......HyperhidrosisAndMe.com is a website for those who have Primary Hyperhidrosis. Find and purchase clothing and products that can help you feel and look good, explore treatment options that can help you, and read about growing up and living with Hyperhidrosis from my personal perspective.
Blessings, Charmaine

Archive for insurance coverage

Sep
21

Hyperhidrosis And Shame: The Unintended Consequences

Posted by: Charmaine · on September 21, 2010 | Comments (1)

I will begin by stating the obvious: We have hyperhidrosis and we are ashamed.  Yeah, me included.

The ways in which our bodies betray us every single day is our own business; our own private hell.  Why should we speak up and expose ourselves to outright sneers or, worse, polite distaste?  It has always been this way, and most of us prefer to guard our secret at all costs.

What’s the harm in it?

Here is a simple fact:  because there are far too few voices telling the public that abnormal sweating is caused by a physical disorder, our society makes unfair assumptions about people who visibly sweat. We are seen as shifty, nervous, self-conscious, and unclean.  The result of a wet handshake?  We are often pitied and dismissed.  In short, the public and the media are, for the most part, indifferent to our plight.

The consequences of this indifference?

  1. There is no awareness about hyperhidrosis in the public eye, and very little serious consideration about hyperhidrosis in the medical community.
  2. It is commonplace that we go undiagnosed for years.  In fact, the average is said to be 9 years.  For me, it was 33.  This results in years of suffering in isolation and all the emotional baggage that comes with that.
  3. Psychologists are often unaware of what hyperhidrosis is and how deeply it can affect the psyche.
  4. There has been little research into the cause and cure for hyperhidrosis.
  5. The tendency to under-diagnose hyperhidrosis has resulted in the health insurance industry’s general reluctance to cover treatments that go beyond Drysol.  Therefore, we are commonly left with two choices: pay for expensive treatments, or go without.

And the biggest consequence of all, in my opinion?

Internet Scams.

Think about it.  We are the perfect type of victims for the Internet scammer.

Too embarrassed to seek advice or treatment, we look on the Internet.  Too ashamed to ask anyone else’s opinion, we believe what is promised.  Desperate for relief, we will spend our money on anything that promises a cure.  Too embarrassed to admit that we were scammed– much less what we were hoping to cure– we do not expose the scam after the fact.

Easy money.

If you have found this website, the odds are pretty high that you have done an Internet search to try and alleviate your sweating.  Have you been tempted to buy a very short but extremely expensive little e-book that tells you to stop sweating and start living?  Have you seen promises that you can stop sweating in three days, guaranteed?  How about all-natural, herbal remedies that will put an end to your sweating?  Did you know you can wipe out facial sweating?  Do I need to continue?

The people behind these miraculous hyperhidrosis cures know a great deal about Internet marketing, and I would guess, precious little about your suffering.  Did you know that some of these e-book “publishers” pay a 65% commission to websites that link back to their very convincing shopping-cart sites?

Stop and think: If ANY of these “miraculous” cures, books, or systems worked, it would be no secret.  The International Hyperhidrosis Society would know about it; any doctor with any knowledge of hyperhidrosis would know about it.  These are all SCAMS.  These people are getting rich off of me, you, and our secrecy.

Our collective shame has made us a target and the victims of our own silence.

The only way to end the scamming, the indifference, and the medical mismanagement of our disorder is to talk about it.  I know it is hard.  Ask my friends on Facebook!

Categories : Awareness
Comments (1)
Sep
07

HyperhidrosisAndMe Weekly Spotlight: Insurance Coverage for Hyperhidrosis

Posted by: Charmaine · on September 7, 2010 | Comments (2)

The spotlight this week is on health insurance coverage for hyperhidrosis.  I know, YAWN.  Please keep reading, though– I have a few points to make that could help with your treatment!

If you have….by any chance… read my report on ETS (on your right, over there → ;) ), you may know that you really MUST be proactive in dealing with your coverage.

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Herewith, a few facts and tips:

  • In case you haven’t noticed (sarcasm alert), hyperhidrosis does not seem to get much attention in society at large, and also is the red-headed stepchild in the medical community as well.  This tends to result in health insurance policies either giving extremely narrow coverage parameters, or ignoring the disorder altogether.
  • You really need to know what your policy does or does not cover.  Absolutely do not, DO NOT, call your insurance company and ask if something is covered.  Read the damn thing yourself.  This was a mistake that I made that very nearly cost my family $20,000.  It didn’t cost me in cash in the end, but the distress it caused was very real and completely unnecessary.  Hypothetically:  You call your insurance company and ask, “Am I covered for Botox treatments for hyperhidrosis?”  The person on the other end (who gets paid whether or not the answer you get is accurate or not) may respond, “Well, is it medically necessary?”  To which you reply, “Yes, absolutely, I think so!” That person then replies, “Well, then you’re covered!”  Then, you merrily go on your way and get the treatment.   Weeks or months later, a letter comes in the mail from your beloved insurance company informing you that you did not take the proper steps to prove medical necessity and therefore coverage for the treatment is rescinded.  And you are left with the bill.  Really.  That happened to me, but the treatment was not Botox.  It was about 20× more expensive.
  • Oftentimes, the aforementioned “proper steps to prove medical necessity” for anything invasive and/or expensive require you to do any number of things, such as taking oral medication, using a prescription topical treatment, iontophoresis, etc.  Skip any of these steps at your own expense.
  • Many policies I have reviewed will only pay for treatment of hyperhidrosis if hyperhidrosis is directly causing skin infections or diseases.  This means that you are only eligible for relief from sweating if the sweating is causing you bodily harm.  Because we are apparently not suffering enough. (sorry, insurance makes me snarky)
  • If your insurance company balks at covering your treatments, a letter of medical necessity from your doctor may change their stance.
  • If your insurance company refuses to cover your treatments or if you feel you are being treated unfairly, do not hesitate to contact the insurance commission for your state.  This is one of the things that I did, and I think it really helped my case.
  • Keep a written record of all communication between you and the insurance company: dates, names, brief outlines of conversations.  Also print out any emails and keep any letters.  Again, that probably factored in my little victory.
  • If it is worth the expense, don’t be afraid to get a lawyer involved.  Once again, I did!
  • For more information and to download letters of medical necessity and other helpful forms, go to http://www.SweatHelp.org, which is the website for the International Hyperhidrosis Society.  See “Insurance Tools”– they have it all covered (pun intended :) )!

Please keep in mind that it costs insurance companies NOTHING to rescind payment or promise of payment for a procedure/treatment you have already received!  My lawyer told me that the vast majority of people who are denied coverage just accept the decision.  Don’t be one of them.

You have a medical disorder:  Your Sympathetic Nervous System does not work properly.  You do need medical intervention to correct it.  You pay for medical insurance; therefore, you have the right to coverage for the medical interventions your hyperhidrosis requires.   It is wrong that you should have to fight for that.  But you may have to–  and I hope you will.

If we don’t fight for what we are entitled to, how will anything change?  Do you want to fight insurance companies for the next 20 years?  I don’t.

Categories : Weekly Spotlight
Comments (2)

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