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!

tube

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

 

Advertisements

Lessons for my high school self

I’ve had HH for almost 28 years now and I think I’ve learned a thing
or two. If I were to travel to the past and meet up with my high
school self, I would share what I have learned.

I approach my high school self. I am in the band room, my second home.
I know that at this point in my life I was slowly starting to tell my
closest friends and teachers about HH. I had a love for playing the
flute, but struggled with my hot, sweaty hands. I also had
difficulties in school, taking tests and writing essays with paper and
pen.

“You inspire me because you are brave. You have talked about HH openly
with your closest friends. You give me hope that people are accepting
and understanding. I hope that you continue to share your stories
about HH with those closest to you.”

I know that once I hit college, I started hiding my HH again. I barely
told anyone about it until my junior or senior year. I can only
think of 5 people I told in college- none were teachers. I think
telling people about it and talking openly, even with a few people, is
so helpful and a real coping mechanism.

“People aren’t paying attention to you and your HH as much as you
think. You may feel that your sweat is obvious and feel anxious about
it, but chances are other people really have no idea and can’t tell.”

People with HH are amazing at hiding it even though it might not feel
like it. I went through college and grad school without any teachers
knowing I had it. I just took a deep breath and did what needed to be done.
Easier said than done, but I’ve learned to at least try to stop worrying about
what people think.

“Don’t give up and follow your passions.”

I didn’t let HH hold me back. I found ways to modify the activities I
loved or talked to someone about it for advice. I have played the flute
for 19 years. All I needed was a fan, a hugely absorbent towel, great
musician friends, and sometimes a tub of cold water to stand in.
I’ve learned to make do with what I have.

“Although it might sound cliche, I promise that it does get better.”

Since graduating high school, I’ve had 10 more years of experience with
HH. I’ve learned different coping techniques, tried new treatments, and
helped the HH community grow. I know there is help and support out there
and have seen it first hand.

I am proud of my journey with HH and am happy that I have learned with it
and from it. I know that I can’t really share what I have learned with my high
school self, but I can share it with you.

How would life be different without HH?

Sometimes I wonder how my life would be different without Hyperhidrosis.

I wouldn’t have to worry about the little things like greeting someone new with a handshake or writing with a pen on paper. I wouldn’t have to worry about holding a newspaper, either deteriorating the paper with sweat or coming away with print on my hands. I wouldn’t have to worry about holding onto a subway rail, taking change back from a cashier, accidentally touching someone’s arm with a cold and wet hand, or leaving an embarrassing hand print behind. I wouldn’t have grown up with other kids not wanting to hold my hand during square dancing in gym class or as their line partner to go to the lunch room. I wouldn’t have had to avoid certain things growing up like playing clapping games with my friends or braiding each others’ hair.

Sometimes I think about life without HH and how normal it would have been. I wouldn’t have had to be anxious about my underarm sweat stains reaching the hem of my shirt, or going to the nurse’s office several times a week just to avoid my embarrassment. Maybe I would have continued taking gymnastics lessons. Maybe I would have joined clogging dance with my sister where there is a lot of hand holding.

Life without HH seems so normal and it’s something I’ve envied for a long time. But thinking of life without HH sure has a lot of maybe’s and  what if’s.

What I do know is that I really can’t imagine my life without HH. It is a part of me and it is a part of who I have become. Without HH, I would have taken all of the above for granted. I feel fortunate that I don’t.

HH has made me a stronger person. It has given me pride in accomplishing even the smallest of tasks. HH has also made me an observer and someone who cares a lot. It has given me an understanding and appreciation for all people.

So how would life be different without HH? I’m not quite sure.
But I think life with HH has made it better.

 

Will my kids have HH?

I’m often asked if I’m worried about passing Hyperhidrosis on to my kids. HH runs in my family, so I know that there is a pretty good chance of passing it on.

I’ve given this a lot of thought for many years. In the past, I was concerned about passing it on because I know the difficulties of HH first hand and I don’t want my children to suffer through it. Children especially have trouble with HH in school and social activities. Years ago, a part of me thought my future children would be angry with me for passing it on.

However, after more thought and discussion with family members, I can say that although there is a high chance of passing HH on to my kids, it doesn’t deter me from wanting to have my own children. I have always wanted to be a mom.

In fact, if my children are born with HH, I will be incredibly well-equipped and be their biggest support. I will be able to share coping techniques and be knowledgeable about treatments. I will be a huge resource and am confident I will be able to help them.

 

Dry Grip No Sweat Lotion Interview

A couple of months ago, I suggested some over the counter treatment options for my younger cousin who also has HH. He is in middle school now and has had HH for his whole life. Out of the options I suggested, he chose to start with a lotion called Dry Grip No Sweat.

He is having great success with the product so I thought it would be a fun idea to interview him about it and his experiences with HH. A big thank you goes out to him for helping me with this post!

Here’s what he had to say:

Caryn: What do you think the hardest part of having HH is?
Cousin:
I think the hardest part of HH is having to deal with it all the time. I mean, unless it was the winter, usually my hands were sweaty. I personally had a really tough time getting used to it, and even now. I just want it to be done with.

Caryn: What difficulties do/did you find in school with HH?
Cousin: It is quite hard to cope with it at school, like when you accidentally touch someone, or when you have to pass something around and you get it really sweaty, or trying to hold a pencil but your hand keeps slipping off, it becomes annoying, and sometimes embarrassing.

Caryn: Do/did you have any difficulties with HH outside of school?
Cousin: I absolutely had troubles with it outside of school. Trying to do sporting activities was a bust, I couldn’t really touch anyone, and eventually I started to get stressed. Stressed that it wouldn’t go a way, no matter what I tried to do about it.

Caryn: How often do you apply the lotion and how does it make your hands feel?
Cousin: I apply the lotion every morning on weekdays, and at first it feels like glue because it’s sticky, but that only last for about 5 seconds. Other than that, I don’t feel it whatsoever, and often forget I put it on that morning.

Caryn: How successful do you think it has been?
Cousin: I believe it has worked quite well, but I like to think of it as brushing your teeth. It’ll only work if you consistently do it, as for most things. Now even though I’m not applying it on weekends, I just do that so my hands don’t get used to it, so I can use the same lotion for longer.

Caryn: How has your day to day life changed since using the lotion?
Cousin: My day to day life has changed for the better, no doubt about it. I hardly notice my hands sweating, and usually that’s after gym in school. I no longer have the problems I used to have in school, and I much enjoy it. It really stinks to have HH, but if you don’t do anything about it, it won’t go away.

Thanks for reading,

Caryn

 

 

Adaptation

When I decided to go back to school for Special Education, I chose a
focus area of visual impairment. I didn’t have much experience with
people with visual impairments prior to choosing this specialization,
but knew they live an adapted way of life. They use Braille instead of
print, canes and guide dogs to get around, and digital audio output to
do work on their computers.

As someone living with HH, I can say that I also live an adapted life.
I wear certain clothes that won’t soak through, I use a towel under my
hand to write with pen and paper, and I keep a fan going wherever
possible to help dry my hands.

Although we share a need for adaptation, we can both live satisfying
and happy lives. This is what inspired me to want to learn more.

I am specifically learning how to be a teacher of students with visual
impairments (TVI). So far, I’ve learned a lot about different
techniques to use.  Since students with visual impairments cannot
observe what people are doing around them, a TVI can model various
actions by using a technique called “hand-over-hand” or
“hand-under-hand”. This involves the teacher to put his or her hand on
top or underneath the student’s hand while demonstrating a movement
like cutting food or spreading peanut butter on bread. This technique
is proven to be very effective.

Again and again, I learned how the TVI interacts with their students
using their hands.

Now, do you see an issue with this? I have palmar HH. What would a
student think if my wet hands?

Although not ideal, this fact does not deter me from this field. I
still want to  continue learning and help people.

Also, my hands have been relatively dry lately. I’ve been having
success with Iontophoresis and hope it continues. I feel like I can
also wear gloves in the classroom if I start having an issue.

From one adaptation to another, we can all help each other. I’m looking
forward to learning even more!

Iontophoresis with Baking Soda

I’ve been using my Iontophoresis machine once a week for many months now with great success! However, in early October, I noticed my hands were starting to sweat a little more than usual. I was really concerned about this and felt like I might have formed an immunity to the machine.

To help, I started doing treatments more than once per week. At one point, I was using it three or four times in one week. Still nothing was working.

I remembered one of my readers from NYC had said that the water here is pretty soft and sometimes doesn’t work well with Iontophoresis. Until October, I hadn’t had an issue with the water or effectiveness of the machine. I was told that adding baking soda to the water can help by adding minerals and electrolytes.

After adding baking soda to my treatments, I noticed a significant difference. My palm sweating is now more under control. Adding baking soda does make the treatments a little more uncomfortable. It irritates my skin a little more, but it’s worth it!

Sweathelp.org has an article dedicated to Iontophoresis. In addition to baking soda, it says you can even try crushing Robinol tablets in the water.

I’ll let you know if the baking soda continues to work!