Hi All,

I have been under enormous stress both very good and extremely bad, which I think makes it even worse. Not to go into all my good happenings and problems I just wanted to say I have had RSD for 8 years just this past Jan 4,
that was my disgnosis day, funny how we remember that. Sorry I got off track. I had to go into see my doctor which I haven't done outside of my routine 3 month visit because I was so sick,increased pain, anxiety through the roof, felt like I was going to throw up, headaches and just plain sick. My husband had to take off work to drive me which is unheard of.This is not my normal behavior so my point is if you are feeling increased symtoms and your under STRESS please take care and step back. I really scared myself I thought I was going to pass out in the shower I was trying to get ready for work yesterday when it just all hit me I just couldn't do it.

He gave me some medication, I don't take much of anything anymore so I had nothing to help my symtoms, wants me to see my specialist in NYC which I'm going on Monday, have some bloodwork done just to rule out anything else, I'm also hypo-thyroid and do nothing for the 3-4 days, which it's cold and snowy so I'm actually looking forward to the break.

I know we have all read that stress is a big contributing factor with RSD but I never experienced it so bad as this past week outside of after I have done ketamine treatments.

So everyone please be kind to yourselfs. I never give myself a break but I won't be doing that anymore. It really scared me.

Everyone have a great weekend and if your a football fan enjoy the games on Sunday. I'm a Jet fan we all know what happen their, but my son is a Ravens fan so go Ravens.

Gabbycakes

gabbycakes,

I'm sorry to hear you had such a bad bought. I know stress makes my rsd worse has well. Usually it is the bad stress that makes it unbearable. Or any kind of emotional triggers.
I hope you are taking care of yourself and taking a little down time. That is important if we were normal not to mention even more important with our rsd.

I'm so sorry that you have been having such a rough time. I think the emotional triggers are the hardest ones for us to control and they can cause such havoc with our RSD. I feel like I am constantly coaching myself to not let certain things get to me, to not get stressed out about things, etc. Most of the time it works but sometimes you just can't escape it. Especially when it comes to work. I am really excited to go back and looking forward to it...but I also know that if I take a laid back easy going approach that some may interpret that as me not caring...which would not be the case. I am not looking forward to the stuggle to balance my medical needs for limited stress and the stressful nature of my job.

Take care and let us know how things go with the doctor. It's good to rule out other stuff...but it's always good to remember how important it is to not let yourself get stressed (if at all possible). I hope you start to feel better soon.

I am sorry to hear that your RSD has given you such a scare. I know others have experienced such a thing. Please be good to yourself. I hope the doctor can help you when you go. Stay warm and do try to enjoy the football games this weekend. I will be watching right along with you. I wish you all the best in your coming appointments, and a speedy solution so you can be more comfortable. I remember I posted to you quite awhile back. I try to remember the people I have met. You will be in my thoughts and prayers. I hope there is less pain today than yesterday. take care of yourself. ginnie

Thanks everyone for the responses. It truly makes me feel better to know there are others out there like myself. I sometimes get out of touch with my condition like it doesn't exist. But I have to really start thinking of myself.

Went for my blood work and will see my Dr. in NYC on Monday. Just hope nothing is going on.

Again thanks and I hope everyone is feeling okay.

Gabbycakes

Hey Gabby, I will pray for you on monday for your doctors visit. Please do the same for me on Wed. I go for an endoscopy, biopsy and to have my throat stretched, fun again....bah humbug. ginnie

Dear Gabbycakes...

I'm very sorry you are going thru such a hard time... Our RSD is nasty enuf...and stress is our ignitor.. I hope it helps you to know you are in my thoughts And prayers...feel better very soon and best wishes for good results on Monday... Take the time you need to rest .... positive vibes!!

Hugs, Kathy

I do stay connected to the RSD site, even though that is not my main issue. I have degenerative joint disease, NP is present, so I have an idea of the RSD pain. I have Cervial, throat, and ankle issues that cripple me. The NP in the foot is rough. I so know how much my own hurts, I reach out to those that have RSD and CRPS. I also have a friend in my area that has this, a cousin with MS and a neighbor that had PD. So I try to stay and help comfort as best I can. I also need comfort right now, as this is my second biopsy for throat cancer, and I am sure scared, just like you are with the RSD. None of our conditions are easy to live with. Pain is no fun. I actually do have a prayer list and I do pray every night for those souls on my mind. I keep the names and conditions, in a Noahs Ark Tin, that I have next to my PC. If I forget, I can then look up each persons name and condition. In this manner I try real hard to comfort those that need a good thought their way. Take care of all of you, and I hope you sleep well tonight. ginnie

Hi, Hope you are feeling well or at least better. I have cervical issues as my main problem (ACDF C5-6 C6-7 12/2/2010). I recently had a diagnosis of RSD by a vascular surgeon at LIJ and then went to a pain specialist who does not feel it is RSD but rather sever Raynauds. I think you stated that you go to NYC to see someone for RSD. It is is allowed can you pass on that information to me. The pain specialist wants to do an EMG and a Stellate Ganglion Block to see if he is wrong and it may be RSD. Not sure how I feel about the block, but willing to have an EMG. Any thought?

Dr. Richman at the Hospital for Special Surgery just opened the Center for Brachial Plexus injury in NYC. He has an awesome reputation.

Good luck.