MEET THE TEAM
Thanai Caesar
Thanai Caesar (she/her) has always been passionate about advocacy, creativity, and building spaces where people feel seen and supported. With a background in youth development, social impact, and community engagement, she’s spent years working with marginalized communities—helping young people navigate challenges, find their voice, and access the support they deserve.
Now, as the founder of This Won’t End Me, Thanai is channeling that same passion into the fight for endometriosis awareness. Living with the condition herself, she understands firsthand the frustration of being unheard and dismissed. Through creative initiatives like guided art and sip experiences, storytelling projects, and awareness-driven events, she’s on a mission to make endometriosis seen—because no one should have to fight alone.
Currently based in London, Thanai’s life is a blend of creativity, advocacy, and connection. When she’s not working on TWEM, she’s curating the perfect playlist for every mood, getting lost in a new book, or mapping out her next adventure. And if she’s off the grid? She’s probably somewhere in nature, soaking up the quiet before diving into her next big project.
Founder & CEO
Amanda Della Giustina
Amanda Della Giustina (she/her) is an enthusiastic and curious person who is constantly interested in learning something different. Her favorite hobbies involve things that bring her relaxation to calm down her busy mind, like handicraft, painting, and being in contact with animals and nature. She also loves travelling, and the best place for her to be is a tropical beach, enjoying sunny days and the sounds of crashing waves.
With a Honours Bachelor's and a Master's in Nutrition as well as a PhD in Health Sciences with a focus on Neuroscience, Amanda used her own experience as a person with endometriosis, her knowledge as a registered dietitian and her research skills to increase awareness of this condition and demystify misconceptions about diet and endometriosis.
Based in Ottawa, Amanda spends her time with her husband and their dog Ella watching movies and TV series, tasting new craft beers, enjoying the good weather outdoors, baking, and trying to get back on painting canvases.
Head of Research & Advocacy
Paige Marsh (she/her) is a thoughtful advocate who brings both professional insight and lived experience to her work in menstrual and reproductive health. Diagnosed with stage 4 endometriosis and adenomyosis, Paige has spent years navigating the complexities of the Canadian healthcare system. Her journey has shaped her passion for education, patient support, and community advocacy.
With a background working within healthcare, Paige has a unique understanding of where the system succeeds and where it falls short. Her personal challenges have strengthened her commitment to helping others feel seen, validated, and better equipped to advocate for themselves.
Paige is based in Canada and continues to stay closely connected to the endometriosis community through peer support, education, and awareness initiatives. Outside of her advocacy work, she embraces her artistic side. She loves painting, music, creative expression, and simple joys like salty snacks and quality time with loved ones.
Director of Health Strategy & Community Liaison
Paige Marsh
Mehreen Rashid (she/her) is based in Ottawa, Ontario. She holds a Bachelor of Science in Neuroscience and Mental Health and is currently researching ovarian cancer-associated cachexia as a Master’s student. Mehreen is keen to apply her science background towards advancing social change and health equity.
She hopes to bring the perspectives shaped by her South Asian and Muslim identity, along with her experience conducting community-based research with Indigenous youth, to help foster a culturally sensitive approach to endometriosis and menstrual-health advocacy. Through TWEM, Mehreen aims to make complex health science accessible, inclusive, and useful for those seeking clarity about their reproductive health diagnoses.
Outside of work, Mehreen admittedly spends too much time on Reddit and YouTube, but she also loves disconnecting from the internet to work out at the gym, knit and crochet, read fiction books, and take plenty of naps.
TWEM Volunteer – Research & Community Engagement
Mehreen Rashid
Keneisha Williams (she/her) is a leader, community builder, and advocate with more than 14 years of experience across the events and impact sector. As the founder of the Black in Events Network and Director of Programs at CILAR, she works to create equitable spaces and opportunities for underserved communities. Her work has been recognized globally, including features in Forbes and multiple industry awards.
Keneisha believes she has lived with endometriosis for most of her life, only learning this much later. Navigating pain in silence has shaped her commitment to visibility, education, and compassionate advocacy. She is passionate about breaking misconceptions and supporting those whose experiences have been overlooked.
Based in Toronto, Keneisha loves cycling to soca, finding comfort in a stack of pillows, and treating herself to ice cream. She unwinds by binge watching classic shows and reading. She is honoured to join TWEM’s board and help strengthen awareness and support for the endometriosis community.
Director of Advocacy & Awareness
Keneisha Williams
Rachel Albert (she/her) is a proud member of the Métis Nation of Manitoba and brings a thoughtful blend of scientific knowledge, cultural awareness, and creativity to her work at TWEM. Based in Montréal, she holds academic backgrounds in biomedical health and psychology, and has worked alongside Indigenous women to improve access to care and strengthen health outcomes in communities facing systemic barriers.
Raised in a big busy family, Rachel learned early the importance of connection, balance, and joyful living. Creative expression became a central part of her self-care, leading her to film photography and baking. She believes art can be both healing and preventive and is passionate about weaving creativity into wellness and community care.
Outside of her advocacy work, Rachel finds peace outdoors, especially running with her Border Collie, Monte. She loves spicy snacks, pretzels dipped in chocolate, and music that fits her season of life. She is honoured to join TWEM as Director of Arts and Health and is committed to helping build creative, accessible, and supportive spaces for the endometriosis community.
Director of Arts and Health
Rachel Albert
Laura MacDonald (she/her) has been obsessed with stories for as long as she can remember—whether it’s a novel, a poem, or a really well-told personal anecdote, she loves them all. With a Bachelor of Arts in English Literature and a Master of Arts in Children’s Literature, she’s spent years making books and storytelling her whole vibe. She turned her love of words into a career in publishing before jumping into the world of marketing and social media.
Laura is an advocate for endometriosis and mental health awareness, using her voice to share experiences, support others, and break stigmas. She believes in the power of open conversations, self-care, and making sure no one feels alone in their journey—because every story, especially the hard ones, deserves to be heard.
Based in Toronto, Laura’s days are a mix of creativity and connection. She spends her time crafting content, scrolling social media (for work and for fun), reading, and binging Gilmore Girls (again). When she’s not doing any of those things, she’s perfecting her status as Dog Mom and Cool Aunt.
Advisory Board Member
Laura MacDonald
Mia Caven (she/her) is a London based author, influencer, and social media strategist who brings creativity, humour, and a love of storytelling to her work. At 23, she has built a vibrant online presence rooted in books, films, music, and community. Her Greek heritage and passion for communication shape much of her creative approach.
Mia was diagnosed with PCOS at 14 and endometriosis at 18. Both conditions have deeply impacted her life, especially during the years when she was hospitalised almost weekly. She often describes the pill as life saving and works to challenge misconceptions about chronic illness, including the belief that endometriosis is not a disability. Her lived experience fuels her commitment to supporting others through honest, accessible content.
Outside of her work, Mia finds comfort in warm, cosy routines. Her flare up essentials include Pepto Bismol, painkillers, a hot water bottle, her Oodie, and a weighted blanket, usually paired with chocolate and an episode of Smosh or Bob’s Burgers. Mia is excited to help shape TWEM’s digital storytelling and strengthen our online community.