Home Actress Chloé Hayden HD Photos and Wallpapers March 2024 Chloé Hayden Instagram - Since 13, my life has been taken by debilitating pain, dismissed as ‘you’re a woman, deal with it’.  So for over a decade, I did. I dealt with waking up vomiting from pain, lying in the bathroom screaming while my stomach back and legs felt like they were being stabbed, passing out, 2am visits to the emergency ward and being turned away with Panadol, with a pain on the same pain scale as heart attacks and labour pains. Every single day.  Finally, I was diagnosed with severe endometriosis and adenomyosis; both progressive disorders in the top 10 most painful conditions in the world, and found on every organ in the body. There is no cure, and our governments lack of education and care for AFAB folk means the average time to get a diagnosis is 10 years, with 2/3 being misdiagnosed first.  50% of endometriosis sufferers will suffer from infertility 1/6 will lose their jobs Excessive bleeding (even when not on your period), pain, fatigue and overall reduced quality of life are just a few things that we go through every day. AFAB folk are taught that pain is normal, to be silent. Recent studies show that women are left out of the equation all together during research, with most researchers refusing to use female rodents in their clinical pain trials as the menstrual cycles of female rats adds too much variability (ha.) 
And after surgery, women are more likely to be prescribed anti depressants and sedatives for pain, while men are more likely to be prescribed actual pain medication when they have surgery for similar things. If you’re autistic there’s a new level of ‘it’s all in their head’ when seeking an endometriosis diagnosis, and is further exacerbated when the autistic person has been societally conditioned to mask, to fear speaking up, or if their body is unable to feel pain. If you are otherwise disabled, BIPOC or living below the poverty line, accessing support statistically grows worse. If you’ve been told your pain is normal, it’s not. If cis men had periods, it would be the ultimate sign of masculinity, they would praise and boast about their cycles and pain would be eradicated. If cis men had endometriosis, there would be a cure. There is no excuse.

Chloé Hayden Instagram – Since 13, my life has been taken by debilitating pain, dismissed as ‘you’re a woman, deal with it’.  So for over a decade, I did. I dealt with waking up vomiting from pain, lying in the bathroom screaming while my stomach back and legs felt like they were being stabbed, passing out, 2am visits to the emergency ward and being turned away with Panadol, with a pain on the same pain scale as heart attacks and labour pains. Every single day.  Finally, I was diagnosed with severe endometriosis and adenomyosis; both progressive disorders in the top 10 most painful conditions in the world, and found on every organ in the body. There is no cure, and our governments lack of education and care for AFAB folk means the average time to get a diagnosis is 10 years, with 2/3 being misdiagnosed first.  50% of endometriosis sufferers will suffer from infertility 1/6 will lose their jobs Excessive bleeding (even when not on your period), pain, fatigue and overall reduced quality of life are just a few things that we go through every day. AFAB folk are taught that pain is normal, to be silent. Recent studies show that women are left out of the equation all together during research, with most researchers refusing to use female rodents in their clinical pain trials as the menstrual cycles of female rats adds too much variability (ha.) 
And after surgery, women are more likely to be prescribed anti depressants and sedatives for pain, while men are more likely to be prescribed actual pain medication when they have surgery for similar things. If you’re autistic there’s a new level of ‘it’s all in their head’ when seeking an endometriosis diagnosis, and is further exacerbated when the autistic person has been societally conditioned to mask, to fear speaking up, or if their body is unable to feel pain. If you are otherwise disabled, BIPOC or living below the poverty line, accessing support statistically grows worse. If you’ve been told your pain is normal, it’s not. If cis men had periods, it would be the ultimate sign of masculinity, they would praise and boast about their cycles and pain would be eradicated. If cis men had endometriosis, there would be a cure. There is no excuse.

Chloé Hayden Instagram - Since 13, my life has been taken by debilitating pain, dismissed as ‘you’re a woman, deal with it’.  So for over a decade, I did. I dealt with waking up vomiting from pain, lying in the bathroom screaming while my stomach back and legs felt like they were being stabbed, passing out, 2am visits to the emergency ward and being turned away with Panadol, with a pain on the same pain scale as heart attacks and labour pains. Every single day.  Finally, I was diagnosed with severe endometriosis and adenomyosis; both progressive disorders in the top 10 most painful conditions in the world, and found on every organ in the body. There is no cure, and our governments lack of education and care for AFAB folk means the average time to get a diagnosis is 10 years, with 2/3 being misdiagnosed first.  50% of endometriosis sufferers will suffer from infertility 1/6 will lose their jobs Excessive bleeding (even when not on your period), pain, fatigue and overall reduced quality of life are just a few things that we go through every day. AFAB folk are taught that pain is normal, to be silent. Recent studies show that women are left out of the equation all together during research, with most researchers refusing to use female rodents in their clinical pain trials as the menstrual cycles of female rats adds too much variability (ha.) 
And after surgery, women are more likely to be prescribed anti depressants and sedatives for pain, while men are more likely to be prescribed actual pain medication when they have surgery for similar things. If you’re autistic there’s a new level of ‘it’s all in their head’ when seeking an endometriosis diagnosis, and is further exacerbated when the autistic person has been societally conditioned to mask, to fear speaking up, or if their body is unable to feel pain. If you are otherwise disabled, BIPOC or living below the poverty line, accessing support statistically grows worse. If you’ve been told your pain is normal, it’s not. If cis men had periods, it would be the ultimate sign of masculinity, they would praise and boast about their cycles and pain would be eradicated. If cis men had endometriosis, there would be a cure. There is no excuse.

Chloé Hayden Instagram – Since 13, my life has been taken by debilitating pain, dismissed as ‘you’re a woman, deal with it’. 
So for over a decade, I did.
I dealt with waking up vomiting from pain, lying in the bathroom screaming while my stomach back and legs felt like they were being stabbed, passing out, 2am visits to the emergency ward and being turned away with Panadol, with a pain on the same pain scale as heart attacks and labour pains.
Every single day. 
Finally, I was diagnosed with severe endometriosis and adenomyosis; both progressive disorders in the top 10 most painful conditions in the world, and found on every organ in the body.
There is no cure, and our governments lack of education and care for AFAB folk means the average time to get a diagnosis is 10 years, with 2/3 being misdiagnosed first. 
50% of endometriosis sufferers will suffer from infertility
1/6 will lose their jobs
Excessive bleeding (even when not on your period), pain, fatigue and overall reduced quality of life are just a few things that we go through every day.
AFAB folk are taught that pain is normal, to be silent.
Recent studies show that women are left out of the equation all together during research, with most researchers refusing to use female rodents in their clinical pain trials as the menstrual cycles of female rats adds too much variability (ha.) 
And after surgery, women are more likely to be prescribed anti depressants and sedatives for pain, while men are more likely to be prescribed actual pain medication when they have surgery for similar things.
If you’re autistic there’s a new level of ‘it’s all in their head’ when seeking an endometriosis diagnosis, and is further exacerbated when the autistic person has been societally conditioned to mask, to fear speaking up, or if their body is unable to feel pain.
If you are otherwise disabled, BIPOC or living below the poverty line, accessing support statistically grows worse.

If you’ve been told your pain is normal, it’s not.
If cis men had periods, it would be the ultimate sign of masculinity, they would praise and boast about their cycles and pain would be eradicated.
If cis men had endometriosis, there would be a cure.
There is no excuse. | Posted on 30/Mar/2024 06:06:07

Chloé Hayden Instagram – Two months with our surprise wedding rescue kittens 🐱 

The four raggedy, terrified, feral little kittens we found under a shed on our wedding day have grown into the most loving, lively, sweet little darlings in the world; Woolbrook (named after our venue) thinks he’s part dog, part human; he only eats with the dogs, wags his tail, follows his big dog brother around like a shadow, will sit on your shoulder and watch intensely if the telly is on, has a personal vengeance against house plants and absolutely must start and finish every day by cuddling you with both paws wrapped around your neck; Freja (named after the Nordic Goddess of Love; and also, a tradition in which the bride is given a cat on her wedding day!) is becoming more and more confident every day, and absolutely loves a snuggle, trying to beat her personal best of fanging it from one end of the house to the other, and is teaching her big sister Beatrix (who was previously our only cat, and has quite severe PTSD from an accident that left her with 3 legs before we adopted her) that other cats aren’t so bad; Beatrix will now even let Freja nap on her bed with her and share her food 🥺
(Mama and Papa took the other two kittens, who are also thriving now and, after having found them at our Disney themed wedding, have been rightfully named Lilo and Stitch) 

Our home is a riot of lil paws everywhere and my heart is so so so full
Chloé Hayden Instagram – Two months with our surprise wedding rescue kittens 🐱 

The four raggedy, terrified, feral little kittens we found under a shed on our wedding day have grown into the most loving, lively, sweet little darlings in the world; Woolbrook (named after our venue) thinks he’s part dog, part human; he only eats with the dogs, wags his tail, follows his big dog brother around like a shadow, will sit on your shoulder and watch intensely if the telly is on, has a personal vengeance against house plants and absolutely must start and finish every day by cuddling you with both paws wrapped around your neck; Freja (named after the Nordic Goddess of Love; and also, a tradition in which the bride is given a cat on her wedding day!) is becoming more and more confident every day, and absolutely loves a snuggle, trying to beat her personal best of fanging it from one end of the house to the other, and is teaching her big sister Beatrix (who was previously our only cat, and has quite severe PTSD from an accident that left her with 3 legs before we adopted her) that other cats aren’t so bad; Beatrix will now even let Freja nap on her bed with her and share her food 🥺
(Mama and Papa took the other two kittens, who are also thriving now and, after having found them at our Disney themed wedding, have been rightfully named Lilo and Stitch) 

Our home is a riot of lil paws everywhere and my heart is so so so full

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