Looking to connect with people who have non-diabetic neuropathy
Would. Like to find people with this issue
Interested in more discussions like this? Go to the Neuropathy Support Group.
Would. Like to find people with this issue
Interested in more discussions like this? Go to the Neuropathy Support Group.
I’ve tried all the creams and nothing helps. I’m taking the Gabapentin because Lyrica made me have seizures and Nortriptyline makes me feel like someone is stabbing my.
What is the medicine you take at night? I’m taking 300 mgs of Gabapentin, 100 mgs 3 time per day and 60 ‘mgs of Cymbalta in the morning with my seizure medicines. Keppra and Clonazepam. They also have me on Quetiapine.
Wow! I take the Tizanandine at night. I also have prescription for Tramadol for pain. I keep trying things. It is so frustrating. I hope you find some relief.
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1 ReactionI have same exhaustion and joint pain- maybe “long Covid”?! Although I test negative! Palo Alto Doctors haven’t got a clue!?! Any pain pill ideas?
My large peripheral nerves were damaged by vasculitis. I have pain and the tingling and the hot and cold and everything else that happens when you have peripheral neuropathy. Nothing really helps except I sometimes use Aspercreme. My neurologist has also recommended that I use ALA alpha lipoic acid. So I started taking that about six weeks ago. I haven’t seen too much relief from that yet but she wants me to double up and so I’m gonna start that right now. It’s tough when one disease causes another disease and you can’t do anything about it. But I’m learning to live with it and it’s just plain annoying. My arms tingle I feel like I’ve got ants and bugs crawling up and down my arms and legs all the time so I’m constantly sweating at myself after while it becomes funny. I don’t know what else to say. I wish you the best and please know that you are not alone in this.
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4 ReactionsI have ms and none diabetic neuropathy.
Susan, I feel the same. Sorry you have to go through this.
Thank you for your reply.
I often used deep breathing to help me fall asleep. Breathing in, holding
for 4 seconds breathing out for 4 seconds. Concentration on breathing
turning my thoughts from pain.
I have read about mantras now that you mention it. I need to practice them.
I walk daily and I think making positive statements may help me from
letting my mind wander. Walking and stretching seem to really decrease
pain. I don't have certain stretches or exercises but I am willing to try
new things or sequences that anyone suggests.
Gabapentin is a miracle drug for many people. Physicians have such few
drugs to use for neuropathic pain. When I was initially hospitalized for
what I now know as small fiber neuropathy, I was prescribeda taporing dose
of Gabapentin. When I was at 1200 mg I began having slight muscle spasms
and sudden depression. It is hard to explain, but it was frightening and
the doctor tapored me off of Gabapentin. The dark depression lifted and
pain increased. The medication was put on my allergy list. In June of
2021, I was placed back on Gabapentin out of desperation for pain control.
I was told that it was rare that I would experience thevsame side effect.I
had the same side effect. Currently, I work closely with a doctor.
Taporing me off of prednisone and Gabapentin would be very bad for my
health. So I will wait. I tell myself that my feelings often reflect
prednisone withdrawal and Gabapentin. Not my true feeling. I am ok and my
future is going to be wonderful. I pray for patience. I guess maybe that
is like a mantra.
Like I said, Lyrica and Gabapentin are wonder drugs. They help many
people. I just was very unlucky. And am lucky to have a husband and a
doctor to hold my hand during my journey.
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4 ReactionsI have neuropathy in my feet as a result of Long-Covid 19 and was wondering if anyone has used neuropathy socks to address the pain?
Welcome @rse77, I know it must not be easy dealing with MS and the the pain from neuropathy.
Have you found any treatments that provide some relief?