Lupron Warriors Victims Hub

​Lupron Warriors Victims Hub

THIS IS REAL LIFE!

Welcome to the Lupron Warriors Victims Hub.

This is where survivors of Lupron and other GnRH agonists unite. Our mission is to give a voice to the voiceless by sharing our personal stories to demand accountability and justice.

Join our community as we fight for change, share vital resources, and heal together. You are not alone.

Make a stand publicly against Lupron !

Lupron Warriors Facebook









Lupron Warriors Victims Hub

 @LupronWarriorsvictimshub  channel

💔 How Many People Are Really Affected by Lupron?

Many of us know someone who has taken Lupron (leuprolide) — for prostate cancer, endometriosis, puberty suppression, or other conditions.

While official reports of side effects exist, new data suggests far more people may be affected than previously understood.

Here’s what we know:

In the U.S., over 60,000 adverse events have been officially reported over the last 20 years.

Research shows that only about 5–10% of people who experience side effects actually report them.

That means the true number of affected people in the U.S. could be between 600,000–1.2 million.

If we include Europe, the combined total could realistically be around 1–2 million people who have experienced problems with Lupron.

Support groups (like those run by families and patients) confirm this:

In a 12,000-member group, only 5% had officially reported their issues — yet nearly everyone had been affected in some way.

What does this tell us?
The official numbers only scratch the surface.

Tens or hundreds of thousands of people may be silently struggling.

Reporting your side effects matters — it helps regulators, doctors, and researchers understand the true scale of the problem and puts more scrutiny on the drug.

“Even small actions — like reporting your experience — can make a big difference in protecting thousands of others.”

If you require more information, please check us out on Facebook and Instagram.

LUPRON WARRIORS VICTIMS HUB

LUPRON WARRIORS

5 months ago | [YT] | 0

Lupron Warriors Victims Hub

 @LupronWarriorsvictimshub 

Lupron has many names. Check the lists attached to see if you or someone you love may have been a Lupron victim.

Please share to beat the algorithms of Youtube

We will NEVER give up on the fight 💪
We are still here. We have removed ourselves from Facebook. This doesn't mean we have given up. In actual fact , it is the exact opposite.

We will not let the public be poisoned anymore. If you have a story to tell. Let us be your voice. Send reels and documentaries to us, and we will make sure you are represented in the best light possible.

Please check out the details on Lupron Warriors & Lupron Warriors Victims Hub on Facebook

As the quote said

" The only thing necessary for the triumph of evil is that good men do nothing."

#deathtolupron
#lupronispoison
#genderreassignmentsurgery
#Endometriosis
#fibroids
#prostatecancer
#precociouspuberty
#gnrhagonists
#health
#foryou
#health

5 months ago (edited) | [YT] | 3

Lupron Warriors Victims Hub

‪@LupronWarriorsvictimshub‬ channel

💔 How Many People Are Really Affected by Lupron?

Many of us know someone who has taken Lupron (leuprolide) — for prostate cancer, endometriosis, puberty suppression, or other conditions.

While official reports of side effects exist, new data suggests far more people may be affected than previously understood.

Here’s what we know:

In the U.S., over 60,000 adverse events have been officially reported over the last 20 years.

Research shows that only about 5–10% of people who experience side effects actually report them.

That means the true number of affected people in the U.S. could be between 600,000–1.2 million.

If we include Europe, the combined total could realistically be around 1–2 million people who have experienced problems with Lupron.

Support groups (like those run by families and patients) confirm this:

In a 12,000-member group, only 5% had officially reported their issues — yet nearly everyone had been affected in some way.

What does this tell us?
The official numbers only scratch the surface.

Tens or hundreds of thousands of people may be silently struggling.

Reporting your side effects matters — it helps regulators, doctors, and researchers understand the true scale of the problem and puts more scrutiny on the drug.

“Even small actions — like reporting your experience — can make a big difference in protecting thousands of others.”

6 months ago | [YT] | 3

Lupron Warriors Victims Hub

‪@LupronWarriorsvictimshub‬

⚠️THIS IS SOMETHING BIG PHARMA OR FDA DONT WANT YOU TO KNOW! ⚠️

🔊🔊🔊🔊🔊🔊 SHARE 🔊🔊🔊🔊🔊

THIS NOW

Lupron Warriors Victims Hub needs to find someone to help us unseal these documents. 🔑

THIS IS SOMETHING BIG PHARMA OR FDA DONT WANT YOU TO KNOW!

#lupron
#pubertyblockers
#makesastandagainstlupron
#deathtolupron
#fightforjustice
#osteoporosis
#bonedestroyer
#eraserbrain
#chemobrain
#endometriosis
#transgenderreassignment
#prostatecancer
#gnrhagonists
#stoplupron

Music #BassettBlue #Lucidvoltage

youtube.com/shorts/psSv8cTFZ0...

9 months ago | [YT] | 3

Lupron Warriors Victims Hub

 @LupronWarriorsvictimshub 

This is my story as seen on Facebook & Instagram ..

please share so one else has to suffer like me.

My Lupron Story – A Warning, A Cry for Justice, A Voice for the Silenced

My name is Cheryl.
And this is not the end of my story — it’s just another brutal, painful chapter.
I’m sharing this not for sympathy, not for attention, and definitely not for profit.

I tell my story as a warning.
I tell it to guide others.
I tell it to stop even one more woman from being poisoned the way I was.

Years ago, I was prescribed Lupron (Prostap in the UK) to treat Endometriosis — a drug that promised relief but delivered devastation.
What was supposed to be “safe” shattered my life.

💔 Lupron destroyed my body.
💔 Lupron destroyed my health.
💔 Lupron stole my independence.
💔 Lupron even took my smile.

🩺 Here is what I now live with – every single day:

• Bone pain throughout my body

• Legs collapsing, knees buckling with no warning

• Narcolepsy-like blackouts and sudden exhaustion

• Total loss of muscle mass – I can no longer walk

• I am now wheelchair and bedbound

• Constant vomiting and bowel dysfunction

• Chronic swelling and inflammation

• Chemo brain – confusion, memory loss, stuttering

• Visual disturbances and full-body tremors

• Tingling in arms and legs that never stops

• Myalgic Encephalitis – a constant flu-like weakness

• Suicidal thoughts and psychological trauma

• Osteoporosis and fragile bones

• Dramatic weight fluctuations

• Endocrine chaos and total hormonal imbalance

• And worst of all… Lupron destroyed my jaw and gums

→ I have now lost all of my teeth and gums..

→ I cannot chew. I have to have liquidised meals, I can barely speak. I am in constant, unrelenting pain.

I trusted the system. I believed the doctors.
I wanted help for my Endometriosis — not to be chemically crippled and mutilated from the inside out.

But this is the truth that no one tells you:

Lupron doesn’t just hurt — it ruins

So now I speak.
For the women who haven't found their voice yet.
For the ones still being dismissed.
For the lives still at risk.

💛 I speak to warn.
💛 I speak to protect.
💛 I speak because silence is no longer an option.

We have gone through Lawyers, social media newspapers etc but no one will take on Lupron its yhe biggest cash cow there is and they are giving this to children too now. Just think of the devastation that will cause in their undeveloped bodies.

We may not win the war against the drug companies…
But together, we can win battles.
We can raise awareness.
And we can save lives — one story, one voice, one woman at a time.

📢 Please read this. Share this. Let others know.

If someone you love is battling Endometriosis and being offered Lupron or Prostap or any other GnRH agonist— please, beg them to research it first.

Doctors do not always have your best interest at heart.

Profit comes before people!

This is not the end of my story. But it just gets worse.
But it is the truth.
And the suffering Lupron causes…
Never. Truly. Ends.

With love, truth, and fire in my spirit,
– Cheryl Newton 🕊️

#LupronSurvivor #ProstapPoison #LupronStoleMySmile #EndoWarrior #MedicalGaslighting #ThisIsNotRare #StopLupron #ChronicPainIsReal #HormoneHell
#makeastandagainstlupron #deathtolupron

I had prostap. Below is a pic of all the other lupron products in the UK 🇬🇧

* Please Note

If you see documentation referring to Leuprorelin Acetate, Prostap, Lutrate, or Staladex in the UK, it is the same drug class as the US-branded Lupron.

9 months ago | [YT] | 4

Lupron Warriors Victims Hub

 ‪@LupronWarriorsvictimshub‬ ​

www.facebook.com/share/p/14H3Qp53znf/

BONE DESTROYER:

The Invisible Damage That Lasts a Lifetime.

​To all our brave Lupron Warriors, we need to talk about the silent, invisible devastation this drug wreaks on our skeletal system. This is a critical warning we must share to protect everyone considering this toxic treatment.

​Horrifying Fact: Lupron is a Bone Destroyer

​Lupron (and Prostap) works by essentially forcing your body into a rapid, chemical menopause. By creating a severe hypoestrogenic state—a sudden, dramatic drop in estrogen—the drug strips your body of the essential hormones needed to maintain healthy bone tissue.

​This is what happens:

​Rapid Bone Density Loss:

Unlike natural menopause, where bone loss is gradual, Lupron can cause bone mineral density (BMD) to plummet quickly.

​Osteoporosis:

This leads to osteoporosis, turning strong, healthy bone into fragile, porous bone. This is not just an older person's disease; this drug gives it to young women.

​Fractures and Collapse:

The result is a dramatically increased risk of fractures and skeletal damage.

We have countless stories of warriors suffering broken bones, stress fractures, and vertebral collapse from everyday actions.

​The Damage Is Often Irreversible

​The most terrifying truth is that for many survivors, the bone density loss is permanent. While "add-back" therapy is often touted as a protective measure, it is often insufficient to prevent or fully reverse the damage done by the drug's initial impact.

​This isn't a temporary side effect;

it's a crippling, life-long health sentence.
​Our Call to Action

​If you are a Lupron victim, demand regular DEXA scans and consult a specialist who understands drug-induced osteoporosis, not just age-related bone loss.

​If you are a patient being offered this drug, you must understand: You are being asked to sacrifice your long-term skeletal health for temporary relief. The risk does not outweigh the reward.

​Stay strong, Warriors. We will continue to be the voice for the silenced bones.

Cheryl Newton assisted by Husband
J.B Newton

Thank s to Kristy Townsend

Email address on bio

Please share 🙏 so we can beat the algorithms

#LupronHorror #BoneDestroyer #Osteoporosis #PermanentDamage #LupronWarriors #FightForJustice
#makeastandagainstlupron #deathtolupron #pubertyblockers #StopLupron

9 months ago (edited) | [YT] | 2

Lupron Warriors Victims Hub

 ‪@LupronWarriorsvictimshub‬ ​


Thank you for your support so far.

A anonymous story Emailed to us at Lupron Warriors Victims Hub.

Please share and stop this happening to someone else... there are plenty of stories to come sadly, each as horrific as the last.

Please share everywhere!

They do not want these stories out in public. This is the same drug used as puberty blockers for children and the same medication that they use for gender reassignment off label.

I would like to contribute my story to your database/documentation. Please find my experience attached / below. I would like to remain anonymous if possible.

Thank you for your time and support.

*************************************

My Story – Lupron / GnRH Agonist Injury

I am a woman from Serbia (Eastern/Southeastern Europe). In 2022, after surgery for endometriosis, I received a GnRH agonist injection (Triptorelin, equivalent to Lupron) as part of my post-operative treatment.

Before the injection, I was fit and able to manage my daily life despite my pain. But immediately after the injection, my health began to deteriorate rapidly. I experienced worsening pain and neurological symptoms, and within months, I became severely debilitated.

Shortly after, I was diagnosed with a rare, hormone-dependent tumour called angiofibroma in my nasal cavity; a condition extremely rare in women. This strongly suggests that the hormone disruption caused by the GnRH agonist contributed to its development.

From 2022 until the end of 2024, I endured immense suffering and medical gaslighting. What made it even harder was the way doctors responded. Many dismissed or minimized my symptoms. The gynaecologist who recommended the GnRH treatment turned away from me. Instead of support, I faced denial and neglect. No one warned me about the risks beforehand, and no one has taken responsibility for the damage done.

In Serbia, there are no adequate resources or specialists to diagnose small fibre neuropathy (SFN), and most doctors are unfamiliar with this condition. Because of this, I had to travel abroad to get a skin biopsy; a necessary test to confirm the diagnosis. This situation highlights significant weaknesses in the Serbian healthcare system and leaves many patients like me without proper care or answers.

At the end of 2024, I was finally diagnosed abroad with severe and progressive small fibre neuropathy, a condition that causes permanent nerve damage and chronic, excruciating, widespread full-body pain resistant to treatment.

GnRH agonists may affect the body in several ways that could help explain these symptoms:

Suppressing sex hormones such as estrogen and testosterone, which normally protect nerves and reduce inflammation, potentially making small nerve fibres more vulnerable to damage.

Altering immune system function, which may trigger or worsen immune-related nerve damage.

Causing autonomic symptoms such as palpitations, temperature fluctuations, and mood changes; symptoms that overlap with dysautonomia often seen in SFN.

Today, I live with a chronic, severe disability and depend on others for daily activities. Medications provide limited relief but cause side effects such as weight gain, fluid retention, and breathing problems.
I have been left with a severe, irreversible, lifelong illness.

I share my story to warn others, support research, and call for recognition and justice. Nobody should have to suffer like this. Those affected by GnRH agonists deserve to be heard and helped.

*************************************

Thank you for sharing your story and emailing it to us.

If you have a story too please contact us. Links on bio

9 months ago (edited) | [YT] | 2

Lupron Warriors Victims Hub

 @LupronWarriorsvictimshub 

Thank you for subscribing and joining us in our fight to make a stand publicly against Lupron and GnRH agonists.

What Lupron does ...

Lupron is a drug that “shuts down” the hormones that come from our ovaries or testes (like estrogen, progesterone, and testosterone). It does this by overstimulating the brain’s hormone switch (the pituitary) until the switch basically burns out and stops working. Once this happens, the body goes into a state like sudden, extreme menopause or andropause.

This sudden loss of hormones affects almost every system in the body:

Bones and gums become weak and start to waste away.

Brain and nerves suffer, causing depression, anxiety, and brain fog.

Metabolism changes, leading to weight shifts, cholesterol issues, or blood sugar problems.

The immune system can get weaker, so healing takes longer.


To be clear — Lupron doesn’t break or damage DNA directly, like chemotherapy drugs do. Instead, it changes which “instructions” in our DNA get switched on or off. Think of DNA as the book of life: hormones are the bookmarks that tell the body which chapters to read. Lupron rips out those bookmarks, leaving the body confused and unbalanced.

Please share.

This information could save someone's life. This information should be disclosed by the doctors to us before treatment is administered, Why isn't it ? It is because they know how bad the drug is. They just don't care.

9 months ago | [YT] | 1

Lupron Warriors Victims Hub

⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️ ⚠️

 ‪@LupronWarriorsvictimshub‬ ​​

Major Risks Associated with Lupron

​1. Bone Density Loss

​Lupron can cause rapid bone density loss, a condition called osteoporosis. This is a well-known risk, as the drug's mechanism of action reduces estrogen and testosterone, which are critical for maintaining bone health. This can lead to increased risk of fractures and long-term skeletal damage.

​2. Neurological and Cognitive Issues
​Patients have reported a wide range of neurological and cognitive problems, including:

​"Chemo brain," which involves memory loss, confusion, and difficulty concentrating.
​Neuropathy, causing numbness and tingling, especially in the hands and feet.
​Visual disturbances and full-body tremors.

​3. Cardiovascular Problems
​For men taking Lupron for prostate cancer, there is a documented increased risk of heart attack, stroke, and sudden death. While this risk is most clearly stated for men, some women also report cardiovascular issues.

​4. Severe Pain and Musculoskeletal Damage

​A significant number of patients report developing new or worsening pain conditions, such as:
​Widespread joint and muscle pain throughout the body.
​Myalgic Encephalitis (M.E.) and fibromyalgia-like symptoms.
​Loss of muscle mass and strength.
​5. Psychological and Emotional Trauma
​Lupron can have profound effects on mental health, with many patients reporting:

​Severe mood swings, anxiety, and panic attacks.

​Profound depression and, in some cases, suicidal thoughts or attempts.
​Psychological distress that is often dismissed by medical professionals as a side effect of hormone suppression.
​6. Endocrine Chaos and Organ Damage
​By disrupting the body's hormonal balance, Lupron can lead to widespread damage, including:

​Hypothyroidism and other thyroid dysfunctions.
​Adrenal problems.
​Dental problems, including significant jaw and gum damage.
​7. Severe Skin Reactions
​In rare but documented cases, Lupron has been linked to severe and life-threatening skin conditions like Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN), which can be fatal.

Now think, is this right?

MAKE A STAND AGAINST LUPRON!

#poisonedbylupron #lupronwarriors #gnrhagonists #deathtolupron #endometriosis #fibroids #genderreassignmentsurgery #prostatecancer #pcos #precociouspuberty

Please fill in poll on Lupron Warriors Facebook link in bio poll attached to featured section.

⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️⚠️

9 months ago (edited) | [YT] | 3

Lupron Warriors Victims Hub

@LupronWarriorsvictimshub

youtube.com/shorts/v1tNlz3dt0...

Please share to support our fight.

9 months ago (edited) | [YT] | 4