Chlamydia Pnuemoniae

After everything Ive read and from what my doctor said, I think this is my worst infection. One website dedicated to CP says that the treatment time is 3 years minimum due to the long life cycle. I don't necessarily consider that to be true for every single person. But it turns treatment into years instead of just months.

It doesn't seem like alot of people have this one, maybe alot of people just don't get tested. I don't feel like my lungs have an infection in them. I'm wondering if sometime during my treatment I'll start to feel it? Or maybe it's just in a different place in my body?

Ugh... I cant wait until my books get here. The internet has way too much conflicting information. It's hard to know what to trust, even if it is written by a doctor. Maybe no one really knows, and the best we can do is antibiotics or strong herbs until people feel better. It doesn't seem like it's very well understood why people get better. I want all the answers!!!!

CPN is the very first thing that kept coming back in searches for my MS diagnosis.

Check here for more information:

http://www.davidwheldon.co.uk/ms-treatment.html

They claim it resides in 95% of the population (their lungs) and is the main cause of asthma. My one PCP knew about it and treated me for it with a Z-Pack. It did nothing of course but i was desperate to get on any antibiotics. The protocol above uses many of the same abx that is used for Lyme treatment and he cured with wife who was diagnosed with Secondary Progressive MS. It's a real good read.

Bad lungs run in my family. My mom died at 57 in 2011 from COPD. I wish I knew about this stuff back then. Maybe her life could've been lengthened. Maybe my family is predisposed to extra sensitive to this infection genetically or something...?

I'm really missing her lately. I figure if she was here and healthy she could help me with my son while I'm so incapable. My world is crashing down around me and I've never felt so powerless... my relationships are suffering, my house is a wreck, I can't pay my bills because I can't work.. I just feel ruined.

Maybe I'm herxing, but depression is starting to take hold. I'm so overwhelmed. I expected relief with getting diagnosed and really all it has done has added more stress. My fiance resents me. My brother acts like I don't exist. My friends don't even hardly talk to me anymore let alone show their faces. I can't comfort myself anymore.

These infections have robbed me of my happiness. My motivation, energy, and laughter are all fading away.. seriously, it hurts like hell to laugh. I'm sure some of you with headaches face and stomach pain can relate.

I'm completely humiliated and filled to the brim with shame. I'm questioning myself and my treatment. A couple years seems like a long, expensive time to see if I'm on the right track. What if I'm not doing the right thing? That would be a pretty monumental mistake.

Ugh... go away lyme disease! And Co infections! And life!