To My Lupus Community: I’m So Glad We Had This Time Together

To My Lupus Community: I’m So Glad We Had This Time Together
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As a kid, I was a big Carol Burnett fan. At the end of her variety show, she would sing a song called “I’m So Glad We Had This Time Together.” When it was over, she would tug on her ear.

Today, I am tugging on my ear and writing to say farewell. In February 2016, I was diagnosed with lupus, and I was clueless about so much. I really thought I was going to overpower my illness.

Shortly after that, I was offered the opportunity to write for Lupus News Today. I have learned a lot, shared a lot, and been truly embraced by the audience here over the years. It’s only fitting that I’m saying goodbye to you all in the month of February, having grown wiser about so much when it comes to battling my own body.

I have also learned from your battles, muddled through because of your encouragement, and come to really appreciate the community here. You will surely be missed.

Although I am leaving Lupus News Today, I will still be on social media if you want to keep up with my crazy life with lupus. I talk about my life abroad with lupus on my YouTube channel, and often share my art projects on my Instagram.

I hope that you will continue to be a part of my community by visiting me in those places. The community I have come to know over the past five years at Lupus News Today has been nothing short of wonderful.

Everyone I’ve worked with has been wonderful, and I will miss them all. I am so happy I was offered a way to share my highs and lows in a truly supportive environment. As I move on, it is with a light heart and happy thoughts. Thank you for reading and commenting over the years.

I wish you all peace, love, high energy, and low pain. Farewell, my friends.

***

Note: Lupus News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Lupus News Today, or its parent company, BioNews, and are intended to spark discussion about issues pertaining to lupus.

Kellie is a lupus warrior who spends her time teaching many about the incurable disease she battles with a smile on her face. She travels the world, writes articles, has an active YouTube channel and creates coloring and activity books for both adults and children. She is known as Queen Bubbly Bee because no matter what is going on with her body, she always manages to find the silver lining.
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Kellie is a lupus warrior who spends her time teaching many about the incurable disease she battles with a smile on her face. She travels the world, writes articles, has an active YouTube channel and creates coloring and activity books for both adults and children. She is known as Queen Bubbly Bee because no matter what is going on with her body, she always manages to find the silver lining.

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