The Seasons Collective is a non-profit organization that brings together people living with PCOS/PMOS and their supporters. We nurture connection through educational and creative workshops, curated gatherings, and reflective sessions.
Embracing the changing seasons
The Seasons Collective is a reflection of how our bodies and lives move through different seasons. From the foods we eat to the relationships we hold close, each season invites gentle adaptation from within ourselves. How might we thrive in each season?
Here, you’ll find seasonal practices, gentle conversations, events and shared reflections that help you connect with your PMOS/PCOS journey and with others in meaningful ways. Wherever you are in your journey, you belong here.
How might we celebrate seasons of joy, courage, resilience and hope?
Could social connection be just as essential to our health as nutrition or exercise?
You are invited!
This collective is for:
🌿 Individuals with PCOS/PMOS who are looking for community and sharing resources.
🌻 Supporters and caregivers who want to learn and be part of the conversation.
💜 Anyone curious about how we can build spaces of collective healing.
We are based in Toronto, Canada, but the spirit of this collective extends beyond geography. You are welcome here. Join us at one of our upcoming events to learn more about this community and become a part of this collective.
Note: This space is not intended to provide medical advice, diagnosis, or treatment. I am not a clinician or healthcare provider, and the information shared here is for community support and educational purposes only. Please consult a qualified healthcare professional for medical concerns.
Thriving with PMOS: Finding strength in social relationships
Hi, I’m Krutika Galgalikar, a Designer and Facilitator based in Toronto, Canada.
My life changed 16 years ago when I first heard the acronym PCOS—Polycystic Ovary Syndrome. PCOS is a hormonal, metabolic, and reproductive condition with no known cause and no cure. Since my diagnosis in 2010, I’ve been on a journey of understanding my body, reclaiming my voice, and becoming a patient advocate seeking deeper conversations around care, community, and recovery.
In 2026, PCOS was renamed to PMOS (Polyendocrine Metabolic Ovarian Syndrome) to better reflect the complexity of the condition. While this change is an important step forward, I also recognize that for many of us, PCOS is more than a medical term; it has been part of our identities, our stories, and our advocacy for years, sometimes decades.
Like many patient advocates, I am still adapting to this change. Language shapes how we understand ourselves, and a new name can bring up mixed emotions alongside hope for progress. As medical spaces begin to embrace PMOS, communities will need time to navigate what this change means for our identities, our experiences, and the movement we have built together. I’m learning alongside you.
The idea for this collective was born from the support I received from my friends, family, and partner. They made space for conversations about PCOS, took the initiative to learn more, and supported me through lifestyle changes that made a meaningful difference. Their care showed me what becomes possible when we center curiosity, connection, and community in our recovery.
Through this collective, I hope to reimagine what healing can look like for people living with PMOS/PCOS; one rooted not only in treatment, but also in relationships, belonging, and shared understanding.
You can learn more about my PCOS journey here.



