Update: frontpaging this since deadline is coming near (August 9)
I just got a PM from GBAtemp regular and tgames site owner Mamule
I am so sorry to hear what is happening to your family Mamule, that is so horrible and unfair...
I will be signing the petition myself and in the name of my wife, this is the least I can do.
Please sign: http://www.petitions24.net/syndrome_dehlers_danlos_nous_disons_non_a_larret_du_diagnosti
*EDIT*
I just got a PM from GBAtemp regular and tgames site owner Mamule
My children and my wife have the Ehler Danlos syndrom, a rare genetic disease that destroys collagen. Collagen is everywhere in the body (bones, skin, organs...) so you can imagine the damage
http://en.wikipedia.org/wiki/Ehlers–Danlos_syndrome
In the world the only place to get treatment is in Paris. For the entire world. The hospital who is in charge of it wants to stop financing the health support so there will be no more treatments, refunds or anything.
Just so you realize, my 36 year old wife will be in a wheelchair within 5 years, my two children are under heavy medication and tons of health checks with specialists.
A petition is in place to attempt to revert the hospital's decision, but we need 50 000 signatures before August 9 in the hope that the french government will even look at the case.
http://www.petitions24.net/syndrome_dehlers_danlos_nous_disons_non_a_larret_du_diagnosti
I am so sorry to hear what is happening to your family Mamule, that is so horrible and unfair...
I will be signing the petition myself and in the name of my wife, this is the least I can do.
Please sign: http://www.petitions24.net/syndrome_dehlers_danlos_nous_disons_non_a_larret_du_diagnosti
*EDIT*
You might want to stick this translation of the form at the top:
You get an email, and the second link is for confirmation.First Name
Last Name
City
Country
Publicize your signature? (Yes is selected by default)