Linsey's Legacy Gynaecological Cancer Foundation

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Linsey's Legacy Gynaecological Cancer Foundation Our foundation is committed to supporting the lives of regional women affected by gynaecological cancers. Donations to Linseys Legacy
BSB 325185
Acc 04085070

We are here and ready to offer hope, healing, care packages and financial assistance. Linsey's Legacy Gynaecological Cancer Foundation

We are an Unincorporated body in honour of Linsey Metcalf and her children. Linsey lost her battle with Cervical Cancer in December 2021. Linsey was 38 and the mother of 3 boys Jaidyn, Blake and Brax and the stepmother of Shilah Smith. The purpose of the foundation is to provide information for the prevention and early intervention of gynaecological cancers and support to families who are required to have extended stays in Adelaide, for treatment. We are recruiting members of the foundation at a cost of $20 per year as the base funding to provide comfort packages for families who are required to have treatment in Adelaide and therefore are required to be in Adelaide for an extended time. The package will include luxury bed topper, quilt, sheets and pillows. We are also aware the Patient Assistant Transport Scheme PATS will only pay for accommodation on treatment days and therefore families are required to travel back home for weekends. In my experience this causes much unneeded stress on families who are doing it tough. Having a base where children and other family can come to support the patient is critical to their wellbeing. It is our intention to provide both the comfort packages, assistance with accommodation and financial support so families can have a home base while having treatment. To do this we will be fundraising and seeking sponsorship. I will be forever grateful for the support and as we are dedicated to preventing women from gynaecological cancers and providing families with support when treatment is required. Deb Katsiavos
Founder
Linsey's Legacy
Gynaecological Cancer Foundation
Ph: 0418 892 417

20/09/2026

💙ZOE’S STORY💙

I am writing this to put awareness out there from my experience leading to my diagnosis.
2025: at the start of 2025 I started experiencing lower abdominal pain, at first it seemed that it was a bit of gas, after that it wasn’t to bad but my gut health didn’t feel good, I went to my doctor as my mum passed from bowel cancer as many of you know so I got all the necessary testing to make sure everything was ok, I have severe health anxiety since mum passed so I have been hyper aware of any sort of change in my body. The testing all came back normal no bowel cancer nothing, my doctor thought it was IBS (irritable bowel syndrome) so I started supplements and everything to help it and that was it I didn’t think of anything else until this year.
2026: still on the supplements at the start of this year, I decided to stop them as my body felt like it was regulating properly again, except I noticed my stomach was constantly swollen and bloated looking like I was pregnant all the time again didn’t think about it as the symptoms from ibs and also weight gain from being on the depo provera needle for 5 years prior to. Around end of July early August I started having this dull ache in my left side pelvic area, wasn’t sure if it was due to my c-section scar tissue or something else, either way it felt a little off I ignored it for a bit but it didn’t go away, so I decided the only way to know for sure is to go to my doctor and request an ultrasound so we could see inside my body, I listened to my gut and I forever will.
26th August I went in and had my ultrasound, the tech thought it could be a cyst wasn’t 100%. Two days later 28th August I got a call from my doctors asking me to go in now to discuss results I knew then that it didn’t look good from past experiences anyway. Dr Fatemeh Ebadi is my doctor I seen and she was absolutely amazing she sat us down and said it is a large mass and they need to see if it is benign or malignant obviously I started balling as everything with my mum came flooding back (I was there from her diagnosis to her death) she said I want you to go for a CT scan so we can see which it is. I went for the CT that day luckily. I had to see a different doctor on the Saturday to get results as I didn’t want to wait to find out. I got my report and it said it’s consistent with an ovarian malignancy but it’s been caught very early which I am soooo lucky because ovarian cancer is usually found when it’s already at stage 4, counting my lucky stars that’s for sure!
On that Sunday Dr Fatemeh rang me on her day off and said she read my file and is sending me for blood tests so we can test cancer markers. I went in on the Monday and got the test done, seen doctor Fatemeh again on Wednesday 2nd September to get blood results everything came back normal except for one marker the CA-125 with me that’s consistent with the mass they found but that marker can go up with any inflammation in your body so again lucky. Then having to wait another week to see the gynaecologist which for me at the moment is gut wrenching because I just want this out of me.
9th September I seen the gynaecologist he was lovely along with the nurse and student in the room. He confirmed that yes it is ovarian cancer early stages again luckily! I will have to have a full hysterectomy which includes exploring of the abdomen aswell to make sure everything else is fine, about 9-10 weeks after surgery I will undergo 6 rounds of chemotherapy to make sure any remaining cells are killed.
Being diagnosed at the age of 33 I never imagined, but in a way I was waiting after mum got diagnosed I thought this is it I’m going to end up with it next because I was closest to her she was my bestfriend, luckily I have her as my guardian angel through this.
Now I want to take a minute to talk about Dr Fatemeh Ebadi, she won’t see this, I told her at my last appointment anyways but she is beyond amazing, she has pushed for me, she sent me for everything I asked for no questions asked and she continues to push, I know that’s her job but you donot get many doctors like her that actually listen to you and advocate for you so I am forever grateful for her, I wouldn’t have got here without her .
So what I thought was IBS turned out to be Ovarian Cancer, ovarian cancer can mimic symptoms of IBS, I was none the wiser but I listened to my body and recognised that something was different and not right. All the symptoms I was having are symptoms of the cancer.
So please listen to your body, if you feel something isn’t right get it checked doesn’t matter if you think it’s silly or nothing get it checked to be 100% sure, if I didn’t go in and ask for the ultrasound when I did, I have no idea when I would have found this cancer.
It pays off being hyper aware of your body and health even though it can drive you crazy at times but it’s worth it.
To many people I love have been lost to cancer it’s not talked about enough, testing is not done enough.

We thank Zoe for sharing her story with us, so we can continue our mission to raise awareness and help those women closest to us.

We continue to support local woman diagnosed with gynaecological cancers and you can help us help them by donating too.

🩵

www.linseyslegacy.au/donate

Send a message to learn more

18/09/2026
Whyalla Girls Alice and Jackie will be running marathons in Melbourne this October in memory of Astro and raising funds ...
17/09/2026

Whyalla Girls Alice and Jackie will be running marathons in Melbourne this October in memory of Astro and raising funds for Ovarian Cancer Research! Please get behind them. We need more research for Ovarian Cancer!

https://melbmara2026.grassrootz.com/ocrf/doing-it-for-astro/?utm_id=97757_v0_s00_e231_tv2_tp1_a1dennhbmvqgmn&fbclid=IwdGRjcAUYq_FjbGNrBRirs3Bkb2YFZXh0bgNhZW0CMTEAc3J0YwZhcHBfaWQMMzUwNjg1NTMxNzI4AAEeULxcyzGv_Uny29RlCc6E3zXiYljW2S4OXtVyO7JqZ7X0A_N2QW5sliP_7vA_aem_GtjSd_bRY5Cr8hfnuBDUnw

Hi there We are raising funds to help the Ovarian Cancer Research Foundation, we’re aiming to raise funds to help spread awareness around this disease and in hope that one day in the near future there will be an early detection test available to help diagnose ovarian cancer. We have chosen to run ...

17/09/2026

💙 PROUDLY HOSTING LINSEY’S LEGACY FOUNDATION 💙

We’re honoured to welcome Linsey’s Legacy Foundation to the Women On Eyre Women’s Health Expo.

Raising awareness of gynaecological cancers, the importance of recommended screening, early detection and recognising unusual or persistent changes, Linsey’s Legacy Foundation is helping women feel informed, empowered and supported when it comes to their health.

Their message is simple but powerful: Know your body. Keep up to date with your screening. Seek medical advice when something doesn’t feel right. Prevention, early detection and timely treatment can save lives.

15/09/2026

A tool that works faster than you can blink, developed by Adelaide researchers is poised to change the way endometriosis is diagnosed and skip the need for surgery. đź”— DETAILS: https://bit.ly/3SYB5l3

14/09/2026
Take notice
11/09/2026

Take notice

Sis, something feeling different... downstairs? đź©·

September is Gynaecological Cancer Awareness Month — a good time to know the signs of cancers that can start near your lower tummy and down below.

Our bodies can give us signs when something’s changed – keep an eye out for:

Bleeding — New or unusual bleeding down there
Fluid changes — New or unusual fluid down below, it might be very watery, pink or bloody
Tummy changes — Bloating or pain in your lower belly, or feeling full quickly
Toilet changes — Needing to go more often, or feeling pain when you do
Skin changes — An itch, sore or lump down below
Most of these signs can be caused by other things too — so don’t jump to the worst.

But when our bodies talk, let’s listen 👂🏾 ✨

Notice something different? Book in for a check 🫶🏾

08/09/2026

đź’™ LIGHTING IT TEAL FOR GYNAECOLOGICAL CANCER AWARENESS đź’™

From 8–12 September, the HMAS Whyalla will light up teal in recognition of Gynaecological Cancer Awareness Month, in support of Linsey’s Legacy Cancer Foundation.
Every year, around 5,500 Australian women are diagnosed with gynaecological cancers, including cervical, ovarian, uterine, vulval and vaginal cancers. It’s estimated that 1 in 23 women are at risk of being diagnosed by the age of 85.

Lighting the ship teal is a symbol of support, awareness and hope, helping spark important conversations about prevention, early detection and support for women across Regional South Australia. đź’™

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Whyalla, SA

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