The effects of Botox can typically last 7-9 months, but I’ve heard it takes longer to build up to that amount of relief (ie, one must have multiple treatments for it to last that long). After my first Botox treatment in April, the effects lasted a short 3 weeks. But let me tell you, it was the best 3 weeks of my life. It was like I forgot I had ever suffered from HH! My confidence was through the roof, and I felt so much less inhibited and held back because of my condition.
But then my sweating started coming back, and I also noticed that while my hands were dry, it was like my body was made to sweat, so it was just going to sweat elsewhere instead. So now my back sweats way worse than it ever did, and I am super self-conscious about my clothing and stuff when I can feel it happening. The Botox has completely worn off now and my body has basically given me the “eff you” gesture. I thought it would be the answer to my prayers, and it was, even if it was only for that short time. I can’t help thinking that maybe my Botox experience was just God’s way of giving me a glimpse of what heaven will be like for me when I get there. I imagine my heaven to be about 65 degrees all the time, with a gentle breeze always encircling me for comfort.
Maybe I am supposed to be going through this here on earth so that I can start to become a voice for people who suffer from this or any other condition who feel like pariahs and like they’ll never fit in. Perhaps this is what musical artist Laura Story calls a blessing in disguise. I can’t help but think that my HH, in combination with me being a Highly Sensitive Person (HSP), allows me to be more compassionate and empathetic with people from all walks of life. I feel like sometimes I’m on a different wavelength and can pick up on the intricacies of people and their moods and feelings, and because I’ve felt like a freak in my own body for most of my life, I am better able to interact with the world in a more loving way. I’m kind of a contemplative person who likes to ruminate on things like this.
While I’m glad I did the Botox, I don’t know if I’ll ever do it again, not just because of the cost but because of the other areas where it caused me to sweat. I am not willing to hope I can get my insurance to cover it and then end up with a bill for more than $1000! However, I know that some insurance companies will cover it, so practice due diligence if you are considering Botox and have health insurance. For more information about insurance coverage, visit the “insurance tools” page on the International Hyperhidrosis Society’s website, www.sweathelp.org. To be a patient volunteer was a great opportunity for me to be exposed to treatment, but it was a catalyst for so many other things for which I am even more grateful! It pushed me the extra step I needed to actually start blogging about my HH, and now I’m volunteering for the IHHS in my local area area and will be contributing to one of their upcoming newsletters, too.
Once I accepted myself for who I truly am, and felt the acceptance from the IHHS and the doctors and nurses who treated me, my soul just opened up. I can share my story with the world now. While the Botox didn’t work for very long in my own body, I certainly want others to try it for themselves since everyone’s body is different and may respond differently. There is hope for treating and finding a cure for hyperhidrosis. Don’t get discouraged if a treatment doesn’t work for you.
My dermatologist called me back the other day to tell me that my biopsy was benign (read the post here if you missed my dermatologist experience) and that after doing some research on the Catapres (clonidine is the generic name) tablets, he called in a Rx for me. I still have to pick it up and try it out, but I’m glad he took the time to do the research. The Catapres is similar to the active ingredient in the Transderm Scop (scopolamine) patches I had used , so hopefully I will get some good results.
My apologies for not blogging this last week. While I would like to be blogging every other day or so, sometimes I just am not able to do so. But life is full of enough could’ve’s, should’ve’s, and would’ve’s, so I am not going to feel bad for not always blogging on a regular basis. However, if you have bookmarked my site and checked back for new posts, thank you for taking the time to do so. I value you as a reader of my blog.
Until next time,
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