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.
My doctors think that I have inherited neuropathy for some sensory and autonomic issues that I've had since childhood, but think there is likely an autoimmune cause of the rapid onset, but they can't find proof. Fighting with BCBS to get IVIG to see if it helps. Anyone have experience with IVIG?
@arcticmark, I am tagging a few members who have discussed an IVIG in a post and may have information they can share with you. Please meet @bburleson1 @gratefulone @mllucas @mllucas @ginifuller @captnick @kdp3186 and @5134177246 -- can you share your experience with IVIG treatments with @arcticmark ?
John
Sounds somewhat familiar. January 2017 diagnosed with small fiber neuropathy. July 2017 I drove from Massachusetts to Missouri, but in December I had to give up driving because I had no feeling in my feet or legs. February 2018, further EMG testing revealed both small fiber and large fiber. Pain, burning, numbness, etc from waist down to soles of my feet, both legs, and getting worse.Neurologist in St. Louis called it idiopathic, which I think of as "Doc, you're an idiot for not listening to me and exploring possible connection to my life-long thyroid issues, changes in my spine, and a history of several genetic glitches. I'm heading back to Mayo in August.
I am scheduled to start IVIG in two weeks. I, too, would appreciate any information shared. Thank you.
my son has been getting ivig for 18 years...it will help
drive with hands...very easy
I have been diagnosed with a skin biopsy with small fiber peripheral neuropathy and read everything I can find about it. What is IVIG? I have tried Lyrica, gabapentin, nortriptyline, and others with nothing but severe side effects.
Hi @cmartinjr, I believe there are others here who can share their personal experience with an IVIG. Here is some information I found that gives a little background information on IVIG.
Patient education: Intravenous immune globulin (IVIG) (Beyond the Basics)
-- https://www.uptodate.com/contents/intravenous-immune-globulin-ivig-beyond-the-basics
John
Thanks!
im a neuropathic patient and I have been suffering from neurological itches for the past one year. Day by day its increasing. Since Iam using Asprin the amount of blood coming out is high. I came to know that there is no specific treatement for this. Anyone having any idea? Pl.share.