by My Life as a Puddle | Jul 5, 2021 | Hyperhidrosis
Are you struggling to find a hyperhidrosis doctor? What about treatments for hyperhidrosis? In the following video, I discuss the difficulties when it comes to finding medical providers and access to treatment options for hyperhidrosis. Prefer to read the transcript...
by My Life as a Puddle | Jan 24, 2021 | Guest Post, Hyperhidrosis
Please welcome Melanie from the United States to the sweaty tribe. She is a brave soul with hyperhidrosis who has chosen to share her sweaty story on mylifeasapuddle.com. Going public about our sweaty secret can be scary, but using our sweaty voices is the bravest...
by My Life as a Puddle | Nov 8, 2020 | Hyperhidrosis, Hyperhidrosis Awareness Month
I’m thrilled to bring you a new video interview. I had the pleasure of speaking with Lisa J. Pieretti, Executive Director & Co-Founder of the International Hyperhidrosis Society (IHhS). She’s a notoriously busy woman who runs this small but mighty...
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...