Neurologist

Yes, I went to a neurologist referred by my PCP and he did nothing to help. He didn't even acknowledge CFS. I ended up two different times in the E.R. and they took MRIs CTScans extensive blood work and nothing came out wrong. The goes to show everyone that they don't know what to look for yet for CFS. Let's pray they find it soon so we can at least get an official diagnosis. I found a rheumatologist who diagnosed me with Fibromyalgia. At least now the government recognizes it and is starting to give people Social Security Disability to those who apply if they cannot work anymore. I'm hoping & praying they'll recognize CFS the same way some day soon! When I went to the E.R. my head felt like it was 100 times bigger and it had lots of pain, and still they saw nothing on those test. I also have trouble with talking when I have full-blown bouts of CFS. Thankfully it goes away and doesn't flare up again until my body gets so badly overworked, so the trick is to take it slow. I can't travel like I used to. Does your PCP recognize the CFS and is willing to send you to other specialists? I recommend asking for a rheumatologist to get diagnosed for Fibro...at least you'll know if you have it or not. All the best.

I had to cancel my appointment because I woke with a bladder infection. but I have a new appointment  on October 9th

  Does any one ever get a lot of bladder  infections because of CFS?

Every 6 months  I get one.

hugs, Caren