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.
Thanks Colleen. I think I get it now. Just want to clarify one thing. I had asked how to initiate a new post vs new discussion. It seems the only way to initiate a new post is via a reply to an existing conversation?? Ooops, now all of a suddent I question myself if I know how to initiate a new discussion! And, is a new discussion the same as a new "topic". Oh Lord, I need a tutor! I'm so embarassed by how compromised my brain/memory/focus/concentration/tracking, etc. is! I've always been on top of those things. This Gabapentin is horrible!
BTW, eventually I would like to share my experience w/ CBD oil. I was under the Tx plan of a world renouned doctor whom Kaiser Permanente invited to speak at their pain conference a couple of summers ago in Hawaii, Dr. Allan Frankel. He works w/ chemists, growers, etc., and is well known for dosing. Since I should post under that CBD discussion, I'm thinking a lot of people won't see it b/c they're used to using the current discussions on the main neuropathy disscussion. Or, am I wrong? I know I don't go back to view specific topics related to neuropathy. My info could qualify for the "pain" topic as well. What do you suggest to maximize visibility on what I have to say since it's pretty good info?
Thanks again so much, Sunnyflower
@busterbrown Please explain as best you can what the foot, toes, ankles neuropathy feels like. Every night I am awoken with horrible pain in my feet, ankle and toes. I am diagnosed with peripheral neuropathy, but this is getting worse. I dread going to bed at night
Me Again, My hubby just created a "rule" for my Mayo Neuropathy emails to go into a folder named that. Problem, not all emails say "neuropathy" anywhere in the email; specifically a "like" from someone. What to do? Thanks so much, Sunnyflower
@sunnyflower, When you look at the emails in your Connect folder that your husband set up for you, the subject of the email contains the name of the discussion. It will also tell you if someone mentioned you in the discussion or if someone liked a post you made.
@sunny-flower, the email does state which discussion it is from. Look below the blue where you click to reply. Also, if you look at the very top of the email it states the topic,
Thx but we looked and there are some that do not contain the word, "neuropathy" anywhere in the email. . Working on it; have n'fied Colleen.
HankB @jesfactsmon
Hello Hank,
In 2012, was the trailer fire. I lost 7 dogs and 6 cats in there. I can honestly say now that my mind is stuck on the fact that it was arsoned and the reason I believe this is because I lived in this trailer for 2 years and when my family would leave we would turn the main breaker off. April 19th 2012 I finally got my bill of sell and made plans to move the trailer into a country area, on April 21st 2012 we left to go and get some flowers and we decided to give our neighbor one of our babies for a surprise, (friend of ours at the time) without him knowing. When we we heading home he called my husband and asked 3 times if we had our daughter which he answered "yes".
When I was told about the fire, I kept screaming "breck in back door, bust in the glass" but he said it too late. A 13 year old female seen it all and told me she tried to save them while others just watched. When I told the person who was supposed to get a pup and he told me "if I had known that, the fire would never have happened."
My mind shut down after that, I had to go through therapy and put on meds to help me to cope of the loss of my fur babies.
Before the accident of getting hit in the head with a log, I also hit my own head with the claw part of a hammer which the doctors claim I did it on purpose. My husband told the doctor he could understand if I hit my head with the hammer twice but 6 times without me knowing I was really doing it?
This is why I'm scared of having brain fog, or clouds, I can't think or communicate when this happens and my husband makes sure that I'm in a safe place and keeps a close I on me so that I don't do harm to myself or others when this happens.
I was told I have chronic issues to where I make myself have medical problems and that I'm looking for attention.
Thank you for the idea about writing a journal on this, and I will start right away, maybe I can pin point where the fog, or cloud started and get to the bottom of what is going on.
SORRY for writing a story.
John, Volunteer Mentor @johnbishop
Thank you I will check this out.
My pain started back in 2010 and got worse after my gallbladder was removed in 2011. Doctors has put me on more medicine to help with the pain but nothing helps. It doesn't matter what I eat, i still get pain and the doctors have no clue what to do, and they offered nerve blocks to see if that will help.
Yes, most do but some definitely do not. Anywhere! Believe me, we looked. Could be it was some replies, but underneath in blue that is usually there, isn't in some. Thx for taking the time. 😊
Yes, thank you. I thought it only tells someone if they were mentioned a discussion if their Mayo name @..... was somewhere in the email/reply/discussion. Take care, Sunnyflower