CFS- Please Help! Every Symptom, but not fatigued or tired?

I have EVERY symptom on CFS. I however am not fatigued or tired. I do sleep in later than I used to daily...but the rest of the day, my energy is just fine. DR. told me that I have every CFS symptom and according to my research, I must agree. I however...have fine energy once I get my butt out of bed. I stay up until 11:30pm at least every night. Physical Activity does hurt alot more than before, but it does not exhaust me. I walked Sea World on Friday for 3 hours. No pain or exhuastion while there. Pain the next morning though. My energy level is just fine? But...I do fit EVERY other criteria for CFS? I believe it all started with seeing the death of a family member, 5 months later my whole body started falling apart. Insomnia, bowels, twitching, rashes, muscle pain ( sometimes really bad )! Recurring infections, etc. etc. Also no STD's and have been tested 3 times. I have very few of the pressure points for Fibro and no skin sensitivity for Fibro. Dr, said MUST BE- CFS? I have lots of energy though? Help!

Were you tested for other illnesses that share many of the same symptoms? Lyme is one that comes to mind. Thyroid, etc.

Yes...No Lyme or Thryriod problems- Been tested. I am not fatigued at all? Does that make any sense?

Been tested for other co-infections if not Lyme?
Remember any kind of bite?
What about parasites like giardia?
Mine began with some type of gastro-intestinal infection that didn't resolve for a very long time. By that time it had become firmly lodged in my nervous system -- at least that is my current thinking.
What about ANA? Autoimmune disorders?

Yes..been tested for all the above. I do appear to have a nervous system dissorder though? I did have c-diff and guardia, have been re-tested and they say both is now gone.

I had Giardia a while back and took meds. They only tested me once for the clearance though? Why do/did you mention Guardia? Does this cause muscle aches in the body?

Visit the Lyme forum...it was suggested to me in the CFS chat room and I am surprised at what I've learned about the inaccuracy of the tests, etc.