Stop trials of puberty blockers on children

The Issue

Puberty is a critical time in the development of a child, encompassing not just physical growth but emotional and psychological maturity as well. The use of puberty blockers, medications that delay the changes associated with puberty, has been a growing practice, yet the long-term effects remain largely unknown. Despite this uncertainty, these drugs are being trialed on children, a vulnerable population who cannot fully comprehend or consent to the potential lifelong impacts of such a decision.

It's crucial to acknowledge that while some advocate for the use of puberty blockers as a means to ease gender dysphoria, we must also consider the profound implications of interfering with a child's natural development. The Food and Drug Administration (FDA) has not approved puberty blockers specifically for the purpose of gender transition, and existing studies on their safety are limited, leaving a significant gap in our understanding of their long-term risks, which may include impacts on bone density, future fertility, and psychological health.

Moreover, children are not developmentally equipped to provide informed consent. Their capacity to evaluate the risks and considered outcomes of such medical decisions is limited. By allowing trials of these drugs on children, we are essentially experimenting with their futures without fully understanding the consequences.

We urge policymakers, medical professionals, and regulatory agencies to halt the trials of puberty blockers on children until comprehensive, evidence-based studies are available to demonstrate their safety and long-term impact. It is only fair to demand a standard of care that prioritizes the well-being and future health of our children.

Together, we can ensure that our children are protected from unproven and potentially harmful medical interventions. Please join us in signing this petition to put a stop to these trials and advocate for safe, evidence-based healthcare solutions for all children.

3

The Issue

Puberty is a critical time in the development of a child, encompassing not just physical growth but emotional and psychological maturity as well. The use of puberty blockers, medications that delay the changes associated with puberty, has been a growing practice, yet the long-term effects remain largely unknown. Despite this uncertainty, these drugs are being trialed on children, a vulnerable population who cannot fully comprehend or consent to the potential lifelong impacts of such a decision.

It's crucial to acknowledge that while some advocate for the use of puberty blockers as a means to ease gender dysphoria, we must also consider the profound implications of interfering with a child's natural development. The Food and Drug Administration (FDA) has not approved puberty blockers specifically for the purpose of gender transition, and existing studies on their safety are limited, leaving a significant gap in our understanding of their long-term risks, which may include impacts on bone density, future fertility, and psychological health.

Moreover, children are not developmentally equipped to provide informed consent. Their capacity to evaluate the risks and considered outcomes of such medical decisions is limited. By allowing trials of these drugs on children, we are essentially experimenting with their futures without fully understanding the consequences.

We urge policymakers, medical professionals, and regulatory agencies to halt the trials of puberty blockers on children until comprehensive, evidence-based studies are available to demonstrate their safety and long-term impact. It is only fair to demand a standard of care that prioritizes the well-being and future health of our children.

Together, we can ensure that our children are protected from unproven and potentially harmful medical interventions. Please join us in signing this petition to put a stop to these trials and advocate for safe, evidence-based healthcare solutions for all children.

Petition updates

Share this petition

Petition created on 23 November 2025