Helen Quayle, the CEO of LaserHQ, is no stranger to advocating for important health issues, and her recent invitation to Parliament for an exclusive event further underscores her commitment to supporting the Endometriosis Foundation. As March marks Endometriosis Awareness Month, Helen’s attendance at the Endometriosis and Reproductive Health: Fair and Inclusive Care campaign launch is a poignant reminder of the ongoing battle for better healthcare for those living with endometriosis.
The event, held at the prestigious Jubilee Room in the Houses of Parliament on March 6th, 2025, was an incredible opportunity to highlight both the personal and systemic challenges faced by individuals living with endometriosis. With attendees from across the healthcare, political, and advocacy sectors, the event set the stage for crucial conversations around improving healthcare practices, reducing waiting times, and ensuring that patients receive fair, inclusive care.
Helen Quayle, who has been dedicated to raising awareness and making a difference for individuals impacted by endometriosis, was particularly moved by the discussions that took place throughout the day. The event included thought-provoking panels and speeches, focusing on the urgent need for better education, mental health support, and improved fertility care for those living with the condition. As a strong supporter of the Endometriosis Foundation, Helen has been instrumental in driving forward initiatives aimed at advancing care and research into this often-overlooked condition.
A Personal Journey of Advocacy
Helen’s involvement in the fight for better endometriosis care is not just professional—it’s personal. Four years ago, Helen underwent her own surgery to treat endometriosis. Her experience navigating the complexities of diagnosis, treatment, and recovery deeply shaped her commitment to supporting the cause. She understands firsthand the physical and emotional toll this condition can have on those living with it, which fuels her passion for advocating for better care.
Her continued advocacy for the Endometriosis Foundation is a testament to her belief that awareness and action can bring about real change. By sharing her own story, Helen hopes to inspire others to join the fight for better care and resources, and to ensure that no one has to navigate the challenges of endometriosis alone.
Endometriosis Awareness Month: A Time for Action
Helen’s presence at this event is especially significant as it coincides with Endometriosis Awareness Month, a time dedicated to raising awareness about the condition and advocating for better treatment and research funding. The campaign launch at Parliament was a pivotal moment in this mission, bringing together key policymakers, healthcare professionals, and patients to drive change.
The discussions held during the event centred on the urgent need for inclusive care, especially when it comes to addressing the fertility challenges faced by those living with endometriosis. It was a powerful reminder of how far we still have to go in ensuring that people affected by this condition receive the care and attention they deserve.
Helen Quayle’s Continued Commitment to Advocacy
Helen’s ongoing work with the Endometriosis Foundation is a reflection of her personal and professional dedication to improving reproductive health care. Through her role at LaserHQ, she has helped amplify the voices of those affected by endometriosis, using her platform to foster greater awareness and to drive positive change in healthcare policies.
The Endometriosis and Reproductive Health: Fair and Inclusive Care campaign is an initiative that Helen fully supports, knowing that better care and research are vital for improving the lives of those living with endometriosis. Her participation in the parliamentary event was an opportunity to contribute to discussions on practical solutions and to be a part of a collective effort to make meaningful change.
A Shared Mission for Change
As Helen’s journey proves, advocacy is not just about attending events or supporting campaigns—it’s about making a lasting impact in the lives of individuals who are affected by conditions like endometriosis. The Parliamentary event on March 6th was an important milestone in the ongoing fight for fair and inclusive care for those living with this condition. Helen’s continued dedication to this cause, both personally and professionally, helps to keep the conversation going and reminds us all of the importance of pushing for better healthcare policies and practices.
For those who couldn’t attend, the event offered valuable insights and a shared commitment to improving the lives of people living with endometriosis. With Helen Quayle and many others leading the charge, we can be hopeful that change is on the horizon.
Let’s continue to raise our voices for better care, increased research funding, and a brighter future for those living with endometriosis. Together, we can make a real difference.
To find out further information and ways to get involved, please visit https://www.theendometriosisfoundation.org/
