would be like. But the flip side, and I do think there is a flip side. See, when you do find the one. She will most certainly be understanding. B/c she will know form the start what some of your disabilities are. Maybe even someone with a chronic condition as you who will actually understand the problems and pain that come with it.
I don't know the answers but I am 40. I have been married for almost 14 years and we had so much fun. Seven years playing before kids. And now even though he is a trooper and tries to get it. He really doesn't. I actually made him say the word today"FIBRO" He is in such denial that his wife could have a chronic condition. He want's to fix it. He want's his old wife back and his old life. And God knows I try. I am not the same. And may never be.
So I guess either way we go here it isn't perfect.
If I were single I may find a support groupfor fibro or cfs. Maybe meet someone there. I don't know.
Being married and getting it is no walk in the park either,
Lots of hugs and prayers
Deena

Last edited by MOMOFBOYZ; 07-04-2006 at 12:55 AM.

 
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