Conditions That May Be Associated With CRPS | Pradeep Chopra, MD, MHCM | RSDSA
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- čas přidán 14. 12. 2021
- Dr. Pradeep Chopra is a Pain Medicine specialist. He completed his Residency in Anesthesia and Critical Care with a Fellowship in Pain Medicine from Harvard Medical School.
Dr. Chopra is currently an Assistant Professor (Clinical) at Brown Medical School and works full time as a Pain Medicine specialist. He has a special interest in chronic complex pain conditions and their associated co-existing conditions including Ehlers Danlos Syndromes (also known as EDS) and, of course, Complex Regional Pain Syndrome.
Dr. Chopra has several publications to his credit and is on the editorial board for a journal on pain. He also serves on the medical advisory board for several chronic pain conditions.
Take a moment to view Dr. Chopra’s slides here: bit.ly/3ma6OvR
To learn more about complex regional pain syndrome (CRPS) and reflex sympathetic dystrophy (RSD), visit Reflex Sympathetic Dystrophy Syndrome Association (RSDSA)’s website at rsds.org.
#RSDSA #CRPS #RSD
![[PART 1] Understanding CRPS: The Truth About it’s Neurobiology and Effective Treatments](http://i.ytimg.com/vi/XBB_7MrJkQA/mqdefault.jpg)
![[PART 1] Understanding CRPS: The Truth About it’s Neurobiology and Effective Treatments](/img/tr.png)
Every medical student needs to review this lecture.
You literally saved my life by discussing LDN, Dr. Chopra. No more wheelchair! It took about 18 months. Thank you!
I'm very thankful for this MD 🙏🏻 Wish more MD's would listen to him and be more teachable 🤞🏻😇🎈
Thank you so much. I have taken so many of your ideas to my doctors over the last few years and it has changed my treatment dramatically, my doctors have started to change their treatments for other CRPS patients as a result. Thank you so much. I have disautonomia with my CRPS. I have learned so much from rsdsa and Dr Chopra.
I believe you may want to look in to Mrs. Alissa Wolfe, pain specialist. She has three incredibly eye-opening videos on CRPS (youtube). It is very cutting edge, and the best break down of this condition on a neurological level I have ever heard from anyone. Also, there is a current study going on in Liverpool England which involves blocking the IL1 antibody (which causes inflammation purposefully in your body) which is very promising.
And that is a human study that is occurring. They already had incredible results using mice.
This was fascinating. Such a knowledgeable doctor with compassion and understanding. I need to listen to this a few more times to digest it all. Thank you for sharing your wisdom.
Very informative. Thank you!
Thank you, very good information. I find my self in these different conditions that are linked, such as eds, pots, macs, small nerve pain, but unfortunatly also aspergillosis.
Broke my foot 3 months ago and have now rcps.
I don't know how this is going further, I also felt it already in my 'good foot' and thought I was going crazy, but thanks to learning from this video I know I 'm not crazy.
I wish there were more docters like you.
You are absolutely not going crazy . What you are feeling is valid . ❤❤ you are not alone fellow warrior
I acquired CRPS 2 in 2018. A cut to my perineal nerve behind my knee during a knee replacement. Since then I've been diagnosed with hypothyroidism, osteoporosis, psoriatic arthritis, anxiety and depression, leached calcium of the bones which manifested as any teeth that I had with crowns on them the crowns broke away from the roots and now I have five missing teeth in my mouth including my two front teeth. Lost these in a 4 month time period.. Also psoriasis that showed up in 3 days from the first tiny itchy spot to about 40% coverage. Scared to see what next.
Thank you so much Dr Chopra 🙏✨💖
Its every thing how well I know 18 very long years
I am so sorry, my friend. For me in February will be 22 years. I do not wish this on anyone.
It's Horrific! 20 years of severe rsd from my brain to my toes. RSD/CRPS SUCKS BIG TIME. PLEASE COME OUT WITH SOMETHING. WERE BURNING TO DEATH!!!🔥🔥🔥🔥🔥Deadly.
All good info, with exception of the perception on discussed immunization.
Is there a transcript from this talk? 🤞🏻🤓🎈 found it !
He says the pain never goes down, but what about those with up days and down days, isn't that pain going down and they are responding via more activity?
Is not Thoracic outlet surgery contraindicated in CRPS type II?
I have CRPS from a failed back surgery in 2010. I do have Hashimoto thyroiditis and encephalopathy and mixed connective tissue diease
45:38-48:24 Doctor Pradeed Chopra answer and comment about stem cells therapies for CRPS. 45:25 stem cells infusion from fat can be very helpful.
I have EDS and CRPS.
Thoracic outlet syndrome could be me!
So if you need a upper and lower from GI Doctor. Is it okay or will my CRPS spread. ? My stomach is so messed up now can't eat without being nauseated. Have loss of appetite and loss weight.I just don't want it to spread through
I caught covid from a vaccinated person though so that advice doesn’t really make sense.
Same …
Very interesting presentation. I disagree with views on the vac seen though. I'm 78 and along with friends and family we have been absolutely fine without wearing masks and getting the jab. I have watched friends getting numerous infections and Covid following it. I have had ME for 34 years and not had a virus since getting Covid 2 years ago. My immune system is working fine. This is an interesting talk nevertheless apart from this misunderstanding about the vac seen. Very knowledgeable doctor.
YOU ARE EXTREMELY MISLEADING WITHNYOUR INFORMATION IN THIS VIDEO. IVE HAD IT FOR 13 YEARS ANDNI FOUND MANY DISCREPANCIES IN WHAT YOU ARE SAYING. PLEASE STOP. JUST STOP.
Video is 2 years old. Why don’t you post what you feel are misleading?