Bindi Irwin, Wildlife Conservationist and CEO of the Australia Zoo
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- เผยแพร่เมื่อ 5 ก.พ. 2025
- 2024 EndoFound Blossom Award
Bindi Irwin is a dedicated wildlife conservationist, who has inherited her parents' passion for protecting wildlife and wild places. She educates millions of people on the importance of protecting our natural world. Born to Wildlife Warriors Steve and Terri Irwin, Bindi is determined to carry on her father’s legacy and make a positive difference on the planet.
Robert sounds and looks so much like his dad. He'd be so proud of his kids and his wife. Great job to the mom.
To me Robert looks more like mom, except hair color, Bindi looks exactly like her dad, always has except hair color,lol.
“I hated looking in the mirror because all I could see was the pain.” Wow. That hit home. It’s a comfort to know that’s not just me.
“Time for men to discuss and prioritize women’s health” - what a statement, thank you Robert!!
Not only to discuss endometriosis, but to allow women to make choices for their own bodies! STOP CRIMINALIZING ABORTION!
@@AaronNickolas7 Bindi should spend as much time raising awareness about animal causes as she does trying to promote herself as a SM darling and promoting her baby bindi ad nauseam.
She uses SM to bemoan about all her personal woes that're no one else's business in the first place for whatever instant gratification she gets out of having her precious ego stroked by perfect strangers as she kept a months long running commentary over her health woes and used her brother to chime in so no one forgets and she claims it's all to raise awareness but that's what they all say when they want attn & sympathy and she proved it when she then turned around and told everyone she wanted her privacy! Gross!
So much for raising awareness. She blabs about her personal woes and then turns around and announces that people should leave her alone??? WOW! Just remember that, all you well-wishers. Leave this poor celebrity victim alone!
@ #troll
ok who else loves that the Australia Zoo energy just never disappears.... its really just always there!
Bindi I am so sorry you’ve had to go through this. I know you are a hugger by nature and to think that you were in so much pain while doing it breaks my heart.
I am so grateful to see this. I have suffered with Endometriosis and finally when I ended up homeless from so much time off of work, the state stepped in and paid for a major surgery which changed my life although I still struggle with this disease, it makes me so happy to see awareness about it. Thank you from the bottom of my heart
well-deserved Bindi of that award your dad would have been so proud of you
I was recently diagnosed with severe endometriosis when my gynecologist went in to take out a troublesome 10cm ovarian cyst. I've had pain and other symptoms (I don't know what's endo and what's IBD, etc), but thankfully not daily, all-consuming pain. Praise God for a diagnosis and medical help and compassionate people.
Thanks for these brave and beautiful ladies for making endometriosis known
I have endometriosis and the pain is extremely real.
Everyone kept telling me I was overreacting and making excuses.
No.... It's really real.
I'm teary eyed watching Bindi.
Thank you so much Bindi and all the brave and beautiful ladies paving the rode with hope for this debilitating disease🙏♥️😭
I was asymptomatic until I was 38 years old. I'm so grateful I found a doctor at the Cleveland Clinic that did excision for my stage 4 Endometriosis. I've been pain free for over 7 years now. My heart goes out to people that have had multiple surgeries, and had their fertility options taken away because of this terrible, often misunderstood disease.
I love the Irwin Family. God bless you all. ❤❤❤
My adoptive mother had Endometriosis. This was over 50 yrs ago, amazingly new treatments and procedures are now available ❤
God Bless the Irwin family
I had it over 30 yrs. ago. No fun. My ovaries ruptured . I know what u went through so sorry u went through this. So glad u found a doctor that cares.
I really hope that Robert finds a lovely girl to marry soon. What a handsome young man he is. I wish Steve was here to see Bindi and Robert , he’d be in awe of his talented and beautiful kids.
Steve is with them all the time, so I believe he is still supporting Terry and the kiddos in a different way, it's just that we who don't have the gift of sight can't see their joy, really wish we could.❤️🕊
Bindy Brave& Courageous 🎉❤🇦🇺👏👏😍
Have been through that years ago. Way to go to make awareness.
God Bles you bindi
I'm 44yrs old and I have had Endometriosis and PCOS all my life. All I ever wanted to be was a mother but after i got married and my husband and I tried for 5yrs to conceive with no results, I knew i had to do something. I live in Texas and luckily enough I had an expert right in town! (Key word- EXPERT!) not your regular GYN or OBGYN, No you have to see a specialist or they won't help! I got my surgery and a couple years later i had my son, then later i went on to have 2 daughters. Finding the right doctor is key! Endometriosis has been around for a long time, we don't have to suffer, we just have to speak up!
Bindi lrwin you are one of my heroes
As I commented before, been there done that! I ended up with a hysterectomy! When I recovered no more pain! And it took a while! But, I got there! I say we have some sort of 5K to benefit Endometriosis!
Every woman in my family has endometriosis. As a transgender man, I myself know exactly what it’s like to suffer through endometriosis, as I have it as well. For me, hormone replacement therapy was a lifesaver because it took my menstruation away, thus taking endo away. But, the other women in my family aren’t so fortunate because they still have to endure it. But, I am grateful I did myself for a time so I could know for a fact exactly what they’re going through. The pain is insurmountable. It’s indescribable. Not only that, but it could and very often does lead to early onset infertility. Which is devastating for those women who dream of bearing their own children.
I always kind of hoped that Bindi would have one day become more hands on in what she did more akin to Steve. Not to the extent of jumping on crocs and flingin' snakes around, but I always hoped to one day see her on tv out in the bush teaching me about Australian wildlife with that same passionate look on her face,
She's too chubby, lazy and self absorbed to do any real conservation work. It's all up to Terri and Robert.
Let her live her life ffs
Robert love you. 💘😍
Thanks God for completing healing and Jesus christ of Nathaniel name,,,❤❤❤Only God grace and mercy ❤❤❤❤
This is not endo but back in October of 2021 I was diagnosed with ogilvie Syndrome what's a syndrome / disease where your colon grows the doctors told me that I was born with it I had gone on diagnosed with it for 31 years and 9 months and that same year the doctor's tell me if I hadn't come in when I did that I wouldn't be here right now because my colon would have popped then the next year February of 2022 I had my colon removed and the doctor said if we don't remove your colon you're going to die sooner rather than later which scared me quite a lot so combined I suffered with ogilvie syndrome for 32 years and 1 month looking back on it now I am really! Glad that I survived this situation and it was scary at the same time
So sad wen a wife looses a great husband and the kids loose a great father terrible feeling
I suffered from the same thing and had a full hysterectomy.
middle of summer hot water bottle on my back. dismissed by doctors etc. pain like hot pokers .etc. Unfortunately, I did not have a child because of this and an early change of life.
Endo sounds horrible. I'm sorry for anyone that has it and the medical gaslighting and ignorance too.
Robert can I be your father please
Robert what’s your poo like? Is it good?
Can I have my reward for my terribly painful periods and infertility too??
She's not getting the reward for her period; she's getting the reward for her fierce work to bring awareness of the disease to the world.
Sure, all you have to do spread awareness and champion the cause and getting famous helps. Someone's got to do it.
Is no one gonna talk about why suddenly so many women have endo ? It definitely wasn’t around as much as this 30 years ago . I knew NOBODY experiencing these kind of symptoms. Now every second woman I know has these symptoms! I think it’s highly plausible that something new that was introduced for women could be the culprit … 💉
30 years ago there was even less information about Endometriosis than there is today and there are still women being misdiagnosed.
30 years ago a woman would’ve been told you’re making it up and sent home, in fact this still happens
I wonder too. It isn't natural for females to be in debilitating pain which also effects fertility. Something in our modern diets or environment? Are you suggesting the warts virus vaccine? Who knows.
People had endo 30 years ago, they just didn’t know or talk about it. It was not common to talk about regular periods ffs let alone periods that caused extensive debilitating issues. Also you seem to be insinuating that we have done something wrong to cause our pain. This is insulting, and mirrors the medical gaslighting that we so often hear in drs offices.
Where is Chandler? Trouble in paradise?
I think he stayed back home in Australia it look after grace
Thay ave a daughter so probably lookin after her, so no trouble in paradise 🤷♀️
Get a life
That's the question you have? I cant
spouses dont have to do everything together 🙄