My Anosmia Stories

My Anosmia Stories: Life Without Smell

I used to not tell anyone about having anosmia and living with no sense of smell. Fortunately, I’ve switched my way of thinking. Now I am an open book! This page is very special to me, as I’ve outlined a couple of my personal stories about my experience living as someone who can’t smell. I welcome you to read on! Click On Each Pic For Each Of My Stories.

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The Girl Who Cant Smell On The Web!


The information contained in my blog posts, stories, memes, webcomics, science articles, drawings and future content, is not intended nor implied to be a substitute for professional medical advice, it is provided for educational and entertainment purposes only.

By accessing this site, you assume full responsibility for how you choose to use this information. My website,’s purpose is to share my OWN personal experience growing up with congenital anosmia. Not as a guide as to how anosmics in general, live their own lives.

Always seek the advice of your physician or other qualified healthcare provider before starting any new treatment or discontinuing an existing treatment. Talk with your healthcare provider about any questions you may have regarding a medical condition.

Nothing contained in these topics is intended to be used for medical diagnosis or treatment.

The Girl Who Can't Smell Show Podcast Now Available

I’m THRILLED to have my own podcast! On my show, you’ll be able to listen in on my personal stories, tips and rants about what it’s like living with anosmia. Also, I’ve recorded all of my previously published articles, so you can listen to them while on the go!