http://www.ilads.org/
If you would like to help and become an ambassador.. please go here...
http://www.ilads.org/
Atteinte de la borréliose chronique persistante , babesia et bartonella ; le déni est grand , battons nous pour la faire connaitre la borréliose de lyme et ses coinfections ; 8 ans de bi et tri therapies d'antibiotiques auxquels j'ai ajouté une partie du protocole Buhner et autres http://francelyme.fr
the ILADS "Power of Us" campaign.
Please help us raise money for the ILADS "Power of Us" campaign. The ILADS is the organization that trains our doctors to become Lyme literate. They also run the Lyme-tap program that pays for testing for those who do not have the means to do so. They cannot do this without our help. They are just asking us to give a few dollars. We would rather see our patients pay a few dollars rather than the huge expense of testing. Insurance does not cover all testing. Please help and "share" this on your walls and ask your friends to contribute and "share" as well. The ILADS cannot do this alone
http://www.ilads.org/
If you would like to help and become an ambassador.. please go here...
http://www.ilads.org/
http://www.ilads.org/
If you would like to help and become an ambassador.. please go here...
http://www.ilads.org/
