I have a urologist appt. this afternoon, so we will se what he says on the subject.I am sure it will be test after test..fun!

Dr. H has me calling IGNEX for the urine collection kit to test for PCR while on meds.

On an up note, he also told me he has someone creating a website for him, so all his abstracts can be posted. He feels this is a great way for non LLMDs with lyme patients to get informed.

This seems to be his mission....talk about passion...everybody needs to know what he and others have found out about the disease.
Its nice to have someone in our corner!

One more question..has anyone out there been diagnosed with neurogenic bladder? This was one of my GPs ideas when i went to her for the pee problem. I know this is a common symptom of MS, Any ideas???

Thank you..hae a great day!.....jellyfish