LimbicRetraining.com is a new satellite blog created by Planet Thrive that will focus exclusively on neural reconditioning for MCS, CFS, FMS, and related conditions.
New blog focused on brain retraining for MCS, CFS, FMS
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NEWS
Summary of MCS meeting on May 13 at WHO headquarters in Geneva
A group of Spanish doctors discuss including chemical and electrical sensitivities in the WHO International Classification of Diseases (ICD), to help patients get legal recognition for their illness.
Wireless network denied our daughter access to her school
by an anonymous father in Sweden | Our daughter Johanna went to school in the Falkenberg school district in Sweden. During the spring of 2006, she was in third grade and experienced headaches and profound fatigue.
Jessica Alba joins fight against toxic chemicals
Jessica is pregnant with her second child and chemicals in the environment are a huge personal concern of hers.
Low-EMF zone in Stockholm suburb defeated on technicality
The Swedish town of Södertälje loses a battle to keep out cell towers in order to create a low-EMF zone.
Vote today for CFS research – only a few days left
by Cort Johnson | Chase Community Giving has given CFS research a kind of life line; a chance to win some big money in a time of dearth and to put that money directly into the hands of excellent researchers.
Our neighbors agreed to turn off their wireless networks
by Ann and Torkel Atterbom (translated from Swedish) | We finally discovered the reason for the months of constant headaches and sleep problems.
MCS activism: How to be represented in an unsafe place
How can chemically and electrically sensitive people do public activism work when the spaces they need to enter are not accessible? E.I. Jane to the rescue!
Homegrown activism for MCS Awareness Month
Planet Thrive member Susi Lippuner shares an educational brochure about non-toxic living with her community in honor of Chemical Sensitivity Awareness Month this May.
Feisty lyme sisters helping each other out
This is what real grassroots activism is about, folks. This is how to raise awareness for an illness, help a patient in a very practical way, and most importantly, to show a friend how much they are loved and cherished.
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