Meningoencephalitis War on Brain
In the first week of September 2012 I developed flu like symptoms which seemed to get worse daily. My eyes turned bright red, a super bloodshot look. Finally, I sought treatment at a hospital ER. When I arrived it was noted I had some confusion so I was given an orientation exam which revealed I didn't know the date, president, etc. I barely remember the next few days before going into a coma. A lumbar puncture revealed a pus pocket in my spine. My cerebral fluid was thick and yellow when it should normally be clear. For a week and a half they had no idea what was wrong with me. Finally, they discovered it was West Nile Hell. I had developed Meningoencephalitis from the virus. There was no treatment for West Nile Virus.Three times they sent me to ICU, I was on a respirator and my husband was told to prepare for the worse. He was told if I survived I would be a vegetable. Miraculously, a month later I started waking up. There were days filled with hallucinations, I couldn't feed myself or walk but was able to start communicating. The doctors were astounded. Finally I was transferred to a rehabilitation facility where I learned to feed myself and walk again. That was excruciating work! The day came when I could go home to my beloved and my furkids. Glory to God! Sadly, I must say today's physicians know little about this disease and the long term effects. On going symptoms are frequently labeled all in the head or drug seeking. There's a wonderful support group on Facebook for anyone looking for information. It's under West Nile Support Group. Best wishes to all who have suffered and continue to suffer from this horrible disease.
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