Chlamydia Pneumonia for CFS and fibromyalgia: 6 Month Recovery

Submitted by SunnyDay on Sun, 2016-08-07 23:38

TO: ANYONE LIKE ME!I write this post not long after finishing the antibiotic routine. I am writing this for other people who are perhaps like me. When I first came here I could see there were many very sick people on this site and although I was quite unwell, I was not in the extreme category. So, this may be worth reading for other people who feel they are in a similar situation to me. SYMPTOMS BEFORE BEGINNING TREATMENT (JAN 2016)

I haven't blogged in awhile...

Submitted by willingtocope on Fri, 2016-08-05 12:26

Yet real further progression.  So, I'm going to call the protocol succesful.  I'm sure, if I'd get off my but and exercise a bit, improvements would come.I did, however, have one of those episodes Aug 2.  I'd been feeling a little off for a couple days.  Low grade fever in the afternoon.  Monday, chills in the afternoon.  Went to bed, couldn't get up again.  Finally, about 5am, I struggled to my feet and then collasped (gracefully) to the floor.  Had to call the care attendants to pick me up.  No damage.Turns out there was indeed a bug of some sort going around the building. Everything seems back to normal now.

Cpn protocol prescriber in Detroit, Michigan, USA

Submitted by Debbie Allen on Thu, 2016-08-04 21:02

Does anyone know how I can get the medication?  My doctor won't prescribe without cpn infection proof.     I am extremely discouraged.    How is everyone on this site getting the meds?  I live in the Detroit, Michigan, USA area.   I was diagnosed with secondary progressive ms in 2001.    

Pulse #33

Submitted by supaguy on Sun, 2016-07-31 18:21

Pulse #33 here we go ...Yes, I am rather late this time but then I have had very little energy; rather like a wet rag.I have been rather depleted lately, so I haven't even logged on for a while. Having just started a pulse, it was necessary for me to log on in order to post. I went out into Swansea yesterday but today I am back to just basically doing almost nothing.  Here in the UK, the popular and universal get-out seems to be Brexit; I don't think I'll be blaming my lack of energy on that.  Hopefully, in a week's time I'll be singing from the tree tops.WinkG.

49 done changed to ramphin

Submitted by froggy 1965 on Thu, 2016-07-14 09:36

ok so started raferpin - not a whole lot of difference so far but seem to have regained apperite which has to be be good, still not walking,pain in feet as gefore sill living in hope.   I hope for more improvements,  especially walking and brains seem tolive in confision - not good anyway still convin yced that I will recover its a very slow process for me  anyway best wishes to all on this marathon, love Suzannne

Keeping a Lid on Cpn

Submitted by raven on Sat, 2016-07-09 16:36

Hello again,just checking in this month. I have been really busy extracting myself from my teaching job. I retired and I'm finally free. Now I will have the time to take better care of my health. Had some Cpn testing done earlier in the year and levels have been rising. I did a few rounds of Ivermectin and it cut the testing amount in half but Ivermectin only goes after the elementary body form of Cpn.