Guest guest Posted October 13, 2007 Report Share Posted October 13, 2007 Hi all, I just wanted to let everyone know what I have been through since my decompression on August 31st so maybe I can help someone else recognize the symptoms of meningitis. 8/31: My surgery at NSUH 9/5: Discharged from NSUH with headache 9/6: Left Variety HOuse with headache 9/9: Arrived Waco TX (Parent's house) still had headache. Trip was pretty miserable but was able to stop or sleep whenever I wanted to 9/10- 9/12: I had the ever present headache, no real change 9/13: My headache intensified, I was no longer able to sit up without great difficulty. My lighht sensitivity became blinding and later I was struck by the nauseau that finally sent me to bed. By 6pm I was asleep and woke up fine by 10pm. I was able to eat a little and then went back to bed. 9/14: I acted about the same as the day before except that when I tried to sleep it off, nothing changed, I didn't feel better and now I couldn't keep any food down. 9/15: After sleeping most of the day, I was woken up by my mother to get me to eat. I refused. This evening I was vommitting and having loose stool. After speaking to Dr. Chan, my father took me to a small hospital in Palestine, TX where they gave me a shot of demerol and sent me home. 9/16: Slept the whole day. 9/17: I received a call from June inquiring as to how I was feeling. I explained the symptoms: Headache, nauseau, vomitting, loose stools, and she surmised that it was food poisoning. I went back to bed, and then woke up with more severe symptoms. My father took me to Providence Health Center in Waco, TX. 9/18: I was admitted after they found antibodies in my lumbar puncture. 9/19: None of the doctors felt they could help me but I did eventually respond well to steroid through the IV. I was released with an oral steroid (prednisone 50mg / day for 5 days then 25mg / day for 4 days). 9/20: The headache started coming back dispite the oral steroid. By 3 pm I was at my PCP's office. She then sent me directly to another hospital ER. 9/21: 7am St Francis Hospital (Tulsa) finally admitted me. I met with Dr. Debra L Murray MD, PHD Infectious diseases and she started a fungul culture on me besides the spinal cultures. She started me on an antifungus called amphrotericin once a day. 9/22-924: I still complained about the headache, so they gave me morphine, demerol, and then finally a dilotted pump. 9/25-9/26: Dr. Murry, against her better judgement gave me IV steroids. They calmed down the headache immediately. 9/27: Dr. Murry received all of her lab tests back, and all were " inconclusive " . She has recommended my release date of 9/28 on the basis that I am not contagious. Sent home with prednisone 40mg twice a day, then taper down quickly. I sent this synopsis to Dr. Bolognese and his responce was that I was suffering from Aseptic Meningitis; that my own red blood cells that were left over in my spinal fluid were causing the meningitis. I hope this helps someone else avoid the many problems I experienced with these small town doctors. The hospital in Palestine, TX could have killed me by their not recognizing the symptoms, they just gave me a shot of demerol and sent me HOME. Meningitis can kill within hours so if anyone has these symptoms seek medical attention immediately. To get a better list of symptoms, go to www.meningitis.org or http://www.cdc.gov/ncidod/dvrd/revb/enterovirus/viral_meningitis.htm. In my case the meningitis was not caused by a virus or by bacteria but by my own blood cells being in my spinal fluid. I have not found any information to lead me to believe that MY aseptic meningitis could have been fatal but it hurt like heck and I lost 12 pounds and spent too may days eating hospital food...yuck! I am still on the steroid for a few more days so wish me luck. Dr. Murray seems to think that the meningitis is not through with me yet. All I can do is wait and see. She did stress that if I have any symptoms at all to go directly to the emergency room...do not pass go and do not collect $200... I am a little worried, I don't know if I'm being paranoid or what but each day that I tapper off of the steroid my neck seems to get a little bit stiffer and sore. I am so afraid that the headache and neausea will come back. Ok, I think that I have written enough...I sincerly hope that this helps at least one person. If anyone has any questions please email me. I tried to be as accurate as I could but I find that I always leave something out that makes people go .... huh??? what's she talking about...LOL Love to all! Take care and have many pain free days!!! Hugs, Sheila FRMLY of West Palm Beach, FL Now in Tulsa, OK (Love it! I'm so close to my family now!!!) 10.5 mm herniation decompressed 8-31-07 Spina Biffida Occulta w/pars defect OTFT surgery scheduled for 11-29-07 @ NSUH Quote Link to comment Share on other sites More sharing options...
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