Postherpetic Neuralgia (Shingles) nerve damage
Postherpetic Neuralgia (Shingles) nerve damage around eye, eyebrow, forehead & scalp (8 years) has anyone had any sucessful treatment other than drugs
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Hello @lakeside26, Welcome to Connect. There is another discussion that you may want to join and meet other members who have posted about hotness of the feet and shared their experiences:
Burning Feet syndrome: https://connect.mayoclinic.org/discussion/burning-feet-syndrome/
Have you discussed the symptoms with your doctor to determine the cause?
I suffer from trigeminal neuralgia and am thinking to try botox. Anyone tried it and have a reduced pain or any side effects?
Thanks
Andre.
My shingles wasn’t to painful but I didn’t know I even had them because of where it broke out. One spot was just below my collar bone on the left side. The other was the back of my arm just above the elbow. I never saw them after showering because I didn’t look into a mirror and my chin was always in the way. This was many years ago and the doctor prescribed a cream to apply to it. If I remember correctly, he said it breaks out on the same nerve side, mine was on the left side. There is a vaccine out for Shingles that may help you and ease the pain, check it out with your pharmacist or GP.
I'm 80. I had shingles in all the same places on my face 5 years ago. I have no problems now except an itchy forehead on the side where I had the shingles and a small white scar from a scab that was really thick.
I don’t know about Botox for that but I do often read that DMSO Gel is very effective at relieving Shingles pain.
Topical 5% lidocaine helps a bit. I have cream and spray. I use the spray on my scalp occasionally. I don't like to use it too often.
Topical 5% lidocaine helps a bit. I have cream and spray. I use the spray on my scalp occasionally. I don't like to use it too often. Sometimes I use cold compress on my scalp.
Have been dealing with similar problem for 3 years. Last time I saw my cornea specialist he told me to look into Botox for the post herpes neuralgia. Had my first injection in early July after Medicare approved the procedure. My PHN is much better! I thought I was going to suffer the rest of my life and now I can’t wait for another treatment. I hope you can find a pain specialist. Most of them at UC San Diego double as anesthesiologists. I hope you can find a provider in your area.
Read my post today. Botox worked for me with no side effects.
I had multiple shingles outbreaks. Post Herpetic Neuralgia is not a common conditiopn. It is permanent nerve damage. I didnt know what it was, until I got it. I have been to numerous doctors - GP, Pain Management (I have seen about 5 different ones), acupuncture, cold laser therapy. I have had a spinal cord implanted and removed. A week ago, I had a peripherial nerve stimulator implanted. I have not been given any relief. I have tried all the standard and not standard meds for pain. No opiates, of course. I would appreciate you moving my post. Information from others with PHN would be helpful.
Thank you.