This organization was created because tens of thousands of women
are choosing to tell their stories and make their voices heard.
JOIN THIS IMPORTANT MOVEMENT
TELL YOUR OWN STORY
SUPPORT OTHERS BY SIGNING A PETITION,
DONATE TO AWARENESS EFFORTS
LISTEN TO WHAT WE HAVE TO SAY
CONTINUE THE CONVERSATION
Sign a Petition
Requesting full disclosure of all side effects caused by the paragard and mirena iud
Change.org Petition - Emma hilditch
Over 5,000 people have signed - They are trying for 7,500!
Testing for Mirena IUD / SkylaIUD : Clotting & Autoimmunity
MoveOn.org Petition - Denise Lineberry
Have over 650 - NEW goal - They need 750 Signatures!
There needs to be more studies and trials to research a potential connection between the Mirena IUD, clotting and autoimmunity. After using Mirena IUD, women are suffering from autoimmune reactions and diseases and other health risks associated with blood clotting. There needs to be thorough research done on the silicone used in Mirena IUD (and now Skyla IUD) and the synthetic progestogen (LNG) used in Mirena IUD (and now Skyla IUD).
If there is a connection, women and their doctors need to be warned by the manufacturer, Bayer — especially women with a family medical history of clotting or autoimmunity.
And women who have been affected need answers.
The Medical Device Safety Act 2017
H.R. 2164 #MDSA17
Over 10,000 Messages Sent So Far! - TAKE ACTION NOW!
Introduced in the house on April 26, 2017 by Congressman Brian Fitzpatrick. It is a bi-partisan bill currently co-sponsored by Rosa DeLauro, Louise Slaughter, and Jan Schakowsky. The bill would amend the Federal Food, Drug, and Cosmetic Act with respect to liability under State and local requirements respecting all Class III devices. Including, but not limited to, essure, nerve stimulators, hip implants, defibrillators, pacemakers, infusion pumps, surgical mesh, cochlear implants, and breast implants.
The purpose of this bill is to restore a patient’s right to litigation should he/she be harmed by a Class III medical device. Even decades after the FDA’s pre market approval of a Class III device, if it is proven to be ineffective or proven to cause harm, individuals still cannot hold the manufacturer liable for injury, even in the case of a recall.
IUDs are classified as Class III Devices.
#NOT IN MY PUSSY
Take the Pledge to Get 1 Million Women
to Remove their IUDs by 2023
Copper Toxicity is a growing epidemic in the modern world more times than not caused by the use of the IUD also known as the Coil. Women are fed false information everyday that the IUD is a safe birth control option when it's making our women and children sick. Sign the pledge now to remove your IUD and spread awareness about Copper Toxicity helping women everywhere take back power of their bodies and health!
MIRENA CONTRACEPTIVE -
Australia Needs a Major Investigation into
Mirena & Bayer Manufacture!
Change.org Petition - Jodie Rowsell
Petition closed with 340 supporters!
Paragard Interuterine Device (IUD):
Do more Studies on the Paragard,
for Safety of Women Everywhere!
Change.org Petition - Michelle Jardine
Petition closed with 232 supporters!
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When Bodies Talk - Cuando los cuerpos hablan
by Flor Kot Hansen
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