We not only have to deal with our illness, but also have to do our own research and educate ourselves about this disease and all risks associated with treatments. We can't blindly trust our doctors. We have to constantly fight to be heard and this is perhaps one of the most exhausting illnesses to have for that reason.
Also for those of us trying to advocate and spread awareness, because we don't look sick, many people assume we just want attention. I myself have experienced this and it makes me hesitant to share my experiences with others or spread awareness.
I think this is great you are doing this! Please send us the link for your channel so we can share and support you and spread the word! Lots of love 😘💜✌🏻

Hi ShaylaNicole,
I can't wait to see it! I hope you are feeling good today ❤️
I have to say, I have had significant improvements in just one week after going off Visanne and switching to a natural, holistic treatment. The side effects of hormones were making me so ill. Now I feel like I'm making a comeback! its the first time in a long time I have hope!
Hope you have a good day, and can't wait to see the video! 😘

Just because you cannot see a illness does not mean its not there.

Hi Dre :D

I wanted to check in on how you're doing lovely. Thank you so much for your contributions to my video. Really, it's not MY video, but rather it is OUR video because it's a journey that we are all a part of. I've just got a decent video editing software so am working on it now, between being curled up in bed with pain today. Needless to say, I'll post you the link as soon as it's done & before I publish it to make sure that you're happy with it too :)
How has your weekend been? I hope that you are well lovely & that endo isn't causing you any grief this weekend. Lots of love xx

ShaylaNicole, yes, of course you may use anything I have written. I am happy to help contribute in any way. I think this is great you are doing this! I can't wait to see the video 😊💜