For the four months I have had two bouts of pneumonia, an episode of
fluAmniocentesis
Atrial fibrillation/flutter
Cerebral spinal fluid (csf) collection
Culture - joint fluid
Fluorescein angiography
Flushable reagent stool blood test
Fta-abs
Gastroesophageal reflux disease
Gastroesophageal reflux in infants
Haemophilus influenza organism
Hiatal hernia repair, hypothermic blood
temperaturesTemperature measurement (with no symptoms, shivering, etc.), temps ranging from 91.5 to 93.5 degrees. The
temperaturesTemperature measurement are always consistent in this range. I have lost my sense of taste, except for a metallic aftertaste when eating and drinking. I have tried taking zinc, but with no resolution. I have difficulty
swallowingPainful swallowing
Swallowing difficulty, and slurred
speechHearing or speech impairment - resources
Speech disorders. My labs have shown low
WBCWbc count of 2.8, low platelet instr 105 among other abnormalities. This has stayed consistent for weeks until a May 13th lab when the WBC went back up to 8.3 and my platelets have dropped to 100. When looking at a flow chart of labs, it seems that my platelets are dropping at a rate of 10 points every couple of weeks. During this time there was a period that I had more muscle strength and had even walked a good distance with a walker for the first time in four years. I was sleepy all of the time…and my strength would come and go. The first couple of weeks of May, my symptoms worsened dramatically, worsened slurred speech, loss of muscle strength, continued low body temperatures, sleep disturbances (vivid dreams at night) extreme lethargy during the day with an inability to stay awake, and continued loss of taste with a metallic after taste. My ability to bear weight comes and goes. I am also dizzy at times. I have seen many specialists who have no explanation and cannot suggest what specialist to see. I feel I may have a medical problem that is exacerbating the MS. I don’t know where to go for help. The specialists have ruled out all they can think of. Any suggestions?
My suggestion would be to go to http://www.Lymenet.org and Click on Flash Discussion and then Medical Questions. There are many folks there who have been diagnosed with MS when they really had Lyme disease.
I have known a couple of people with MS and most of them are not as sick as you are. Most of the Lyme patients I know(including hubby) are very very sick like you.
Hope you find some answers soon.
Best Wishes