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.
I tried a hemp product once, I think I need a FULL SPECTRUM product and a little more persistence. Thanks for your input.
Hi am mike i had a mirodicectomy at the age of 38. In Indiana workmans comp. Had 4 doctors lie to me and tell me I was crazy. And I had no pain. One day close to the end of my claim. One of there doctors showed me the problem . He used a 3 year old MRI . He told me that the only treatment was a stimulator. After 3 years of lies, they put me through a syic exam. Said I couldn't handle the surgery. After completing was over, closed. My wife's insurance paid for it and I went 18 years with no meds. More to come!
Are you saying that you eventually got the spinal cord stimulator and it wored pretty well for you?
I had a Medtronic intrathecal catheter for 6 years. It caused arachnoiditis, causing pain worse than my original diagnosis. It was not a success for me
Hi, I am Kathy (WNC). Hoping to get info and guidance for pherpherial neuropathy and CRPS, on my right foot, ankle, leg and groin. Had leg bypass surgery 4/22 and my life has never been the same since. Pain and issues are beyond miserable everyday. Praying I can find someone, some Dr., Someplace that can help me. Will not be confined in wheelchair and relaying on someone to ,"take care of me" etc -just not that type.
I'm sorry that happened. Thank you for sharing. I hope you can find some relief and peace. I know we keep trying for better outcomes. Blessings to you.
Hi Kathy @kathr, Welcome to Connect. It's good that your are just not that type and don't want to be limited by relying on someone to take care of you. Connect is a great place to learn what others have shared about their experience with neuropathy and other conditions. Here are a few discussions you might want to scan through and you can always type in the search box at the top to locate others with specific experience.
-- Living with Neuropathy - Welcome to the group: https://connect.mayoclinic.org/discussion/living-with-neuropathy-welcome-to-the-group/
-- CRPS: https://connect.mayoclinic.org/discussion/crps-6/
Kudos to you! I’ve actually told myself the same thing, but , unfortunately, only intermittently find it helpful.
Keep up the good work.
Aahh! I forgot I get headaches from humidity and could not figure out why I was waking up these past few days with a headache. Our overnight humidity has been in the upper 90%, as high as 99%, this last week.
Thank you @busylady. Knowing is (almost) half the battle.
I’ve heard that repeated cortisone shots can damage muscles or ligaments but I’ve never had them. Ask the people at the pain clinic about the side effects AND do a little research on your own. There are online sites like this one and WebMD and others that have info, not just opinion.