Showing posts with label healthcare. Show all posts
Showing posts with label healthcare. Show all posts

Sunday, January 27, 2019

The Art of Eligibility

This post is a bit of a throwback, but it feels relevant with some of the work I'm involved in right now.  Before I moved to Boston, I lived on my own for a bit (with a roommate), and during that time, I went through my first "eligibility assessment," to continue to receive Medicaid services, and the minimal nursing help I had with my medical tasks.

It was an odd, exhausting process, and it led me to write this.  I realized it never was published anywhere, but my mom blogger friend posted it in her blog.

Recently, I've been supporting in some state level efforts to actually make this process more person centered, so while it has taken some time, I like to think perhaps we are getting there.  I have shared this with many of my co-workers as a way to show them the other side of the assessment, that it is emotional, taxing, and more than just a tool. It's a lot of mixed feelings sometimes, bringing so many perspectives to the table, whether I choose to or not.
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“Are you able to get on and off the toilet by yourself? Any trouble urinating, or with your bowels? Do you wear pads or anything, or just for your menses?”

These are just some of the invasive questions that pop up during an “eligibility assessment” while trying to get healthcare services as a young adult with “special healthcare needs.”

On a typical morning, I wake up, head into the kitchen where I hit the buttons on my Keurig one cup coffee brewer with my eyes half open and settle in front of my Macbook to pour over emails and celebrity gossip until I can see straight. Usually this is followed by a shower, and all together an hour or so of blow drying, hair straightening, eye lining, lip-glossing, and perfume spritzing. But not today. Today I’m playing a part. Sort of.

In my life, my illness is not at the forefront. My LIFE is. I power on day-to-day, working to change the healthcare system for others in similar situations. I network, I spend time with my family, I get coffee with my friends, I rot my brain with reality TV, I do things every other 25 year old does. Then at the end of the day before heading to bed, I happen to get hooked up to an IV for 12 hours when I sleep. No big deal. Another day in the life.

But when it comes time to prove eligibility it’s ABOUT being sick- not able to be independent or successful. It’s not about proving how hard you have worked to achieve a level of good health and independence. It’s playing a game, to see if you “win” the services you need to ultimately be independent… and alive.

My phone rings, and the “assessor” tells me she has found my apartment. When I hang up, I throw my coffee mug in the sink, and stash my pink jewel encrusted iPhone under the pillow on the couch. As someone who meets the “income requirements,” I certainly shouldn’t have things like an iPhone. Ditto for my Macbook, which I quickly put to sleep and close off to the side so it won’t draw attention.

Today there is no eyeliner, no mascara, and no lip gloss. I haven’t showered, my hair surely is not perfected, and I’m wearing the same tank top and shorts I slept in.

I open the door for her, and my first thought is offering her something to drink (as any good hostess would) but I hesitate. Is that the right move in “the game?” If I can get her a glass of iced tea, then surely I can get some for myself… which means I can probably cook my own meals… which would probably deduct points in however the scoring of this sick game works. I don’t offer her anything.

We sit down at the kitchen table, and I wait for her to initiate conversation. I direct her to a plug so she can plug in her laptop where she will undoubtedly be recording all of my answers. I feel like I’m on a very unrewarding game show. I sit quietly, secretly hoping that some of yesterday’s mascara has successfully created dark circles under my eyes to make me look more like someone with “a condition.”

Finally we start talking. I keep my answers short and simple, only emphasizing the negative- like how hard it is for me to go up and down stairs, that of course I am able to shower by myself, but not forgetting to mention the complex dressing change that must be done after.

I know the script by now, and after awhile I just start to go with the flow, and even make light of it, in my own head, thinking of how I could joke that the only assistance I need while grooming is the occasional wax or highlights I just can’t seem to perfect myself.

I continue to choose my words carefully however, and avoid sounding too articulate.
“Do you have all your own teeth? Are you missing any?”
I raise an eyebrow, and answer “Yes. No….”

“That’s wonderful!” She says, as if having all of one’s teeth is an oddity, but considering the region, and that the assessment is done by “elderly services,” I suppose maybe it is.

I start to follow it up with “Actually, I just whitened them last night, and they are fabulously straight since I just got my braces off in November…. Which I paid for myself, and are completely paid off!” They absolutely do not want to hear that. I actually bite my lip so she can’t see how good they look.

“Have you had to see a foot doctor at all? Can I look at your feet?”

“Um… no, and sure.” I swiftly cross my ankles, hiding the one foot that is emblazoned with a tattoo, and point my toe of the other foot at her. My self applied turquoise nail polish glitters.

“Oh, you have little nail polish on it, and your hands too!” I immediately regret the touch up I did the night before, then get over it. It’s exhausting trying not to be yourself. Can’t catch it all.

The questions continue, and she begins explaining to me that my current insurance company cannot be billed retroactively, and I will have to fill out yet another application and apply for another program to prove I’m eligible for services I have already been receiving.

My brain starts buzzing, and the words on the application become a blur. “Wait… what?” I ask, striving for clarification.
“Do you want the number for the Department of Health & Human Services? I have the number for all of them!” She offers, as though telling me I just won the Powerball so none of this even matters.

“I have all the numbers.” I shrug. “I just am trying to understand what I need to do.”

We spend about twenty more minutes of me trying to clarify what I am asking, and her trying to answer. She then promises me she will relay the information to all the parties who need to be notified since once again, I’m not even sure I get it, but in a last ditch effort to not spend my entire day unshowered, sitting with this stranger in my house, I tell her I do.

Finally she prints another sheet of paper and with her arms raised says “Well! Of course you qualify for a nursing home level of care! But I know you choose home! Home home home!”

I cock my head to the side wondering if she really just said that sentence as if it were some deranged cheer they learn in “eligibility assessing school.” I try to keep my jaw from visibly dropping as I sign my name on a line under a checked box that said “I understand my options within this program and choose to stay in my own home to receive care.”

“Yea. I do.“ I said bluntly. It had been two hours and my act of playing nice was wearing off. Playing sick and tired I could do (since the tired part was not acting), but pretending this whole process isn’t the most unhinged, psychologically damaging thing I’ve ever seen…gets old. “And we’ve worked HARD for the past 25 years to see that this is the way it could be.”

She drops the cheerleader act and gathers her things, and wheels her laptop-carrying suitcase to her car. “I hope everything works out for you. Good luck.”

“Thanks,” I replied. “Have a good day.” And I meant it. We were both back to just being human again. And I could take a shower.

I close the door, and shake my head. Of course I choose home. I choose independence, grad school, work, and success… I choose having a LIFE. And I can only hope that some day, that is what the system is based on, being rewarded for being healthy and successful, instead of deprived of services that make it possible. 

Maybe someday.


Wednesday, June 20, 2018

Rare patient seeks doc.


I have a doctor’s appointment tomorrow, and I need to prepare myself emotionally.  I haven’t had a GI specialist since that one time in Boston when I had to break up with one.  For those who are new here, I like to compare healthcare to dating.

I have to take an Uber, schedule a time that works for both of us, and pray it’s a good fit.  Much like men prior to the fiancé, GI Specialists don’t really know what to do with me, and much like I was during that time period, I don’t want to be fixed.

I’m strong, I’m vocal, I do things my way and this works for me.  Doctors (and most men) don’t know how to handle this.

And let me just Internet shout:
I DON’T NEED A CURE. I’M NOT LOOKING FOR A CURE, AND I DON’T WANT TO TRY YOUR EXPERIMENTAL DRUG THAT IS GOING TO RUIN MY QUALITY OF LIFE I HAVE WORKED HARD TO ACHIEVE.


So phew.  Now can we just talk like people? I don’t want to pay for a bunch of expensive, invasive tests because YOU’RE curious.  Sure, go ahead and google me, I highly recommend it.  Don’t be afraid to say “I don’t know.”  Nobody does, and sharing vulnerability makes us equal.

Don’t judge my choices, my life, or reprimand me for living the way I choose- for swimming, for traveling, for enjoying a cocktail with brunch. While you’re googling, look up “dignity of risk.” 

Cause guess what? I’m living my life for me. You may be super excited because I’m “rare” and maybe you can write a paper.  One for the books. I write too.  I have letters after my name even.  So stop looking at your watch, and listen.  Learn from me.  Soon we can get the check, and I can get back in my Uber.

Then we’ll decide if we want to keep seeing each other.



Friday, June 23, 2017

#SaveMedicaid Part I

Ok.  It’s time to get real.  I usually try to gloss over some of the healthcare, and advocacy stuff, but with things as scary as they are, that may be pretty much impossible.  I made a vow when I relaunched this blog, that it would encompass ALL parts of myself, and that’s a pretty big part, regardless of how well I may hide it.

Unless you live under a rock, you know that health care is in SERIOUS danger.  The proposed “health care” bill was unveiled yesterday with the new “administration,” and let me just say, I use the term care loosely.  Take a gander at the summary and make sure you have your barf bucket nearby, as it is basically a mass murder bill.

While it’s a dumpster fire all around, I want to discuss Medicaid.  Rachel Maddow spells it out perfectly, as really Medicaid is the country’s LARGEST insurance plan and covers 74.5 MILLION people- mostly women, children and people with disabilities. SEVENTY FIVE MILLION OF THE PEOPLE WHO GOT OFF THE TITANIC FIRST.  SEVENTY FIVE MILLION.  LET THAT SINK IN.

Medicaid is NOT welfare; it is one of the best insurance plans in the country that covers things that private insurance does not cover. Things that are essential for people with any “beyond average” health needs require to be alive… or be in their community instead of a hospital.  These can include wheelchairs, life sustaining IV nutrition, assistive devices or PEOPLE to help with eating, going to the bathroom, communicating, GETTING AROUND.  You know…. Those things most people do every day without batting an eye. 

So here’s where I get real.  This is the first time in my life I have NOT had Medicaid.  I have also had private insurance.  I have a rare genetic disorder, and I rely on IV nutrition to LIVE.  I get 7 bags of IV fluid delivered to my apartment every week.  My love, Owen Reese puts this in the fridge and helps me prepare it every night.  I keep a stock of medical supplies to administer said IV (these all cost money and are not available at Walgreen's).  The cost of my daily existence is roughly between $7,000-$10,000 every two weeks, and this is when I am at my very BEST health.

I could very easily end up in the hospital for an infection because of my disease.  I get frequent Iron infusions.  I get regular bloodwork that costs $1,500.  For now, my private insurance covers most of that (MOST).  Here’s the plot twist.  I work for our state Medicaid program right now.  I can’t get into that, BUT for the sake of irony, it’s important.  IF I lost my job due to Medicaid cuts, since this new bill wants to make blood thirsty $800 BILLION cuts to Medicaid, I would NEED MEDICAID.  If one of us ever had a medical crisis, we may need in home supports to STAY IN OUR HOME.   Here’s the thing I often don’t talk about.  On paper, I am "nursing home level of care," or “hospital back up.”  I would qualify for the program I work on. What that means, is, if all of a sudden, I didn’t have the support, or the ability to care for my own medical condition as well as I do I would need to be institutionalized. Yes, I said it.

When my sister and I were little, our parents wanted to take a vacation and because our needs were too high for “respite,” (which probably was not even a covered benefit under their plan, they suggested my parents “PUT US IN A NURSING HOME FOR THE WEEKEND.”







FOR. THE. WEEKEND.  Two, young, vibrant, independent girls who happen to have a few extra steps due to their medical diagnosis.  This story still grosses me out to this day, that was even suggested as a solution.  Needless to say, my parents did not go that route, and we were fortunate to have the natural supports that we found someone to stay with us so my parents could have some grown up time. 


But I digress.

The point of this is to say, the cuts to Medicaid would be life threatening to thousands of people.  This is not “lazy people living off the government.”  Once you are over the age of 18 this is NOT AN ENTITLEMENT PROGRAM.  You have to apply for it, you have to fight for it, and you have to justify your needs over, and over again.   It is not “free money,” it is not “disability.”  It is necessary healthcare coverage so people with disabilities, and other complex medical needs can maybe be CLOSER to achieving some sort of quality of life when our society is still riddled with obscene barriers every step of the way.

When I was little, growing up, with more medical needs than my family ever thought we could handle? I WAS ON MEDICAID.  When I was in college, trying to further my education so I could have a job, and a fulfilling life as an adult? I WAS ON MEDICAID.

When I was in grad school, working in public health and operating a small business?  GUESS WHAT? I WAS ON MEDICAID.  And guess what?  I pay taxes.  I pay a lot of taxes.  If my health care coverage is taken away so that I can no longer work?  Guess what…. Then I am “living off the government.”  And the government CHOSE THAT.

This is definitely just the beginning of how I feel about this entire debacle, but I needed to begin by setting the stage.  $800 billon cuts in Medicaid is just one terrifying piece of why the proposed bill is unacceptable.


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And my story is just one of 75,000,000 that will tell you why. 
#SaveMedicaid








Monday, May 16, 2016

Life is a Highway Part II

Here is the full saga of my adventure trying to transfer my out of state license after the big move. I will warn you, it's a SAGA. My hope is that maybe it can save other people some of the nonsense I went through. Feel free to read on if you have time. Prepare to get frustrated...


Five years ago, I got my driver’s license.  As some of you may know, it took me about ten years.  


What I didn’t think about was that after that, I might be moving to another state (two different states actually) and what that would mean for said driver’s license.


LUCKY FOR YOU.  Once again, I am here, to provide transition “lessons learned” so that if any of you driven, ambitious young people want to get the hell out of your home state you will know the steps to go through to eventually transfer your out of state license, be a real citizen of that state, and MAYBE have to make less ridiculous trips to the DMV than I did.


Let me back up a little bit.  


We moved to Colorado in August of 2015.  My license expires May 28, 2016.  I got my Colorado license today… with 12 days to spare, before my Maine license would expire


I made my first trip to the DMV in October of 2015.  There were a couple of reasons I waited to start the process a little late in the game.  The first one, is similar to why I waited to  transfer my healthcare when I was living Boston.  Because I just wasn’t sure.  As I have mentioned before, I am most definitely my own worst enemy when it comes to believing in myself, and my life choices.  WHAT IF I FAIL!?!?!?  What if I lose all my money and my job, and everyone hates me and we lose our apartment, and I have to move back to Maine!?!?!!? I might as well keep my Maine license, juuuust in case.


The second reason- let’s just be clear about this.  I AM NOT ACTUALLY DRIVING IN COLORADO.  My car, Lily, is happily in Maine, hanging out with my sister, because logistics, and I take the bus, and it’s fine.  Otherwise, I would have had to renew my out of state license within 30 days of changing my residence to Colorado (this may vary per state, so be sure to check)


Anyway, so one day in October, I took the morning off from work, and took an Uber to the specific DMV that does driver’s license (cha ching- $20).  I had done my research on the website, and had my proof of residency, my passport, my current license, a blood sample, my first born, etc etc.  
It really didn’t take that long to get called and go through the process, so I figured I was good to go.  However, when they called me up to get my photo taken, they had me review my information to make sure it was correct.  And my apartment # was wrong.  UGH. So, I mentioned it (come to find out, I managed to grab the ONE piece of mail that actually had my address wrong…but somehow it got to me so go figure) When I mentioned it was incorrect, they had me sit back down.  So I did, and waited, and waited.  And I knew I was not leaving with a license.


Sure enough, they called me back up, and having looked at my file, explained to me that I needed to have a form filled out by my doctor, because it said on my license that I needed accommodations in my vehicle THAT IS NOT EVEN IN THE STATE OF COLORADO.  I will say the staff was super nice, and even checked with the manager if this was the case, but it was.  Then they sent me on my way, with the form.

It’s kind of funny because I try not to be a big nerd who is like “Everything has to do with health care,” but you guys, everything has to do with health care.   


At this time, I was also transitioning to my second PCP because my first one just did not have follow through that I needed (that’s another blog).  I ended up switching to an Internal Medicine group, that is a lot better, so when I got my first appointment, I brought in the form, to this poor doctor who has never even met me.  She was nice, and didn’t ask many questions, and filled out the form.  


Then the holidays, work, and life happened, and I didn’t have the opportunity to take ANOTHER morning off to go to the DMV and do this again.  But, since the clock was ticking, I found a day.  I made sure all my mail had the correct address, paper-clipped all my crap together, took another Uber (cha-ching) and went back to east middle of Nowhere to the Driver’s License office.


This guy was also super nice, but as he examined the form, he told me that it didn’t include the specific information it needed explaining my particular accommodations that I need IN MY VEHICLE THAT IS NOT IN COLORADO.


I asked him (still being my super nice, Advocate self)  “Ok, well does it say to include that information on the form?”


DMV Dude: “Well, no.  But the doctor is just supposed to know.”


Clearly, they teach mind reading in med school.  I wish they had taught that in Public Health school, then maybe I would have known what I needed before I went to the DMV twice


I know he was just trying to help, but clearly not understanding how healthcare works, this kind young man said “Well if you can go back today and have them fill it out, and come back, I can help you right away.”


My doctor’s office is a half an hour in the OPPOSITE direction from my house, so about an hour from the DMV, which is in the middle of nowhere in the other direction.  Also,  you don’t just stroll into Internal Medicine and say “Hey, I need someone who can just jot some words on this form.  AGAIN.”


This was also the day of the Super Bowl parade, so getting anywhere in the city would take twice as long.  I ALSO need to mention, that in my current job, I do not have paid time off.  Not only am I paying to Uber each time, but I’m missing valuable work time that I am not getting compensated for.  My choice, but still, another factor that makes each DMV trip even more painful.


After they sent me away the second time, I had a very long moral dilemma.  I had a form with my doctor’s signature, and we had discussed my accommodations and everything I needed, technically I could just write in the notes section, whatever they needed and save myself a trip BACK to my doctor’s office.  I also didn’t have health insurance during this time, so I was not about to be billed for a dr filling out a form they ALREADY FILLED OUT.


Finally, I decided I was just going to fill in the information, and make another trip to the DMV.  Well, apparently the universe didn’t think that was a good idea because the form was blank.  After my second trip, the guy at the DMV had TAKEN THE FORM THAT WAS SIGNED and given me a blank one, without even telling me.  I was literally back at square one.  Are you kidding me?


At this point, I had lost much of my motivation to even make this happen.  The other reason that I was in such a panic to get my CO license in the first place was because I was going to be applying for jobs with the state, and having a CO license is a requirement.  At this point though, I had gone through the process and checked with HR, and since I already worked at the state, and could prove residency, as long as I was working on it, they told me it wasn’t as urgent.  That helped me relax a little bit, but I still just wanted to get it done.  The clock was still ticking, and as I mentioned, after spending 10 years trying to get my license, I will be damned if I was going to sacrifice it because the system is completely inefficient.


Fast forward to May, after four months of not having health insurance (another blog), and I make an appointment to see my new PCP, and figure i’ll have her fill out the form ONCE AGAIN.  Please note- this was AFTER I had been messaging with my team (who are all residents so I never see the same person twice) and they said I could mail the form, and they would fill it out and send it back.  Then they told me I needed to make an appointment EVEN THOUGH THEY ALREADY FILLED IT OUT ONCE.  But whatever, at this point I had other issues I wanted to discuss anyway so I actually just took a whole freaking day off in the name of wellness and took the bus to the doctor.  Because Eff Uber when the sun is out and I have nothing but time.  


I go to the doctor, and wait… wait… because healthcare is inefficient.  Then I get in with the doctor, and she says, “So you’re here for some paperwork?”  


“Yes, and you have the paperwork.  It was in an envelope with a note that included very specific instructions on what to write and it had a note that said, DO NOT LOSE THIS FORM.”


“I’ll be right back.”


I’m sure you know where this is going.  They couldn’t find the form.  I decided before I even went, I was not leaving without this form so I told them to find it.   They were super gracious, and they did find it.  Let me re-emphasize. I WROTE DOWN what I wanted them to write on the form.  This was another person who had never met me, so I basically did all the work and they got to bill my insurance.  CHA- CHING.  I left with the form.


Today, 2 weeks after that appointment, I decided to just take the plunge.  I gathered all my documentation UH-GAIN.  Left the house at 7 a.m. in the rain and Ubered to the DMV.  Luckily, I had the same girl I had the first time, who raised both eyebrows when I said “Maybe third time’s the charm?”


In less than 20 minutes, I was waiting to get my picture taken.  I was a little worried when she disappeared for a little too long, that there was some other reason I wouldn’t be leaving with a license, but I made a vow to myself I was not leaving until it was complete.  I was done playing games.  


So now 6 months later, I left with my Colorado license and and a goofy picture because apparently in Colorado you can’t show your teeth when you smile, BUT I DON’T CARE!!  Now that this is behind me, next time I can just renew this baby online!  The Maine chapter of my identity is officially off the books… there you have it!


Best of luck to all of you as you move into your new lives, and new identities.



For those of you who want the TL:DR version, here are my top five lessons learned from the Driver’s License Saga Part II:
  1. Don’t trust the internet.  If you have an adapted vehicle or any sort of your driving experience was a little different, call ahead of time to see if there is any additional documentation you need (I went back and looked, and that part of the website was down. Of course)
  2. Make copies of everything and stay organized!!!!! I wish I would’ve asked for a copy of the form before they took it away (But I thought I was getting the same one back) JUST SCAN OR MAKE COPIES.  After my first trip, I just kept the documents I knew had the correct information so if I did have time to go back, I could just grab my “DMV packet!”  It saved everyone time once  got there.
  3. Keep your cool.  Whether TSA or the DMV, if there are added steps for you, even if you are annoyed, take a deep breath and be clear on what you need to do.  It’s ok to mention there are gaps in the process or how it can be improved, but leave with a smile or at least a “Thank you.” and  you’re more likely to get what you need eventually.
  4. DIY. Always.  If  you want something done right the first (or second time) DO IT YOURSELF. Clearly my PCP who I was meeting for the first time is not going to know about my car in Maine.  Write the exact language you want them to put on the form, this goes for any sort of eligibility requests, or Medical Necessity as well.  Any guidance you can provide, saves them a lot of time and will get you your form back a lot quicker.  If you don’t know the language to use, find an advocate or someone who can help you make sure you’re “playing the game” correctly.  Hit me up, I minored in this!
  5. DON’T GIVE UP.  Seriously.  Cheesy as it sounds.  Figure out what you need, and the people who can help you get it, and keep at it.  The system is broken, but we can’t let it win.  I will definitely be writing a letter, since if that form had been on the website, it would have made my life a lot easier, but ultimately I got what I came here for, and I can now take a deep breath and enjoy my new Colorado life.  



All in a day’s work!