Vick’s Vapor Rub for Neuropathy Pain

Hi friends in pain… 🙏

Thank you for the VICKS..

I wear socks everyday...
Please try 100%wool and see the difference...
You see, wool, keeps the Boddy temp consistent to ours.
Amazon has 3 sets for $ less then $20. Next day....free.

also mentioned
to wear sleepers 2-3 hrs before night night... thus keeping ft at body temperature. Add the VICKS.. Am on it tonight.

Thank you all.

Ps
Have you ALL LOOKED INTO PROTOCOL 525?

Am on it... Just read and watch YOUTUBE INFO ETC...

Blessings
Carlos, Here. In HOUSTON TX.

Fascinating idea! I have had PN for 23 years. My symptoms have changed dramatically over the years.

My feet, calves, and knees were numb to just above my kneecaps. Over the past two years, the feeling has returned to my shins and feet. The pain also returned! Now my shins are in such pain. My legs feel so cold I literally shiver sitting in my living room. Our temperature is set at 78 degrees. My husband is melting. He wears shorts, no shoes or a shirt! I am in flannel sweatpants, two t-shirts, and a flannel robe with a hood. I have an electric blanket over my legs.

I will try Vicks tonight! This forum has given me so much help. I am feeling very hopeless. All my doctors say nothing can be done. I do not accept this. I have an appointment with a pain specialist physician for an evaluation and hopefully a nerve conduction test. I have had several over the years which all confirmed PN. My neurologist told me I do not have PN and she could not help me as my condition is not PN. She accused me of drug seeking. I broke down uncontrollably sobbing I was so devastated. She did not blink. I asked if she would do a nerve conduction test. She replied, "well, if you insist". Every neurologist I have seen has always done this test. I have been with a pain management physician for 3 years. She referred me to this neurologist. I have been using Hydrocodone for many years.

Bless all of you on this forum! For the first time in many years, I feel hope! This group is so positive.

Sorry, this is long and rambling! I just got so excited to see this post about hammer toes!

Yes, Vicks helps with neuropathy pain and burning. It did for me and I pray it will help you as well. Neuropathy socks has helped more than anything! Please give them a try🙏🏻

Fascinating idea! I have had PN for 23 years. My symptoms have changed dramatically over the years.

My feet, calves, and knees were numb to just above my kneecaps. Over the past two years, the feeling has returned to my shins and feet. The pain also returned! Now my shins are in such pain. My legs feel so cold I literally shiver sitting in my living room. Our temperature is set at 78 degrees. My husband is melting. He wears shorts, no shoes or a shirt! I am in flannel sweatpants, two t-shirts, and a flannel robe with a hood. I have an electric blanket over my legs.

I will try Vicks tonight! This forum has given me so much help. I am feeling very hopeless. All my doctors say nothing can be done. I do not accept this. I have an appointment with a pain specialist physician for an evaluation and hopefully a nerve conduction test. I have had several over the years which all confirmed PN. My neurologist told me I do not have PN and she could not help me as my condition is not PN. She accused me of drug seeking. I broke down uncontrollably sobbing I was so devastated. She did not blink. I asked if she would do a nerve conduction test. She replied, "well, if you insist". Every neurologist I have seen has always done this test. I have been with a pain management physician for 3 years. She referred me to this neurologist. I have been using Hydrocodone for many years.

Bless all of you on this forum! For the first time in many years, I feel hope! This group is so positive.

Sorry, this is long and rambling! I just got so excited to see this post about hammer toes!

I first read about using Vick's Vapour Rub a while ago, and it works for me. I put it on before going to bed, as I find that is when the burning and irritation and pain become the worst. I will re-apply in the night if needed, and it always seems to calm things down. I would be interested to know what is in it that makes it work for us neuropathy sufferers.

I believe it is the menthol in the Vicks Vapo rub, because it is also in other pain rubs I've tried.