I thought I would share another very interesting theory with you on what cause our fibromyalgia, I keep searching for a cause and have uncovered a likely source I think?!
prohealth.com/library/showa...
Again it is a bit heavy to read but it will certainly make you think!
If you find this interesting, I posted yesterday and there is another very fascinating link to look at too.
Happy reading and soft hugs
Xx
I read your post yesterday,I also did some research and found today's post, very interesting, not sure how we've ended up with it?
Good research
Regards nicki xxx
Hello Homer,
I am pleased you find the postings interesting it is amazing what the dr.s don.t tell us!
I am not too sure either how we got it, however I am going to keep digging, the info must be out there?!, Was we sprayed? Was we bitten? Has it spread from others? Has it been triggered by this myoplasma?
And if so does anyone know how we get our gp.s or consultants to give us the correct blood tests to identify it with out us been sent from pillar to post?!
And not be incorrectly treated has we have all been done over the past years we have had this fibro!
It will be very interesting to see if anyone has any good ideas.
A theory I have is do we contact an army doctor, they are obviously helping gulf war victims? It is just a thought!?
They will have all the right measures in place to identify the myoplasma, because these victims were either vaccinated with the stuff or were subjected to biological warfare, and are now being treated for the conditions they are suffering from which is not dissimilar to our condition?
Which I gather they are getting good results?.
Happy researching
Soft hugs xx
I read your post yesterday,I also did some research and found today's post, very interesting, not sure how we've ended up with it?
Good research
Regards nicki xxx
I read your post yesterday,I also did some research and found today's post, very interesting, not sure how we've ended up with it?
Good research
Regards nicki xxx
I read the articles concerning Mycoplasma. What I find remarkable is that all people with ME/CFS/Fibromyalgia at some stage are given blood tests including Full Blood Count. If the red blood cells are changed in the way suggested then this should show up in Mean Cell Volume (MCV), Mean Cell Haemoglobin Concentration (MCHC) and other haematological parameters.
Famous people 
It's all mashed up in my head from over the last few months and i cant really make sense of any of it. Good luck lol
If Two People With Fibromyalgia Had A Relationship Would It Work ?
Hello
Sleep programme last night!
