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I have done IVF that ended in a miscarriage. Our idea of multiple children or any at all seems like an unattainable dream. It's heartbreaking to think that we may not have a family of our own. However, I'm also afraid that if we have...

Health care for endometriosis needs to be more common in smaller towns or cities, as in more specialists need  to help more patients than just the one or 2 specialists that are available and you have to wait for 6 months to a year to...

I finally made it to an endo specialist and I feel lucky to be here - awaiting some treatment but I can tell you - my anger and fear are still there. I worry about a system that may deny me help again is this...

On my worst pain days I can't go to work. This is about once a month. I always hope it falls on a weekend so I don't have to call in sick. I can't run or workout several days a month for the pain. I...

I have lost relationships and jobs because people didn't or don't believe how deliberating and crippling this illness does to you, I was mistreated and disrespected a lot. I also developed fibromyalgia after my surgery and this is year 2 of me still learning to...

I am fortunate that I am still able to work with endometriosis. I have had to adapt my exercise regime as running makes my abdomen hurt. Two to three days a month I do stay in bed in pain, which affects my social life. ...

Since I first got my period they were heavy and long and painful. 10 years ago, as my chronic pelvic pain persisted, I was told that I was being dramatic, that my pain wasn’t real. After countless doctor visits, bloodwork, ultrasounds, colonoscopy and emergency room...

It took 17 years for me to get diagnosed with endometriosis. Lots of adhesions - I lost my left fallopian tube. Fighting with infertility. This is a tough and emotional journey. ...

Many of the pharmaceutical remedies that are used in the treatment of endometriosis are not available to me as I'm a hormone positive breast cancer survivor. We've been treating my endometriosis with pain medication....

Since I first got my period they were heavy and long and painful. 10 years ago, as my chronic pelvic pain persisted, I was told that I was being dramatic, that my pain wasn’t real. After countless doctor visits, bloodwork, ultrasounds, colonoscopy and emergency room...

I have always been capable of so much from working out to to being a straight A student, and participating in numerous sports teams. This illness has changed everything that was personal to me and has stripped my identity to the point where fertility is...

I was very lucky to have been diagnosed and undergone surgery in less than a year. During the surgery the doctor referred to my internal situation as a “war zone.” She had to also remove my appendix since it was covered in endo cysts. I...