Hi everyone- I don't want to retell my entire story. If you like, you can go back and look at my past posts. Suffice to say, I have tried everything including Pudendal nerve surgery.
For the past two years, my PHN was mostly gone with occasional flare ups that I believe were viral flare ups. After a week or so, it would go away.
But, it was always mild compared to the 4 years I had it after the initial exposure.
Well, for the past week, it has been back with a vengeance....much like it was those 4 long years. I am very worried. I don't know what I could have done to trigger it and I know that there isn't anything I can take that will make a difference.
This sucks. I have been taking 2000mg of valtrex for the past 3 days in the hopes that it may reduce the amount of "damage" or "agitation" it may cause my nerves.
I am going to also take BHT, Vitamin A, and Lysene.
I am not very hopeful considering my 4 year battle previously. I don't know why it went away(thought it might be the surgery) and I sure don't know why its back.
Just wanted to vent.