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by: Theresa Flaherty - Monday, May 13, 2013

In our local newspaper today is a letter to the editor that made me laugh. The writer called out Congress on its hypocrisy when the sequester began to impact air travel.

The letter states:

For the first time in recent memory, both houses of Congress responded in prompt bipartisan fashion. And while the White House bemoaned the sequester, they announced the president would sign this legislation.

 

By coincidence, today I also clicked on a LinkedIn discussion (which I rarely do). The question: MPP alternative is relaunched. Does anyone think it has any chance to succeed this time? Many of those in the discussion were cautiously optimistic about the bill's chances. As one provider said: We've got to give it our best shot.

Another commenter pointed out that Congress remains in complete and utter gridlock, which I think will be a huge problem for MPP.

And then, this was depressing. www.govtrack.us keeps users updated on how the bill is progressing. Some lowlights: MPP has only a 3% chance of being enacted. Only 11% of House bills made it past committee and only 3% were enacted in 2011-2013.

Looks like the mountain the industry is pushing that bill up just got a little steeper. With bad weather looming overhead.

It will be interesting to see who attends the AAHomecare conference (is that next week already?!). My guess is it's the same providers who go every year. (BTW, there was a bit of association bashing on this thread as well. Are you listening, association leaders?).

Speaking of listening, provider Chris Rice suggested the industry's message on competitive bidding needs to cut to the chase. His suggestion? We just auctioned off your healthcare to the lowest bidder. Any questions?

He's got a point. Providers can talk to lawmakers until they are blue in the face but I think it's the beneficiaries who would have the most impact. 

Of course, it would still take an act of Congress to get Congress to act.

Theresa Flaherty

 

by: Theresa Flaherty - Monday, April 29, 2013

Against all odds, I found myself temporarily sucked in today by the video of last week's hearing on Medicare and DMEPOS, led by Sen. Claire McCaskill. Now I see what one industry insider, who attended the hearing meant, when I inquired how it went: "Sen. McCaskill is totally uninformed."

Now, to be fair, I didn't watch most of the hearing, just a snippet. While I understand (and support) McCaskill's concerns around shady marketing tactics, the snippet I saw showed a lawmaker getting caught in the weeds in my opinion. In referring to a company called Med-Care, she honed in the fact that, on the phone, it might sound like "Medicare." OK. I guess I can see that, now that she's pointed it out. Did the company do that to be deliberately confusing? I don't know, but neither does she.

She certainly talked about it a lot, though, going so far as to press CMS' Peter Budetti on why they would let a company name themselves as such. I gotta give Budetti credit for answering with a straight face when he told her he didn't think CMS has the authority to dictate what folks call themselves.

McCaskill then went on to question why physicians aren't supplying HME (this whole discussion cued off a beneficiary's letter about CPAP supplies)? I think she thought that would be better than the guy in the middle who stands to make all the money. (That would be YOU, the HME provider she was referring to).

I mean, is she suggesting scrapping the whole HME system? And what about drugstores? And labs? Should doctors do all of this?

I am still scratching my head.

Theresa Flaherty

by: Theresa Flaherty - Friday, April 19, 2013

You may recall my brief and failed attempt at using a diabetes app to record stats.

Well, I was reminded of that when I saw this study about how technology doesn't translate to lasting behavioral changes for people with diabetes. The study only focused on those with Type 2 diabetes but I bet you'd find similar results in the Type 1 population.

On the plus side, technology gave study participants better understanding of the disease but on the minus side, and this is kind of major, technology didn't promote changes in diet and exercise.

Let me tell you what works for me. A stack of nutrition reference books, cookbooks that list nutritional content, measuring cups, a scale, several sets of containers of varying sizes and cupboard full of spices instead of fats and sugars to add flavor. I also have sneakers and a gym membership I occasionally use. A subscription to Diabetes Forecast. You get the picture. And don't worry: I've been doing this long enough that a lot of this information is in my head, I am not constantly weighing and measuring. I can also identify a carb count at 20 paces but sometimes it helps to refresh my perception by measuring it out.

You can have all the technology you want but it can't cook for you, work out for you or go the grocery store for you (by the way, when are grocery stores going to change their layout so that the fresh food is together, not wrapped around all the aisles of processed stuff?).

There's no app for that.

Speaking of technology, I'd like to give a shout-out to Bryan who made my Monday with his email instructing me how to change the annoying beep on my new meter. My co-workers thank you, too!

Theresa Flaherty
Type 1

by: Theresa Flaherty - Tuesday, April 16, 2013

I am obsessed with a Slate advice column called "Dear Prudence." In fact, after I first stumbled upon it, I engaged in a few marathon sessions reading through the archives (not at the office, Liz). Sample headlines: I've been banned from my vegan grandbaby, how will she get her meat and cheese; Since starting on antidepressants, my wife has been cheerful and optimistic. I hate it; and this recent fave: Help! A neighbor has been poisoning our cat colony.

So imagine my joy at finding an opportunity to incorporate Prudie into an HME News blog. It's from about a year ago, I believe.

Q. New Job: Back in May of 2011, I decided to get back into truck driving. A large faith-based company agreed to hire me. I went through orientation, and was in the process of putting my belongings in a truck when I was called up to the safety department. The director of safety had found out that I have mild sleep apnea (my roommate snitched on me). He wanted me to travel back home, undergo another sleep study, and get a letter from my doctor stating that I could drive without any restrictions. Here's the problem: The safety department never had me sign any release for them to discuss this matter with me, or anyone else, let alone even look into it. I asked a lawyer friend about this, and he told me that it's a violation of my HIPAA rights. I am currently driving for this company, but I am tempted to quit, and file a lawsuit against them. To sue, or not to sue?

A: I often get chastised that I don't suggest more often that people just sue. But your letter beautifully encapsulates the litigious world we live in. You're considering suing over the fact that the trucking company that employs you discovered you have a medical condition that could result in your falling asleep at the wheel. I'm wondering whether in the papers you signed for your job there wasn't a line about disclosing relevant medical information that you neglected to note. In any case, your roommate snitched presumably not out of malice, but out of concern for the other people on the road. Instead of entering the legal system, enter the medical system and find out if pursuing this line of work could mean you're a danger to yourself or others.

Now, it's not the most interesting letter, but it does show how far there is to go in many cases, with understanding sleep apnea. In the May issues (coming soon to a mailbox near you) I have a feature on some soon to arrive guidelines from the Federal Motor Carrier Safety Administration geared to just this population.

Another thing about Dear Prudence, is because it's an online forum others will weigh in with their two cents. In this case, 2 cents that isn't worth the copper it's stamped on:

Q. RE: Sleep Apnea: Prudie, I believe that you are a bit confused as to what sleep apnea is. It is a sleep disorder characterized by abnormal pauses in breathing or instances of abnormally low breathing, during sleep. Each pause in breathing, called an apnea, can last from a few seconds to minutes, and may occur five to 30 times or more an hour. So, it would have no bearing on his ability to drive a truck, it is not like he has narcolepsy and is just going to fall asleep at the wheel!

Now this person obviously knows what sleep apnea is, but note the last sentence! Really?

By coincidence, Dana Voien, of SleepSafe Drivers, sent me a study link over the weekend. Sleep apnea patients are--wait for it--more likely to fail driving tests. So, there's obviously still room for growth in this market.

Meanwhile, if you want to check out Dear Prudence: "Help! My girlfriend kisses her cat and it grosses me out!" 

by: Theresa Flaherty - Thursday, April 11, 2013

So, I finally switched over to a FreeStyle meter after using the Lifescan products since, well, diagnosis. 

To start, I couldn't find the darn thing (I had packaging, instruction booklets, a testing log, lancets and even the dreaded lancing device). But, no meter so I went off to the (local) pharmacy to get another one for $19.49.

I am happy to report that, working on instinct (I loathe reading technical instructions), I was able to use the meter, although I did put the test strip in backward on the first try. I do have a complaint: the meter has an annoying high-pitched beep the likes of which I haven't heard since the early 2000s. It is especially annoying at 4 am.

I will also pay a compliment: the strip, once I turned it around, was much easier to use, a bonus here in still chilly New England, where somedays getting blood from my finger is akin to the old turnip saying.

It seems somehow appropriate that I switched over this week, right about the time CMS announced the names of the mail order contract suppliers. There were a few (very few) known names, which is an improvement over Round 1. A quick perusal of the manufacturers they carry shows that they are all offering at least one of the most popular brands, although, as one provider asked me: It's one thing to offer it, but will they stock it? That is not a question I can answer, my Mayan friend. 

I did speak with one winner today who said that he planned to be compliant with CMS rules about providing popular brand product but who also says he doesn't think that will last long for most of the companies.

It's simply unworkable, from a financial standpoint. So, while there are plenty of folks who will switch without giving it too much thought, I am sure there will be some unhappy customers, but I guess we will have to wait and see.

Theresa Flaherty
Type 1

by: Theresa Flaherty - Monday, April 8, 2013

The more I think about the mail-order program for diabetes, the more it ticks me off. I mean, every week folks (not just in the diabetes space) come up with all sorts of creative ways to criticize the program or question various technical aspects. And, while I have covered this in depth, the more I think, the more questions I have.

For example, by its own estimates, CMS has said that about 6 million beneficiaries are expected to be impacted by the mail order program (that's in line with the percentage of beneficiaries who use mail order anyway). But isn't that estimate based on bennies having ample local choice if they so, uh, choose? If you consider that CMS changed gears mid-stream (like, after the bids were submitted) and decided to apply mail order pricing to everyone, than wouldn't that mean CMS should, to use one of its favorite words, extrapolate those numbers? After all, even before the Round 1 rates (56%) came in, before the Round 2 rates (72%) came in, CMS has said that bennies would have that choice, indeed that safety valve of your friendly local diabetes dealer?

With such a drastic cut, it's a good guess that a lot of those safety valves are going to plug the drain that is Medicare diabetes. Leaving, oh, let's take a guess, a few million more beneficiaries to switch to mail order providers who were awarded contracts based on smaller capacities.

Also, and this could apply to all categories, but, if providers submitted bona fide bids, based on what they could afford to offer a product for (and submittted the invoices to back it up), and then accept contracts at far below what they bid, how is that supposed to work? I mean, call me naive, but if wouldn't they have bid lower if they thought they could afford that? Is CMS requiring contractees to prove they can still honor contracts at those much lower rates?

Theresa Flaherty

 

by: Theresa Flaherty - Wednesday, March 27, 2013

I recently (reluctantly) returned from vacationing on Vieques, a tiny island in Puerto Rico where horses roam free, on the beaches and in the twisty, winding narrow roads.

On Vieques it was easy to avoid all talk of competitive bidding, MPP or Medicare in general, mainly because internet access is so spotty, there are no local papers (and if there were, I suspect they'd be in Spanish) and I didn't travel all that way (3 airplanes and two rental cars) to watch my hosts' TV. They could have cancelled the bidding program and I wouldn't have had a clue!

While all that lack of access was welcome, I am, still, a reporter for HME News and at some point during my stay I realized what else I hadn't seen: home medical equipment ('cept for my own diabetes stuff). I saw no oxygen, no wheelchairs, no walkers, not even any canes. Is this because islanders don't need HME? Is it not readily available? Maybe those aforementioned twisty roads make it difficult to get around in a wheelchair (it was certainly difficult in our Jeep and I have the bruises to prove it). 

It's truly the first time I have gone a whole week without seeing some sort of HME. Even during my annual week in Cape Cod I have seen wheelchairs on the beach (I didn't however, get close enough to see if it sported an "I heart Cape Medical Supply" sticker). 

Where am I going with all this blather? I just wanted to post a vacay pic 

Theresa Flaherty

 

 

by: Theresa Flaherty - Thursday, March 7, 2013

As I edit the pages of the forthcoming April edition of HME News, I come across interesting tidbits. Take, for example, the Richard Barnes commentary on employee engagement.

Did you know that, according to a Gallup Poll, only 29% of employees are fully engaged in their work? And that 54% have mentally checked out (Hey you with the computer solitaire, we see you). Our fave stat here at HME News world HQ (which we share with a few other folks on a sister publication) was this one: 17% of employees are actively disengaged AND sabotaging the efforts of coworkers. With about 22 folks here in the office we estimate that four of us at any given time are saboteurs (smart money's on the new-ish guy).

As Round 2 continues to wreak havoc throughout the industry, I would imagine some of these numbers will rise among HME employees. After all, it's tough to work in an environment where folks are losing jobs, pay is being reduced and uncertainy is the only certainty.

For those employees left standing, here's a few signs that they are actively engaged: they are 26% more productive, twice as likely to be top performers, and miss 20% fewer days of work. Simply put, if you "bring it" to work and don't play hooky on a regular basis, your coworkers probably won't be giving you the fishy eyeball wondering if you are out to get them.

The commentary also says that constant complaining about the company is a bad sign, but I don't know. Isn't that just cubicle nature?

by: Theresa Flaherty - Tuesday, February 19, 2013

Providers are always talking about how beneficiaries have trouble learning new things or are resistant to new brands. I am no Medicare beneficiary (though I still can't get off the darn AARP mailing lists) and I have many times, while not scoffing at this notion, said of learning a new meter,  "it's not rocket science."

Well. A few weeks ago I picked up my new Freestyle meter and strips from my local pharmacy. The switch is solely because it's the preferred brand of the insurer's, but it's still a top brand with the features I demand (I sound like a commercial). I have twice opened up the box with the meter and twice stuffed it back into the box and back into the diabetes basket under my dresser (if only I could actually stuff my diabetes in that basket). It's not the meter, it's the stupid lancing device that has proved the sticking point. It has two separate pieces that look like they cover the lancet but I can't figure out how to make them fit.

Now granted, I haven't tried too hard, and it's not in my nature to read(yawn) instructions. The second time I tried it was because I realized I had left my meter at the office and needed to check my sugar. I was so irritated that this wasn't as simple as I thought it should be that I broke out the meter I inherited from Big Ed (alas, I only inherited one vial of strips from him).

But, I am getting near the end of my supply of One Touch strips and it's time to retire the meter and make the switch already.

I hate change.

Theresa Flaherty, Type 1

by: Theresa Flaherty - Friday, February 1, 2013

Did I really say, in my last blog, that expected payment amounts for Round 2 for diabetes test strips would about $15? Boy, was I (and, apparently, pretty much everyone else) wrong. The strips came in at $10.41. How did the price get so low, especially since Medicare implemented its 50% marketshare rule for Round 2. Did some bidders offer to supply them for free?

My first reaction was one of shock, quickly followed by dismay, not for myself but for all the wonderful providers I talk to that will be impacted by this. In fact, I had talked to several of my "sugar peeps" in the days before the announcement. I wanted to know what they thought of the plan to reimburse all Medicare diabetes supplies at the new mail order rate. While none of them were happy, they also weren't wailing and hand-wringing.

I have a feeling that's changed (if you are reading this and supply diabetes products, save me a dime and call me). CMS likes to spin the benefit to the bennies, but I think we'll find, you get what you pay (or in this case, don't pay) for.

Speaking of diabetes, I picked up my new brand of meter and strips the other day. The pharmacy billed it through as a 90-day supply, even though it was supposed to be 30. I hope that was an honest error but really, 200 strips to last a Type 1 90 days? I don't think it will last me 30 days. To give credit where it's due, my new insurer called the pharmacy right away and straightened it out.

It will be interesting to see how quickly I master the meter. Confession: The lancing device looks tricky already.

Theresa Flaherty
Type 1

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