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Living with Neuropathy - Welcome to the group

Neuropathy | Last Active: Oct 27 5:51pm | Replies (6152)

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@sallymagint

Thank you Colleen and John, I'm hoping I can learn as much as possible about Neuropathy and how others are living with and managing their symptoms effectively.
From my point of view the care and treatment provided by my medical team is likely to have more positive outcomes if have a positive approach and try to help myself as much as I can -I guess it's a team approach and I'm a vital player. It's not easy, in fact it's damn hard a lot of the time and some days I wonder how I'm going to get through it but I don't have any other option.
I have a numbee of medical conditions which leave me with a fair amount of neuropathy. I have altered sensations in most parts of my body affecting my sensitivity to temperature, pain, touch, taste, smell. My legs, arms and extremities have significant weakness and a degree of paralysis which may or may not be permanent. I'm in the process of undergoing treatment with neurosurgery planned in the not to distant future. It's hopeful surgery will reduce the risk of further permanent damage and then the focus will be on retraining/repairing the brain. There's no guarantees and it's still a long road to travel but I'm crossing my fingers I can reverse some of the damage.
Thank you so much for giving me the opportunity to talk about my situation. Although I haven't delved into it too much due to the complexity, it's helpful to chat about the neuropathy part of it.
I live in Australia and knowledge/experience amongst the medical profession about my conditions is limited. It has made it very tough and I've been confronted with a fair amount of ignorance. It is soul destroying when you know there is something wrong but you're made to feel it's in your head. But I'm not giving up, I can't give up and through perseverance I've found some amazing specialists who are familiar and experienced and are hopeful they can help me. And I want to raise as much awareness as I can. Awareness is power and power makes change. If less people experience the degree of emotional trauma like myself and others have faced simply by increasing education and knowledge, it can only be a win for all involved

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Replies to "Thank you Colleen and John, I'm hoping I can learn as much as possible about Neuropathy..."

Have you looked into Stem Cell therapy?

Hello 👋 I am from Australia 🇦🇺 and have just started on this journey of discovery. This week I learnt a bit about what is happening. Still in shock, and not wanting to believe it. I hope 🤞 I will hear from you if not I do understand. I am living in QLD Thanks Teresa

I just found out why I've been feeling more pain ... I picked up my rx for gabapentin at the usual pharmacy but it looked different - it's a large white tablet, it's usually a yellow-beige capsule. I asked the pharmacist why it looks different -- she read the labels and said that it's 600 mg, the other is 400 mg. My doctor changed my rx to 600 mg months ago and sent the rx to the pharmacy but they kept filling the old rx until it ran out without asking me or the doctor if they were supposed to discontinue the old one and start the new one right away. The old rx just ran out so they finally filled the new one -- perhaps I will feel less pain in a day or two. Do any of you have a good system for staying on top of your medications, doctors, appointments, and pharmacists? Something that's portable, easy to update, easy to read ... ? Peggy

Hi Sally, I am new to this site and just learning to navigate it. Whereabouts in Australia are you? I am on the Gold Coast. I would be eager to have any information you can share. Neuropathy has destroyed my life and losing my independence is confronting. Look forward to hearing from you. Patricia.

Consider the spinal stimulator . You should pain doctor and or a neurosurgeon.

John 2nd time
Initial blood test mean corpusclar hemoglobin up .4 Dr. Called me.they said other labs will come tommow.question: is this common with P N. ??