MS Hug

I have been diagnosed since 1997 and regularly going to our MS Clinic as well as using Avonex for 5 years... I have spent the last 3 weeks dealing with what appeared to be a heart attack and had been admitted to hospital twice to no avail. ALL cardio work ups & chest X-rays were negative. My wife had found what appears to be most of my symptoms on line as something called MS Hug. Is this real? Do the neurologists' discuss this... anyone have similar experiences?

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