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 | Dec 18, 2020 | Clinical Trials, Hyperhidrosis
This piece has been entered in the Patients Have Power Writing Contest run by Clara Health and designed to raise awareness about clinical trials. As a member of their Breakthrough Crew, I am passionate about this cause and hope it will help raise much-needed awareness...
by My Life as a Puddle | Nov 29, 2020 | Hyperhidrosis, Hyperhidrosis Awareness Month, Hyperhidrosis Conference
If you missed the Hyperhidrosis Conference last weekend, you can still watch my session below. I moderated session 2 and spoke with Courtney, a fellow hyperhidrosis patient and advocate from London, Ontario. Watch Session 2: Hyperhidrosis and Mental Health Maria...
by My Life as a Puddle | Nov 15, 2020 | Hyperhidrosis, Hyperhidrosis Awareness Month
Is your hyperhidrosis causing you to have anxiety, negative thoughts, or depression? Dr. Claudia Luiz, a psychoanalyst in New York, helps us unpack the mental aspect of living with an excessive sweating condition and what we can do to help ourselves cope. Scroll down...
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...