B.C. woman speaks out about living with rare, stigmatizing genetic condition


A Port Moody, B.C., woman is speaking out about a rare and stigmatizing genetic condition in the hopes of raising awareness.

Kirsten Anne was diagnosed with neurofibromatosis when she was only two years old.

“So, I don’t really know what it is like to not have this,” she told Global News.

Neurofibromatosis, or NF, Type One, affects one in every 2,500 Canadians. It is a rare genetic disorder that causes the uncontrollable growth of non-cancerous tumours on the nerves.

“It can also impact your hearing and vision, you can have scoliosis, bone deformities, airway blockages, you are at higher risk for certain cancers like breast cancer,” Anne explained to Global News. “And because it is so individualized, it does impact everybody differently.”

In her case, her tumours are concentrated on her back and torso.

Story continues below advertisement

Growing up, Anne said the physical differences were hard to explain and hard to hide.

Receive the latest medical news and health information delivered to you every Sunday.

Get weekly health news

Receive the latest medical news and health information delivered to you every Sunday.

“As a child going through that and being called names and other awful things, that does also stick with you,” she said.


Click to play video: 'BC denies funding for drug to help treat rare blood disorder'


BC denies funding for drug to help treat rare blood disorder


However, Anne is now taking those experiences and channelling them into her art, while advocating for others navigating the disorder.


She has toured elementary schools, teaching children about acceptance and empathy, as part of an educational puppet troup.

“My ultimate goal one day is to have an NF puppet show, so I can educate people,” she said.

“As a puppeteer, I find that even adults — it’s just easier to reach them with any sort of message with a puppet. It’s non-threatening, it’s just a little bit easier to digest.”

Story continues below advertisement

May is also Neurofibromatosis Awareness Month, which helps start the conversation about improving care and quality of life for those navigating a diagnosis.

“It does require a multi-disciplinary clinic,” Dr. Sarah Lapointe said.

“And there are a lot of trials out there in the pipeline to, you know, have hope that we can manage this syndrome and this condition, every day. So, yes, I think the future is bright.”

Anne said she hopes her message allows her to take centre stage.

“I want to be a voice for them and to uplift them, so they know that they aren’t going through this alone,” she said.

&copy 2026 Global News, a division of Corus Entertainment Inc.



Source link

  • Related Posts

    SpaceX to reward Elon Musk if he gets 1 million people living on Mars

    In January, the board granted Musk one billion performance-based restricted Class B shares split into 15 equal tranches. To get the full award, the company will need to have achieved…

    University of Alberta’s Abby Guezen, Ryder Rattee sweep 2026 U Sports awards – Edmonton

    By Staff The Canadian Press Posted May 20, 2026 9:09 pm 1 min read Descrease article font size Increase article font size The University of Alberta swept the U Sports…

    Leave a Reply

    Your email address will not be published. Required fields are marked *

    You Missed

    Famously secret about its finances, SpaceX opens its books for the first time

    Famously secret about its finances, SpaceX opens its books for the first time

    Fashion’s Brand Management Evolution: Cavalli Deal and Authentic IPO Buzz

    Fashion’s Brand Management Evolution: Cavalli Deal and Authentic IPO Buzz

    News of U.S. Indictment Slow to Reach Cubans Waiting for a Breakthrough

    News of U.S. Indictment Slow to Reach Cubans Waiting for a Breakthrough

    Canada Gazette – Part I, February 15, 2020, Vol. 154, No. 7

    ValOre Metals Announces Non-Brokered Convertible Debenture Financing of up to CAD$2 Million

    SpaceX to reward Elon Musk if he gets 1 million people living on Mars