Back for 2024!

Happy New Year! 

First off, I want to let you all know that I am alive and well. It’s been five years since I last posted on my blog. I hope you are all doing well. I’ve missed you! While I wasn’t active on this platform, I was still involved in the Hyperhidrosis community. 

Most recently, I was featured on NPR podcast, Audacious with Chion Wolf as I talked about what living with excessive sweating meant for me. I was so grateful for this opportunity. When I was first approached, I almost said no. It was my gut reaction. It’s hard to talk about Hyperhidrosis publicly. I wasn’t sure I was up for it. But after learning more about the series Chion was doing on rare conditions (although Hyperhidrosis really isn’t as rare as it was once thought to be) I gathered my courage to say yes and help bring Hyperhidrosis awareness and understanding to a larger audience. 

Chion was down to earth and personable. She really wanted to learn about my experiences and her interview questions were so thoughtful. She even stumped me when she asked, “What would you want someone to say to you if they noticed your excessive sweating?” I remember thinking about that question long after the call ended and realizing that I really just wanted my excessive sweating to be invisible. If no one saw it, no one would need to say anything. I’ll just deal with it myself, as long as no one else knows what I’m going through. But Hyperhidrosis has a way of sneaking into our daily social lives. By the way, I don’t think that question made it to the final cut in the podcast. I’d love to hear how you would answer that question. Please let me know if there’s anything someone has said to you that has helped or something you wish they would say.  

Also last year, I had the honor of counseling a branding firm that was going to help relaunch Dove Clinical antiperspirant deodorant. It was a humbling experience to teach Hyperhidrosis from my first hand experience to a group of people trying to gain a deep understanding so that they could communicate it to the world. We talked about the spectrum of Hyperhidrosis and how every person is unique. Products may work differently for each person. Discussion about the Hyperhidrosis spectrum was really interesting to me and a topic I would like to dig more into.

Over the past five years, I have also had meaningful conversations with many of you! Although I wasn’t active on my blog, I had lovely emails, phone calls, and video calls with many of my readers about Hyperhidrosis. If we haven’t met personally, I’d love to hear from you! You can reach me at justalittlesweat@gmail.com

So…five years. 

A lot has changed! I am basically a new person haha. I’m a mom! 

I have two boys – a 4 year old and a 1 ½ year old. My husband and I are living the family dream and we’ll be celebrating our 8 year wedding anniversary in April!

You may be wondering – do my kids have Hyperhidrosis? What is taking care of babies/kids like with excessive sweating? Have you told them you have Hyperhidrosis? Do they even notice you have it? How do you feel about all this? 

Well, so far I am happy to report that I do not notice excessive sweating in my kids’ hands or feet. First of all – yay!!! You may have read about Hyperhidrosis and heredity. It can be hereditary. My aunt on my mom’s side has Hyperhidrosis. Her two boys have it. 

Hyperhidrosis can appear at birth/shortly after birth, or even later in life like during puberty. My parents noticed that I had excessive sweating at least by my first birthday. So, I guess this is to say that I’m not ruling anything out. I’m keeping an attentive, but not obsessive, eye on my kids for excessive sweating. I will say that although not confirmed, my older son does express some cranial excessive sweating symptoms. This is brought on with exercise. He’s an active and athletic kid, so this is all probably normal, but I do notice he’ll be sweating more than the other kids along his hairline, and pretty noticeably too. The good thing is that it has not bothered him once and besides me, I don’t think anyone has said anything about it. The other kids haven’t commented to him about it. 

What’s it like taking care of my kids with sweaty hands? It hasn’t been too much of an issue. Sometimes their clothes will get a little wet from me changing them or holding them, especially when they were babies. Most notably, their little hands can easily escape mine when we’re holding hands to walk across the street. If I’m able to, I ask my oldest to hold on to the stroller instead or hold my husband’s hand if he’s with us. 

I haven’t told my kids that I have Hyperhidrosis or what it is. My oldest might be at a point where I can start that conversation. Where we are right now, they haven’t really noticed. I think it’s just them being young and not aware of it yet. 

I fear the day one of my kids may recoil with disgust if I try to hold their hand in my sweaty own. This is why I need to get ahead of it. I will start speaking out loud about sweat positivity. I want it to be normal in our house. So far, I’ve hinted at it a little – like when it’s bath time after breaking a sweat at the playground. I remember doing a double take when I was talking with my son. I had said something like “we need to wash the sweat away,” but then I caught myself and said, “but sweat is normal and healthy!” Sweat will be a thoughtful topic in our house and an ongoing conversation. I’ll let you know how it goes and please feel free to send any suggestions for talking with kids about sweat. 

As for me, I’m still working from home. I have told others that it’s been my “cure” for Hyperhidrosis. It’s a place where I can manage my own temperature and environment. There are no unexpected handshakes or high fives. I still sweat, but it’s a lot more manageable when I’m in a controlled environment. Outside experiences are a different story. 

I started taking piano lessons. I’ve been taking lessons for a little over a year now. Piano – and most musical instruments – have their challenges as someone with Hyperhidrosis. I am proud of myself for having the courage to start and continue. The lessons are at my house where I can control the temperature. During lessons, I turn my heat down or AC up so I can be cold. Sometimes I am too cold, and worry that my teacher is uncomfortable, but it helps my hands from sweating too much when playing. When my hands are sweating, playing piano is incredibly uncomfortable. It’s a negative cycle physically and mentally. It’s also really not enjoyable if my hands are sweating, so I try to control the temperature and what I’m wearing so that I can get ahead of it as best I can. At times, I’ve had to stop and take a step away to get a towel or run my wrists under cold water. If I’m able to control my sweating with these techniques, which really is more than not (thankfully), I do enjoy playing and plan to continue. 

I’m still fanning my sweaty hands with anything I have on me, wiping them off and holding on to towels. I’m not currently using any treatment. My next trials may be with lotion that helps excessive sweating. Please let me know how you’re coping with Hyperhidrosis and what techniques or products you are using. 

Thank you for reading and finding my blog. I am so humbled that many of you reached out to me over the past five years even when I stopped writing here. Thank you for sharing your stories. I wish you all a happy, healthy, and dry 2024! 

Caryn

My Secret Isn’t So Secret Anymore

For Hyperhidrosis Awareness Month this year, I had the amazing opportunity to share my story of living with Hh on a larger scale. The International Hyperhidrosis Society approached me earlier this year to ask if I would consider being a part of their Awareness Month campaign and tell my #HhStory. Although I am usually pretty secret about my condition, I decided to take the leap and trust that a video like this could help others living with Hh and spread awareness and understanding. It’s always important to me to portray Hh as NOT just a little sweat. The video really captures the struggles I’ve faced and the obstacles I’ve had to overcome to get through each and every day. My story is just one of many from millions of other Hh sufferers all over the world. You are not alone. We are in this together.

So, without further ado, here’s my story.

So, I guess my secret isn’t so secret anymore…and that’s okay.

Thank you to the International Hyperhidrosis Society for this opportunity and to my husband and mom who joined me to share their experiences of having someone with Hh in their lives.

To all my family and friends – thank you for your never-ending love and support ❤

Caryn

November is Hyperhidrosis Awareness Month

I live with Hyperhidrosis in a private way. It is my secret life. My palmar and plantar Hyperhidrosis can be invisible to others. I’ve also become so good at hiding it that there’s a chance that the people I interact with on a daily basis might never even know I have this condition.

I have lived with Hyperhidrosis for 31 years. I am used to this life. But sometimes it doesn’t seem to get any easier. As I sit and write this, I am fanning my hands and soaking the sweat up with paper towels. I am trying to breathe through my discomfort. I am alone in my room, not anxious or nervous about anything, and I’m still struggling just being me.

One of my most successful coping techniques for Hyperhidrosis has been writing about my experiences on this blog. It has helped tremendously getting my thoughts and frustrations out about living with this condition. Another way I cope with Hyperhidrosis, is to tell people in my life about it.

November is Hyperhidrosis Awareness month. It is our second annual month and I am so thankful that this condition has reached the point to have an official month. It is a very big accomplishment in the world of Hyperhidrosis and it’s an exciting time to be a part of it.

I encourage us all living with Hyperhidrosis to get out there and tell someone about this condition and what it means to have it. Not only will telling someone about Hyperhidrosis spread awareness and understanding, it could give you the relief and support you need. For me, telling certain people about my Hyperhidrosis has made my quality of life better.

One really impactful example I have for you happened just last week.

For some backstory, a few years ago, I decided to start mentioning my Hyperhidrosis in my job interviews. I was at the point in my life when I was starting to switch careers and go into Special Education. Hyperhidrosis was my biggest inspiration for my decision, and as scary as it was to talk about, I found it fitting to explain why my life experience has led me to this point.

So, my current boss has known about my Hyperhidrosis since the first day I met her. Since starting this job a year and a half ago, little by little, I explained what living with this condition means to me. I’m thankful I told her about my condition right away because it allowed me to be myself.

I work from home now, which has been a huge help in managing my own room temperature and always having a fan at the ready. But this fall, I have been traveling to the office more frequently. Last week while I was in the office, I was part of a group meeting. The room was very warm and I knew immediately that I was going to have an issue with my hands sweating. I had a paper towel with me, but I was worried it was not going to be enough. At any other job, I would have just dealt with it and melted away, not being able to focus on the meeting at all. I’ve had those meetings where all I could concentrate on was my sweat and how uncomfortable I was – and how nervous I was for my secret to be discovered.

My boss was part of this meeting and I asked if I could bring a fan in to help with my Hyperhidrosis. She didn’t question or give it a second thought. I brought the fan in and positioned it at my hands. I don’t think that anyone else in the meeting thought it was weird or different. It may seem small, but this fan helped my hands stop sweating and allowed me to focus on the meeting. It made me feel normal.

It’s funny how something so small like this can be so impactful to me. I think of it and smile even now. One person who knew about my Hyperhidrosis made me feel comfortable enough to bring in an accommodation for myself – something I knew would help me. Telling people about my Hyperhidrosis has made my life better.

That is just one example of how Hyperhidrosis awareness has helped me personally. I believe that Hyperhidrosis awareness and understanding will make the world a better place for us. We are all in this together. This month, I encourage you to tell someone about your Hyperhidrosis journey. Be strong and have courage. I know you can do it. I can’t wait to hear your stories!

Happy Hyperhidrosis Awareness Month,

Caryn