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Which advice would you give to someone who has just been diagnosed with Wartenberg's migratory sensory neuropathy?
See some advice from people with experience in Wartenberg's migratory sensory neuropathy to people who have just been diagnosed with Wartenberg's migratory sensory neuropathy
Ask for a referral to a pain clinic, they can then help you try out different types of pain relief such as drugs, tens machines etc, to create a tailored program that suits you. This can come with other co-disorders, so it is necessary to separate what pain is due to WMSM and which is due to these other conditions. WMSN is often felt as a sharper pain than, for example, arthritis where the body is attacking the cartilage instead of the the nerves. This allows each type of pain to be dealt with, for a better cumulative result.
Posted Dec 5, 2017 by Kristin 5220
