Why Join the CKOS Network?
If you’ve been exploring the CKOS website, you might not yet know about our Network—a welcoming community for people with smell loss. The Network is designed to connect you with others who understand your experience, provide support, and share practical advice.
I’m Chrissi Kelly, founder of CKOS, and I’d like to invite you to join this unique community. Whether you’ve lost your sense of smell due to COVID-19, a head injury, or another cause, the Network is here to guide and support you.
Getting Started in the CKOS Network
Once you join the Network, you’ll have access to a vibrant community space filled with resources, conversations, and shared experiences. On the main page, you’ll find four years’ worth of posts covering topics such as parosmia, smell training, and coping strategies. You can use the search icon at the top of the page to dive into specific subjects or scroll through recent discussions to see what’s on people’s minds.
Don’t be shy—introducing yourself is a great way to get involved. Post your story, ask questions, or join ongoing conversations. The Network is a judgment-free zone where we encourage everyone to participate and share what’s on their mind.
What’s Inside the CKOS Network?
1. Monthly Zoom Drop-Ins
I host monthly Zoom sessions where members of the Network can meet, share their stories, and hear from others. These sessions are a chance to connect with people who truly understand what you’re going through. While every person’s smell loss journey is different, we all experience the emotional ups and downs that often come with it.
2. Free Online Courses
I also run free, two-hour online courses tailored to the needs of people with smell loss. Whether you’re looking to understand parosmia, benefit from smell training, or manage the emotional impact of sensory changes, these sessions are packed with practical advice. Check the Network for details on upcoming courses.
3. A Supportive Community
Joining the CKOS Network means becoming part of a community that truly gets it. Smell loss affects more than just your ability to smell—the impact on mental health is one of the most underrated aspects of what we are going through, as well as the effect on our relationships and overall quality of life. We get you! Here, you’ll find understanding, encouragement, and real solutions to help you navigate these challenges.
Helpful Resources to Explore
If you’re not ready to join the Network just yet, the CKOS blog is a great place to start. Here are a few articles that might address your questions:
You’ve lost your sense of smell from having Covid, and you are still not better?
Not again! What to do if you catch Covid a second (or third) time
New Swedish study examines the social impact of smell loss after Covid-19
How to benefit from smell training
Parosmia: understanding it and helping yourself
These posts cover topics ranging from the social effects of smell loss to actionable steps you can take to support your recovery.
Why Community Matters
Together, we’re building a community that understands, supports, and uplifts. By sharing our stories and experiences, we create a space where everyone feels seen and supported—no matter where you are on your smell loss journey.
We’re so glad you’re here and can’t wait for you to become part of our supportive community.
