May 2014 archive

So “Let’s Talk About Lyme”…

The “Let’s Talk About Lyme” awareness event was a huge success, and there was standing room only in the Community center! I met so many incredible patients, physicians and community members, although it was hard to move around the packed house (no complaints!). I learned so much from the incredible speakers, particularly Gwen Barlee’s detailed presentation on the Lyme disease situation in Canada, and the other Lyme patients & families whose powerful stories touched the audience and brought home why we were all there. It’s hard to get that many people with chronic illnesses in one place, so Lyme disease awareness events are usually have a ‘family reunion’ feel to them :).

I’m the one in the green speaking, with the fabulous Gwen Barlee at the podium
I feel our personal stories are the most powerful tool in a patient-cum-activist’s arsenal. You can read about how Lyme disease in on the rise and that there are all these awful symptoms, but it’s much easier to imagine yourself in a patients place, than hear faceless statistics. I’d encourage everyone to share their story with everyone you can; your words just might save a life. Below is a copy of the speech I gave at the event (just imagine me talking eagerly with an exclamation point after pretty much every sentence, and it’ll be like you’re right there!)

“Let’s Talk About Lyme” May 10, 2014 @ Fairfield Community Center Welcome everyone. My name is Nicole Bottles, and I’m 21. When I became mysteriously ill at 15, I imagined I would keep going to specialists, peeling back layers of symptoms, until they discovered what was wrong, and I’d get back to my ‘usual’ life; Dr. House style. That was 7 years ago, and I still am waiting for a diagnosis in Canada.  After going downhill daily, in 2008 we turned to our southern neighbors for help and saved my life. I learned I not only had Lyme disease, but 3 other life-threatening tick-borne infections. 

giant clay ticks to make with kids!

I was a hobbit on an epic quest; to regain my health, of course, but also to ensure no one else suffer from what should have been a simple infection, curable in it’s early stages with $100 of antibiotics. An infection which in it’s late stages has no cure.  Instead we have spent tens-of-thousands of dollars on my on-going treatment. I’ve made great progress with my treatment, but still have a long way to go. As a young girl, I’d always wanted to ‘change the world’, but I had no idea how. I decided to embrace this opportunity in disguise, and “make lyme-aid”. That means educating, and advocating for change, without letting a chronic illness keep me from experiencing all life’s wonderfulness.  For 2 weeks we discussed challenges Lyme patient’s experience with 80 MP’s & Senators in Ottawa. It opened my eyes to the power of legislation, compassion and human connection. Many already knew about Lyme disease, and all quickly understood the gravity of our situation and wanted to help.  Since becoming ill, I’ve wanted to give back to organizations that have helped me immensely.  Channeling my passion for creativity, I’ve been able to financially support the incredible work of CanLyme & the Dr. Murakami Center for Lyme by knitting IV covers and creating original photography cards.  On difficult days, I remind myself “to dwell in possibility”, as Emily Dickinson wrote. On the good ones, I keep moving forward, optimistic that if we believe we have the power to create change, it will happen.  (STAND)  So “Let’s Talk About Lyme”.  Let’s spread the facts.  Let’s engage our politicians.  Let’s keep talking to our doctors.  Let’s keep the conversation alive.  Because the conversation can only stop when Lyme disease is cured, and prevention becomes second nature to all Canadians. ~ *rolls off of pillbox* I am so lucky to have the support and love of friends. I could never thank them enough! One of my best friends, Morri, came to the event and later created this amazing video, sharing what she learned (omg. the gal is a sponge! such accurate information too! high five!), and also how to create a fabulous “Lyme-Look” eyeshadow. So cool. Check it out the video on her Youtube Channel!

Let’s Talk About Lyme ~ Awareness Event

If you hike, bike, garden, play outdoors with pets or kids, this event is for you!


I’m really pumped to invite you all to our local Lyme Disease Awareness month event: Let’s Talk About Lyme. If you call Victoria, BC, Canada home, or are close by or visiting we would love to share an afternoon of uplifting stories, hope and awareness. This is the event I wish I’d gone to before I got sick! 
We have some amazing speakers lined up (The MP’s Elizabeth May & Murray Rankin, and Jim Wilson of CanLyme will be there! And some seriously cool activists – like Gwen Barlee…and Lyme disease patients. I will be speaking as well!). 


Saturday, May 10th from 12:00 pm- 3:00 pm
At the Fairfield Community Place, 1335 Thurlow Road, Victoria, BC Canada (behind Moss St. Market!)

Invite your friends, family and neighbours and local groups. Check out our Facebook Event, and share and invite to your heart’s content!


Want to help out? We’re looking for volunteers to help set up & take-down, and help with kids craft (we’re making modelling clay ticks! and doing a faux-tick drag for kids…and there is a colouring table…just saying…it’ll be a blast.). If you’d like to help out, please email me for more information @ bitemeback@live.com.


feel free to share the poster with friends, family, neighbours, co-workers…everyone. let’s stay safe this tick season.

Lyme-infected ticks are here on Vancouver Island! Join us for an afternoon awareness & prevention event featuring awesome children’s activities, amazing guest speakers, prevention and awareness booths and videos, and speak with local health care practitioners.


See you on on the 10th of May!


Ps: Visit the Victoria Lyme Disease Awareness & Support Group’s website at: www.LymeVI.ca

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