Well so much for a happy new year. My pm drs NP and new rheumatologist both said that they believe I have rsd spread. Rheumatoid was ruled out last week. My rhuem dr noticed the excessive hair growth on both of my arms. I noticed them about a month ago and was going to ask my pm dr on my next med check, but saw her first and she said it was probably rsd spread. I have had burning in my rsd wrist and my other wrist and both feet for the past few months and limited range of motion in my left wrist and right hip lately. The spread has gone down my right hip, leg, knee, ankle, foot and toes and to my left foot, toes, ankle, calf and hip. I have burning, redness, shiny skin on my left foot, swelling, limited rom, and excessive hair growth on both of my arms. I have osteopenia in my right hip, osteopersis in my both hips and dengerative disc disease in three spots on my lower back and neck per xrays my rheum took last week. I'm getting an MRI this week so she can check further. Tomorrow I go to my Gastroendo dr to see why my stomach is so bad. I already cancelled once because of fear of an endoscopy and what she may find, but I have to go because I can't eat too much without being nauseas. Hopefully it's just the gallstones and gallbladder that need to come out. Then I have to make an appt with podiatrist to check on the bone spur in my left foot. And I just noticed last night after feeling pain in my gums that I have another cracked tooth. This time it's the front one. And to top it off, I accidentally hit my head on a shelf in my deceased Great Aunt's house while cleaning out her closets and I have a really bad headache now so I'm contemplating whether or not to go to the dr to check for a concussion. (Like it's not bad enough to have go to her house knowing I will never see her again.) I'm sorry I'm whining alot, I just needed to vent. I know some of you are worse off then me, but the rsd spread is scaring the heck out of me. And when I told the NP at my pm drs office last week about what she thought, she said she thought I probably have spread too but to wait until spring (when it's warmer out) for that. I can't wait for my pm dr to come back from vaca so I can ask him. I really didn't care for her response. Why would I want to wait. It may spread more by then. Well, I see him next month so hopefully he'll have a better answer. In the meantime, I'm trying to take things a day at a time, keep my emergency rsd flare kit and list nearby, and pray a lot. Thanks again for listening to me whine. Sorry again for complaining. I hope you are all having a better year then me. And hopefully things will get better for me too as long as I hold onto my faith. Take care.
PS: My rheum told me that she thought fentonol patches (sp?) might be better than percocet for long term chronic pain like rsd. I was wondering if anyone has tried the patches and/or percocet and which one they think helps more with rsd pain. Also what side effects they may have. I told my NP at the pm drs office last week I wanted to try weaning of my percocets anyway because of their side effects and brain fog, and she said to wait until spring for that too. I think I'm going to just see my pm dr from now on and ask him what he thinks, but any advice that any of you may have would be greatly appreciated. Thanks again for listening.

Renee,
It's perfectly o.k. to whine here. i think we've all done it.

I'm fearing spread as well to my foot. Like Vrae I have cold RSD/CRPS2 too.

I wish I had advice on patches, I have never tried them or been given the option to by my P.M. Dr. Right now, I'm relying on a few meds. & nerve blocks.
If you can, I think weaning off the percocet is a good idea if there's an alternative that works for you.

Thanks AZ-Di,
I have CRPS I. I know that it's not the same as CRPS II, but I do have coldness in my initial site which is my right wrist, hand and and fingers, but not really anywhere else. I'm sorry you may have spread too. I will pray that it's not though.
I think I am going to try to wean of the percs too if I can. I know I'm paranoid by nature, but I can't help but feel that the drs want me to stay on it to make money off of me, because they make me come in every month for an office visit (1 1/2 drive to and from there) for med checks on the percs which costs me more money and I have to give urine tests every few months to confirm I'm taking them and the lab tests also cost money. I"ll check with my pm dr next month and if I don't like what he says, I may start looking for a new pm dr. I thought I could trust my pm drs, but the longer I see them, the more doubts I am starting to have about them. Thanks for your advice. Take care.
From your friend, Renee.

Hi Renee, I'm sorry you are having such a lot of spread...it is very scary stuff, and talking about that isn't whining

I've got cold CRPS too, although I get my fair share of burning too , and mine has spread from the original site in my left knee, to my whole left side, and my right foot and hand. Only recently it's spread across into my left breast. That's a barrel of laughs...

I don't know. It's impossible not to panic a bit Renee, it's perfectly understandable. I try to live day to day and not think too far ahead. Looking ahead seems pretty scary at times!

Take care,

Bram.

Sorry to hear Renee...
I know all to well how scarry spreading can be. I wish you well in your battles and that we all find comfort and relief...

So sorry you are dealing with spread on top of all else that you are dealing with Renee. This is the place to vent and whine....most of us have done a bit of that lately (present company included ).

I am allergic to percocet. I tried the fentanyl patches and you'll never believe this....I had an allergic reaction to them too It's a shocker, I know. I would give them a try if I were you, I have read on here that some do use them and they are very helpful. I would try anything at this point...well most anything. I really hate that only getting 30 days worth of meds and having to go back monthly for a refill and a drug test. I refused to go to one PM doctor because the way their drug policy was written, made me feel like I was a junkie or something. Bad people ruin it for the good people. I can't tolerate much so I do not take much. I have been taking demerol when I get to a point that I just can't take the pain any longer. It gives me a bad headache and makes me nauseous, so I have to take promethazine with it.

Anyway, I hope you can get some answers from you drs soon...and that you can get some relief!

Nanc

Renee - so sorry this scary stuff is happening to you. NO you are not whining. You are always so sweet to others on this forum, you deserve to vent a bit. I have cold CRPS II, similar to Vrae. I was on a Fentanyl patch for 2 years. It is a powerful narcotic. I came off it because of the side effects and I wasn't convinced it was helping a whole lot. I experienced constipation, brain fog & short term memory loss and withdrawal symptoms on patch change days (usually every 3rd day). And, as far as the spread goes, I am terrified of spread so don't think you are whining!! Be well, Lottie

I wanted to thank all of you for your caring and helpful advice on rsd spread and fentanyl patches. I am really nervous about the spread, but am more scared about the fact that my pm group doesn't seem to be treating it right away. I don't have many pm drs to choose from in this area, but will have to do my research and see if I can find another one. And as for the fentanyl, I don't know if I want to try that either. I sort of want to wean off narcotics. I didn't know that was one of them. I don't know if I can do this with the increased spread and pain I have, but want to try to at least take less. I have to compare the two with my pm dr if I go back to him, and also look into the longer acting percs (if they have one, I think someone told me that there was, but I'm not sure. my memory is so bad these days). Maybe I can take less of percs if I take a time released one instead. My neurologist as well as some of you here have thought I was taking too many pills. My neurologist and gp have also recently said I should try to wean off the percs, xanax and neurontin too if I can. I'm going to try. My pm dr and pscyhiatrist said what I'm taking is okay. It's so confusing, but I can't help but feel that all the meds I'm taking are taking a toll on my stomach. I have to see my Gastroendrocronologist (sp?) today because of the terrible stomach pains that I have. I was up half the night again with stomach pain. I felt so nauseas. I wanted to trust my pm drs, but now I just don't know if I do anymore. Anyway, I'll see what my gastro dr today thinks is going on with my stomach. I'm soooo scared. I don't want to go and it's soooo cold out, but I can't cancel again. I have to face my fears. Thanks again for all of your support. I hope you all have a blessed day. Sincerely, Renee.