by My Life as a Puddle | Jun 2, 2025 | HealtheVoices, Hyperhidrosis
I’m thrilled to announce that I have been selected to attend the 2025 HealtheVoices Patient Advocacy Conference. After years of applying, hyperhidrosis will finally be represented at this conference by advocates, for advocates. Watch my video update below or on...
by My Life as a Puddle | Mar 28, 2025 | Hyperhidrosis
I’m honored to be featured on Sweaty Girl Society as a Hyperhidrosis Hero for International Women’s Day. You can also meet two of my fellow sweaty friends if you visit Karina’s blog. Here’s my interview excerpt. What led you to become a...
by My Life as a Puddle | Mar 5, 2025 | Hyperhidrosis
Greetings, my fellow sweaty friends. It’s been awhile, hasn’t it? I’m hoping to blog more on a regular basis soon now that I’ve completed treatment for thyroid cancer, enrolled my son in preschool several days a week, and am finally coming up...
by My Life as a Puddle | May 10, 2024 | Hyperhidrosis
Do you or your child suffer from hyperhidrosis (excessive sweating) and it’s affecting your education in the classroom? If so, you may be able to request what is called a 504 for accommodations (in the U.S.) or an Educational Health Care Plan (EHCP in England)....
by My Life as a Puddle | Apr 28, 2024 | Hyperhidrosis, Social Health Awards
The #SocialHealthAwards celebrate patient leaders who positively impact the lives of patients and caregivers. I’m honored to announce that I have been nominated this year for Advocacy Trailblazer and Lifetime Achievement Award! I’d be so grateful if you considered...