Neurological problems from lymes
I have posted on here beforeabout my symptoms. I was wondering on here from everybodys expirience from lymes disease how many have neurological problems as one of there main complaints of lymes. I am going on my 4th year of what I have been told from Dr.Weisbren as chronic lymes disease. My nero problems are getting so bad now I can hardly see at night and I can barley read a sentence anymore. It's getting worse because were I am from is Minnesota and my Dr here won't treat me from Dr. Weisbrens findings because it isn't showing up in my blood work. Dr. Weisbren even wrote me a prescription for the picc line and to start getting treated imediatly because it was so bad. But to get treated from him would not be paid by insurance. If I could convince my Dr. here to treat me it would. Dr.Weisbren even wrote out oral treatements witch my Dr. here prescribed for me But I could not take them because I work outside and the antibiotics caused alot of sunburn.
But even with the oral's it has been to long for them to even do what I want them to do because I am having so many neuro problems. From what I have been reading IV treatment is the only way to go. I have been going to a neurologist for has long as this has been going on because they thought this was MS at first but my neuro doesn't believe that it's MS. So I am a huge believer that it's lymes because I have had just about every symptom that it says.