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Believing women’s pain shouldn’t be revolutionary — it should be the standard.

Let’s keep pushing for a world where every story is heard and every symptom is taken seriously. 💛

A huge day for endometriosis research!

We’re thrilled to announce the launch of the Seckin Endometriosis Research Center for Women’s Health at Cold Spring Harbor Laboratory @cshlnews — the first facility of its kind, dedicated exclusively to decoding the mysteries of #endometriosis.

Alexis Roderick Joel was there to help launch this historic center, and we are deeply grateful for her voice and support on this incredible new step for #endo research.

Founded by world-renowned surgeon Dr. Tamer Seckin @seckinmd, this groundbreaking center will unite top scientists and clinicians to drive real progress in diagnosis, treatment, and hope for the 200M+ people worldwide living with endometriosis.

With a $20M investment fueling 10 years of cutting-edge science, the future of endometriosis care begins here — and it begins with all of us.

🎗️Tap the link in our bio to learn more🎗️

Power the Science - Fuel the Hope!

Photo 📸: @levradin

A huge day for endometriosis research!

We’re thrilled to announce the launch of the Seckin Endometriosis Research Center for Women’s Health at Cold Spring Harbor Laboratory @cshlnews — the first facility of its kind, dedicated exclusively to decoding the mysteries of #endometriosis.

Alexis Roderick Joel was there to help launch this historic center, and we are deeply grateful for her voice and support on this incredible new step for #endo research.

Founded by world-renowned surgeon Dr. Tamer Seckin @seckinmd, this groundbreaking center will unite top scientists and clinicians to drive real progress in diagnosis, treatment, and hope for the 200M+ people worldwide living with endometriosis.

With a $20M investment fueling 10 years of cutting-edge science, the future of endometriosis care begins here — and it begins with all of us.

🎗️Tap the link in our bio to learn more🎗️

Power the Science - Fuel the Hope!

Photo 📸: @levradin

A huge day for endometriosis research!

We’re thrilled to announce the launch of the Seckin Endometriosis Research Center for Women’s Health at Cold Spring Harbor Laboratory @cshlnews — the first facility of its kind, dedicated exclusively to decoding the mysteries of #endometriosis.

Alexis Roderick Joel was there to help launch this historic center, and we are deeply grateful for her voice and support on this incredible new step for #endo research.

Founded by world-renowned surgeon Dr. Tamer Seckin @seckinmd, this groundbreaking center will unite top scientists and clinicians to drive real progress in diagnosis, treatment, and hope for the 200M+ people worldwide living with endometriosis.

With a $20M investment fueling 10 years of cutting-edge science, the future of endometriosis care begins here — and it begins with all of us.

🎗️Tap the link in our bio to learn more🎗️

Power the Science - Fuel the Hope!

Photo 📸: @levradin

A huge day for endometriosis research!

We’re thrilled to announce the launch of the Seckin Endometriosis Research Center for Women’s Health at Cold Spring Harbor Laboratory @cshlnews — the first facility of its kind, dedicated exclusively to decoding the mysteries of #endometriosis.

Alexis Roderick Joel was there to help launch this historic center, and we are deeply grateful for her voice and support on this incredible new step for #endo research.

Founded by world-renowned surgeon Dr. Tamer Seckin @seckinmd, this groundbreaking center will unite top scientists and clinicians to drive real progress in diagnosis, treatment, and hope for the 200M+ people worldwide living with endometriosis.

With a $20M investment fueling 10 years of cutting-edge science, the future of endometriosis care begins here — and it begins with all of us.

🎗️Tap the link in our bio to learn more🎗️

Power the Science - Fuel the Hope!

Photo 📸: @levradin

A huge day for endometriosis research!

We’re thrilled to announce the launch of the Seckin Endometriosis Research Center for Women’s Health at Cold Spring Harbor Laboratory @cshlnews — the first facility of its kind, dedicated exclusively to decoding the mysteries of #endometriosis.

Alexis Roderick Joel was there to help launch this historic center, and we are deeply grateful for her voice and support on this incredible new step for #endo research.

Founded by world-renowned surgeon Dr. Tamer Seckin @seckinmd, this groundbreaking center will unite top scientists and clinicians to drive real progress in diagnosis, treatment, and hope for the 200M+ people worldwide living with endometriosis.

With a $20M investment fueling 10 years of cutting-edge science, the future of endometriosis care begins here — and it begins with all of us.

🎗️Tap the link in our bio to learn more🎗️

Power the Science - Fuel the Hope!

Photo 📸: @levradin

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

You’re not just imagining it. #Endometriosis is whole-body.

If you relate to these symptoms ➡️ you’re not alone - and you deserve to be heard. #Endo is so much more than ‘just bad periods.’

#themoreyouknow #endometriosisawareness

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

“I sat in my car and cried, wondering if I was being dramatic.”

That line stayed with us. Because so many people with endometriosis know exactly what that moment feels like. When pain is minimized long enough that you begin questioning yourself instead.

For six years, @kristennlarose lived with daily pain, exhaustion, anxiety, GI symptoms, inflammation, and the exhausting reality of trying to function while feeling like her body was constantly working against her. She was dismissed, doubted, and told it was “just a bad period.” Even minutes before surgery, she was still being told they likely wouldn’t find #endometriosis.

They did.

Last week, she stood on Capitol Hill advocating for new women’s health legislation, using the same voice she once had to use just to convince doctors something was wrong.

Her full story is deeply honest, heartbreaking in parts, and ultimately hopeful.

Tap the link in our bio to read her #endostory

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

What a great day! Thanks to everyone who joined us to support Cold Spring Harbor Laboratory and learn about endometriosis and the vital partnership between Semir Beyaz, PhD, and Tamer Seckin, MD. A special thank you to Alexis Joel for sharing your story and reminding us what matters most: the patient. Establishing the Seckin Endometriosis Research Center for Women’s Health couldn’t happen without support from this community. Together, we are building a future with real hope for those living with endometriosis.

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

Endometriosis doesn’t just affect your body, it can shift your entire world.

The exhaustion that no one sees. The unpredictability of never knowing how you’ll feel from one day to the next. The constant calculations, canceled plans, self-doubt, and questions of “Is it really that bad?”

When pain and symptoms become part of daily life, they can start affecting more than your physical health. And because so much of it is invisible, many people carry that weight quietly.

If you’ve ever felt frustrated, isolated, overwhelmed, or like you don’t recognize yourself anymore, you’re not alone. The impact is real, and it deserves to be acknowledged just as much as the physical symptoms💛

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

“Nothing is wrong. Just keep trying.”

For years, that was the answer @bryndalynnnn kept hearing while enduring five miscarriages, unexplained digestive symptoms, surgeries, injections, and the quiet heartbreak of feeling like her body was failing her.

Then came a four-hour surgery and a diagnosis: stage IV #endometriosis “absolutely everywhere.”

What followed wasn’t just answers, it was a completely different future. Two children. Relief from symptoms she had lived with for years. And the realization that so many things she had accepted as “normal” never were.

Sometimes persistence changes everything. Read her full #EndoStory at the link in bio.

Today at the New York State Capitol, we stood together for a future where no young person suffers for years before learning that their pain may not be normal. Thank you to the incredible endo warriors, advocates, Miss New York @thelaurennorris, and the members of EndoFound’s UpEndo Coalition for showing up, speaking out, and supporting this mission.

Now we need your help.

If you couldn’t join us in person today, you can still make an impact by signing our petition urging the passage of Assembly Bill A7557. This bill would bring endometriosis education directly into New York classrooms helping students recognize symptoms earlier, understand when something may be wrong, and learn how to advocate for themselves.

The average #endometriosis diagnosis still takes 7–10 years. Education can help change that.

📣 Sign the petition at the link in our bio and tell the NYS Assembly: Pass A7557 📣

Today at the New York State Capitol, we stood together for a future where no young person suffers for years before learning that their pain may not be normal. Thank you to the incredible endo warriors, advocates, Miss New York @thelaurennorris, and the members of EndoFound’s UpEndo Coalition for showing up, speaking out, and supporting this mission.

Now we need your help.

If you couldn’t join us in person today, you can still make an impact by signing our petition urging the passage of Assembly Bill A7557. This bill would bring endometriosis education directly into New York classrooms helping students recognize symptoms earlier, understand when something may be wrong, and learn how to advocate for themselves.

The average #endometriosis diagnosis still takes 7–10 years. Education can help change that.

📣 Sign the petition at the link in our bio and tell the NYS Assembly: Pass A7557 📣

Today at the New York State Capitol, we stood together for a future where no young person suffers for years before learning that their pain may not be normal. Thank you to the incredible endo warriors, advocates, Miss New York @thelaurennorris, and the members of EndoFound’s UpEndo Coalition for showing up, speaking out, and supporting this mission.

Now we need your help.

If you couldn’t join us in person today, you can still make an impact by signing our petition urging the passage of Assembly Bill A7557. This bill would bring endometriosis education directly into New York classrooms helping students recognize symptoms earlier, understand when something may be wrong, and learn how to advocate for themselves.

The average #endometriosis diagnosis still takes 7–10 years. Education can help change that.

📣 Sign the petition at the link in our bio and tell the NYS Assembly: Pass A7557 📣

Today at the New York State Capitol, we stood together for a future where no young person suffers for years before learning that their pain may not be normal. Thank you to the incredible endo warriors, advocates, Miss New York @thelaurennorris, and the members of EndoFound’s UpEndo Coalition for showing up, speaking out, and supporting this mission.

Now we need your help.

If you couldn’t join us in person today, you can still make an impact by signing our petition urging the passage of Assembly Bill A7557. This bill would bring endometriosis education directly into New York classrooms helping students recognize symptoms earlier, understand when something may be wrong, and learn how to advocate for themselves.

The average #endometriosis diagnosis still takes 7–10 years. Education can help change that.

📣 Sign the petition at the link in our bio and tell the NYS Assembly: Pass A7557 📣

🎙️ New episode just dropped: *Living With Endometriosis: The Diet, Fatigue & Flare Reality Nobody Talks About*

“I truly felt like I was dying — and every doctor kept telling me everything was normal.”

This isn’t a conversation about quick fixes or miracle diets. It’s about what life with endometriosis can actually look like… and the tools, understanding, and validation that can help make the journey less isolating.

After a 12-year diagnostic delay, clinical nutritionist and endometriosis patient @savannahregensburger joins @dianafalzone for an honest conversation about the parts of endometriosis that often happen quietly: debilitating fatigue, brain fog, gut issues, fertility struggles, inflammation, and the unpredictability of flares.

Listen now wherever you stream your podcasts — Spotify, Apple Podcasts, and more. *tap the link in our bio*

#endometriosis #lifewithendometriosis #hope #endometriosisawareness #endowarrior

NEW YORK: we need your voices in Albany!

The NY State Senate has already passed legislation supporting menstrual health and endometriosis education in schools. Now, Assembly Bill A7557 remains stalled in the Assembly Education Committee — and we need advocates, patients, families, and supporters to help move it forward.

Join us in Albany THIS Wednesday, May 20 for a press conference and advocacy day alongside legislators, clinicians, the endometriosis community, and Miss New York @thelaurennorris, as we urge the Assembly to act.

📍 New York State Capitol, 4th Floor Lobby – Outside of the Gallery
🕚 11:00 AM
📅 Wednesday, May 20, 2026

Endometriosis is far more than “just a bad period.” It is a complex, whole-body disease that can impact every aspect of a person’s life, yet symptoms are too often dismissed, misunderstood, or normalized for years. Education is one of the most powerful tools we have to change that.

Come stand with us. Bring signs. Share your story. Help us advocate for earlier recognition, awareness, and better outcomes for future generations.

#endometriosis #endoawareness #menstrualhealth #UpEndo #endoadvocacy

NEW YORK: we need your voices in Albany!

The NY State Senate has already passed legislation supporting menstrual health and endometriosis education in schools. Now, Assembly Bill A7557 remains stalled in the Assembly Education Committee — and we need advocates, patients, families, and supporters to help move it forward.

Join us in Albany THIS Wednesday, May 20 for a press conference and advocacy day alongside legislators, clinicians, the endometriosis community, and Miss New York @thelaurennorris, as we urge the Assembly to act.

📍 New York State Capitol, 4th Floor Lobby – Outside of the Gallery
🕚 11:00 AM
📅 Wednesday, May 20, 2026

Endometriosis is far more than “just a bad period.” It is a complex, whole-body disease that can impact every aspect of a person’s life, yet symptoms are too often dismissed, misunderstood, or normalized for years. Education is one of the most powerful tools we have to change that.

Come stand with us. Bring signs. Share your story. Help us advocate for earlier recognition, awareness, and better outcomes for future generations.

#endometriosis #endoawareness #menstrualhealth #UpEndo #endoadvocacy

NEW YORK: we need your voices in Albany!

The NY State Senate has already passed legislation supporting menstrual health and endometriosis education in schools. Now, Assembly Bill A7557 remains stalled in the Assembly Education Committee — and we need advocates, patients, families, and supporters to help move it forward.

Join us in Albany THIS Wednesday, May 20 for a press conference and advocacy day alongside legislators, clinicians, the endometriosis community, and Miss New York @thelaurennorris, as we urge the Assembly to act.

📍 New York State Capitol, 4th Floor Lobby – Outside of the Gallery
🕚 11:00 AM
📅 Wednesday, May 20, 2026

Endometriosis is far more than “just a bad period.” It is a complex, whole-body disease that can impact every aspect of a person’s life, yet symptoms are too often dismissed, misunderstood, or normalized for years. Education is one of the most powerful tools we have to change that.

Come stand with us. Bring signs. Share your story. Help us advocate for earlier recognition, awareness, and better outcomes for future generations.

#endometriosis #endoawareness #menstrualhealth #UpEndo #endoadvocacy

NEW YORK: we need your voices in Albany!

The NY State Senate has already passed legislation supporting menstrual health and endometriosis education in schools. Now, Assembly Bill A7557 remains stalled in the Assembly Education Committee — and we need advocates, patients, families, and supporters to help move it forward.

Join us in Albany THIS Wednesday, May 20 for a press conference and advocacy day alongside legislators, clinicians, the endometriosis community, and Miss New York @thelaurennorris, as we urge the Assembly to act.

📍 New York State Capitol, 4th Floor Lobby – Outside of the Gallery
🕚 11:00 AM
📅 Wednesday, May 20, 2026

Endometriosis is far more than “just a bad period.” It is a complex, whole-body disease that can impact every aspect of a person’s life, yet symptoms are too often dismissed, misunderstood, or normalized for years. Education is one of the most powerful tools we have to change that.

Come stand with us. Bring signs. Share your story. Help us advocate for earlier recognition, awareness, and better outcomes for future generations.

#endometriosis #endoawareness #menstrualhealth #UpEndo #endoadvocacy

For many in the endometriosis community, hearing the word “endometriosis” included in a national conversation around women’s health is meaningful.

Progress in this field has never happened overnight. It is the result of years of advocacy from patients, physicians, researchers, and organizations working tirelessly to push this disease out of the shadows and into the broader public health conversation.

At EndoFound, our mission has always been nonpartisan and patient-centered: advancing research, education, early diagnosis, and access to proper care for those living with endometriosis.

#whitehouse #endometriosis #nationalawareness #EndoFound #DrSeckin

New podcast just dropped!

On this episode of EndoTV, @dianafalzone speaks with Nicoletta and Jessica of @elysaramedical about the often-overlooked reality of life after excision surgery and why endometriosis requires long-term, multidisciplinary care beyond the operating room.

Together, they explore the links between inflammation, hormone imbalance, nervous system dysregulation, nutrition, and persistent symptoms after surgery.

Listen wherever you stream podcasts 🎧

#endometriosis #excisionsurgery #livingwithendo #womenshealth #endo