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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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#1 | |||
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Sorry guys, I'm just venting, I don't expect anyone to fix anything. My emotions got the better of me right now and I know you are the only ones who can relate.
I get nerve blocks in my neck for my CRPS arm and hand about every 2 weeks and I have to be sedated so I need a driver. Last week my older son took me because my husband was just too slammed at work. Well, he didn't really have time for me either, He kept pacing around the room saying how weird he felt not working mid-day. He just opened his own firm & only a few clients so far. I FELT LIKE SUCH A BURDEN! If you knew me you'd know that's the last thing I ever want to be. Now because my P.M. Dr. will be out of town for 2 wks. & she really pushed for me to get one this week as well. I already tried to cancel, but the office staff told me that the Dr. had notes to keep my slot no matter what. My husband says "why do you need one this week" when I already told him all of the above. He says "I can take you if I have to, but please try to cancel again tomorrow." My son already gave him a break last week. Then he orders me not to get upset because then he'll get mad and won't be able to sleep. Now here's the rant: I thought everyone in my family understood that this is a chronic disease, no cures only treatment options. Now it feels like they think "OMG can you be well already, this is such a drag!" I ALWAYS SWORE I WOULD NEVER EVER BE A BURDEN! I'VE ALWAYS TAKEN CARE OF EVERYONE ELSE! I STILL DO TAKE CARE OF ALMOST EVERYTHING - I JUST NEED A DRIVER! What is this the support that's promised just becomes too hard? I'm sure some of you have felt this. Part of me just wants to give up say He** with it all, give up all treatment. I guess if I can't always be the happy, happy, joy, joy chearleader of the family I can just feel worthless now. ![]() |
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#2 | ||
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AZ-Di, I completely get what you mean. I hate the slightest feeling of being a burden too, and of course sometimes it's just there no matter how hard you try - because you DO have a chronic condition and you just can't do everything you would want...
Sorry if any of the following sounds like I think I am some kind of counsellor - I'm just trying to say something that might help! ![]() Sounds like your husband is stressed out and has maybe taken his eye off your situation a little. It happens with my husband too - it's when he gets stressed and worried and feels like the world is on his shoulders that he seems to almost resent my problems. Makes me feel so bad. Cheers for that ![]() Has he ever been in the room while you have the procedure? If he has then ask him if he thinks you like having it done. If he hasn't then show him a YouTube video of one being done. Might help him get a little perspective...? Oh I so know the happy happy joy cheerleader thing! I had exactly that talk with my husband last weekend - why is it always down to me? Why can't you manage to try to remain cheerful when I am feeling bad? It makes me feel so responsible for everyone else's happiness.....yet sometimes I am just trying to find some for myself. Keep battling on girl. Talk to him and tell him the rants make you feel horrible. Ordering you not to get upset because he'll get mad and won't sleep?! That's not very considerate at all! If things get really bad I occasionally have to remind my husband of the 'sickness and health' part of our marriage - if HE were the one to have got sick, does he not think I would care for him and try to ease his burden? Would I not have tried to hide my frustrations about the difficulties it caused in order to save him from feeling worse than he already did? Normally stops him in his tracks. I think sometimes they just get into a little pit of self-pity and have to be helped out. A bit of flattery, thanks for what they do and a nudge in the direction of guilt and what's right and wrong help us get out of those times. I really hope you feel better soon, and can keep that appointment. It's important that you go, so try not to feel so bad about it. I'm sure he'll come round again - have you ever read 'Men are from Mars, Women are from Venus'? It's so true it's almost funny ![]() Remember that this is not your fault and you didn't choose it. You are coping as best you can with everything it throws at you, and personally I think you do pretty darn well girl. Be proud of everything you do despite your CRPS, and we're right behind you ![]() Bram.
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CRPS started in left knee after op in Aug. 2011 Spread to entire left leg and foot, left arm, right foot. Coeliac since 2007. Patella femoral arthritis both knees. Keep smiling! . |
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"Thanks for this!" says: | AZ-Di (09-18-2013) |
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#3 | ||
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Don't let it get you down. We all have off days. I had one just the other day. He is slammed at work, he is probably worried about you too. If I could I would go get you and drive you, but I'm on the otherside of NM. I have felt that I need to be happy happy joy joy too. We all do. It suck royal boogers that we are stuck in a body that feels so much pain. We are so use to helping everyone else we don't even think about us. I have been there many times. I had one of those days just a few days ago. Im not saying my pain is worse than yours or we have to suck it up. We can all use a day to vent. Just remember they love you. They really don't mean to make you feel bad. They are also venting about their lack of ability to help you. I have had to get my husband to take time off also to go to med appts. I don't understand why he would want youmto change the appt if your PM is going out of town, but then again I do. He wants to be there but with the way work is he can't. I'm not justifying why he said it the way he did. I'm just saying I can understand why he would prefer the following week when things are calmer and not so stressful. They may not have CRPS but they also feel the effects. Keep your chin up. We do have a tendency to let this get our heads all jumbled up and start thinking it would be better if we weren't around, but I also think we try to be the same person we were before because then we were normal and not this crud we have now.
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"Thanks for this!" says: | AZ-Di (09-18-2013) |
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#4 | |||
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Oh AZ-Di, I am so sorry hon! I/we do know how you feel and this just stinks for you. You did all that you could do, and at some point EVERYONE in the family will have to come to grips (just like you’re trying to do)with the fact that you are going to need help. What they truly don’t realize is that you hate this as much as they do! You might tell them that the next time this is needed that you’ll just grab a cab. No matter how expensive and uncomfortable that would be. (I’m such a rebel aren’t I) Perhaps a softer approach would be better and a family meeting, called by you might be appropriate. Explain (again I’m sure) that this is the gig guys. I’m going to need you to pencil me in from time to time, because without this treatment, things are only going to get worse for ALL of us. Gosh this is such a hard thing… My instincts are to get mad, and so I should probably quit my post response now because it really does make me upset for you.
Again, I am so sorry. Please hang in there girl and know that you’re not alone. Great big soft hugs AZ-Di!v ![]() Ps. For me, sometimes the children are the toughest to make understand. I have several children and my oldest (my son) seems to operate in denial. It frustrates me to no end sometimes. |
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#5 | |||
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"Thanks for this!" says: | AZ-Di (09-18-2013) |
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#6 | ||
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Quote:
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CRPS started in left knee after op in Aug. 2011 Spread to entire left leg and foot, left arm, right foot. Coeliac since 2007. Patella femoral arthritis both knees. Keep smiling! . |
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#7 | |||
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Thanks so much! I know all of you have dealt with these feelings too. I sure don't mind feeling counseled or even preached to. I was just so upset and I knew I needed to take it down & react more like the mature woman that I am.
I want to be the person I always was, I just hate how this disease changes life. I DO KNOW from all your posts that you all truly know that feeling as well! ![]() |
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#8 | ||
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Magnate
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It might make sense to hire someone to drive you to your appointments and even run errands and help you clean a few hours a week.
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"Thanks for this!" says: | AZ-Di (09-19-2013) |
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#9 | ||
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Az-Di we all wish we were the same people we were. I would give my left arm to be able to go outside and run and roll around with my son. To be able to do a ton of things I used to do. I can't even walk my dog. So I get her to run around the back yard which is tiny. I have problems even driving into town some days and thats only about 2 miles off this stinky base I live on. It sucks we have to give up so much because of this (yes I am going to say it) damn disease that has attacked us. Thats what this is. Warfare. We are at war with our pain to try to have a semblance of normalcy for us. I am going to fight this war as hard as its trying to bring me down. Sorry for cursing, but some times we have to get it out. We are here for you at anytime.
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"Thanks for this!" says: | AZ-Di (09-19-2013) |
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#10 | |||
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"Thanks for this!" says: | Brambledog (09-19-2013) |
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