New Product Review: Carpe Antiperspirant Hand Lotion

Hi all,

I was recently introduced to a brand new product called Carpe. It is an antiperspirant hand lotion for sweaty hands! I received a sample of this product in the mail a few weeks ago and immediately felt results. I was recommending this product the day I tried it and I am happy to write a review for my blog!

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What’s great about this product is that it is a non-invasive solution for sweaty hands. It’s something you can take on the go and use as you need it. It can be used daily and will keep your hands sweat-free for hours (4+).

Carpe is an opaque white lotion with a pleasant scent. It smells like eucalyptus and mint. One of my first observations when opening the lotion was that it had a mild scent and didn’t smell like medicine. I feel like a lot of similar lotions don’t have as nice of smell.

Carpe should be applied to clean and dry hands.  You apply a pea-sized amount to your palms and rub together for 15 seconds. The lotion is pretty tacky when going on, but it disappears within the 15 seconds and leaves no residue. I was able to resume typing on my computer keyboard after the 15 seconds and did not need to rinse my hands. The lotion sunk in for a while and my hands were dry.

I find this product especially good for people with HH who have not yet explored other treatment options, children with HH, and people who have occasionally sweaty hands.  For people who  haven’t explored any other treatment options, a lotion is the perfect way to start. Carpe is sold over the counter and is very affordable. One tube costs $14.95 and will last for 1.5 months. For children with HH, I think a lotion is absolutely the way to go. Since HH is hereditary, I’ve given a lot of thought to how I will approach HH with my future children if they get my HH gene. I would not want to put them through Iontophoresis or give them Robinol until much later. Since the lotion is topical and can be reapplied throughout the day, it’s a great tool for kids at school and during after-school activities. Same goes for people who do not have HH, but have occasionally sweaty hands. The lotion is great for them because they won’t need the more intense treatments like Ionotphoresis or Robinol.

Last week, I had the pleasure of speaking with the co-creater of Carpe, David Spratte. He started working on this product when he was a senior in high school because of his frustration with sweaty hands. Now, a junior at the University of North Carolina, his product is on sale and ready to help the HH community and more! I was quite impressed to learn how much David had accomplished at such a young age and I was inspired by his story. I love that this product was created by someone who was struggling with sweaty hands himself.  He took his experiences and knowledge of sweaty hands to create a product he knew would work. David uses Carpe every day.

Something unique and special about Carpe is that long-term sweat reduction is possible if it is used regularly. David says that based on efficacy studies, 60% sweat reduction is achieved long-term if used once a day. Carpe is FDA-certified and non-irritating, so it is safe to use daily. Additionally, I was very happy to learn from David that Carpe also works on sweaty feet and foreheads. If you use the product on your feet, wait 10-15 minutes before putting on a shoe or sock to ensure the lotion sinks in.

Last, I would like to mention how much I love the name of this product. Carpe is short for Carpe Diem – Sieze the Day. David uses ‘Sieze the Moment’ on his packaging. Having this association with the lotion completely correlates to what I mention in my blog: Don’t let HH limit you and what you want to do in life. This lotion can provide  much needed relief as you face challenging and potentially embarrassing daily situations. Whether it be a handshake or highfive, playing sports or musical instruments, or simply taking a test with paper and pencil, Carpe can be a solution for you.

Please let me know if you have any questions about Carpe and please check out their website!

Thanks for reading,

Caryn

 

My Experience on Dating Someone with Hyperhidrosis

Happy New Year!

My boyfriend had been talking about writing a guest blog post for Just A Little Sweat for a while, and on Christmas day, he surprised me with his beautiful and inspiring take on his experience dating someone with Hyperhidrosis. His words mean a lot to me and show me how supportive he is of me and my blog. He also shows support for you, my readers, and that is just as important to me.

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It’s probably not Hyperhidrosis. Caryn says it might be food induced HH but I’m not entirely convinced. Sweat pours down my forehead when I eat spicy food. I don’t eat it very often but when I do, I constantly have to wipe my face from becoming such a mess. It’s not really a hindrance though. I can easily stop eating spicy food (not that easy to give up chicken wings). I could just eat it in the privacy of my own home so people don’t see the sweat on my head. If only it was that easy for Caryn.

I don’t claim to understand Hyperhidrosis. But as silly as it sounds, it’s my small attempt in putting myself inside her shoes. (Which is a lot to ask for since she has a lot of shoes.)

I never heard of Hyperhidrosis until I started dating Caryn. And as hard as it must have been for her to tell me, I feel awful that I don’t remember the first time she told me about her condition. I probably didn’t even ‘get’  how big of a deal it was when she told me. But what know now is how much it affects her in everyday life and how she’s managed to overcome those struggles. Yes, there are some days that are easier than others. Her hands get more wet when she’s anxious and since she’s even more anxious when her hands are wet, the situation practically snowballs from there. But despite all of those things, she reels in those feelings, adapts and keeps moving forward.

It wasn’t always easy for her though. Well, I can’t say it was ever easy for her at all. There were times where I simply didn’t “get it” to completely help her in some situations. But what really helps her is having solace to all those who read this blog. Sharing her experiences with all of you has such a positive impact in her life and outlook on HH. Before this blog, she was afraid of letting anybody know about her condition. But after writing a couple of entries, she became braver and more inspired. While she didn’t tell every stranger out in the street (it doesn’t stop her from talking about it out in the subway though), she managed to muster up the courage to tell her closest friends. They’ve all been supportive and I feel like it gave Caryn the relief she always wanted.

Coming from someone who doesn’t have it, I can’t even begin to imagine how hard it must be to tell someone about HH. Caryn once gave me hand lotion that stayed wet for about 5 minutes. It was definitely uncomfortable and it’s probably the closest experience I could equate it to. But what I can say if you’re someone who hasn’t told your closest friends and family, mustering up the courage to tell them offers more support than what you thought you had. In Caryn’s case, she was so worried telling some of her friends that when she finally told them recently, she forgot that some of them already knew. She didn’t realize she had the support all along and she just needed to open up to people.

My friend once told me one of the best pieces of advice I’ve heard: “People aren’t judging you as much as you think they are.” It’s slightly different than ‘stop worrying about what others think’ because this outlook shows that people aren’t as negative as you think. If shaking someone’s hand makes you embarrassed with what they think, chances are they probably didn’t think much of it. If you think people can tell your hand is getting sweaty, chances are most people aren’t even paying attention to it.

If HH is preventing you from getting close with anyone, remember that HH doesn’t define you. Just like how I said people aren’t judging you as much as you think they are, that special someone will get past it, accept it and love you for who you are.

In the beginning of our relationship, Caryn kept asking me if her hands grossed me out. All I would have to do is hold her hand tighter to show that spending time with her was more important than her hands. Besides, who else could laugh with me when I sweat profusely while eating chicken wings?

Irish Dancing Update

Hi All,

Sorry I’ve been quiet lately! I was on a family vacation on a cruise to the Western Caribbean! It was a fantastic trip and I was sad that it had to end.

Now that I’m back, I’ve been catching up with emails and work. Slowly but surely, I’ll get back in the swing of things.

I wanted to write a quick update about the team Irish step dancing class I took.

It was really fun, but I won’t be continuing. I was so anxious during class because my fingers were sweating like crazy and I had to hold hands with the other girls. We were all sweating a ton, (and it didn’t help that we were in a classroom with no air conditioning or windows!!) but I was still too self-conscious about my hands. I couldn’t relax and have fun. I was checking the clock every 5 minutes to see when class would end. It’s unfortunate because the dance part is actually pretty cool, and apparently I am needed for a competing team.

No one said anything about my hands or gave me funny looks, but I still couldn’t get past it. I’m sure you all know how I feel!

Anyway, I’m still taking 2 hours of Irish dance a week (soft and hard shoe) and love it. I’m lucky I found a dance where I can keep my hands to myself, down at my sides.

I wish HH didn’t have to be my deciding factor with something I love, but I guess I’d prefer to not be anxious and self-conscious so that’s how this one has to go.

My next goal with my partially dry hands- learn knitting! 🙂

Thanks for reading and enjoy the end of summer!

Caryn

More Irish Dancing!

Hi All,

I’ve been taking Irish step dance classes every week now since February and I continue to love it more and more. I even added on a hard shoe class, so now I’m taking 2 hours of Irish step a week!

Recently, my teacher invited me to a free introductory class for team Irish Dancing called Ceili. This looks really fun, but it features hand-holding with your team while you dance.

Tomorrow is the class and what a great time it is to test out my “new hands”!

I never would have considered this type of dancing if my hands were still sweating profusely- although I have to say I’m still pretty nervous! I just hope my sometimes clammy fingers don’t get in the way!

I have finished the initial treatments with the Iontophoresis device, but Bill Schuler from the R.A. Fischer company suggests I still treat my hands and feet once a week. After a while, I can gradually increase the time between treatments. So, maybe I will do a treatment tonight if I have time, just to be safe for tomorrow!

Check out the type of dance I’m going to be doing! Looks fun, right? Wish me luck!

Thanks for reading,
Caryn

He Said, She Said

Today I thought I would give you a little glimpse into some of my conversations with Francis!

While hanging out together with my cat:

Francis: Why is Grace’s tail wet?

Me: Because her tail is resting on my foot.

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Near the end of a long run together:

Francis: My feet are all sweaty in my shoes. Do you get that too?

Me: Oh, I can’t tell the difference anymore – sweat is my normal.

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While holding hands at my friend’s wedding:

Me: Sorry my hands are so wet.

Francis: Every time you say that, I’m just going to hold your hand tighter.

Happy Reading,

Caryn

Photo Booth from Friend's Wedding

Me and Francis- Photobooth photos from my friend’s wedding this weekend!

 

Luann Comic- Hyperhidrosis

Hi All,

This weekend, the popular Luann comic strip mentioned Hyperhidrosis! Thank you to my Aunt (who also has HH) for bringing this comic strip to my attention!

I am so happy and surprised that HH is mentioned, and by name too! I feel like this comic strip just made HH history. So many people read the Luann comic. It was my favorite comic strip growing up!

Greg Evans (Luann creator) was just able to reach thousands about HH. I am so curious what the response is! Thank you!

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All best,

Caryn

I was featured by the International Hyperhidrosis Society!

I wanted to share some exciting news!

Today I was featured in an article in the International Hyperhidrosis Society eNewsletter! Sharing my HH story with others has been a really rewarding experience and I thank the International Hyperhidrosis Society for giving me the opportunity to share with so many of you!

Please click HERE to read the article.

The International Hyperhidrosis Society is a fantastic support site for people with Hyperhidrosis. They share a wealth of information including HH education, tips for coping, stories from others with HH, deals and discounts on sweat-helping products, research studies, treatment information, a comprehensive search for doctors, ways to get involved and more! I have had a really positive experience communicating with them in preparation for this article and always find their website helpful. Please check it out!

All best, and stay tuned for an entry about the Iontophoresis machine that was just donated to me from R.A. Fischer iontophoresis devices !

Caryn