Shingles and Postherpetic Neuralgia and Pain
Has anyone suffered from LONG lasting neuropathic pain as a result of Shingles, and what treatment do you use for the pain? My daughter had shingles at 21, a spinal cord stimulator inserted and removed, many trigger point injections, all of which may have contributed to the thoracic pain she has. She is now 34, and teaches yoga, but is still on a compound prescribed by a pain management Dr. in NYC what is basically Oxy. I am paying for this, since neither she nor her husband can afford it at around $500 a month. She could not find a physician in Fl. I know who would prescribe this medication after 10 years, thus the use of an out of state physician. I do not want to see her suffer, nor can I discuss much with her since we barely speak, but this expense, coupled with paying for asthma inhalers that are expensive is becoming more and more of a strain. Any thoughts for alternatives are appreciated.
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I wish you lots of good luck!
Will you please send me information to order. I am willing to try again. Thank you.
I'll try to figure it out so you get the 25% off and I get the $30, but if it doesn;t work easily (a friend had a problem) You can just order direct at the regular price.
I have another thought, why don't you call them and ask wha they think will work best for you. I'll get you their phone number.
Phone number 844-550-8699 I and my friends use the Liberty Patch. I also have some of their socks that are handy because i don't run out of socks and they are good to go out shopping in. I put another sock over them so the heels don't wear out.
https://voxxlife.com/superpatch/
Thank you. 🙂
Where did you find information regarding your plant based diet. I am in such misery, I have to try. How long until you noticed a change in your pain level. Thank you.
I don't want to discourage you as tens units do help people. For me with PHN. It was just another item to buy with many others. It did not help.
I am still trying. That is the best thing to do. One day, something will lower your pain to a tolerable level. I feel very bad for you because I completely relate to your post.
I have tried most everything but stem cell. Good luck.