Living with Neuropathy - Welcome to the group
Welcome to the Neuropathy group.
This is a welcoming, safe place where you can meet other people who are dealing with neuropathy. Let’s learn from each other and share stories about living well with neuropathy, coping with the challenges and offering tips.
I’m Colleen, and I’m the moderator of this group, and Community Director of Connect. Chances are you’ll to be greeted by volunteer patient Mentor John (@johnbishop) and fellow members when you post to this group. Learn more about Moderators and Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let’s chat. Why not start by introducing yourself? What concerns would you like to talk about?
Interested in more discussions like this? Go to the Neuropathy Support Group.
@wilcy So...did you also find folks to help you make your selections? I hope it goes well and that you experience some relief. Thanks for checking in with us. Have a restful sleep. Chris
@barbbie, it is great to read that you have a good and trusting relationship with your pain management doctor. Congratulations for making the effort and being a cooperative patient. Sleep well tonight....Chris
Hope it goes well - keep me posted!
For many years I spent probably 60-70% of my day in bed. Pain meds made me tired. My quality of life diminished. Socially, I pulled way back because when others saw my pain they were helpless and I wanted to hide. I tried to continue to work and was in such a brain fog. Fortunately, I had an office and would shut my door and rest on the floor. I pushed thru exercise classes and would get painful spasms that would draw attention. I explained that they would pass and one day the instructor said in front of everyone that I freak her out. I stopped. I’ve never had such pain in my life as I’ve had from shingles. I was 56 at the time and am now 71. The saddest thing is there are many worse off than I am. I fake my way thru social events. Smile, laugh and act like I’m enjoying myself when in reality I just want to be home and in bed.
This is the place I come because no-one in my life can possibly understand what goes on inside my body with SFN. I find comfort and support just reading through yours posts. Thank you for sharing and helping me make a connection of sympathy, encouragement and guidance.
@rwinney, Some beautiful and genuine thoughts in your post. Thank you. Chris
So far, not doing anything!
Thank you. It's so true though as I sit here crying reading everyones responses and likes. You all do help me. I'm at the hospital now hooked up to my 6th lidocaine infusion, after taking my hydrocodone for comfort and pain relief. I hate taking a narcotic! I'm so against it. I've never drank, smoked or done drugs and here I sit going through the motions with lidocaine that doesn't help this far, just trying to reduce the hydro.
It was such a hard weekend...my daughter's graduation from high school party. I live for my kids and these moments and powered through so much. It didn't kill me but boy oh boy did it all hit me super hard. I had so much pain and moments of removal from the party due to dizziness, over heating, palpitations, and shortness of breath, along with migraine mid day which thankfully Cambia aborts. I just really miss life as it used to be.
So sorry truly feel for you!❤️