January 23, 2020

New State, New Healthcare, New Life



Adios, Texas

Two years ago today, I wrote an op-ed piece for the Texas Tribune about my son Charlie and our journey with Medicaid for medically fragile children in the Lone Star State. The sub-par coverage we received from Texas was one of our chief reasons for leaving. The piece was published as a result of a post I penned here on my personal blog called Moving, Medicaid, and Motherhood

Here’s a little taste: 

“When the state of Texas denies a Medicaid renewal application for a medically fragile child, they are making a bet. The bet is that the family doesn't have the resources to appeal - that they don't have the hours to spend, or the ability to navigate the system, or a vehicle to pick up copies of medical records, or access to a fax machine to send letters from doctors and appeal application materials. They are betting that the families are tired and otherwise engaged with the work of caring for a child with special needs. And guess what? That's a good bet. Most of the families who have medically fragile children on Medicaid cannot jump through all of these hoops. The state wins. Parents stop fighting. The state doesn't have to pay. And that was their plan from the beginning.”


Hola, Oregon

Our family has been living in Oregon now for two years and I’m ready to report back about our experience of arriving in a new place, applying for care, enrolling in state-run programs, receiving medicaid through the Oregon Health Plan, and re-enrolling. For those of you who told me that care was the same in every state and that medicaid expansion states weren’t any better than those that refused money as part of the Affordable Care Act, this might be a disappointing read. 


Enrollment

The state of Oregon is committed to medically fragile children. I know this because of how our family was treated by the state and how they responded to our application. The system is by no means perfect but it is humane and fairly easy to navigate, especially when compared with our multi-step and sometimes dead-end process in Texas. Oregon’s goal is to get your child the care they need. 

Here in Oregon, our enrollment process was completed either online or by talking to a real human in real time. I didn’t have to track down hard copies of paperwork, get things notarized, or personally fax documents from specialist to specialist for signatures as I did in Texas. 

Everyone we have talked to through the Oregon Health plan has answered our questions in a straightforward manner and when needed, referred us (in real time by connecting our call) to another real human who could help us out. After a few days, Charlie was approved and the system was set in motion to get a local pediatrician who could attend to his special needs and refer us to specialists in the area. 

The process of enrolling for Medicaid through Oregon Health was a breeze compared to the 6-year waiting list that Charlie sat on in Texas. Granted, we are a computer savvy family with access to previous medical records. (But this was also the case for us in Texas.)


Receiving Care

Our family lives in a very rural location. The nearest clinic is an hour away and the nearest hospital is and hour and 45 minutes away. Most of our specialists are in Boise, a nearly a three hour drive. When we moved here, many family members were worried about our remoteness as it pertains to Charlie’s maintenance and care. Rest assured that our new medical team is all within a reasonable distance. (It used to take me an hour and a half to get to the Children’s Hospital in Dallas traffic, so this isn’t much different. Just fewer cars and a prettier drive.)

As a side note, our family has access to emergency services via helicopter that can get Charlie to urgent care in Boise in about 30 minutes. We pay a little extra for that coverage, but not much.

Once we were approved for Oregon Health, Charlie was connected to a pediatrician in La Grande, OR. After seeing her, she connected us with a pediatric neurologist in Boise. We were initially worried that Charlie’s care wouldn’t follow him across the state line from Oregon to Idaho, even though they are our closest specialized care. In Texas, even though we were near the Oklahoma border, Charlie was not covered in another state. Oregon has made provisions for those who live on the borders and medical care follows the patient to their closest care-giver; in our case Boise, Idaho. 


Quality of Care

Our care in both Oregon and Idaho has been excellent. The doctors and nursing staff are thoughtful, personable, informed, and helpful. We’ve also received great therapy services in Eastern Oregon through the school. Charlie sees a physical therapist, an occupational therapist, and a speech therapist through our very rural school system. They drive out from the closest town to see him, manage his therapy, and train para-professionals who are on site. Everyone has been proactive and attentive.


Re-Enrollment

In Texas, re-enrollment was always terrifying. Because of their massive budget cuts in 2015 and again in 2017, the state was always leaving medically fragile children by the wayside. Kids like Charlie who had coverage, could find themselves kicked off due to changes in eligibility rules. 

This October, we re-enrolled Charlie. He was approved online in real time. The best part was that his re-enrollment form already had last year’s information entered into each section. The form asked for updates, rather than an entirely new application. (Not so in Texas.) 

We did run into a little snag. There was a discrepancy between some of our income numbers and we were unable to progress through the application without assistance. We hopped on the phone and talked with an enrollment specialist who walked us through our income verification in real time. He was eager to get Charlie approved right away and gave us some helpful follow-up information. Within 48 hours, the application was complete and Charlie’s new healthcare card was in the mail. 


State-run health care is not just about the money. Its about intent. If your goal is to get care to your state’s most fragile citizens, families FEEL that. If your goal is to find any and every reason to deny access to care for your most vulnerable populations, families FEEL that. They feel it in their pocketbook, in their wait-times, in their commute time, in their personal interactions with care-givers, and most importantly, in their aspirational capacity. And this makes an enormous difference in their quality of life. It is a game changer for a family like ours.

Again, I know that the system isn’t perfect. I also know that Texas has far more people on Medicaid than Oregon (although the ratio of state population to those covered by Medicaid is the same). I also know that there are folks having a hard time navigating the Oregon Health website and enrollment process. Maybe it seems great because Texas was so awful. Whatever the reason, we are very happy with our choice to move. Charlie has what he needs, which means that I’m free to just be his Mama again. 

March 9, 2019

Re-emerging

It's been a million years since I shared anything on this blog. Perhaps its because Charlie has been through some incredible transitions in the past 18 months. Or maybe its because I have been through some huge transitions as well. Either way, its been pretty quiet around here.

Charlie is 8 years old now. In December of 2017, our family moved from Dallas, TX to Halfway, OR. Its a very rural place and many of our friends and family members wondered if we'd have the right kinds of services out here to support Charlie's needs. Would there be therapists? Orthopedic specialists? Neurologists? Would he have support at school? Aides? An adequate special needs program?

Well, there was no need to worry, friends. I did my research and I knew we'd be well cared for. And our new community, our new school, and our new support team has exceeded our expectations in every way. Are there hiccups? Sure. That's true anywhere. But across the board, Charlie has everything he could possibly need.

The best news of all is that Charlie is walking most everywhere he goes now. We haven't had his wheelchair at home for months. Its stays at the school in case he needs it for long distant walks. We even took a trip to California for a week and didn't bring the chair.

Now that we've settled in and Charlie has a new routine here in Eastern Oregon, I'd like to start writing more about the day-to-day stuff. In the previous 8 years of this blog, it seems I was always writing when there was trouble or struggle. And while it was so valuable to have this line of communication with our community during those hard times, I'd like to pay it back with some of the joyful and more positive parts of life with Charlie. Because there are so many!

You'll be hearing from me again soon, but until then, thank you.

Just... Thank you.




August 4, 2017

Charlie Turns 7



It's been another impressive year for Charlie Fighting Bear. He completed the 1st grade, had some medical help from the Medicaid program, and best of all began walking with AFO leg braces! His vocabulary has been steadily improving (he's now using two word sentences) and he's learned to use an iPad. Another huge bonus is that he has remained mostly seizure free. Like we said, its been a big year.

HAPPY BIRTHDAY, Charlie!


February 14, 2017

Charlie is WALKING

Charlie has been making huge gains this winter. The biggest change has been his dexterity and ease with his gait trainer - a type of walker that Charlie uses to walk upright. Charlie's original stroke caused severe damage to his corpus callosum, the part of the brain that assists in balance and communication between the brain's two hemispheres. This rendered Charlie unable to walk. In fact, most of our doctors were unsure if Charlie would ever be able to walker. 

But this week, Charlie proved us all wrong. Not only did he take multiple steps in free air with only the use of this leg braces, but he took 45 steps! And there's no stopping him now. Charlie is ready for more more more! Take a look...



September 12, 2016

Reach, Charlie, Reach

This month, Charlie discovered that he was tall enough to climb up to the kitchen counter and reach to the UPPER cabinets and open the door. What? Yes.







March 5, 2016

Help Charlie WIN a Bike!

Charlie has just been entered into the Great Bike GiveawayDo you remember the day you learned to ride a bike? The Great Bike Giveaway is about giving children with special needs the same feeling you had when that shiny new bike arrived at your house. The Great Bike Giveaway is a campaign started by Friendship Circle of Michigan giving children and teens with special needs an opportunity to win an adaptive bike. The Great Bike Giveaway was started in 2012 and has grown each year. In 2016 we hope to give away 600 adaptive bikes. 

Charlie has registered for the bike below. This is a bike that his parents would pedal and charlie would ride. The best part is that the chair can detach and be used as Charlie's wheel chair! Please visit Charlie's personal bike giveaway site and sign up to be an ambassador. Charlie needs 10 people (you must have a Facebook account) to be eligible to receive a bike. And here's the kicker - we have to have the first 5 signed up within the next 48 hours. So we have until Monday at noon to get five Charlie fans on the roll call. This is a great program that helps hundreds of special needs children across the country. 

Learn more or sign up to be an ambassador for Charlie HERE.



June 22, 2015

Crowd Funding for Charlie's New Ride


We've just launched a crowd funding campaign for my Charlie's handicapped accessible van!
Please watch the video below and check out all of the details HERE.


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A LITTLE ABOUT CHARLIE: 

Charlie Greenman was born on August 4, 2010. It was soon discovered that he had suffered two strokes in utero. He has since been diagnosed with Cerebral Palsy and Epilepsy - all complications due to stroke.

When Charlie came into the world, doctors told us that Charlie would probably never walk or talk. As of this summer, Charlie is doing both and showing no signs of slowing down. This is due, in part, to the excellent physical and occupation therapy Charlie receives.





THE SITUATION: 

However, a new conundrum has come up for our family. Charlie's efforts to be mobile require all sorts of assistive equipment. We need space for both his wheelchair and his gait-trainer when we travel.

Also, Charlie has just hit 50 pounds and is in the 90th percentile for height. My husband, Jack and I carry him everywhere, lifting him in and out of wheelchairs, gait-trainer, grocery carts, chairs and cribs. But the most difficult transfers take place when we need to get Charlie through the car door and into his car seat.


THE SOLUTION: 

A handicapped accessible van for Charlie! We have just purchased a used Toyota Sienna from a neighborhood family. There is plenty of room for his equipment, but the best part is that it's already adapted for handicapped accessibilty. A new, fully adapted van, would have cost in excess of $60,000. We feel very fortunate to have found a used one in great condition for $26,000. 

But now we're in a bind - one which so many families of special needs children find themselves. We simply do not have the financial resources to pay for both Charlie's life changing therapies and also cover the necessary cost of his handicapped accessible van.






 THE GOAL: 

We're hoping to raise $26,000 for Charlie's new ride. Every dollar we receive goes directly towards paying down our car loan and allows us to continue our monthly payments towards Charlie's many therapy treatments.

THANK YOU to everyone for your past, present and ongoing support of our son, Charlie! Our family could not do it without you. And a special thank you to Kenna's Kids for their amazing support for Charlie over the past three years.


Visit our Go Fund Me site to donate and share our story on social media.




.......................................

Full disclosure: Go Fund Me takes 8% off the top of your donations, 
while Paypal only takes 3% in fees. Charlie's Paypal donation button is below
if you prefer that to Go Fund Me.

Thank you for all your love and support!


June 11, 2015

Talking the Talk

Charlie's verbal skills have been severely delayed due to his perinatal stroke. And while we know that he understands more than he can express, this verbal delay can sometimes prevent Charlie from interacting with people outside of his immediate circle. As of September 2014, Charlie could say between 10 and 15 words. As of June 2015, that number has risen to over 80. Needless to say, this year of school and therapy was instrumental for Charlie Greenman's speech.

Just for fun, we've included a list of all Charlie's words to date. Most of these words are not intelligible to the average listener, but Charlie's teachers, therapists and family can see that he is using these words with consistency with a growing level of accuracy. Keep up the good work Charlie!




Charlie's Word List June 2015:

Charlie
Greenman
Walker
Mommy 
Daddy
hi
hello
How are you?
good
great
eat
yogurt
oatmeal
cheese
muffin
apple
water
bowl
table
chair
bed
night night
pillow
light
on
off
walk
up
down
bye bye
be back
name
my
I
want
Griffin
doggie
cat
sheep
cow
baby
outside
swing
wind
rain
thunder
run
friend
white
yellow
red
purple
orange
green
happy
grumpy
hungry
bear
house
home
car
bus
school
teacher
more
bite
wiggle
signing time
street
Elmo
cookie
bonk
hat
glasses
ear
eye
chin
cheek
hair
head
shoulder
knee
toe
quiet
sleep
help
nice
sun
moon
star
sky
rainbow
tree
bug
grass
day
show
word
shoe
sock
boot
pants
shirt
shorts
bird
creep
clap
Leah
Rachel
Michelle
Alexis
Katy
Jessica
kitchen
room
bath
go 
delicious
me
tickle
crunchy
please
thank you
all done
no
yes / yeah
twist
spin
sing
twinkle
round
wheel
shut
where
what





January 27, 2015

Registration is Open for the 2015 Kenna Cup

The 8th Annual Kenna Cup is here!

Friday, June 26th 2015
Saturday, June 27th 2015

at the Golf Club at Frisco Lakes
7170 Anthem Dr, Frisco, TX

The format is an 18 hole 2-man scramble.

$125 per player / $250 per team
-includes golf, range balls, goodie bag, tournament t-shirt,
multiple hole-in-one contests, 1 mulligan, food & drinks on the course
and BBQ from Randy White's after the round!

Register HERE






Kenna's Kids is a fantastic nonprofit organization that reaches out to individual families with children experiencing life's medical challenges at a young age. Charlie Greenman was a beneficiary in 2012 and Kenna's Kids continues to be a big part of his life. Please support this organization. There are lots of ways to participate. Visit their website for more information!




January 16, 2015

Last Semester of Pre-School

Hi Charlie fans, its been a while since I last posted, but I thought I'd check in with an update about our teeny-little-super-guy. Charlie is just starting his last semester of preschool. He loves riding the bus, seeing his friends, working with his therapists and playing games with his teacher. He still adores music and all manner of books.

The biggest growth for Charlie this fall and winter has been in the verbal category. He is attempting any and all words. His mimicry is getting a lot more accurate and we can tell that parts of his throat and tongue are loosening up. When Charlie first arrived, his brain MRIs showed extensive damage to his language center and our doctors gave us grim forecasts as to his future ability to comprehend language and make words. But in the past few months, Charlie has shown us all that he is ready to talk talk talk. Besides, he has to keep up with his chatty brother.

In December, Charlie had two seizures, which were both small and contained. A recent visit with our neurologist helped us to understand that as Charlie's brain changes and adapts, especially when he's in the throes of rapid skill acquisition, seizures are normal. Still, we're going to have another MRI in the spring to take a look at Charlie's brain again. We're mostly interested in seeing how the scar tissue from the stroke site has changed as his brain has grown.

As always, thank you so much for all of your support and love. We couldn't do it without you! We have some exciting developments in the coming months; we'll be welcoming a therapy dog into our home and we'll also be buying a used wheelchair accessible van for Charlie! So we'll keep you updated as we know more!




October 17, 2014

Preschool & Charlie's Gait Trainer

Charlie has been enjoying his second year in preschool. His teachers and therapists are all so heart-centered, so educated, so enthusiastic - a perfect match of Charlie Fighting Bear. One of the physical goals this year is to get Charlie comfortable in the gait trainer. We would like for him to be mobile by the time he starts kindergarten. This will aid in his ability to participate, play and interact with the children in class and the world around him. It also allows him some autonomy and choice making.

Here is a video of Charlie in his gait trainer. Only 6 weeks into the semester and he's already reaching his physical goals for the school year!



June 1, 2014

Charlie's Upsee

Charlie received his Upsee harness last week! Sarah, Jack and Charlie have spent the past days getting to know their new equipment and learning how to move together.

Like most new adaptive equipment, Charlie was apprehensive at first. His initial try was uncomfortable and ended in tears with lots of bucking and kicking and hanging in the harness. The second try was more successful resulting in a two minute walk around the house. By the third try, Charlie was ready to head outside.

This morning was Charlie's fifth day in the Upsee. He and his dad, Jack, took a spin around the neighborhood and through a nearby parking lot. Charlie is becoming more confident and eager the more he uses the Upsee. After his first few attempts, it was clear that Charlie didn't need the shoes that came with the package. Charlie is already able to move his feet and bear weight without assistance. Charlie's issue is one of balance and stamina, which the Upsee addresses beautifully.

And as for Charlie's walking partners, Jack and Sarah are able to stand up strait and bear their own weight while still assisting Charlie. No more back aches and pulled muscles from bending over to hold all of Charlie's weight.

Here are some photos from this morning's walk:















Learn more about the Upsee HERE.

May 2, 2014

May is Pediatric Stroke Awareness Month

Hi dear readers. As most of you know, Charlie had a stroke before he was born. About a week before I delivered, Charlie had a massive hemorrhage on the right side of his brain. The stroke affected his motor skills, cognitive and language development. He has since been diagnosed with Cerebral Palsy, Hemiplegia and Epilepsy.

But we were lucky. Charlie presented signs of his stroke immediately and we were able to locate the bleed and begin the hard work of helping him attempt some kind of recovery. Many children who have strokes at such a young age go undiagnosed for months, even years. Why is this? The answer is simple. People don't think that babies and little children can have strokes. The fact is that 1 in 4,000 children will suffer from a stroke.

So, in honor of Pediatric Stroke Awareness Month, 
Charlie would like to remind you that...




Lear more about pediatric stroke by visiting the Children's Hemiplegia and Stroke Association.



April 23, 2014

The 2014 Kenna Cup Needs our Support!

As most of you know, Kenna's Kids has been a GODSEND for our family in helping us face Charlie's medical bills. This astounding organization is now in need of our assistance. Please read on to learn how you can help out:

The 7th Annual Kenna Cup Golf tournament is going to be awesome this year. There are only a handful of spots left for players so act fast if you're interested. Register HERE. Kenna's Kids has five amazing beneficiaries this year and we want to do all we can to help them and their families with the soaring cost of medical care.

Meet the 2014 Kenna's Kids: 







SPONSOR the KENNA CUP

The Kenna Cup needs more than just players for it's tournament. Kenna's Kids needs sponsors. If you or someone you know has a business interested in participating, please contact Jeremy Pigott for information at JBP@kennaskids.org. We need you!





THE BALL DROP

If you are not in the DFW area, please consider participating in the Ball Drop!  
Balls are only 10 dollars a piece and can be purchased HERE.



Let's show these kids how very much we love them!
Support the 2014 Kenna's Kids by 
visiting their website and donating to the cause.

April 7, 2014

Upsee Adaptive Harness for Charlie

Hello Charlie Fans!

Charlie is soon going to have another piece of adaptive equipment in his arsenal. We have just ordered an Upsee Harness! Jack and I are very excited about this new development, not just for Charlie's increased mobility and access to the world around him, but for ourselves. Jack and I have spent lots of time and money on yoga, chiropractic care and medical appointments to treat our ever declining back health. Helping Charlie learn to walk, even with his gait trainer, is murder on our bodies. The Upsee might be just the answer to our prayers!

This harness, invented by a mother whose son, like Charlie, has Cerebral Palsy, became available to the public today. After showing it to one of Charlie's many enthusiastic therapists, we've decided to make the purchase. Charlie is the perfect candidate for this kind of equipment and the harness will work beautifully in tandem with Charlie's orthotic braces. Of course, our insurance will not cover this kind of device, so we're paying out of pocket. If you're interested in helping us cover the cost of the Upsee ($489), please feel free to contribute to Charlie's fund. Thank you so much for your ongoing support. We are ever grateful!



In the meantime, we can't wait to receive Charlie's Upsee and do things like THIS with Charlie in his new Upsee. There's a whole world for Charlie to explore and we can't wait to explore it with him!

All my love and gratitude,
Sarah









April 1, 2014

Something to Chew On

Whole foods for Charlie? Yes, please! Charlie has been eating whole bananas and the tops of muffins during snack time for the past four weeks. His preschool teacher has been slowly feeding Charlie bite-by-bite with lots of success. He is doing some light chewing (a big physical leap) and also waiting until his food is small enough to swallow (a big mental leap). Charlie is so happy to finally be eating some of the foods that other kids his age are able to consume with ease. Hopefully, there is more to come!


March 6, 2014

Charlie's New Orthotic Braces

Charlie visited the therapy clinic at Children's in Dallas yesterday to receive his new orthotics! Big brother Walker picked out the orange and yellow case color! Charlie was a little skeptical at first, but eased up once they were secure on his legs. Then we headed to New Balance to find a shoe that would fit over his braces, which turns out to be a lot more difficult that you might imagine. But here he is, outfitted in his new gear and ready to rumble.





February 19, 2014

Botox and Braces

Hello Charlie Fans,

Charlie had a big week. He started off at the orthotic clinic for a physical assessment and brace measurements. He's being outfitted with an entirely new set of gear. By March, he'll have two new leg braces, an elbow brace and a wrist brace! He'll look like the bionic boy. All of this bracing is to assist in alignment and limb articulation. It will be especially helpful for him while using the gait trainer.

Then Charlie had a visit from United Seating & Mobility because his wheelchair needed re-tooling to compensate for his rapid growth. Charlie is really off the charts for length and at 43 pounds, he needs more room to roll. Charlie responded to his wheelchair adjustment with a big smile and a loud, "Yeah yeah yeah!"

And finally, Charlie paid a visit to Children's Hospital this week to receive a round of Botox injections to combat his over-toned muscles due to Cerebral Palsy. The doctor injected Botox directly into his affected muscles to artificially relax them. The idea is this will aid in Charlie's limb extension and control of his body. The Botox lasts for about 3-6 months, so he'll likely repeat this process again. While the injections were painful and somewhat frightening for Charlie, his family hopes that the benefits will outstrip the initial discomfort.

The Greenman Family insurance is covering 80 percent of the cost of the Botox treatments and 60 percent of the cost of Charlie braces. If you're interested in helping the Greenman Family pay for their portion of Charlie's medical bills, feel free to contribute to Charlie's fund by clicking the button below.

Thank you for your good thoughts and support!





P.S. This winter, the Greenman family built a wheelchair path and gate through their back yard so that they can more easily get Charlie in and out of the car. Creating wheel chair accessible details for their home will be a long process, but this is a great start. Charlie is pictured above in front of the new gate. Yay for mobility!


Big brother Walker, helps the clinician measure Charlie's legs for the new braces.

Charlie in his therapy swing.

January 28, 2014

Kenna Cup 2014

Registration is now open for the 2014 Kenna Cup! As you all know Charlie joined Kenna's Kids as a beneficiary in 2012. Since that time, this organization has played a major role in helping Charlie achieve success in his battle against the effects of his stroke. They have paid off bills for our family, funded adaptive equipment and more more more.

Kenna's Kids has just announced open registration for their annual fundraiser, an enormous golf tournament in Frisco, Texas. This event is the largest of its kind in the state and every year, hundreds of players convene on Frisco to raise money for families who are buried in overwhelming medical bills related to their child. The men and women of Kenna's Kids are angel people!

Don't miss out on the fun!
Go HERE to register.