Added: 2 years ago
From: timsgirl1099
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  • Thank you soo much for making this song for her. I have endometriosis I am 25 and I also already have had cancer because of it. I thank God everyday I listen to my body and not the Dr. saying its okay. We need to get more Son's like you. Just thank you I cried so hard listening to this song you touched my heart. Thank you. xo xo

  • Video well done. I too suffer from Endometrosis. Went thru 3 laproscopy tests. I also have a blocked tube because of the Endometrosis. I also wi be bringing awareness to Endometrosis, and hope to raise money for the costs of IVF. Wish me Luck!

  • i love everything about this!!! but i especially have to thank you for remembering those who lost there battle, endo lead my mom to addiction, she was taking approx 30 loratabs a day when she passed. we ha our issues but she was my one support system when it came to endo, she understood, our patterns where almost identical even tho she didnt raise me nor did i see her much until i was a teen. it scares me to take something for pain b/c of this. i wont take anything until i am about to die.

  • Wow this video is so well done and yes sometimes you have to be harsh to be heard in this world. love the video and the song I pray for a cure for us all,God bless you and all endo suffereers

  • Thank u so much for this video tear, tear...im having surgery sept8th,2011 and I'm scared to death. This is no joke it really hurts cry cry.

  • =(

  • your welcome, thats brilliant! not known is awful ask for a Laparoscopy thats the only way to diagnose it. good luck. my appointment went as well as it could i guess he is fitting a mirena coil and putting me on HRT and has prescribed Dihydrocodeine for pain he wants to review it in 6months with more surgery he cant give me a definitive answer on fertility due to the severity of it but has promised to do everything in his power to help me due to my age and gave me the option to freeze my eggs xx

  • @stacygallagher i am not trying to scare you or deter you from the mirena, but please do your research! mirena as any iud can cause infertility.& the RARE side effect of it growing into your cervix isn't as rare as they make it seem, mine was beginning to grow in me when i had it removed (after 2 yrs),& that was one of the most painful & traumatizing experiences of my life, he pretty much did a DNC on me with no meds or happy stuff. i yelled MOTHER FUCKER at the top of my lungs when he got it :(

  • Doctors need to let any girl with undiagnosed stomach pains know about endo. For SEVEN years I have suffered with stomach pains which I tried to ignore because doctors just thought I was attention-seeking. Now my symptoms almost 100% mirror those of endo. If it is endo and it is a later stage I'm going to find a way to make sure more people know about this. Nobody deserves to suffer endo. Even if I don't have it it's a horrible disease which needs more awareness.

  • @BlaiddDrwg2009 your story is very simillar 2 mine it took 8yrs for my diagnoses. keep pushing your doctors sweet heart they done the same 2 me pushed me from pilla 2 post, by the time it was found it was at stage 4, i always think if they had listened 2 me earlier it wounld'nt have got so bad ,very frustrating. Today i meet my consultant 2 discuss my surgery and find out if i will ever be able 2 carry a child, im very anxious! but i hope 2day i will get the answers i need. best of luck hun xxx

  • @stacygallagher Thank you. =) I've got an appointment on the 23rd so I'll be sure to let you know how it goes. Hopefully I can finally get to the bottom of this. Good luck with your appointment xx

  • :'( I had laparoscopy surgery on friday 2 find the cause of adominal pain (suspected endo), whilst under he found extensive endometriosis stage 4, so he done excision of the endometriosis & ureterolysis cos i even had adhesions on my urethra&kidney thx 2 endo, not the news i expected wen i woke 3hrs l8r, am 23 & DEVASTATED, i will b under the consultant 4 the rest of my life, i had a chemical preg last yr due 2 endo & find out in 3mon if i will b infertile, 8yrs it took 4diagnosis.cruel disease!

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  • Anyone watching this video radio jockys or just wanna help please email me at maureenclynch63@aim.com trying to raise money for a nationwide commercial for love someone with Endometriosis.

    Please Help these women

  • Thank You for this video. Its time people know what we all REALLY go through. 

  • thanks everyone for sharing. I am unable to sleep because I can't stop thinking about this horrible disease. I was diagnosed about 17 years ago, I had a hysterectomy in 2005, I'm left with one ovary. This disease is killing my insides and my sexual drive is shot. It hurts in my legs, arms, chest, back and where ever it finds itself in the body. I am able to control the pain with alternative treatment from the health food store; I find Don Quai helps a lot once taken regularly. God bless us all.

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  • Are the lyrics for this song anywhere?? I'd love to share it with my girlfriends who have this disease along side me also! beautiful song =)

  • actually,i was diagnosed with stage 3 endo.it has been already 8 months since i had the surgery but the pain came back and getting worse.the last time i went to my ob-gyn/surgeon,i asked him why the pain was slowly coming back and he said that there is something wrong with my bowel movement and it's not anymore the endo that's causing the pain.

  • @AimeeLG11 where might i find the stages? i was diagnosed at 18 yrs old and now 32 yrs old. seemed that i was pretty much ok with my endo till bout a yr ago, something is changing cause this pain is crippling me again, yet i still refuse surgery, at what point is enough just enough! Im actually considering RX pain meds again so i can take care of my lil kid and go back to work

  • @taleana2002 i was diagnosed with stage 3 endo by my ob-gyne after i underwent hysterectomy.one month after that operation,the pain came back but he told me that it's not anymore the endo that's causing the pain.now i have ovarian cysts.

  • @AimeeLG11 i feel for you girl, ive struggled with the pain of ovarian cysts for over 10 yrs. My first surgery was for a hemorragic ovarian cyst, second surgery was for the adhesion i got from the first surgery. 3 was a dnc from endo scaring, ovulating is turning into a nightmare for me again, calmed down and is out of control. I am going to attempt a new job tomarrow and nonmedicated for pain..will see how this goes. Im very stubborn :)

  • Remember everybody is different that is what makes this horrific disease confusing.there are some woman who have everything removed and have no more pain ..i say GOD BLESS THEM ..Then you have woman like me who had that to except theirs still so much pain except its worse!!!! I would love to see a Endometriosis Commercial like other illnesses .God Bless All My Endosisters

    Sharon.

  • thanks for posting this video.i was crying while watching this.i had this chronic disease 2 years ago.i had laparoscopic surgery and underwent total hysterectomy last year but i'm still in pain.there's no cure for endo so it means that i could have this for the rest of my life!

  • @AimeeLG11 :""( im the owner of this video

    im Sharon Mayer denverbroncofox@aol.com

  • @timsgirl1099 thx for a great video, i cried cause the reality of what is going on with myself and my sister in law is scarey! I have a family doctor that understands its real and hasnt ever treated me badly because of chronic pain that is hiddin inside of me. He also respects i dont want a specialist or more surgeries, i have chosen to "suck it up" and avoid tomatoes, they are the worst for me, became lactose intolerant many years ago, didnt know it may be endo related. Thx again becky

  • ty for this video and yes its very true i have endometriosis to and i am living in unbearable pain everyday but my endo doctor is sending me to pain clinic for the pain

  • ayo I jus educated 2day...can't believe dis is not something more looked n2...

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