It is so refreshing for someone to be open and honest about Endometriosis. You really do have to fight with the doctors to get a diagnosis. I think it is important that people are aware of illnesses which are not visible. Thankyou for the video
Thank you so much for this videoband your previous ones. I have been referred to gynecology but had to push my GP to make this referral! This video has given me information about what i need to ask about/for at my upcoming appointment. Hope your second surgery works xxxx😊
My period blood is thicker to now and burgundy shade with purple to so yeah sadly no family doctor taking and to get women doc in my town can take years months
My sister has this my sister wants me to get checked my Alberta Canada doctor suck with women heath she didnt get her diagnose until she moved to France when I was 30 4 years ago
@@Mathildebarkercan I ask why you came off it please ? I was offered to be put on it and I was sceptical so didn’t .. have always shyed away from the pill when offered? I worried about it affected my already severe pmdd/pms xx I was diagnosed at age 33 after fighting for answers since the age of 15 years
@ aww okay thank-you and sorry you had to go through that! They push pills but don’t often explain the potential side affects. I’m now with a Endo specialist and they want to do another surgery and I too am contemplating the benefits… long journey indeed and also can feel isolating.. so great to watch your video which makes you feel less alone about a taboo subject to some xxx
Yeah I have pmdd sever PMS hot flashes night sweats chills peeing non stop low blood sugar smell smoke not there pale fever restless legs arms sever cramps lower back thigh pain I'll cry shaking sweating rocking I have heating pad extra strength pain meds and Livia pain machine naproxen dose shit for me from the doc at all only help is vodka right now lol drinking my pain lol witch I can't always do so lol 😂
![My Endometriosis Story | How I Was Diagnosed with Endometriosis [CC]](http://i.ytimg.com/vi/Cfs_XoWhMTA/mqdefault.jpg)
It is so refreshing for someone to be open and honest about Endometriosis. You really do have to fight with the doctors to get a diagnosis. I think it is important that people are aware of illnesses which are not visible. Thankyou for the video
I love these daily uploads
Thank you so much for this videoband your previous ones. I have been referred to gynecology but had to push my GP to make this referral! This video has given me information about what i need to ask about/for at my upcoming appointment. Hope your second surgery works xxxx😊
Thanks for explaining and sharing your story Mathilde.
My period blood is thicker to now and burgundy shade with purple to so yeah sadly no family doctor taking and to get women doc in my town can take years months
My sister has this my sister wants me to get checked my Alberta Canada doctor suck with women heath she didnt get her diagnose until she moved to France when I was 30 4 years ago
My sister will be 30 still no kids herself but she dose want kids
Sorry your endo is tormenting you so much. Do I remember you starting on Dienogest at one point? Did that not help at all?
Yes, had to come off the deinogest straight away!
Ah that’s a shame, sorry to hear that. It did wonders for me so I’m always hoping it will help other people too but we’re all different
@@Mathildebarkercan I ask why you came off it please ? I was offered to be put on it and I was sceptical so didn’t .. have always shyed away from the pill when offered? I worried about it affected my already severe pmdd/pms xx I was diagnosed at age 33 after fighting for answers since the age of 15 years
@@laurentb100 it gave me really bad side effects to the point where I couldn’t leave my bed. Lightheaded etc !! They advised me to stop xx
@ aww okay thank-you and sorry you had to go through that! They push pills but don’t often explain the potential side affects. I’m now with a Endo specialist and they want to do another surgery and I too am contemplating the benefits… long journey indeed and also can feel isolating.. so great to watch your video which makes you feel less alone about a taboo subject to some xxx
Yeah I have pmdd sever PMS hot flashes night sweats chills peeing non stop low blood sugar smell smoke not there pale fever restless legs arms sever cramps lower back thigh pain I'll cry shaking sweating rocking I have heating pad extra strength pain meds and Livia pain machine naproxen dose shit for me from the doc at all only help is vodka right now lol drinking my pain lol witch I can't always do so lol 😂