I was initially told I have PCOS, then they confirmed it is endometriosis. There are good days and bad days. I'm trying to do what's within my power and live and eat more holistically and mindfully while I wait for my surgery 🙏🏽

Holly I've been going through this exact same thing for the last two years. It's so isolating and mentally draining. Thank you so much for making this video because it's so comforting to see someone else going through the same experience. I'm definitely going to push for some hormonal blood tests after watching this!

You're really sweet, Holly, thanks for sharing your journey. Makes me feel less alone and stuck. It sounds like the absolute worst and hardest. Hope you've been having some good, happy days lately! 💖

Holly, honestly thank you girl for putting this video out there. I currently have Stage 4 endometriosis & i have 4 cysts at this moment in time. I had open-stomach surgery last year in July and am currently waiting to see a specialist surgeon who will be able to do my second surgery this year. I am a 21 year old women & the fact i have such bad endo has honestly changed my life. I am a shell of who i used to be🥺 Thank you for telling your story and putting the word out there. Not enough awareness is out there & we need to do more & that is my goal for this year. Thank you again & i look forward to seeing your journey and seeing how the treatment works for you❤️

Thankyou for sharing your journey holly as I was diagnosed with PCOS a couple of years ago and I was crying and felt alone and frustrated and didn't know anyone else suffering like I was. I remember having my internal scan on a full bladder and I nearly weed myself 😂 when they had finished I ran to the toilet. I'm so happy that your getting the right help and understanding your symptoms a bit more

Thank you so much for this Holly!! Was diagnosed with PCOS last year

Hey! Well done for speaking up about it. I’m a nutritional therapist and I have PCOS. I can relate! For anyone struggling, I’d highly highly recommend finding a PCOS or Endo nutritional therapist. With both of these conditions, it’s key to get to your root cause. Everyone’s is different. This way you can find what’s driving your symptoms and causing them to keep returning. Whether it’s the excess androgen hormones or insulin resistance with PCOS, or recurrent Endo cells growing outside the uterus. The frustrating part about surgery is that it might remove the cells at that point in time. But it won’t stop it happening again 😢 There are things you can do with your nutrition and lifestyle to help ❤️ You’ve got this! And to anyone else out there struggling, you’ve got this ❤ There are lots of free PCOS and Endo communities on Facebook you could try to join and ask others for advice. You’re not alone 😘

Thank you for this Holly ❤ currently waiting for my first surgery, but very aware it will probably not be my last so seeing this is extremely useful. Sending all the best energy 🌸

Love this video, and I’m literally going through the exact same thing have pretty much cried every night for similar reasons to you! It’s horrible, but appreciate you sharing your journey so much ❤

I appreciate this video sooooooo with 1thousand O's, much even your tears and all of that I appreciate it because I can literally say truthfully know how you feel I've thought the same and have been struggling too thank you for making me feel less alone and motivating me to get my ass up and get in with getting better❤

Thank you for bringing awareness. Currently going through the pain and GP just refers painkillers. But I know I have it because the pain is just abnormal, I know my body. I have a few of the symptoms incl painful sex.

This is so helpful ❤️ I take the mini pill to try control my endo until my operation, really hope this new treatment works for you

This is so helpful, hope it gets better for you!x

Hey!! Holly today is my birthday and I love your vlogs so so much you are my inspiration and I wish you reach 30K Subscribers very very soon!✨❤️☺️

I wish you the best of luck on your journey 🤗

You helped me so much . Thanks a bunch my dear❤

I bursted into tears when you mentioned phisical pain....

I'm currently 3 weeks post laparoscopy. I'm so glad others are so vocal about endometriosis and it inspired me to make a video too. And thank you so much for sharing the non-surgical options. This is something I'm currently reading a lot about rn. I have a question for you though... how did you find coming back to training? I'm a triathlete and I can barely find anything on KZfaq and instagram about returning to training!

In Germany, it is common for women to visit a specialized doctor one to two times a year just to get everything checked. All women in my family have endometriosis, and i am really relieved that I am (and all other women are) getting a free ultrasound from the inside two times a year. Not all, but most of the things these doctors are doing are paid by our health insurance. Wishing you just the best for your journey ❤️

Love you!❤

It's been great watching this .I'm on a waiting list to go to stmarys ,Manchester and been waiting a year .I'm now thinking about going privately can I ask which hospital yiu went to ? I feel like I've been to every hospital in the northwest for my endo but it's looking now that Manchester is the best .x ❤

Hi Holly, thank you for this video. Followed you for a while. Have you got any PCOS updates since this? Any food recommendations too, I am finding diet really hard with my PCOS.

Hi Holly I went on the Web site and the treatment is £120 for a 45 min consultation for me that's to expensive

Can you do an update on this? Did it help you at all and how often do you have flareups?

Hey Holly this is so insightful! Can I just ask are you on birth control? I am struggling massively with similar symptoms and am not on the pill. Thanks!

Can you just get endometriosis? I never had painful periods, but the last year my periods we're extremely painful and also when I don't have my period I feel period pain.

Goodmorning my love My love, all the beautiful flowers of the world got their beauty from your unique beautiful soul. You're so sweet, my heart doesn't deceive me when it says you are. I love you.

You’re right, feeling how it began to shrink and eventually disappear within 2 months was so liberating. I followed the steps I mentioned, and within the first 2 weeks the bloating was gone. I simply go'ogled Tilly Strankten's Ovarian Cyst Guide and it's like I hit the feel-good reset button lol.

❤

I have all the symptoms of endometriosis but the surgery showed no sign of it:( and ultrasound scans haven’t shown pcos. Does anyone know what else it could be? I just want an answer I’m struggling so so much 🥲❤️