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THE OGONI FILM
THE OGONI FILM Project Vote now☑️
THE OGONI FILM Project Vote now☑️
THE OGONI FILM Project Vote now☑️
It is unbelievably devastating and debilitating, which I knew nothing about until recently. In my 20s, I worked for an OB-GYN for about a year. I'd heard of endo but knew next to nothing. I'm 57 now. I should have known more. Everyone should know more. That's why I voted for the endo project.
My name is courtney I'm happily married with a wonderful 3 year old and 1 more daughter on the way. I have stage 4 endo and adenomyosis, which is all over my bowels, uterus, ovaries, it has spread to my kidneys. I also have IC. We need more outreach. We are in pain everyday!!!
THE OGONI is a must watch film for those who want to know about the situation of environment in the Niger Delta region of Nigeria and the impact of crude oil extraction on the lives of those who depend on the environment and directly benefit nothing from the airport oil firms like Shell. Vote for and donate to support this film production.
Endo What? For me and the other 176 million women who suffer in silence and our voices aren't heard.
Endo What? For me and the other 176 million women who suffer in silence and our voices aren't heard.
Endo What is very empowering! This type of exposure is what the awareness through education movement is all about. We need an earlier means of diagnosis, better support by the medical professionals, and a search for a cure! Many young women suffer in silence too long. Finding livable employment is nearly impossible when stopped in your prime by this condition. For some, it is dibilitating, others have a more positive prognosis. It effects not only the women who suffer, but everyone!
I am also one of 176 million women worldwide who suffer from this and I want to make it part of my life's work to put an end to it. Pieces like this are a major help. Please vote.
I voted for endo what? Endometriosis is a major disease worldwide and the need for more knowledge about it to be able to treat victims properly.
I have read that the roller coaster of emotions and chronic fatigue a woman experiences with endo can be likened to cancer patients going through chemo yet there is little recognition or support for this condition. As an endo sufferer I have the added curse of endo affecting my fertility adding more heartache to an already emotional journey. More money needs to go into researching this debilitating condition and helping the significant percentage of women diagnosed to have informed doctors available to help them make the right decisions and receive the right treatment in what is notably a grey area in the medical field.
I am one of the 176 million women diagnosed with endometriosis. I also was diagnosed with adenomyosis and endosalpingiosis, endo's evil sisters. The spotlight needs to shine on endometriosis, I've battled this horrid disease for 26 years and lost my uterus, fallopian tubes, both ovaries and my gallbladder due to endo. The battle rages on, I will be having another surgery next month, appendix is likely going and possibly part on my bowels. We need more awareness!!
I have suffered from Endometroisis for almost 30 years. It's a debilitated disease that effects millions of women world. It's a extremely painful condition that effects my everyday life . daily .
I suffer from endometriosis and infertility because of it, I also suffer from IBS, Fibromyalgia, and Chronic Fatigue Syndrome because of Endometriosis. Im 26. Diagnosed last year after 11 years of suffering and I was already at stage 4 and infertile. I only wish I could have known sooner like if I had seen a video like this in school! It really needs more awareness so, so many girls and women will know what to do sooner. Lets not forget all the Doctors, partners, and others that need to be informed. Things need to change. Endo what will change lives, lets vote for something that will change lives for so many. Please vote and share ????
I suffer from endometriosis and infertility because of it, I also suffer from IBS, Fibromyalgia, and Chronic Fatigue Syndrome because of Endometriosis. Im 26. Diagnosed last year after 11 years of suffering and I was already at stage 4 and infertile. I only wish I could have known sooner like if I had seen a video like this in school! It really needs more awareness so, so many girls and women will know what to do sooner. Lets not forget all the Doctors, partners, and others that need to be informed. Things need to change. Endo what will change lives, lets vote for something that will change lives for so many. Please vote and share ????
For myself and the thousands of women around the world that suffer from Endometriosis. We should not have to suffer as much as we do. Let's teach the world more about our incurable disease! Maybe our dream of a cure will become a reality.
Voted so more awareness can be done for endometriosis, it is a life changing debilitating disease that took me over 20 yrs to be diagnosed. The first treatment I had for endo didn't help, at best it last 2 years and this is the treatment most women receive (ablation ) which results in yrs of surgeries doing more damage than good. Harmful drugs are also pushed on endo suffers (lupron- it's harmful side effects don't always go away such as joint pain, chronic fatigue, loss of teeth). More research needs to be done to diagnosis earlier , better treatments need to be front of the line offered such as excision vs ablation. Lupron is a bandaid over a bullet hole when it comes to endo.
Very informative!
For my daughter
Informative....
On y va tous!!!
On y va tous!!!