Bec 🌻
Region: GB
Monday 12 January 2026 12:16:01 GMT
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gracep_m :
honestly women’s healthcare sucks so much that it makes me so happy to know you’ve had a good ish experience! i was told to come back when i wanted kids when i got diagnosed with pcos 😭
2026-01-12 14:39:34
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sharisse1913 :
So brave! As if you was a slimming world consultant I’ve prob sent you kit in the past then 🤣 I work at head office xx
2026-01-12 13:40:44
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mais 🐅 :
you have amazing eyebrows sorry this is so far from the point of the video
2026-01-12 12:28:51
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Kirst. :
Endo and adeno has quite literally ruined my life. I’ve been medically going through the menopause for a year now. I’m 32. I don’t feel 32 I’m miserable no therapy helps I had pre cancerous cells couple of months back which got removed it’s just one thing after another and won’t give me a hysterectomy. Went private for my laparoscopy 6k coil put in, left ovary and fallopian tube removed as the endo was bad!! Got the coil removed after 11 months as it didn’t agree with me. Had to fight to get it out. for years I was going doctors with periods lasting 2/3 weeks few days break same cycle. I went from 14 stone to 5 stone in less than 2 years. I feel so so lost. And I’m back at square one can’t financially go private again. It’s so stressful. I started my periods at 10. My daughter is 12 and for her to starts hers gives me such a dread but I’ll also be looking out for signs and be her biggest advocate incase she does get it to! X
2026-01-12 14:59:48
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Toniii :
this is crazy because my mum is struggling insanely with her periods. They make her stomach swell and she looks pregnant and she bleeds for weeks and weeks on end really heavily. They won’t give her a hysterectomy. She’s 50.
2026-01-12 12:43:33
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maggie531 :
Thank you soo much for being so open and sharing your story. I just wanted to say I feel like your a friend, i love your videos
2026-01-12 23:18:17
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Mel :
Bless ya heart sweet when you were telling your endometriosis story it was if you were telling mine from start to finish. I had a total hysterectomy ended up septic with a itu admission for 6 weeks multi organ failure I was 27 family and husband were told I wouldn't survive. Luckily I did. I felt i had to fight for them to believe there was anything wrong in the first place was told i didn't have endometriosis so many time I moved from notts down south new consultant did an exploratory lap once inside she looked stitched me back up and within 2 weeks i was having a total hysterectomy. I still suffer today with the scar tissue and hernias.No surgeon will go inside my stomach due to previous issues unless its a medical emergency us endo ladies have to stick together and fight xx
2026-02-19 18:42:06
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lindsaychild817 :
oh wow, you've really been through the wringer. I'm so sorry you've suffered so much.
2026-01-12 13:07:01
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nakitamaxine :
gosh bec! what a story! brave of you to share. Bec, if you could go back, would you have gone straight for the hysterectomy?
2026-01-12 14:13:44
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leyla_plays :
I'll be back to watch this 2nd part. I watched the first with captions as I'm out and about but a very important message x
2026-01-12 12:20:47
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Dark Cherry 🖤🍒 xoxo :
You are amazing Bec. ❤ Thank you for sharing. Lots of love ❤❤
2026-01-12 12:33:57
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Cait (BishBashBosh Version) 💜 :
Prostap was absolutely horrific! I've never felt more miserable and anxious and so much anger! Worst 18 months ever! And it triggered my iih 🫠🫠
2026-01-12 13:00:59
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Em 🩶 :
Oh bec that's a lot ❤ I'm 6 weeks post abdominal hysterectomy and the pain straight after was horrific so god knows how much pain you would have been in bless u 🥰
2026-01-12 14:25:58
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Gemma 🐆🍒 :
Bless you, it’s hard isn’t it. I was diagnosed with endometriosis when I was 21. I’m 34 now! I went on Zoladex for a bit to go into a temporary menopause and you’re sooo right about the heightened emotions. I just remember everyone my age was out enjoying the summer, and I was sat at home crying during the heat wave having hot flushes etc. Endometriosis is no joke!! For something so common, it’s so misunderstood and dismissed by doctors x
2026-01-12 12:43:07
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leelopodloo :
I've had 2 laps in a year still feel absolutely dreadful all the time. think it time for a hysterectomy I know it's not a cure but I can't take the pain & bleeding anymore, even if it just helps a little. 🥹
2026-01-12 13:42:43
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Nadia :
Your gynae history is similar to mine,with years of bleeding and 1 point 2 yrs continuous. I got my period age 9 too. I had Endo and Adeno and the ethicon mesh was inserted, resulting in a hysterectomy. Il be on lifelong pain medication for chronic pain due to adhesions caused by 17 abdo surgeries. It really is a silent disability, Thankyou for sharing xx
2026-01-12 12:51:57
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phillippa5 :
I'm currently in hospital for a an accidental od for 2-3 weeks I've been taken painkillers none stop for my stomach as it's been so painful currently needing treatment to sort my liver out since I was 16 I've been ignored about my pain and it's got to the point I've accidentally done something and I'm still in pain
2026-01-14 06:57:56
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Maddy Askey :
thank you for sharing, I'm at the start of my journey of diagnosis, after 10 years of hell I'm finally seeing a consultant next month. it's crazy how much ticktock has shown me how many women are going through it. fingers crossed I get under the knife soon 🙏
2026-01-12 16:58:18
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beth :
im waiting on gyne tbey canvelled my 1st appt. i have stage 4 DIE and endometrioma. 32 yrs waiting for diagnose and possibly adyemosis
2026-01-12 17:09:26
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ru ˚ʚ♡ɞ˚ :
that blue makes your eyes look beautiful !!
2026-01-12 12:23:11
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chloe💛 :
i’m 23, i’ve had two surgeries, so many different types of contraception. they’ve even bought up a hysterectomy to me?! i’m honestly at a loss. the pain i go through everyday is unbearable, with both endo and adeno 😢
2026-01-12 18:52:33
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Amber :
I had a coil fitted last April to help with Endo symptoms having it removed because its doubled the pain and bleeding since its been fitted. im waiting to see a gynecologist because I need a second lap
2026-01-12 19:22:25
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Charmain✨️ :
🥰
2026-01-12 13:13:11
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Goldengirl❤️ :
Thanks so much for sharing your story ❤ I've been fobbed off for years that all my problems are related to my pcos which I've been diagnosed with. I have a gp appointment tomorrow and I'll use your advise for sure 🥰
2026-01-12 15:33:37
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sades🌞 :
Oh Bec, you’re an absolute warrior! Thank you for opening up about this, I’m sure it’ll shine some light for women who are struggling with similar issues xx
2026-01-12 14:45:36
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tayler :
I have endo and the doctor had to separate my uterus from my cervix. So painful can’t imagine all the pain you’ve been through! Xo
2026-01-12 13:24:36
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Gem :
🥰
2026-01-13 08:11:29
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Lauren :
I have endometriosis, had my first laparoscopic surgery about 5 years ago to remove a 12cm cyst off my ovary and it off my bowl and other places and after that I was symptom free but they couldn't get it all the endometriosis but now I'm on the coil and I'm having a flare up today, got told the coil would stop my periods but haven't and the stuff that comes out from my body, I'm on a referral to gynecology but that will take as long as it takes, I've been to GP but then just want to refer and that's it. I think there is not enough research around it ❤️thank you for speaking out about your experience ❤️
2026-01-13 14:36:42
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Meagan Mcbean 🎗️💛 :
I got diagnosed last May after a 9 year fight with them to take my pain seriously.. It got so much worse after having my last baby nearly 5 years ago.. Basically my consultant said he didn’t believe I had endometriosis or adenomyosis as all my scans/mri was clear.. Turns out I have extensive stage 4 endometriosis and adenomyosis too, I’m currently week 24 waiting for my next surgery to hopefully remove it all.. I’m like you needing bowel, urinary surgeons, normal surgeon and my gynaecologists in theatre whilst I’m in there so maybe that could factor why it’s a long wait but I was told in August that I’ll be looking at a years wait time. Meanwhile the pain and bleeding is getting worse, it’s literally affected everything in my life. As a working mum of 4 it’s not easy, I’m lucky I have an amazing partner who picks up where I can’t as sometimes I can’t physically move from the pain. I feel like it doesn’t get talked about enough sometimes.. Thank you for sharing your story 🩷🩷 x
2026-01-13 12:31:28
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antoniaexox :
💋💋💋
2026-01-13 10:04:00
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xkellyxf :
I’m waiting for my appointment for the endometriosis centre in Bristol alongside having Crohn’s. Thank you for sharing your story it honestly helps so much! Finger crossed things get a little under control for you 2 xxx
2026-01-13 09:16:32
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Shirley Mccabe :
It is hereditary my mum had it I had it and my daughter is just about to go for her first surgery for it. In my and my mum’s day there was not so much knowledge of it so I am glad my daughter is getting dome treatment and hopefully it helps xx
2026-01-13 19:35:33
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' :
I have adenomyosis just starting this process pre menopausal at 32 I cannot cope with the pain every day im in pain its vile I have my first gynecology app this friday
2026-01-13 06:44:14
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NicolaEndoGirl🎗💛 :
I was diagnosed last year with endometriosis neuropathy after having surgery in April I’ve seen a specialist and had an mri which I’m waiting for the the results as they’re not sure if it’s too deep to operate on I’m on the iud which was put in during my surgery I bled for 6 months straight but I’ve stopped now but the pain is so unbearable 🥺 I phoned the gynae yesterday they haven’t received the mri I had done in November so I’m none the wiser but when I saw the specialist he said if I do have surgery I’m going to have to learn to walk again because I can’t feel anything from my knees down and suffer with severe back pain. Honestly my mental health over the years hasn’t been good but the last year has been the hardest I cry ever day I’m on morphine patches and other meds but nothing works 😢 I tell my husband I don’t want to live like this especially with ends as well as my fibromyalgia on top it’s the worst 🥺😢 but thank you for making this video xx
2026-01-13 06:19:30
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Em :
is it hereditary or do children have a higher chance to get it if their parents have it I know a few people in my life who have it but have never been able to ask questions to understand it thank you for sharing your story
2026-01-13 02:40:49
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Mary Danny Loveridge :
🥰
2026-01-12 22:54:29
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Katyybuxtonn :
currently waiting for my surgery. ive been told before the end of January but it all started 5 years ago. definitely not spoken about enough
2026-01-12 22:44:42
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Dani&Keeva :
endo warrior to endo warrior thank you for sharing your story and awareness 🎗💛
2026-01-12 22:09:52
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Benita Martinez :
I have pcos ( my ovaries look like a chocolate chip cookie) along with fibroids…. I travel with cyst growing constantly on my ovaries
2026-01-13 17:24:25
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chlo 🤍 :
i’ve been dealing with endometriosis and pcos for a while, finally diagnosed 2 months ago. i’m wanting to help others around me and create a digital planner which helps with endometriosis, pcos and other cycle related issues. i would love to know who would be interested in this if i have created it! anyway, sending positive and healing vibes your way, hope you’re doing well!
2026-01-13 20:41:35
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Julie Attwood :
😳😳😳
2026-01-13 21:38:29
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Michelle :
🤍🤍🤍
2026-01-14 00:42:35
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Santa :
On a side note your eyes are beautiful!
2026-01-14 06:35:16
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Megan ☆ PhD Student :
Thank you so much for sharing your story! It is so nice to hear that your concerns were taken seriously and acted upon quickly when so many others are being medically gaslit by healthcare professionals!!🫶🏻
2026-01-14 13:23:49
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Jilly Owens art 🖼🎨 :
I have been diagnosed with stage 4 endometriosis and adenomyosis with just an MRI. However you can feel my adenomyosis through the skin and also see it as it’s caused deep dark bruising on my skin. Currently waiting surgery xx
2026-01-14 21:10:23
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shelly :
I suffered for years with this am 38 now had go have full hysterectomy at 36 they took me ovaries and tubes too.
2026-01-17 16:29:15
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Caitlin :
thank you so much for sharing your story x
2026-01-21 19:16:03
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Beth☁️✨ :
😁😁😁
2026-01-23 22:01:24
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