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> <channel><title>Comments on: Sympathetic Nervous System</title> <atom:link href="http://www.myexcessivesweating.com/sympathetic-nervous-system.php/feed" rel="self" type="application/rss+xml" /><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php</link> <description>Experiences and tips for those suffering from excessive sweating</description> <lastBuildDate>Fri, 03 Feb 2012 22:11:07 +0000</lastBuildDate> <sy:updatePeriod>hourly</sy:updatePeriod> <sy:updateFrequency>1</sy:updateFrequency> <item><title>By: sy</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-8141</link> <dc:creator>sy</dc:creator> <pubDate>Sun, 11 Sep 2011 05:59:54 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-8141</guid> <description>I&#039;ve suffered with excessive sweating since I was a teen.  As I age it is getting worse. My scalp, face, armpits, chest and groin sweat to the point that it is clearly visible through my clothing. Nothing sexier than a sweaty crotch huh? I&#039;m glad to know I&#039;m not alone but I would like to know if anyone has any info on the teas. I won&#039;t go the mediinal route because it seems to have too many side effect and I know the deodorants cause me skin irritation. Anyone have any real answers?</description> <content:encoded><![CDATA[<p>I&#8217;ve suffered with excessive sweating since I was a teen.  As I age it is getting worse. My scalp, face, armpits, chest and groin sweat to the point that it is clearly visible through my clothing. Nothing sexier than a sweaty crotch huh? I&#8217;m glad to know I&#8217;m not alone but I would like to know if anyone has any info on the teas. I won&#8217;t go the mediinal route because it seems to have too many side effect and I know the deodorants cause me skin irritation. Anyone have any real answers?</p> ]]></content:encoded> </item> <item><title>By: HH Mom</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-6662</link> <dc:creator>HH Mom</dc:creator> <pubDate>Tue, 12 Apr 2011 20:54:15 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-6662</guid> <description>My 18 year old son takes glycopyrrolate (Robinul) 6 mg each morning and another 2 mg in the evening if necessary. He also uses Drysol anti-perspirant. He finds this combo of treatments very effective for hyperhidrosis which for him was severe. We decided against surgery since many people online said CS was a problem. My son hasn&#039;t tried botox and probably won&#039;t since his current treatment is working well, is non-invasive, minimal side effects in his case, and very inexpensive (generic drug copays via health insurance).  He used iontophoresis in the past (Drionic) but found it too time-consuming for a teenager and the other methods work better for him.</description> <content:encoded><![CDATA[<p>My 18 year old son takes glycopyrrolate (Robinul) 6 mg each morning and another 2 mg in the evening if necessary. He also uses Drysol anti-perspirant. He finds this combo of treatments very effective for hyperhidrosis which for him was severe. We decided against surgery since many people online said CS was a problem. My son hasn&#8217;t tried botox and probably won&#8217;t since his current treatment is working well, is non-invasive, minimal side effects in his case, and very inexpensive (generic drug copays via health insurance).  He used iontophoresis in the past (Drionic) but found it too time-consuming for a teenager and the other methods work better for him.</p> ]]></content:encoded> </item> <item><title>By: T.C.</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-5921</link> <dc:creator>T.C.</dc:creator> <pubDate>Fri, 21 Jan 2011 00:37:50 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-5921</guid> <description>I have been cursed with this problem all my life. I am 39. I have have it bad, as it affects, my underarms, my hands, my feet, my head (yes my head, when I wake up in the morning, my hair looks like I just got out of the shower), and the most embarrassing place, my butt!
I have tried clinical deodorants, loose clothing, wicking socks and clothing, botox, pills (herbal), and a few other things but none worked completely. My Insurance was HMO and would not cover the pills that drys out everything but I was finally able to switch to a &quot;real&quot; Doctor so hopefully that will change.
In the meantime I wanted to try the tea. All of the responses are about people buying it but no one has posted back stating if it worked. Would like to no how it is working for everyone.
Thanks,
T.C.</description> <content:encoded><![CDATA[<p>I have been cursed with this problem all my life. I am 39. I have have it bad, as it affects, my underarms, my hands, my feet, my head (yes my head, when I wake up in the morning, my hair looks like I just got out of the shower), and the most embarrassing place, my butt!</p><p>I have tried clinical deodorants, loose clothing, wicking socks and clothing, botox, pills (herbal), and a few other things but none worked completely. My Insurance was HMO and would not cover the pills that drys out everything but I was finally able to switch to a &#8220;real&#8221; Doctor so hopefully that will change.</p><p>In the meantime I wanted to try the tea. All of the responses are about people buying it but no one has posted back stating if it worked. Would like to no how it is working for everyone.</p><p>Thanks,</p><p>T.C.</p> ]]></content:encoded> </item> <item><title>By: Phil Foster</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-4204</link> <dc:creator>Phil Foster</dc:creator> <pubDate>Thu, 09 Dec 2010 01:11:46 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-4204</guid> <description>I&#039;m very relieved to see so many others going through what I&#039;ve been going through as well for the past 22 years of my life.  My armpits are completely fine, its my hands and feet that give me a problem.  I&#039;m not as concerned with my feet as I just wear moisture wicking socks to help stray away the sweat, but my hands are always sweaty at inopportune times.
I see on here that to some it happens all the time, and to others not so much.  For me it is definitely a physiological problem because I will get nervous out of nowhere for very simple things not to my own wishing of course.  It is only when I am completely confident that my hands are not sweaty...and even then they can get sweaty in a matter of seconds if I am caught off guard.
I&#039;m ordering the herbal tea tonight and hope very much so that it has a positive effect!</description> <content:encoded><![CDATA[<p>I&#8217;m very relieved to see so many others going through what I&#8217;ve been going through as well for the past 22 years of my life.  My armpits are completely fine, its my hands and feet that give me a problem.  I&#8217;m not as concerned with my feet as I just wear moisture wicking socks to help stray away the sweat, but my hands are always sweaty at inopportune times.</p><p>I see on here that to some it happens all the time, and to others not so much.  For me it is definitely a physiological problem because I will get nervous out of nowhere for very simple things not to my own wishing of course.  It is only when I am completely confident that my hands are not sweaty&#8230;and even then they can get sweaty in a matter of seconds if I am caught off guard.</p><p>I&#8217;m ordering the herbal tea tonight and hope very much so that it has a positive effect!</p> ]]></content:encoded> </item> <item><title>By: Hope</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-3518</link> <dc:creator>Hope</dc:creator> <pubDate>Thu, 28 Oct 2010 16:45:10 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-3518</guid> <description>I have been suffering from the same problem ( hands and feet) for as long as I can remember. It usually only happens when I&#039;m nervous and at the most inopportune times. So I finally decided to try and find a cure. But before I try ets I&#039;m gonna give hushed sea a shot. I ordered it this past Monday and it came in last night. About 3 days for delivery.
I drank a glass as soon as I got it and one this morning. I don&#039;t see any results thus far but I know it takes a little while. The first glass was hard to drink on account of it tasting like crap. The second went easier cause I chugged it. I&#039;m wondering if drinking it iced with a little flavoring takes away from its medicinal qualities. Does any body know? Or have any suggestions? My hh isn&#039;t too severe but has enough of an impact to effect my personal and professional life. thanks for the support. I&#039;ll keep ya posted</description> <content:encoded><![CDATA[<p>I have been suffering from the same problem ( hands and feet) for as long as I can remember. It usually only happens when I&#8217;m nervous and at the most inopportune times. So I finally decided to try and find a cure. But before I try ets I&#8217;m gonna give hushed sea a shot. I ordered it this past Monday and it came in last night. About 3 days for delivery.</p><p>I drank a glass as soon as I got it and one this morning. I don&#8217;t see any results thus far but I know it takes a little while. The first glass was hard to drink on account of it tasting like crap. The second went easier cause I chugged it. I&#8217;m wondering if drinking it iced with a little flavoring takes away from its medicinal qualities. Does any body know? Or have any suggestions? My hh isn&#8217;t too severe but has enough of an impact to effect my personal and professional life. thanks for the support. I&#8217;ll keep ya posted</p> ]]></content:encoded> </item> <item><title>By: rohan</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-3120</link> <dc:creator>rohan</dc:creator> <pubDate>Sun, 24 Oct 2010 03:11:28 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-3120</guid> <description>Hi All,
Give it a shot for Classical homeopathic tretament.May be it can help.Its a long process but will work.Hope for the best.</description> <content:encoded><![CDATA[<p>Hi All,<br
/> Give it a shot for Classical homeopathic tretament.May be it can help.Its a long process but will work.Hope for the best.</p> ]]></content:encoded> </item> <item><title>By: ana</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-1039</link> <dc:creator>ana</dc:creator> <pubDate>Sat, 07 Aug 2010 16:04:12 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-1039</guid> <description>Hi kiesha,
I have this terrible problem, please where did you buy the Hushed sea tea?
This is an emergency!!!!!
ana</description> <content:encoded><![CDATA[<p>Hi kiesha,</p><p>I have this terrible problem, please where did you buy the Hushed sea tea?</p><p>This is an emergency!!!!!</p><p>ana</p> ]]></content:encoded> </item> <item><title>By: Hate_ETS</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-1022</link> <dc:creator>Hate_ETS</dc:creator> <pubDate>Sat, 31 Jul 2010 08:07:03 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-1022</guid> <description>7-30-10: I had ETS surgery six years ago due to facial blushing.
&lt;strong&gt;&lt;strong&gt;This surgery was the WORST decision in my life. PLEASE – anyone considering it, DON’T DO IT!! &lt;/strong&gt;&lt;/strong&gt;
The CS side effects will make your life miserable. My energy level and endurance have gone down, and I feel I have became fatigue a lot more often. I used to be an avid athlete (primarily roller skater). My days of skating were over soon after surgery. I’d soak in sweat just 15 minutes into my rigid work out.  I switched to ice skating – after all, the temperature in ice rink is cool, and I get to cover my body with a jacket (another layer to cover the damn embarrassing sweating).
I eventually started having chest pain (I guess the cold sweat-soaked cloth?), so I stopped ice skating as well. Since then, I have lost most of my muscle tone and gained weight. Note I was in excellent shape prior the ETS surgery. My closet had also gone through a major change – all skin tight and/or light color clothing had to go (well, at least my sister was thrilled).
Over the past few years, I have learned to monitor the weather on daily basis, planning ahead what clothes to wear each day. I am lucky to work in AC’d office environment (even tho stressful and uncomfortable situations make me break down in sweat, primarily on my chest and back). I always liked black color, but now I am &quot;forced&quot; to wear it most of the times (it does cover the sweat the best).
I started working out again, but I must wear a tight shirt with a lose one on the top. I used to love dancing – cannot do it all that much anymore. Walk outside on a sunny day had become very dreadful for me, etc, etc, etc….!!
My fiancee is very understanding and tolerates my problem. We are getting married and our big day is being planned for April. I always envisioned June/July wedding, but that would be a nightmare. This weekend I will be shopping for that special wedding dress. I am becoming extremely anxious, because, under normal circumstances I’d love to have a strapless dress with my back exposed – well, this is not possible because my back gets moist when I get even just a little nervous. So, once again, I gotta hide and cover myself. I hate this soooo much. I wish I could wake up out of this nightmare…
So today I heard about the Hushed Sea Herbal tea. &quot;The herbs in Hushed Sea (Valarian Root, Astragalus, St. John’s Wort, Sage) have a long history of use in western and eastern medicine combating excessive sweating.&quot; Tomorrow morning I am heading to Whole Foods store. I hope they have the tea. I would order it online, but don’t want to wait. I really hope this &quot;magic&quot; tea will help control CS. Will keep you posted.
Good luck to you all!</description> <content:encoded><![CDATA[<p>7-30-10: I had ETS surgery six years ago due to facial blushing.</p><p><strong></strong><strong>This surgery was the WORST decision in my life. PLEASE – anyone considering it, DON’T DO IT!! </strong></p><p>The CS side effects will make your life miserable. My energy level and endurance have gone down, and I feel I have became fatigue a lot more often. I used to be an avid athlete (primarily roller skater). My days of skating were over soon after surgery. I’d soak in sweat just 15 minutes into my rigid work out.  I switched to ice skating – after all, the temperature in ice rink is cool, and I get to cover my body with a jacket (another layer to cover the damn embarrassing sweating).</p><p>I eventually started having chest pain (I guess the cold sweat-soaked cloth?), so I stopped ice skating as well. Since then, I have lost most of my muscle tone and gained weight. Note I was in excellent shape prior the ETS surgery. My closet had also gone through a major change – all skin tight and/or light color clothing had to go (well, at least my sister was thrilled).</p><p>Over the past few years, I have learned to monitor the weather on daily basis, planning ahead what clothes to wear each day. I am lucky to work in AC’d office environment (even tho stressful and uncomfortable situations make me break down in sweat, primarily on my chest and back). I always liked black color, but now I am &#8220;forced&#8221; to wear it most of the times (it does cover the sweat the best).</p><p>I started working out again, but I must wear a tight shirt with a lose one on the top. I used to love dancing – cannot do it all that much anymore. Walk outside on a sunny day had become very dreadful for me, etc, etc, etc….!!</p><p>My fiancee is very understanding and tolerates my problem. We are getting married and our big day is being planned for April. I always envisioned June/July wedding, but that would be a nightmare. This weekend I will be shopping for that special wedding dress. I am becoming extremely anxious, because, under normal circumstances I’d love to have a strapless dress with my back exposed – well, this is not possible because my back gets moist when I get even just a little nervous. So, once again, I gotta hide and cover myself. I hate this soooo much. I wish I could wake up out of this nightmare…</p><p>So today I heard about the Hushed Sea Herbal tea. &#8220;The herbs in Hushed Sea (Valarian Root, Astragalus, St. John’s Wort, Sage) have a long history of use in western and eastern medicine combating excessive sweating.&#8221; Tomorrow morning I am heading to Whole Foods store. I hope they have the tea. I would order it online, but don’t want to wait. I really hope this &#8220;magic&#8221; tea will help control CS. Will keep you posted.</p><p>Good luck to you all!</p> ]]></content:encoded> </item> <item><title>By: Eric</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-1011</link> <dc:creator>Eric</dc:creator> <pubDate>Tue, 20 Jul 2010 16:39:15 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-1011</guid> <description>Yeah I been dealing with this for some time also. the palmar version of this is horrible because when you want to hold your girlfriends hand or shake a girls hand that you meet they give you a funny look and treat you different due to this. But I recently tried the hushed tea. I only had it for a day but most of my night sweats and head sweating has stopped! My palmar however is still occurring but i expect it to go away. So don&#039;t worry, I know how you feel. I know their are worse issues but it doesn&#039;t feel that way to us, does it?</description> <content:encoded><![CDATA[<p>Yeah I been dealing with this for some time also. the palmar version of this is horrible because when you want to hold your girlfriends hand or shake a girls hand that you meet they give you a funny look and treat you different due to this. But I recently tried the hushed tea. I only had it for a day but most of my night sweats and head sweating has stopped! My palmar however is still occurring but i expect it to go away. So don&#8217;t worry, I know how you feel. I know their are worse issues but it doesn&#8217;t feel that way to us, does it?</p> ]]></content:encoded> </item> <item><title>By: Artist</title><link>http://www.myexcessivesweating.com/sympathetic-nervous-system.php#comment-940</link> <dc:creator>Artist</dc:creator> <pubDate>Wed, 09 Jun 2010 20:09:40 +0000</pubDate> <guid
isPermaLink="false">http://www.hyperhydrosis.us/?p=35#comment-940</guid> <description>I&#039;m just back from Brazil where I had surgery by [link removed] for my compensatory sweating (CS). He was able to cure my upper body, from the waist up. I had T2 and T3 cut in 2004 and my hands and feet became dry but CS began right away and increased in severity over the next 5 yrs..I&#039;ve read this can be common. It can also diminish after 5 yrs from surgery.
I still have CS on my legs, currently it is a little more severe that before but the Dr&#039;s other patients did not get a good read on the results for 1-6 months after.  [snip] does not cut the ganglia but takes the time to cut further away from the spine yielding less side fx as the ganglia is left intact.  I am able to sweat from my head during exercise only and asked to keep that as I like the feeling....and I still have that.
I found [snip] to be an extremely caring and skilled surgeon and recommend him to all of you if you choose surgery as a solution. He has developed techniques to cure armpit, facial blushing, palmer, and auxiliary hyperhydrosis with little or no CS. He is the true pioneer in this area. I wish I had found him for my original surgery.
If my lower half&#039;s CS does not improve with time I will seek a solution with him. There is hope there. Right now the technique needs some work to avoid sexual side effects and still give the body some sweating as it is a necessary bodily function. I have faith there will be more advances here, meanwhile I will be patient.
I came across this study from a different doctor.  He surgically treated a patient and cured his CS on his entire body. I am going to contact this doctor and see get more details about side fx and follow up results.
[link removed]
So there is hope. I share with all of you the mental anguish this as caused me. For me it started with armpits and then moved to hands and feet, mostly hands. I wish I had tried botox on the hands or met [snip] as his surgical solution would have far less chance of CS. But what can you do?  I refuse to let this bring me down and will continue to search for solutions. Thanks to all of you for posting your experiences here.
---------------
Note from moderator: We receive a number of comments by websites trying to promote their product or service by including links. This testimonial contained multiple links and were removed. This comment may or may not be legitimate. - as the Artist pointed out, it can take years before you know the result of treatment, and recommending the procedure immediately after treatment is jumping the gun.</description> <content:encoded><![CDATA[<p>I&#8217;m just back from Brazil where I had surgery by [link removed] for my compensatory sweating (CS). He was able to cure my upper body, from the waist up. I had T2 and T3 cut in 2004 and my hands and feet became dry but CS began right away and increased in severity over the next 5 yrs..I&#8217;ve read this can be common. It can also diminish after 5 yrs from surgery.</p><p>I still have CS on my legs, currently it is a little more severe that before but the Dr&#8217;s other patients did not get a good read on the results for 1-6 months after.  [snip] does not cut the ganglia but takes the time to cut further away from the spine yielding less side fx as the ganglia is left intact.  I am able to sweat from my head during exercise only and asked to keep that as I like the feeling&#8230;.and I still have that.</p><p> I found [snip] to be an extremely caring and skilled surgeon and recommend him to all of you if you choose surgery as a solution. He has developed techniques to cure armpit, facial blushing, palmer, and auxiliary hyperhydrosis with little or no CS. He is the true pioneer in this area. I wish I had found him for my original surgery.</p><p> If my lower half&#8217;s CS does not improve with time I will seek a solution with him. There is hope there. Right now the technique needs some work to avoid sexual side effects and still give the body some sweating as it is a necessary bodily function. I have faith there will be more advances here, meanwhile I will be patient.</p><p> I came across this study from a different doctor.  He surgically treated a patient and cured his CS on his entire body. I am going to contact this doctor and see get more details about side fx and follow up results.</p><p>[link removed]</p><p> So there is hope. I share with all of you the mental anguish this as caused me. For me it started with armpits and then moved to hands and feet, mostly hands. I wish I had tried botox on the hands or met [snip] as his surgical solution would have far less chance of CS. But what can you do?  I refuse to let this bring me down and will continue to search for solutions. Thanks to all of you for posting your experiences here.</p><p>&#8212;&#8212;&#8212;&#8212;&#8212;<br
/> Note from moderator: We receive a number of comments by websites trying to promote their product or service by including links. This testimonial contained multiple links and were removed. This comment may or may not be legitimate. &#8211; as the Artist pointed out, it can take years before you know the result of treatment, and recommending the procedure immediately after treatment is jumping the gun.</p> ]]></content:encoded> </item> </channel> </rss>
