[Diabetes-talk] update on Denial of Insulin Coverage

cheryl echevarria cherylandmaxx at hotmail.com
Sun Oct 31 14:28:24 UTC 2010


Well I had switched to the pens 3 years ago when I overdosed on Humalog instead of my lantus, and I believe at the time that Robert Stigle and ss if I spelled last name wrong. In California, they trying to change the government or the insurance companies to change the bottles so it is indicated.

I myself find the pens accessible, I hear the clicks on the pens for the units, it is easier for me to screw on the needle rather than trying to figure out how to use the syringes.

Plus, it is not like the insurance company wasn't covering the Lantus, they were not covering the pens of the Lantus to different issues.

I mean you may like the vials okay fine.

But suppose it wasn't insulin and another drug, why can't we be informed prior to this happens.

I am one of those people because of my transplant I cannot take other drugs and have to take a certain drug like lantus over another insulin.

We should have the choice Michael, just like the sighted community, whether it be this or any other issues.  Accessibility to it, and not say oh we sent it out in the mail months ago, well they didn't, whether I can read it or not, Nelson is sighted and can read it as well.

The biggest compliment you can pay me is to recommend my services!

Cheryl Echevarria 
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  ----- Original Message ----- 
  From: Mike Freeman<mailto:k7uij at panix.com> 
  To: Diabetes Talk for the Blind<mailto:diabetes-talk at nfbnet.org> 
  Sent: Sunday, October 31, 2010 10:16 AM
  Subject: Re: [Diabetes-talk] update on Denial of Insulin Coverage


  Cheryl:

  I'm glad you were able to get your lantus in the SoloStar pens you prefer. 
  Do you have any idea whether or not your pesky insurance company would have 
  paid for the cartridge lantus pen whose name escapes me at the moment made 
  by Sanofi-Aventis?

  This gives rise to a question -- and I wish to publicly assure you that in 
  posing it I mean no criticism:  what should our stand be in light of NFB 
  philosophy if an insurance company refuses to cover the pen one likes? 
  Should we insist that we *need* (as opposed to preferring) that pen in light 
  of the fact that the Count-a-dose exists again?  Put another way, is this 
  really a matter of blindness or is it merely a matter of preference and 
  blindness is a convenient leverage point?  I honestly don't know the anser 
  myself as I use, like and prefer insulin pens.  But I bought a Count-a-dose 
  some time back in case Regence BlueCross got upity. (smile)  There may 
  indeed be no set answer.

  Let the discussion begin.

  Again, I'm glad you were able to get an override and I agree with you that 
  email on some subjects but not others strains the imagination a bit.

  Warmly,

  Mike Freeman

  ----- Original Message ----- 
  From: "cheryl echevarria" <cherylandmaxx at hotmail.com<mailto:cherylandmaxx at hotmail.com>>
  To: "Diabetes Talk for the Blind" <diabetes-talk at nfbnet.org<mailto:diabetes-talk at nfbnet.org>>
  Sent: Sunday, October 31, 2010 6:55 AM
  Subject: [Diabetes-talk] update on Denial of Insulin Coverage


  >I finally got my insulin. not to the help of the insurance company, who is 
  >not raising the premiums on my husband's insurance coverage at his company.
  >
  > My doctor had to call the insurance company and put in an over ride to the 
  > right department because the insurance company gave me the wrong one and 
  > then they had to contact my mail order pharmacy company and do this as 
  > well.
  >
  > I finally got my insulin Friday, I had to forego a few days of my lantus, 
  > making my readings reach over 300 some mornings.
  >
  > I am writing this up for the New York State Affiliate and work on this 
  > with our local government and see what happens.  All depends on what 
  > happens after November 2nd, 2010 elections.
  >
  > I do have a case work with Congressman Steve Israel's office but haven't 
  > heard a word from them, I will call on Monday and find out what is 
  > happening on there end.  I realize that I got my medication, but at the 
  > same time HIP is saying that the durable Medical supply company here on 
  > long island sent out this in the mail.
  >
  > Explaining to them, I don't get my durable medical supplies from that 
  > company since my primary insurance is Medicare.  I also informed them that 
  > they sent out each month or every 3 months via e-mail when I need to 
  > refill a certain prescription but they cannot send me an e-mail that they 
  > are no longer covering a drug.
  >
  > That makes no sense.
  >
  >
  > The biggest compliment you can pay me is to recommend my services!
  >
  > Cheryl Echevarria
  > http://Echevarriatravel.com<http://echevarriatravel.com/<http://echevarriatravel.com%3chttp//echevarriatravel.com/>>
  > 1-866-580-5574
  > Reservations at echevarriatravel.com<mailto:Reservations at echevarriatravel.com<mailto:Reservations at echevarriatravel.com%3Cmailto:Reservations at echevarriatravel.com>>
  >
  > Affiliated as an Independent Contractor with Montrose Travel 
  > CST-1018299-10
  > Affiliated as an Independent Contractor with Absolute Cruise and Travel 
  > Inc.
  >
  > join my yahoogroup
  > echevarriatravel-subscribe at yahoogroups.com<mailto:echevarriatravel-subscribe at yahoogroups.com<mailto:echevarriatravel-subscribe at yahoogroups.com%3Cmailto:echevarriatravel-subscribe at yahoogroups.com>>
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