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Originally Posted by Nogutsnoglory
Thanks for the replies. I haven't been diagnosed with PN yet but my neurologist is thinking my pain and parasthesia may be due to this. I am going to have an MRI and multiple blood tests.
I have Crohn's disease and latest bloods don't show any indication as to why this may be occurring.
My doctor didn't advise me on the compression socks and they only help a bit. The brush is rough but feels like scratching an itch. I'm just going nuts and need some way to deal with this tingling sensation. I'm afraid overtone the brush will get me so sore and ill develop an infection.
My left leg and foot is worse but I wish there was some device or cream. Sally I eat high carbs because I'm trying to gain weight. Hopeful Epsom baths don't do a thing but what's that lotion and where could I get it?
I have tried Neuragen, Bengay, Capzasin, Lidocaine, Cortizone, Arnicare and a TENS device. Nothing helps so far.
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Hi,
If your doctor did not advise the compression socks I would try going without them. I would try to go without the brush also. I am also worried that you will break the skin and develop an infection.
I see Mrs. D. let you know where to get the espsom lotion. Try that. Have you talked with your doctor about Lidoderm patches. I am not certain what area you would need to place them to stop the tingling in your toes. Possibly some others could give you that info.
I believe that some of the medications for Crohn's can cause PN. Many cases of PN are autoimmune as is Crohn's. I have PN and my sister has Crohn's.
I hope you find something that works for you.