1. < Neuropathy
Moderator

Living with Neuropathy - Welcome to the group

Posted by Colleen Young, Connect Director @colleenyoung, Jul 14, 2017

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.

Mentor
Rachel, Volunteer Mentor | @rwinney | Jul 31, 2019
In reply to @johnbishop "Thank you for the kind words!" + (show)
@johnbishop

Thank you for the kind words!

Jump to this post

John, you really are...
THE MAN!

REPLY
1 reply
Mentor
John, Volunteer Mentor | @johnbishop | Jul 31, 2019
In reply to @rwinney "John, you really are... THE MAN!" + (show)
@rwinney

John, you really are...
THE MAN!

Jump to this post

Now I’m really blushing 🙂 @rwinney

REPLY
Mentor
Chris Trout, Volunteer Mentor | @artscaping | Aug 1, 2019
In reply to @mlross4508 "Hi. I’m also looking for PN relief. I’m not sure how to get a group or..." + (show)
@mlross4508

Hi.
I’m also looking for PN relief. I’m not sure how to get a group or talk time started, but I can suggest you research Mayofascial Release Therapy, or MFR. I’ve had bad neuropathy in my feet from a couple of failed back surgeries and developed CRPS which started this pain.
I’ve had 4 MFR treatments and it has given me a new lease on my life with 75-85 percent reduction in my pain. My pain started to go away after the first treatment!
Then you do self treatments on your own to help heal what ails. You have to put time in to get positive results.
It might not work for everyone but when I read about this on this discussion group, I soon tried the therapy and I go once a week and feel better after each session.
Good luck with this and your other suggestions on this post.

Jump to this post

@mlross4508, Wow...you are an MFR hero. Thanks for trusting our guidance and for reporting back to us that the MFR treatments have improved your neuropathic feet. Keep it up. Chris

REPLY
Leonard | @jakedduck1 | Aug 1, 2019

Generic Lyrica (Pregabalin) Capsules and solution have recently been approved.
25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg, 300 mg

Oral Solution
20 mg/mL

Jake

REPLY
1 reply
jimbotch | @jimbotch | Aug 1, 2019
In reply to @jakedduck1 "Generic Lyrica (Pregabalin) Capsules and solution have recently been approved. 25 mg, 50 mg, 75 mg,..." + (show)
@jakedduck1

Generic Lyrica (Pregabalin) Capsules and solution have recently been approved.
25 mg, 50 mg, 75 mg, 100 mg, 150 mg, 200 mg, 225 mg, 300 mg

Oral Solution
20 mg/mL

Jake

Jump to this post

What pharmacy has it?

REPLY
Vradi Fegariou | @vradifegari | Aug 2, 2019
In reply to @etipton9756 "Cynthia; I'm looking for a MD or specialist who can advise my doctor about the validity..." + (show)
@etipton9756

Cynthia; I'm looking for a MD or specialist who can advise my doctor about the validity of Gabapetin for PN. Could you provide his/her name and contact info?

Eddie Tipton

Jump to this post

Hello Etipton:
What is a MD specialist?
Best regards,
Vradi

REPLY
Vradi Fegariou | @vradifegari | Aug 2, 2019

I have 3 questions:
Which is the test I need for determinate my Magnesium levels?
Do you know a trustworthy seller of Fibro Malic and Epsom salts? Amazon sells bouth but I am not sure.
I have vitamin supplement: Multi Women. Energy + antioxidants. Manufactured by: Alfa Vitamins Laboratories. Do you know it?
Good day and thank you.
Vradi

REPLY
dstewart318 | @dstewart318 | Aug 8, 2019
In reply to @confused1955 "I think I'm in here somewhere but my diagnosis has changed and I don't know if..." + (show)
@confused1955

I think I'm in here somewhere but my diagnosis has changed and I don't know if I'm in the right group. I finally received a second opinion and unfortunately it's worse. I have Complex Regional Pain Syndrome CRPS. Nicknamed the suicide disease as the on the long scale it's 42 out of 50. I have read reports that attempts and success range at almost 70%. So far no favorable prognosis. Same deal Gabapentin and pain killers. I've been promised I would be kept comfortable but no one knows how to do that. I live 24 7 in my dark room because the light affects my head. Is there anyone in this group that has had this disease for over 2 years as I believe we would have more in common. After 2 years your not eligible for testing anymore because after 2 years there is no chance of a cure. You are too alive to be helped by dying with Dignity because I suffer with my hands 24 7 it feels like they are in boiling oil. Because I'm not eligible I have to suffer forever. When your reading and they say rarely children get this but they do and it's vicious on our little warriors. HELP

Jump to this post

I am a 43 yrs old female. Diagnosed 9 years ago when they called it Reflex Sympathetic Dystrophy Syndrome. They new VERY little about it. So I put it by the way side. Suddenly 2 yrs ago it hit me like a freight train. This pic is what my hands do during just a typical flare up. You are not alone. Feel free to talk to me anytime!!! I need support as well. Mayo clinic in Jacksonville, FL has a CRPS specialist on staff. They can do all the diagnostic testing and any treatment there. But they require a $5000.00 retainer, not including lodging. I live in Atlanta, GA and I'm gonna go out on a limb here and say....my name is Dana. Feel free to private message me. I am truly just trying to figure out where to even start with all this. And I have a 6 yr old son and 12 yr old daughter. But Im someone who understands what you are going through. Day or night. God bless!! Dana
REPLY
1 reply
Mentor
Rachel, Volunteer Mentor | @rwinney | Aug 9, 2019

Hello and nice to meet you Dana, I'm Rachel.
I'm so sorry for the pain you endure. It sounds like the inspiration in your life must be your children! They have the ability to make us stronger and keep us focused even through the misery. I hope this message finds you with a smile on your face, if only for a moment. Know that you are not alone.

REPLY
Mentor
John, Volunteer Mentor | @johnbishop | Aug 9, 2019
In reply to @dstewart318 "I am a 43 yrs old female. Diagnosed 9 years ago when they called it Reflex..." + (show)
@dstewart318

I am a 43 yrs old female. Diagnosed 9 years ago when they called it Reflex Sympathetic Dystrophy Syndrome. They new VERY little about it. So I put it by the way side. Suddenly 2 yrs ago it hit me like a freight train. This pic is what my hands do during just a typical flare up. You are not alone. Feel free to talk to me anytime!!! I need support as well. Mayo clinic in Jacksonville, FL has a CRPS specialist on staff. They can do all the diagnostic testing and any treatment there. But they require a $5000.00 retainer, not including lodging. I live in Atlanta, GA and I'm gonna go out on a limb here and say....my name is Dana. Feel free to private message me. I am truly just trying to figure out where to even start with all this. And I have a 6 yr old son and 12 yr old daughter. But Im someone who understands what you are going through. Day or night. God bless!! Dana

Jump to this post

Hi @dstewart318, I would like to add my welcome to Connect along with @rwinney and other members. I don't know much about Reflex Sympathetic Dystrophy Syndrome other than it is a subdivision of Complex Regional Pain Syndrome - CRPS type I (reflex sympathetic dystrophy). I did find some information about it on the National Organization for Rare Disorders database here:

https://rarediseases.org/rare-diseases/reflex-sympathetic-dystrophy-syndrome/

I also found some other information that may be helpful if you haven't already seen it.

NIH - Complex Regional Pain Syndrome Fact Sheet
-- https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-Sheets/Complex-Regional-Pain-Syndrome-Fact-Sheet#How%20is%20CRPS%20treated?

Have you found any treatments that help you when it flares up?

REPLY
1 reply
View MoreView Less
Please sign in or register to post a reply.