Fibromyalgia Support Group
You're not alone in your pain. Fibromyalgia is a condition that can be difficult to diagnose and manage. If you're trying to cope with pain throughout your body, sleep problems, general fatigue, or other common fibromyalgia symptoms, you're in the right place. The community is here for you to talk about therapies and share your challenges.

My husband finally admitted this morning that the fibromyalgia has strained our relationship. He complained about me not having energy most nights to do things together, but he also doesn't suggest many ways that we can spend time together either.
I had a picture come up in my Facebook memories yesterday. It was a picture of me strapped into gear waiting to do some rock climbing with my husband. Oh yeah, and I was also 30 lbs. lighter. Seeing it was a jolt of a reminder of what my life was like before. It was only three years ago.
I've come to accept that my body can't handle the strenuous exercise that I used to do. I don't mind walks or hiking when I have the energy. I'm still struggling with the extra weight and feeling that this is now my new normal.
My hubby and I were both very active before. He has been less so lately due to diverticulitis, but he will be having surgery soon to remedy that and will be able to go back to doing the things he loves. I won't be able to and I'm afraid of being left in the dust.
I know that all people gradually age and have less ability over time to do the things they used to do, I just didn't think my days would come to an end so soon in my life as I'm sure many of you experienced as well.
If my hubby and I don't have ways to interact and bond with each other we will continue to grow apart as we have begun to do.
What are some ways that you spend time with your spouses/ significant others despite this? I am definitely looking for any suggestions.
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Another day, another ouchie?My bruised achilles tendon (don't ask) makes my foot numb. Wonky on meds, whacked it.Now, as to fibro:A lot of reports are going around some parts of social media that fibro (and dang near anything else) are caused by post-Covid, post-flu, post-vaccinations, post-pick-something.1. Your risk of death or serious complications beyond "ow, that shot hurt!" are typically...
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check out that smoke ring. It tasted really good. I smothered it with Maulls BBQ sauce which is Local to St. Louis and one of the best I ever had.....


Men want to fix stuff and when they can't they get frustrated. As my mobility has deteriorated due to severe OA and now my lower back (DDD with severe arthritis) we do different things. He takes me for drives around the countryside, we go out to lunch or breakfast and do small projects together around the house. Being my primary caretaker is stressful. If he wants an afternoon or night off to do something away from home, I'm fine with that. He can't always be focused on me and whether I am going to fall again, have a new health problem etc. That's not healthy.
It's important that you speak up and tell him that his comments were upsetting. Especially since he didn't seem to invite any input from you about how to change things. When I got sick, I retooled my interests to better suit my limitations. I have three butterfly gardens that are set up to be fairly maintenance free, I work on genealogy (I have a tree of his family history too), and a variety of other things. Some people walk together, do puzzles, play board games, go to movies, concerts, join a book club etc.
If nothing else, maybe some joint counseling is needed. Under ideal circumstances, marriage is hard work. It take two to tango. I hope that you can get it figured out. Hugs!
I do agree that if the tables were turned he would want me to be obliging and accepting.
I do like your idea of long drives and picnics. There are so many nice places to visit nearby me. I think I had almost forgotten that simplicity can be just as nice and fulfilling as more lavish pursuits.
I do hope you can find answers that suit you.
As empty nesters and before I knew I has fibro. I thought we are growing apart but in reality, we weren’t.
He had his hobbies with his friends, golf, sports etc.
He’d go out with the guys to see a game at the bar. I dont do bars because I have an alcohol problem.
I had my lunches with my friends and rubber stamping expos we’d go to.
The hubby and I fell into a normal beat.
We had date night one or two nights a week.
We would shop...he would shop, I’d just look, haha!
Or we’d do a movie and perhaps a dinner or lunch or a walk with the dogs.
Then we’d puts around the house.
If he was yardworking I would make lunch of his favorite food.
He was 53 when he died and I was 51.
I was recovering from Back fusion surgery and one of my favorite days was
A long drive to the eagle place.
We didnt talk much, I wasnt sure I could finish the drive down there but I did and all we did was look, walk a little and eat lunch.
I’d tell him often how I felt with my pain and energy.
I said I’m not complaining although I am, haha, but I want you to understand I wont be able to walk a mile anymore or ride my bike anymore. And you saw the photo of my fat grandma....that is what is happening to me since I am not active. I can try and that’s the best I can do.
Great response Fantod.
I learned about his fanatic love for old bands and music.
I was learning all about all the electronics he had, receivers, tape players to record the radio to a tape to a cd etc...
The year before he died we were getting immersed into our church and the Bible.
This could be a good outlet for both of you as well to strengthen your marriage vows and expectations. Just a thought.
This story sounds familiar, though. But I met my husband after fibro came into my life. When we were dating, he was the most supportive guy, so sweet and helpful. But then when we got married, all that went away and he acts like he's sick of me most days. He's never home and when he is, always ignores me. He complains that I'm incapable of doing/ handling anything, yet he dumps all of the house chores on me because he works and I don't (I'm on disability). Several times we almost decided to separate.
I encourage my partner to go out and do things with friends and family that she enjoys. She isn't sick and deserves to have a life without guilt. I also go with her at times and just sit and watch while she enjoys activities. When we are able to go out and enjoy a movie or eat out I make a point of thanking her for supporting me. She needs to know that I don't want her to fix it but just to listen and be aware of the challenges I face at the time.
It is good to do things apart and then come together and share your ideas or things you have done. Hobbies are a good thing. If your partner sees you are filling your life with things you can do then they will fee more like allowing themselves to do things they like without judging themselves or you. I hope this helps in some small way.
It's been difficult for us to find things to do together because most of the things we used to do were physical in nature. We just have to find some new hobbies.
He knows that he can go out with his buddies and I won't mind. I have a book club and do things here and there with my girlfriends.
We were in couples counseling last year for a while and it helped some, but the progress ebbs and flows. I think that this time if I do counseling it will just be for me.
I also need to find some of my own new interests too. Being home and doing a lot of nothing besides resting, when I'm not working, tends to make me hyperfocused on only what's going wrong.
Try to see yourself as a victor instead of a victim and get out of the house and into nature whenever you can. It will do you both good, even if it's just sitting on the shore by a lake or the ocean and listening to the surf or reading a book under the sun on a warm day. Plant a garden if you are able....Just being outside enjoying mother earth is healing.
God Bless