Does CRPS (Complex Regional Pain Syndrome) Spread?

If you or a loved one is suffering from Neurological Dysfunction, nerve pain, Complex Regional Pain Syndrome (CRPS), Postural Orthostatic Tachycardia, Ehlers Danlos Syndrome or Fibromyalgia there is hope!
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Suffering from a Neurological disorder can be incredibly isolating, hopeless and frightening and we understand that. Our treatment protocols are not meant to directly treat CRPS. What we work to achieve is the rehabilitation of the central nervous system.

[@jennaleigh33]

After 10 years of suffering the physical pain and spread from crps 2, the absolute mental Devastation of being dismissed by doctors who didn't even believe it was a real condition, they are coming around a bit but are now saying there's no way it spreads but trust you me I know. They say it can't happen.. it's impossible to get Quality Care and treatment for a condition that they are still unwilling to accept. It's cruel and heartbreaking. My prayers go out for others that are struggling with similar issues. Ty, for continuing to give us hope for remission someday. Love, light and many blessings.💚🕯🙏

[@jaybee5794]

We are stronger than we think. We have control of what our brain does. If this is just nerve pain and not physical pain, it can be controlled. I have it now but I’m going to take control and make it stop through overloading my attention on it and distract it. I did think with a tooth ache once and it worked

[@DS-fi4hf]

How do you treat CRPS when it occurs in the face after dental trauma?

[@stephanienorizsan6679]

Is there anyone in the New York capital region that treats CRPS as you do? I have had it for 4 years and it has spread from right side to left. Since it is a WC case, I have to stay in NY. Thank you

[@dorenehendricks6627]

Yes can spread fast or slow it sucks good days but more bad days then good

[@rockymountainpublicsafety1397]

Yes it spreads! I have full body CRPS. Started in right ankle. Spread within 1 year. Been feeling stabbed and burnt to death in every cell of my body for the last 22 years

[@Truerealism747]

Have you tryed ldn what's the difference than fybro apart from skin changes

[@sicknarty9457]

@tom I have been diagnosed with fibromyalgia formally for about four years now. I am new to my CRPS journey, and I can say the severity of the pain I typically feel with CRPS is about x20 worse than my worse days due to fibro. Not sure if thats helpful at all

[@Truerealism747]

@@sicknarty9457 I've had on for 25 years now fybro shoulders armpits which is very hard where is your crps did it change colour

[@sicknarty9457]

@Tom Sale I am experiencing it in my entire right arm . Yes I have already noticed some modeling and coloration changes, for me so far some days it can be quite red and angry and some days blueish. The integrity/texture of the skin itself has changed a little as well

[@Truerealism747]

@@sicknarty9457 have you tryed ldn.starting soon mine is in my shoulders armpit s constant heal pain pelvic pain mines built up over time but say it's central sentization myofacial pain

[@jaybee5794]

Could it be that during the healing process you didn’t take pain relievers so your brain sent down to much pain relief chemicals? What if you target the pain to other parts of your body so the brain stops sending it to one location

[@ronosama]

My spear in one year all body 😢

[@tarawilson6126]

I was diagnosed with CRPS in both lower extremities in August of 2023,and it has now spread to my left hand.😢

[@Bitachon]

*Symptom imperative?*

[@Truerealism747]

You mean tms

[@normamercado5420]

I to have CRPS for two years.

[@Truerealism747]

What's the difference in fybromyalgia apart from skin colour changes etc