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HNPP: My story by Ms J, Eu.

I was diagnosed with hnpp back in 2005, after many years of going back and forth to the doctors (so many ive lost count), been accused of lying, and almost giving up, finally a doctor, recognized the symptoms and sent me for the test, my broken back, had always been a bit of a red herring when it came to my nerve pain, and doctors, failed to understand why, I was still in pain, even after 2 surgeries.

In 2014, I was diagnosed with painful peripheral neuropathy, finally an explanation to why, I was suffering so much with burning sensations, and nerve pain, from the top of my head down to my toes, something that I live with on a daily basis.

Over the years, I have had many hospital visits, through loss of power and feeling in my legs, to a migraine that blinded me, and closed my throat, I have days where im so exhausted from being in pain, or just that general feeling my body is fighting against me, and stopping me from doing what I love.

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