Hi, everybody:

I would like to know if RSD can cause hypothyroidism.

If anyone knows about Internet documents showing a link between these two syndromes, please share them so I can get educated and educate my doctors as well.

Thank you very much for your help.

Oh no, no answer again! Am I the only RSD patient on this forum to have hypothyroidism?! If yes, puh-lease say so, so I do not come back here, expecting an answer and being very, very disappointed when there is none. It is PURE HELL to live with generalized RSD, AND epilepsy, AND hypothyroidism! So, someone, please help!

I am relatively new to RSD (diagnosed in May and started symptoms in December 2010). I don't have hypothyroidism. I am interested to see if anyone else has something to say. I just wanted you to know I was here. Btw, what is "generalized RSD"?

J

Hi, 6kiddos:

Generalized RSD is the technical term for full body RSD. There are two kinds of generalized RSD: external (which does not touch the internal organs) and internal (which does touch the internal organs). I have reached stage 3. Hopefully, I will never reach stage 4 because, like my anesthesiologist and pain management doctor said, stage 4 is equivalent to a "death sentence".

Thanks for being there, 6kiddos. I am really scared because it seems like my hypothyroidism came out of nowhere. I blame my generalized RSD for "attacking" my thyroid, the same way it "attacked" (or spread to) my lungs and gastro-intestinal tract. This is why I would have appreciated an answer to my original message to be absolutely sure RSD spread to my thyroid also.

Thanks Kitty.
I guess I have never heard it called "generalized RSD" before. I am sorry it is so bad for you. Mine moved from the right foot to the left within the first month and a half...though at the time we didn't know it was rsd. lovely. Anyway, since then (Jan-Feb) the burning spread from just my feet and was creeping up my legs to just below my knees. Since my nerve blocks, the burning is much less (though it seems it has been increasing again). I also have to wonder if it has spread to my akles and lower legs. They hurt as bad as my feet at times and today they hurt more. =( Oh well, right?

I hope someone can answer your question. goodnight.

J

Kitty, why not try changing your settings so you'll get Instant Notification (it's at the bottom each time you post)? Then you'll know if you've gotten a response without checking in.

Try not to worry when you don't get a response right away. A lot of us just check in intermittently. This forum moves slowly enough that your question usually won't get totally buried and you'll hopefully get your answer within a few days.

To answer your question, no, I don't have hypothyroid, but I have CRPS-Type II and it's localized in my left leg.

Good luck!

Hi, 6kiddos:

I think I was really, really stupid and this saddens me. Why? My Duragesic (fentanyl) patches and my MSIR (morphine sulfate immediate release) were controlling my icy and burning pain so well that I assumed my RSD could not and would not spread anywhere. How wrong I was! How stupid I was! Now my RSD is generalized. Not only it is external, but it is now internal also. My RSD started "attacking" the following internal organs: brain, lungs, and thyroid. What organ is next? My heart? Another organ? If it continues this way, my RSD is going to end up killing me. I do not know if RSD can be a deadly syndrome when it attacks certain organs, but I do not want to die. I only have one life and I want to enjoy it as much as I can.

Thanks for your answer and kind words. I sincerely hope your RSD will never spread to your whole body and attack your internal organs. A nurse practitioner and other health care professionals told me it was quite rare for RSD to become generalized and attack organs, so hopefully you are safe.

Hi. I just joined this. I have been diagnosed and treated for hypothyroidism for over 35 years. And have had RSD for almost 11 years which is now spreading. Living Hell is putting it mildly. You are NOT alone.

Hi. I just joined this. I have been diagnosed and treated for hypothyroidism for over 35 years. And have had RSD for almost 11 years which is now spreading. Living Hell is putting it mildly. You are NOT alone.

I am new to this support group. I have had the RSD diagnosis since an auto accident in August 2009, by a man who who had no insurance!! Just my luck!! Over two years of dealing with this disability and I still often have times I just want it GONE!! The RSD is in my entire right arm (i.e., shoulder, arms, hand, and fingers). I am one of the "rare cases" that has mirroring in my left hand also. The original injury/damage was to the right upper quadrant of my body because that was the only arm on the steering wheel at the time of the accident.
I am a psychologist for a school system, and I missed almost an entire year of work (2009-2010). I then returned to work full-time this previous year. I am back to needing P.T. again because my shoulder is freezing up again. The part that really "ticks me off" is that the driver that caused the accident has no frigging idea what I will deal with for the rest of my life. I am on several pain, depression, and anxiety medications because my pain level is usually about a 7 or 8.
As the title to the post indicates, I realize that I am slowly losing my fingernails. The white portion is increasing back over the "quick." Does any other RSD patients have the same thing?