I had ETS for excessive palm sweating in 2012 and 2013. Then in 2014 I had a lumbar sympathectomy for excessive foot sweating. Then in 2015 I developed severe compensatory sweating on my back and legs and spread to my stomach, sides and chest.
This compensatory sweating has a huge negative impact on life. I can often only walk for approximately five minutes before I am sweating excessively all over. It made my everyday life extremely difficult. This also has led to my depression and very low self-esteem, morale and confidence. I think it really is unavoidable.
Surgery, in my opinion, was wrongly presented to me by the my healthcare provider as the only alternative to a lifetime of extremely sweaty hands and feet. The surgeon I recall told me about the possible side-effect of compensatory sweating.
My doctor assured me that it was just my body adapting and thing will get better in time. But until now my situation has only got worse. The compensatory sweating has spread and I have spent thousands of dollars over the last years on a vast range of products and natural treatments none of which has helped.
It is quite frustrating trying to function on a daily basis with this situation. I believe that ETS is sometimes being presented to people as the only alternative to living with their original hyperhidrosis condition in full, when in reality there are several non-surgical treatments available to help.
I hope that my story is helpful for someone who might be considering surgery. Based on personal experience, I believe that these operations often cause a lot more problems than they solve.