by My Life as a Puddle | Jul 19, 2020 | Hyperhidrosis
Update: I’ve been nominated for three awards now. It’s that time of year again! Endorsements are now open for the 2020 WEGO Health Awards. But you only have until July 31 to help me grow hyperhidrosis hope and awareness one drop at a time. How can you...
by My Life as a Puddle | Nov 2, 2019 | Hyperhidrosis, Hyperhidrosis Awareness Month
Please welcome my very special friend Jess from Liverpool, England. She is six years old and has hyperhidrosis, and she might be the youngest hyperhidrosis advocate in the world. Jess’ parents, Hayley and Kevin, submitted their story to my blog last year. Right...
by My Life as a Puddle | Feb 5, 2019 | Hyperhidrosis
A few months ago, I had what Oprah would call “a full-circle moment.” I found myself on a jet plane headed to Cranbury, New Jersey, and we all know how much fun traveling with hyperhidrosis is. Not. I went to New Jersey for less than 24 hours for a very...
by My Life as a Puddle | Dec 15, 2018 | Hyperhidrosis
To wrap up the second annual Hyperhidrosis Awareness Month in November, I sat down with Lilly Stairs, Head of Patient Advocacy at Clara Health, to record a podcast all about hyperhidrosis. Find out what the most embarrassing thing I’ve ever talked about with...
by My Life as a Puddle | Nov 12, 2018 | Hyperhidrosis
Confession: Sometimes I cuss like a sailor. Just ask my cousin Jim. I debated whether to use the title of this post for awhile, but then I decided NOPE, I’m not going to filter myself here. Because this word implies that hyperhidrosis (Hh) is serious (which it...