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.
@faithwalker007 Sending much love your way....
@sunnyflower. No, the laser doesn't hurt. There's a wand attached to the machine and the PT uses the wand to go over the area of your body that needs it. It's slightly warm but not burning. Sometimes I don't even feel it. The PT wore dark glasses to protect their eyes. I'm always on my tummy when they laser my back so I don't need glasses. They basically laser me every time. I believe it helps. These machines are very expensive and not too many PT places have it. I know them bc they used to be my clients when I was working in a bank. I've been going there for over 10 years. They treated me for all kind of issues. Once I had a knee problem and an orthopedic doctor suggested surgery. I went there for therapy instead and they fixed it.
I have to be positive about this whole situation, some days I think it'll never get better and feel sorry for myself which is a bad thing. Pain can mess up one's mind. Thank you for your good wishes.
@jimhd What kind of SCS do you have? Why isn't it working? Was it installed at Mayo Clinic?
@faithwalker007 Oh, please don't "dial it back." Good writing is becoming harder and harder to find, and I appreciate it wherever it appear.
@steeldove
I have a Burst DR spinal cord stimulator, implanted by a local surgeon and guided by an Abbott rep. It was great for a year, then during the second year it had to be adjusted every 3 months. After that it didn't have any effect on my pain. I've never met the surgeon except in the surgery prep bay.
Jim
@jimhd Jim, please tell me exactly what you mean when you say "adjusted"...the implanted device? your remote? During my trial with the Medtronic SCS, I could reprogram the stimulator using the handheld remote device.
Hello David, I would have to disagree with you that I 've lost my way. If anything, I have found it more than ever learning so much great information here and having so much encouragement, support, inspiration etc.
I worked in healthcare for 20+ years and have been a patient for about 35. I have many specialists who tell me what a complicated patient I am. As time goes on, I am becoming more and more afflicted.
My career goal was to become a physician assistant aka diagnostic care provider before becoming too ill.
I have tons of diagnostics, procedures, surgeries, etc. I research, research, research until the cows come home bc I love to learn so much.
Before Connect I had no one in my life who could relate to not only my unrelenting severe many types of pain, the self -care to manage a diseased, weak body and the limitations of life. Now I do! So it means everything to me! I am so grateful to have found Connect!
Many blessings to you, Sunnyflower
@faithwalker007 @lorirenee1 @jimhd Interesting information from the Hospital for Special Surgery in N.Y.: https://www.hss.edu/conditions_pain-management-myths-facts.asp
SCS infection is only for specific types on euro Pain in the periphery. Doctors are trying to use it for fibromyalgia.
@sunnyflower
Sunny, we are grateful you found Connect also. You have been an absolute treasure! To me and dozens of others as well. Best to you always and always, Hank