Chronic Pain members - Welcome, please introduce yourself
Welcome to the new Chronic Pain group.
I’m Kelsey and I’m the moderator of the group. I look forwarding to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Why not take a minute and introduce yourself.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
Thank the DEA for the Opioid fiasco. As for a drug? They have some good ones but I can’t take them because I have grand mal seizures. I can’t take Ketamine either. CRPS is a rare disease and incurable. Type 2 or Causalgia has been around since the Civil War but because not many people have it, the medical community doesn’t make a lot of money treating us—therefore no cure? Probably.
@faithwalker007 I am so sorry you have to deal with this!
@cb772
Hi, just thought I'd pass along a small tip for you. If you just click on @jerid right here (in blue) it will take you to her profile. Then scroll down to see all of her posts. The one's where she describes the Cold Laser Light Therapy device are not far down. You can do this with anyone, go to their profile and see their recent posts. Hope this help. Hank
@faithwalker007 @bustrbrwn22
I don't know if that is it. CRPS is still a nerve related disease. As is neuropathy. There are a lot of different avenues of research ongoing trying to find something that will totally or partially cure neuropathy. They just are having a hard time cracking it. The nervous system is, along with the endocrine system, probably the most cryptic system in the body. As much as they have studied it, the science of the brain is still in its infancy, and nerves are just brain matter scattered throughout the body. They might stumble onto something however, and that is my hope, such as all of this talk lately about pirenzepine and how it "might" be able to reverse or at least prevent neuropathy. I feel that something will come along in the remainder of my lifetime. There is A LOT of money at stake if they find something good. Believe it, they want to. But in the meantime there is just the same mediocre treatments they've been pushing for years unfortunately. Best, Hank
@bustrbrwn22 I do not think you are whinning at all. There have been times I told myself I just can't take this pain anymore. Day, night, always. Make me THINK about what I can do. It wears on you and suicide becomes the thought that that is all there is. I thank God and my faith in God for getting me through the rough times. I understand though. Thankfully I have a pain management doctor that prescribes percocet. It helps alot. I pray FDA doesn't interfere.
@lorirenee1
You bet Lori, will keep you posted on both things. BTW, Linda had a good experience with kratom yesterday. It helped her a lot at a time when she really needed it. Yay!
I am so very sorry about your DRG. I don't understand this thing about using different leads. I would think that would be a key question for your Abbot rep. Also, perhaps a little searching on the web for info about others having a similar situation, i.e. lead switching with their DRG. I guess one problem is not having that many people who've had one at this point.
Hope you are having a low pain day. Hank
With all the injections and eight surgeries and going through PRC at the Mayo I have surrendered. I had a herniated disc on my last go-around which one bad at the Mayo which cause a severe spinal leak which then cause a condition called a Arachnoititis. This condition is not curable there's no research on it and it's caused by injections and surgery. The only way to find out if you have it is to get a MRI with contrast of your lumbar area wherever you're hurting and to see if you have it. If you had it or have it you're in trouble because the pain will increase and if it gets to be a he Civ when is spinal pendants touch each other your pain will be like stage 4 cancer. Keep away from the stimulators and find a good pain doctor that understands your pain and able to treat you. You might want to get an MRI with contrast to see if you have any of this condition I just told you about because there's millions of people who are walking around who don't realize I have that condition. Just want to tell you about it. Thanks and be well
Good morning, Is this @esperanza22? I am happy to give you the information. The THC rich Releaf Balm is from Papa and Barkley. I have been using their products since this medical cannabis journey began. https://weedmaps.com/brands/papa-and-barkley The homepage is papaandbarkley.com.
P and B has just come out with a larger size of 50 ml. My yoga teacher uses it herself and my MFR therapist uses it on her patients,
as well as on herself after a shoulder injury so that she could continue treating. It is great at bedtime to take away all the tingles or needles in your hands.
Good luck with it.........and may you be free of pain and suffering.
Chris
@donfeld I can’t believe you are going through this! My heart goes out to you. Thank you for the warning!
@jesfactsmon @lorirenee1 I am so glad for Linda - send my best to her. Lori, you deserve a pain free day. Couldn’t even morphine help your pain? I feel so bad.