Feel like I'm losing my grip!So tired of my daughter having to see me sick and in bed all the time

So Easter weekend came and went without me. I'm so tired of being absent but to tell you the truth....at the moment , I'm happier to be by myself ... not having to inflict my misery on the people around me. Holidays are suppose to bring families together but when one is approaching , I'm dreading the event rather than looking forward to it. I'm tired of my daughter having to see me in bed all the time , not being able to participate in ANYTHING really....

It's been a very dark weekend and by last night the pain in my back and ribs took my breath away. I was pleasantly surprised when it was gone by this morning,considering how intense it was and for the first couple of hours that I was up I was feeling pretty optimistic about my day. Now....I feel sick to my stomach,exhausted and want to crawl back into bed. I have things I need to do today...pick my daughter up from school,bring her to choir practice...ect,ect...I don't know how I'm going to do it!

As I sit here,my hubby just came down the stairs and got mad at me because he told me to go for a walk and when I tried to tell him why that's not a viable option at the moment...he accused me of getting mad at him for trying to help and walked away saying that he's not even going to bother finishing his thought. So once again,I'm left feeling bad...and sad.

I agree with lovett, fightergirl. We so much want to see you get some relief. Phoning the doctor is a good way to start.

Awe, Sweetie...I get what is happening to you and I'm so sorry. Sounds like my hubby when he tries to"help" It's more like the absolute worst scenario he could come up with like...go off all your opioids, here's a little flag you can wave when you're symptomatic and we will spritz you with water to cool you off! SERIOUSLY? How bout taking me out back and shooting me?...because if that's all the understanding you have about my conditions...I'd be better off...offed. Right?

My family actually has been in cahoots to get me off the Oxycontin...felt it was making me a different person and just plain didn't like me on it, no matter that it's for pain they can't even comprehend! They got their wish...cept Doctor turned around and put me on morphine instead...that one kinda bit them in the hiney huh?

Anyway, Ms. Fightergirl...your name says it all and I know that fighter spirit is in you. Have you ever tried to make a routine list for a normal day? things that you can or try to get done? I know when I have a routine to follow, even though I may have to omit a thing or two from the list depending on my ability for the day, I feel better about myself, just having tried and accomplished even a few things on the list. I live with 8 other people in the house, most quite able bodied so if it's something that HAS to be done and I can't get to it, they can do it for me. It's the asking that is the hardest part for me. It's like admitting defeat. I have to erase that kind of thought from my head, it's no good for me to tear myself down any further.

So, dear friend, you need to try to get to a point where you don't blame YOURSELF for what you cannot do..it's the damned Fibro and you've got to start blaming Fibro, get mad at Fibro. If it wasn't for the Fibro, I could do many things but Fibro will limit us from time to time, accept that and take the break it gives you from the things too difficult to do today.

Perhaps hubby should take that walk with you, let him see for himself your inabilities....sometimes it just takes a visual aid for our spouses to get where we are coming from. My hubby had to get reamed out by our doctor before he understood.

There are some very good DISCUSSIONS about a thing called the "Spoon Theory". If you enter that in the DISCUSSION search box the story will come up for you to read. It is very good and has helped me so much to cut myself some slack about what I think I should be getting done every day in my condition.

You know your body and it's responses to stress, illness, chores, etc. You know what it takes to get even the smallest of tasks done in your condition. Hopefully this story will help you to gauge your abilities, accept them and dole out the effort where YOU best think it will be utilized/needed.

Fightergirl...you hang in there. Sounds like you need to educate your loved ones about Fibro, maybe even read them some of the discussions that other members have written. My husband is always blown away by some of the accounts I read him here..it helps to put a face on this disease, for them to understand. Just this last week, I was going through withdrawals from meds, about out of my mind with pain that I couldn't get a handle on, and my knee decided to not support me anymore. So I'm limping, crying, sweating, ornery, bitchy...but I never got a "how ya feeling or anything I can do for you" not a one. They felt bad for me but couldn't even look at me for the guilt they felt for secretly being together on the Oxycontin withdrawal thing. I finally bitched, for all it was worth. Like I said, they were left scratching their heads because of the switch from oxy to morphine. Big Meanies!

Sweetie, trade that sadness in today...congratulate yourself for even getting up out of bed...all the little things that nobody but us understand, brushing teeth, combing hair, etc. Every step you take on these bad flare days is an accomplishment, a spoon that you spend. You decide how many spoons it takes you to get through a day and then only ever give yourself that much. You will learn what takes more spoons than others and you will be able to tell your loved ones how this works, your daughter will be able to understand how the spoon theory works and I bet will gladly join in on the tally and hearing what you spent spoons on today.

I'm sending you just a TON O LOVE today and I ask that you be sweet to yourself today...and every day for that matter. Start Now!

If ever I can help you, please, just ask!

PeacenLove ~ Always~Laurel aka Northwoods

I’m going to have to break down and make the call. I keep thinking "1 more day and I’ll be feeling better. There’s a lot of problems that need to be addressed. My diet…I have to force myself to eat during the day, I don’t know what makes me think my body will function with no fuel. Routine…however limited, I had developed a routine and I know the importance of it. but it somehow got lost along the way over the past year.I’m a perfectionist and don’t do anything half way. It doesn’t matter what it is, exercise,food,alcohol, (which as I know I gave that up 2 yrs ago, yay for me).
I joined the depression/fibro group in hopes of communicating the emotional issues but I was disappointed because there’s next to no activity there, so when I get into discussions in the main group,I get sidetracked because of the emotional turmoil and I think people don’t know how to react and then I feel embarrassed for going on.
I’m waiting to hear from my therapist about my next session. My 1st plan off attack is reassessing my plan of attack and putting plans into action. You can have all the knowledge in the world but unless you put it into action, it’s not going to do you any good. So it’s time but getting started is the hardest part,especially when having to deal with the pain and exhaustion that FM&CFIDS adds to the mix.
I wouldn’t talk this honestly with anyone outside of here because they don’t understand the kind of strength and determination it takes. This just came to me… The Serenity prayer…I’m not religious in the biblical sense but I do believe in a higher power. The Serenity prayer is so simple but it really helps to keep things organized in my mind … And maybe it might be helpful to others.
Grant me the SERENITY to ACCEPT the things I cannot change,
The COURAGE to change the things I can, and the WISDOM to know the difference.

Hugs and much love
Carolyn

Thanks guys...just talking about it make me feel a bit better.

I left a message at my doctors office. She's pretty good about getting back promptly. After hearing your responses it's become very clear that I'm not going to be able to "ride it out" on my own. I'll let you know how it goes.

Lots of love and Hugs

Carolyn

Hi hun
I hope things have improved for you. I just wanted to say keep your chin up. Fibro didn’t know or care that it was easter, unfortunately it doesn’t know christmas or any other special time either. Give yourself a break, you are doing great, you are up even through the pain. Thats an accomplishment. We all know how much bravery and strength that can take.

I can abuse your hubby for you from the uk if you like lol but it is not really helpful. I don’t know how understanding your hubby is but it doesn’t hurt to let him read some of the posts on this site if he hasn’t already. Unless you have fibro you cant understand even if you want to. How many of us struggle to understand so its not really his fault.

It is ok to have had enough and be down and quit for a day or two and give in to the pain. You cant give up but you can have a holiday from the fight. Its even ok to be angry. How old is your daughter because there are things you can do with her. The fact that your worried about her and her quality of life shows your a good mum. Kids understand a lot more than you think and are a lot less judgemental. Be ok with what you can give her because it sounds shes not short on love.

You are not losing your grip you are just having a rough time but it will end i promise you.
Love and hugs from my uk sofa.
Nicola

I also dread school hols. I hate my 3 kids seeing me ill im eating up with guilt cos it feels fibromyalgia has stole the life 2. Keep smiling we will bet this altogether x