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.
Good Evening, @cariloo ~
Thank you for such a poignant and tender reply and look into your life in northern Ontario. You sure are familiar with cold, wet weather...my granddaughter, with her husband and baby live just over the Canadian border in Rainy River, Ontario. Their colder weather arrives early and ends later, also.
How wonderful that you can walk bare-foot! I can't take more than one step without leaning on or touching something really sturdy. I do use a cane 100% of the time because of balance issues, and like you, have 3 walkers ~ using the various styles as you do, according to the need and circumstances.
I think Ray's (@ray666) suggestion of one thing at a time is really wise. My faith has a saying, "the duty of the moment" that could also fit a similar approach, although it seems more of a prioritizing system than an organizing one. All of this sounds very cerebral, doesn't it?!
I can relate to what you said about how much time is spent caring for oneself. Gosh, I never thought it would take me a full hour morning and evening to prepare for the night or day ~ to say nothing of taking a shower! ~ and this is without makeup or any making myself to look presentable - lol. But this has become the case.
Still, I am so very content with the life God has given to me. I can maintain my own home with outside help of the yard in summer and snow removal in winter. And the support of folks with similar life circumstances on Connect is priceless. Sometimes we take one day at a time, sometimes one hour, sometimes one moment. And to add to what Ray said, one step at a time.
Blessings to you,
Barb
Mine is chemotherapy induced; Stage II ovarian cancer. Lyrica and duloxetine have been prescribed by my neurologist. I would say mine is basically tolerable. I take 6 Lyrica and 2 duloxetine throughout the day. It feels like my left foot is swelling past the size of my shoe sometimes when I am at work. I definitely know when I have forgotten a dose. Balance is poor, but I try not to run into doors and corners in walls. Some days are better than others.
hi
I appreciated your reflections on living with PN especially the last sentence. with CMT at 76 I am wondering how I will care for my husband who is showing memory decline and will need a hip op soon. 2 cats keep my busy and are good company. thanks for your thoughts.
Hello @he9, Welcome to Connect. I smiled when I read your post and saw "some days are better than others". It may not seem like much but I'm sure a lot of folks here on Connect can relate to some days definitely being better than others. I thought you might like to scan through the following discussion to learn what others have shared:
-- Chemotherapy-induced neuropathy: What helps get rid of it?
https://connect.mayoclinic.org/discussion/chemotherapy-induced-neuropathy/
A search of Connect lists quite a few members sharing what they have found helpful for chemo induced neuropathy. Here's the link that shows the comments - https://connect.mayoclinic.org/search/comments/?search=chemo%20neuropathy%20what%20helps
Have you had any PT or balance exercises to help with the balance issues?