Showing posts with label rare disease. Show all posts
Showing posts with label rare disease. Show all posts

Wednesday, September 27, 2017

Can You be an Advocate and Still be a Christian? ~ Guest Blogging Day

There were also two others, criminals, led with Him to be put to death.  And when they had come to the place called Calvary, there they crucified Him, and the criminals, one on the right hand and the other on the left.  Then Jesus said, “Father, forgive them, for they do not know what they do.”

And they divided His garments and cast lots. And the people stood looking on. But even the rulers with them sneered, saying, “He saved others; let Him save Himself if He is the Christ, the chosen of God.”
Luke 23: 32-35 NKJV



Lately, as I've been sitting in church and listening to sermons, or taking a walk and listening to a podcast, I have been bombarded by messages that make me question my purpose as an advocate for my daughter who has special needs.  
I've received the message that God wants us to put others before ourselves.
I've received the message that God wants us to LOVE His people (which includes everyone...even those I may not necessarily "like".)
I've received the message that, when I make the world about ME, I am taking my eyes off God.
Logically I started to question my motives in EVERYTHING.  
  • Is this about me?
  • Is this just about my kid?
  • Am I advocating out of FEAR or am I actually making the difference that GOD wants me to make?

CAN I BE AN ADVOCATE AND STILL BE A CHRISTIAN?


Continue reading on Comfort in the Midst of Chaos...

Friday, May 19, 2017

A Good Punch in the Face

Image courtesy of num_skyman/www.freedigitalphotos.net

I've never punched anyone in the face...
Let's get that clear right now.  
But I've wanted to.  In those very "Ally McBeal" moments when you picture yourself following through on your basic animal instincts to lash out at anyone near you when you are injured or threatened...oh, yes...I have wanted to punch many people in the face.

the 8th grade classmate who said, "Tammie, the only reason you get good grades is because you don't have any friends".

the 8th grade classmate who wrote me a note saying that she wanted to become popular that year, and that meant she couldn't be friends with me anymore.  (yeah, 8th grade sucked).
the people who typed the anonymous letters from graduate schools and turned me down because of my GRE scores (although I'm glad you did because I never would have started dating my husband had you accepted me at THOSE schools).
everyone who worked at the Gerber Grow-Up plan because I got a letter from you in December 2004 saying that our daughter couldn't get life insurance through you...(hmmm...a rare disease does that, I guess...hence, why you were forthwith known as the Gerber THROW UP plan).

a couple of Wisconsin's 'civil servants' whose names appeared on letters declining Evie for some county services.  That was unfortunate...but, the courts overturned your decision. :P

the parents who shush their children when they ask me very logical and appropriate "children type" questions about Evie.  Your SHUSH communicates shame...and there is no shame about my daughter.  Your SHUSH is what makes her question what IS SO wrong.
the lady at McDonald's who approached me as we frantically were trying to usher Evie out of the restaurant during a wicked meltdown after a long day of traveling....you approach me and all you do is suggest fish oil for my child's behaviors?  Open the friggin' door for us and help us OUT!
the old man who told me I should have folded up Evie's white cane BEFORE boarding the plane because it was a nuisance for him.  Clearly you don't understand WHY we use a white cane...it's HOW we GET on the plane.

the eye doctors who have treated Evie as if she has no intelligence and that we shouldn't even be in your office...well, guess what...we aren't in your office anymore.  It's actually worth flying back to Wisconsin to see our eye doctor THERE, 1,800 miles from home; than drive two hours and waste our time on you.

I didn't have to, and don't have to, punch any of these people in the face.  They are of no consequence to us.  

This is a great big world, and we serve a GREAT BIG GOD and because of His victory WE have victory.

Today.

No punching required.

Written in response to writing prompt 182 on thewriteprompts.com 



Thursday, May 18, 2017

We Interrupt Your Regularly Scheduled Life ~ Guest Blogging Day

Evie in the Hospital following her Wilms Tumor diagnosis in 2005
When he had finished speaking, he said to Simon, 
“Put out into deep water, 
and let down the nets for a catch.”
Simon answered, 
“Master, we’ve worked hard all night 
and haven’t caught anything. 
But because you say so, I will let down the nets.”
Luke 5: 4-6 NIV

This past weekend I had the pleasure of attending a conference in Redding, CA called GrowU.  One of the "top billed" speakers of the event was Chris Brown, who is one of my favorite storytellers because he has a tremendous gift for bringing scripture to life.  

On Saturday night he retold the story of Jesus choosing his first disciples.  And, when Mr. Brown re-tells this story, you suddenly realize how God chooses us today in the very same way as He chose people back in biblical times.  

When you read Luke 5, you read about some fishermen who are cleaning their nets and Jesus asks Simon to take him out in his boat so he can speak to a crowd who has gathered on the shore.  Now, fishermen fish at night, which means, if Simon was in and cleaning his nets, he had just been out fishing all night long.  

Working hard.  
He was exhausted. 
And Jesus comes along and says, "Hey, can you take me out in your boat?"

Ugh.

Continue reading on Comfort in the Midst of Chaos...

Thursday, February 9, 2017

When a Friend Speaks the Truth ~ Guest Blogging Day

Kathryn with Evie
Many are the plans in a person's heart,
but it is the Lord's purpose that prevails.
Proverbs 19:21 NIV

I was driving home from the hospital with my baby girl in the car.  My heart was racing and my blood pressure was high.  How could God do this to us?  Just when we had reached the finish-line of chemo...boom, another punch in the gut.

I dialed my friend Kathryn and she answered.

"Can you believe it, Kathryn?  We just finished chemo and now she has pneumonia?  Oh my gosh, are you kidding me?"  I say in response to her, "Hello".

"Tammie Jo," she replied, "This is your life...stop waiting for it to change."

Continue reading on Comfort in the Midst of Chaos...

Monday, May 16, 2016

While I was at the Funeral for My Old Dreams



it was spelled out in black and white...
there was a difference in her DNA...
this would not be a "normal" life for our first and only child...

our life was now a query and a question mark rather than an exclamation with a point.

while i was at the funeral for my old dreams,
jesus came and sheltered me
with loving eyes and gentle hands,
with peaceful breaths and merciful words.

while i was at the funeral for my old dreams,
i slowly realized the new,
dreams don't always come true,
but god's unfolding promises do.

while i was at the funeral for my old dreams,
i knew that he'd designed this beautiful journey,
it would not look like my plan,
my plan was now under the earth, and somehow that didn't hurt.

while i was at the funeral for my old dreams,
i began to smile...one day,
after a while,
i settled into today and suddenly we are miles away from the graveyard where we left the old dreams.

those old dreams do not fit us now anyway...

Thursday, February 25, 2016

I Didn't Find What I was Looking For ~ Guest Blogging Day


“The Spirit of the Lord is on me, because he has anointed me to proclaim good news to the poor.  He has sent me to proclaim freedom for the prisoners and recovery of sight for the blind, to set the oppressed free, to proclaim the year of the Lord’s favor.”  Luke 4:18-19 NIV

A couple of weeks ago this passage in Luke piqued my interest in a sermon at church.  It really struck me because, well, my daughter is blind. 
Now, I’ve read plenty of the stories about the blind being healed in scripture, and that has never bothered me.  I’ve never thought, “Why would God heal one blind person here and another here, but not my daughter?”  I already knew that the answer would be, “He has a different purpose for her, and that does not include being healed at this time.”  
But, this particular verse stood out to me as peculiar because it seemed like a type of mission statement for Jesus, yet it seemed quite limited to me in the use of the word BLIND.
Why not say he would heal lepers, raise the dead, and cast out demons?

Continue Reading on Comfort in the Midst of Chaos... 

Wednesday, June 10, 2015

I'm Sorry, Ma'am, Your Child is Broken~Guest Blogging Day


I appeal to you therefore, brothers, by the mercies of God, to present your bodies as a living sacrifice, holy and acceptable to God, which is your spiritual worship. Do not be conformed to this world, but be transformed by the renewal of your mind, that by testing you may discern what is the will of God, what is good and acceptable and perfect.  Romans 12: 1-2 ESV

Color inside the lines, brush your hair, don't let yourself start to smell bad, one scribble on the page is not artwork, and don't forget to smile nice for your picture! 
That's what the world wants, right?  
I shrink inside every time I hear my daughter say, "Finished" and I see the scribble of one color across the white paper.  Her artwork.   But it doesn't look like the artwork that MY CHILD should be creating...no, surely she'd be more creative and want it to look nicer, right?

Continue reading on Comfort in the Midst of Chaos...

Wednesday, May 6, 2015

Blessed Enough to be Speechless ~ Guest Blogging Day

Image "Mother Giving Hand to Child" Courtesy of David Castillo Dominici/freedigitalphotos.net
While he was saying this to me, 
I bowed with my face toward the ground and was speechless.  Daniel 10:15  NIV

A few weeks ago we were at an ophthalmologist's office.  My daughter was meeting this specialist for the first time as she has several eye conditions which include, but are not limited to; aniridia (no irises in the eyes), and glaucoma (high pressure within the eyes).

If you've never seen how doctors measure the eye pressures in children and infants, they typically use an item called a tonopen.  This pen must be placed directly on the eye ball, right where the iris and pupil are located.  The pen takes several readings which reflect how high the pressure in the eye is. 
Because my daughter doesn't have irises, she is photosensitive; meaning, she has extreme sensitivity to light.  She wears sunglasses at all times when she is outside, even if the sun is low on the horizon or behind clouds. 
Keep in mind that my family just moved from the Midwest to the far West under a year ago.  We have become acquainted with all of our new doctors, but don't know them NEARLY as well as we did our doctors in Wisconsin.  Often, I just assume that the doctor knows what he or she is doing; but that's not the best thing when it comes to rare diseases.

For example, when the doctor was trying to check my daughter's eye pressures with the tonopen, she made her tip her head back and stare straight up into an overhead fluorescent light.  It didn't dawn on me to tell the doctor to turn the light off, nor to ask her to dim the light.  My daughter kept closing her eyes while the doctor had the tonopen set on the eye ball attempting to get a reading.  
I watched, silently, as they both struggled to do their jobs:  my daughter was struggling to protect her eye from the blinding light and the doctor was struggling to get a reading as quickly and accurately as possible.
It was excruciating to watch.  

Continue reading on Comfort in the Midst of Chaos...

Tuesday, April 21, 2015

Why the New "Full House" may NOT Work for Us~WAGR Wednesday

I'm listening to Evie upstairs... 

It's been a bad 1/2 hour.  Just 45 minutes ago, I was watching her sit in the recliner with her legs tossed carelessly over the arm in a "regular kid" kind of way.  She had her iPad in hand and was watching "Sam and Cat."

"Do you want to watch that on the Apple TV?"  I asked.  

"No, I just want to watch my iPad."  

Ok...no big deal.

        Until...

"Mommy, can we watch "Sam and Cat" on the Apple TV by mirroring?"  

Now, for any Apple households out there, that didn't sound like a foreign language.  But, for those who don't know, the Apple TV allows you to watch things from your iDevices on your TV...you can simply watch the videos and TV shows on there through your iTunes accounts.  That's what we normally do. 

However, what Evie was requesting was a feature called "mirroring" where you can transpose your iDevice screen onto your TV via the Apple TV.  So, either way, you could watch something on your TV that you would normally watch on your iPad.

Except tonight it wouldn't work. 

The iPad was giving us some message about the show being protected and couldn't be "shared" onto the Apple TV.  No problem, right?  Nope.  BIG PROBLEM.  She didn't want to just watch her show on Apple TV...she wanted it MIRRORED!!!

Seriously, watching it ON the Apple TV rather than mirroring?~It would have looked the same, sounded the same, lasted the same amount of time.  It would have been EXACTLY the same. 

But not to Evie.

      Because of anxiety.

            Because of WAGR.  

Because something happened today, or happened over the past two or three days which built up, and built up, and built up into one great big colossal meltdown. 

We went from Snow White dancing 
while the bluebirds perched on her shoulder 
to the girl in Poltergeist spewing vomit 
while her head spun around 
in a split second.

So, this takes me to why the new "Full House" on Netflix just might not work for us.  It may...don't get me wrong.  We'll give it a shot...but, I'm preparing myself for the disappointment.

First, if the entire cast is not there, we will be asked over and over again WHERE the missing characters are.  "Why isn't Joey there?"  "What happened to Rebecca Donaldson?"  "Why is there no Comet?"  As we try to answer the questions we will be missing the entire new episode which will lead to even greater confusion. 

Secondly, the actors, if the same actors return, will have aged and may be unrecognizable.  Did any of you parents out there live through the changing of the Marinas on "Fresh Beat Band?"  You know what I'm talking about!  Let's face it, we KNOW that Jesse and Rebecca's twins won't look the same, and we know that DJ will not likely have married Steve...

Thirdly, they won't all live together.  Even now, Evie watches, with great angst, the episode where Jesse and Rebecca consider moving out on their own.  "Where will they go?"  "Are they going to move, Mommy?"  "Where will Jesse live?"

Ev, you have seen this episode a number of times, 
you KNOW they don't move out.

So, as much as I'd like to believe that the new Netflix continuation of "Full House" will be a thrilling event in our home, I have my reservations.  Evie's brain gets into nervous knots, and the best way to untangle them is with things that are familiar and repetitive and predictable.  Life rarely appeases that need.  But, we try to safely introduce new and exciting things which can eventually become familiar and predictable as well. 

Well, it's now an hour later.  Things are a bit quieter upstairs.  I still hear her crying.  I still hear her trying to talk herself into a comfortable place in her brain.  In the midst of the meltdown I gave her medicine and Daddy has brushed her teeth, given her eye drops.  She's been back downstairs to apologize for hitting me and having a tantrum, because she "really misses Peppa [Pig] and really can't go to bed without watching an episode."  

She's slept in a hotel, traveled hundreds of miles to San Francisco to be examined and have bright lights shined in her eyes, been talked about regarding her vision, been to the cardiologist and had her weight, her heart surgery discussed, been up early and in bed late, and been to school where they are prepping for major testing next week.  I KNOW this kid is under stress.  I wish I could take it all away from her and tell her that she'll never have to worry about another doctor taking pictures of her heart, or her belly, or her eyes...but I can't.  

I can't help but to be there and to let her watch a "Peppa Pig" episode despite her behavior, because it's the best thing for her soul right now~that...a maybe mommy or daddy saying in that "Full House" sort of way:  

I'm there for you, Babe.

Tuesday, February 24, 2015

The Waiting ~ WAGR Wednesday

Handsraised for #rdd2015 #rarediseaseday on Lake Tahoe

There is a lot of "waiting" that comes along with having a rare disease.  First, my husband and I waited at the hospital for the doctors to figure out where to refer us when my daughter was three days old.  They drew blood and sent it off to Texas for a special FISH analysis and we waited for weeks for the confirmation that she had WAGR Syndrome.

We waited in the ERs and Urgent Cares for doctors to come in and ask the same ridiculous questions which had nothing to do with our visit. 
  • Was she full term?
  • Any complications during pregnancy?
  • Was it a  normal delivery?
This was not necessary questioning when we knew it was pneumonia or a UTI, but, as the "3 Ring Circus" that drew observers from all over the hospital, apparently we needed to be patient and wait for them to satisfy their curiosity.

We waited while our daughter would be under sedation for eye exams and ultra sounds; we waited through eye surgeries, chemotherapy appointments, surgeries, and recoveries.  We wait for blood tests to figure out how her hormone levels are, and how her kidneys are functioning.

Waiting for medicaid approval and acceptance into the county programs was and is hard, because financial concerns heaped on emotional duress only multiplies exponentially one's fear of the future. 

Life with a rare disease can be lonely as we wait.  Waiting for the next diagnosis, the next medication, the next referral to a the next specialist.  We wait for researchers to show interest, for pharma to release the "affordable" generic, for the FDA to "approve" it for children.
We wait, and wait, and wait some more.
On Saturday, February 28, 2015, if you would, please take a photo of you with your hands raised as a sign of solidarity with those living with one of the 7,000 rare diseases~let us know that we don't wait alone.  Post your photo to Facebook, Twitter or even on the official Rare Disease Day website with the hashtag #rdd2015 and #rarediseaseday to join hands around the world and make our rarest voices heard.

Sunday, February 15, 2015

What Did I Do to Deserve This? ~ Guest Blogging Day

Photo "Tomb" courtesy of  Tiverylucky/freedigitalphotos.net

 Near the cross of Jesus stood his mother... John 19:25 NIV

It's amazing to study the life of Jesus and to see how he fulfills the Law and becomes our High Priest who has walked the earth and knows what we go through while living here.  But, lately, I've had to come to terms with another piece that God, in all His wisdom, included in the Gospel.
The fact that Jesus's mother watched him die.
Being parents of children with special needs, many times, we have to face the fact that we could out live our children.  Yes, all parents have to face this; but as parents of children born with certain genetic conditions or medical conditions; we have to live with the fact that our children are more medically fragile. 

Continue reading on Comfort in the Midst of Chaos...

Wednesday, January 28, 2015

The Ticking Timebomb They Sent Home from the Hospital


I'm sure no one thought that when they stuffed the folders at the hospital to send home with new parents they were placing in those folders a time bomb.  

Tick...tick...tick...

A free ninety days (or something like that) of a life insurance policy for your baby named after a popular baby food brand.

Tick...tick...tick...

We took our folder and our baby home, having just learned that she had something wrong with her eyes called aniridia (lack of iris in the eye) and that she might have a rare disease called WAGR Syndrome.

Tick...tick...tick...

WAGR...W~Wilms Tumor (Kidney Cancer), A~Aniridia (Possible Glaucoma, Cataracts, Blindness, and more...), G~Genitourinary Abnormalities, R~Range of Developmental Delays.

Tick...tick...tick...

We were told by our doctor that babies normally eat, sleep, and poop.  If our little girl was doing that, we were just fine.  In the meantime, we were waiting for the results of her genetic testing to confirm or lay to rest the theory that our lives were about to change dramatically.

Tick...tick...tick...

One day, I decided to go through the folder from the hospital.  My maternity leave was filled with fear; I was learning to be a mom for the first time, but at the same time, I was afraid that our baby wouldn't grow old enough to even wear an 18 month sized dress we had received as a gift.  I kept myself as busy as I could, and even filled out the flimsy leaflet that was the application for the life insurance plan with a perfect baby face on the front of it.
"List any health conditions the baby has..." it said...

"Aniridia and possibly WAGR Syndrome" I wrote...
Wasn't I naive?

Tick...tick...tick...

A letter arrives in the mail with a perfect baby face on the front, and the perfect baby lips shaped so naturally I could almost hear the coo.
"We regret to inform you that your baby doesn't qualify..."
Tick...tick...tick...
"This by no means is any indication that we don't believe your child will live a healthy life..."
Kaboom...

...This is life with a rare disease...
...This is life when you feel you may be the only ones...
...This is life before we found the International WAGR Syndrome Association...
...And this is why I, from that day forward, refer to the "anonymous" company's insurance policy as the "Blankety-Blank Throw Up Plan"...

BTW, Blankety-Blank Company, she's 10 (and a HALF) now!


Telling Your Story



If you've never written about receiving a rare disease diagnosis for you or your child, now is a good time.  Rare Disease Day is just a month away, and you can share your story to a large audience and put rare disease on center stage for a day. 

  •   Start by identifying your theme.  Do you want to talk about receiving the rare disease diagnosis?  Handling appointments with doctors, therapists, etc?  How your friends and  family responds to a rare disease diagnosis?  Difficulty in accessing good medical care?
  • Draft a timeline.  This helps to get your thoughts in a chronological order and will help you recall details that you might otherwise forget to include.  The timeline could be your child’s life up until now, or could just be a specific timeframe like infancy, school years, Wilms Tumor treatment, etc …
  •   This is the step I call:  “Throw-up on the paper or the screen”.  In other words, just start typing or writing now that you have laid out a timeline of the events surrounding your theme.  It’s much easier to “tweak” your writing once you have something written out.
  • Read through what you’ve written.  Have you made it personal by writing “I” and “we”?  You want to when you are sharing your story.  Have you used all your senses to describe events you wrote about?  Sights, sounds, smells, and the feelings they generated within you.  Have you identified who, what, where, when, why and how?  Be sure to keep privacy for doctors and others by either saying Dr. S or using alias names if you haven’t asked their permission to write about them.
  • Have another person read and make grammatical corrections and other suggestions for helping to expand or condense your story.
  • Make sure the first paragraph and the last paragraph engage the emotions of the reader, and also point to the theme of your story. 
  •   Ex.  Our daughter’s rare disease diagnosis came on the third day of her life.  We had all of our dreams and securities ripped from our hearts.  Suddenly our lives; rather than filled with plans of visiting friends and family to show off our newborn, became filled with doctors appointments, therapist visits, and a scramble to obtain additional insurance to cover our new medical costs.
  •   Ex.  While we are 10 years into our journey, we still wrestle with fears of the unknown future for our daughter and her rare disease.  We rely on researchers and lawmakers to take notice of the rare disease community to grant us more security here on earth and to help point us toward and brighter tomorrow.
  • Share your story!!!  There are a number of ways to do it, but first visit http://www.rarediseaseday.org/tell-your-story/ and click on the “write your story” icon…you can copy and paste your story and share it with the world.  Post your story on Facebook in your Notes section.  Send your story to your state and national leaders-e-mailing them is easy off of your government’s website.  Be sure you use #raredisease #rarediseaseday and #NORD if you are sharing your story on social media.

Saturday, January 24, 2015

Her World, My Mystery


What is it like to live there?
Lying down and staring up,
Watching Full House or singing with K-Love, 
Rocking back and forth, 
Creating a rat's nest to brush out later with tears.

What is it like to live there?
Knowing enough, but not knowing enough,

Knowing you're different, not just unique; 
But very, very different from your friends.
Knowing that your health has never been good, 
And that this will never change.

What is it like to live there?
Trapped behind eyes that don't hide the light,
In a mind that struggles to find her senses;
The senses to make sense of it all,
In a body that struggles to run, jump, and play,
With a mouth that can't say for sure how you feel.

I want to know what it's like to live there, 
In your own world, in your own struggles, in your own thoughts.  
It is a mystery to me...a painful mystery I try to solve,
Taking one clue at a time, as they come, 
And piecing them together to be a better mother for you every day.

Written in response to Sunday Scribblings 2 Prompt:  lost in her own thoughts

Wednesday, December 10, 2014

Sometimes it's Not the Lions; It's the Flies~WAGR Wednesday

When you first learn that your child has WAGR Syndrome, there are a few things that stand out and cause fear deep within your core:

Your child's heightened risk of developing cancer (Wilms Tumor)
Your child's heightened risk of being blind
Your child's heightened risk of experiencing kidney failure (Focal Segmental Glomerulsclerosis)

But, sometimes, it's not necessarily these "big things" which cause the most heart-ache.  Sometimes it's the "little things" that can eat at you day after day. 

What makes me think of this is an article in the New Yorker from April of 2014 which reveals that a recent study found the most likely reason that zebras have stripes is to prevent biting disease-carrying flies from landing on them.
Flies?
Really?
What about lions?  
         Wildebeests?  
                   Cheetahs?
Zebras, having each of them a unique pattern, size, distribution, and boldness of stripes, appear to have more stripes and a bolder pattern in the areas of the world where they would run the risk of being bit by flies.  According to biologist Tim Caro, "We found again and again that many stripes or intense striping is associated with areas that tend to have many biting flies over the course of the year."  (New Yorker, 4/2014)
This started to make sense to me as I thought about the "little things" that tend to take up a lot of time and create a lot of heart-ache as a parent of a child with WAGR.
Developemental Delays:  As our babies grow, become toddlers, become school aged; we start asking, "When should they be walking?  When should they be talking?  When should they be potty-trained?"  We have NO CLUE what developmental milestones our child will meet, or IF she will meet them at all.  I recall getting mailings every few weeks from the hospital where Evie was born in Madison.  They would say, "Your baby should be...." and it would list all the things she should be doing at that age.  What a horrible mailing to receive while I watched my child fall further and further behind her peers.  I began to just dump those mailings in the trash upon their arrival. 
Ouch...fly bite.
Sensory Processing Disorder:  Head-banging, biting, hair pulling, hitting, screaming...Evie did all of these as she transitioned to her toddler years.  Where had she learned this from?  We felt helpless, and, at times, frightened by how we would live day to day with these kind of behavior issues.  I never wanted to go out, I never wanted to take her anywhere that would "throw her off."  Once I read "The Out of Sync Child," and started to realize that Evie's issues were sensory in nature, and not just a complete hatred of me, her mother; I started to look for ways to LIVE with SPD.  We got Evie into out-patient occupational therapy at a hospital in Madison and life became so much more enjoyable.  But, up until that point, I felt like I lived in a tremendously deep hole out of which I could not climb.
Ouch...fly bite.
Loss of Friends:  As much as people want to be "open to it" and want to say, "your child is no different," we have seen friendships fade after having Evie.  You start to realize that your "group of friends" got together without inviting you.  The reason?  "We know it's hard for you to get out."  "We understand that it's hard having a child with disabilities."  "We didn't want to pressure you."  No.  That's a nice reason which helps these people sleep at night.  It's actually that they don't know how to relate to us anymore.  They don't understand WAGR, or disabilities, or blindness, so they don't want to have us ALL get together, and have no idea how to answer their OWN kids' questions; so, to avoid the uncomfortable situation, they no longer invite you.   You really DO learn who your real friends are when you have a baby born with special needs.

Ouch...fly bite.
As was pointed out in the New Yorker article, "while a single bite from blood-eating flies extracts just a tiny droplet of blood, thousands of bites per day can add up to significant blood loss."
I can't reiterate that enough.  Our daily "fly bites" are Significant.
It's hard to sleep at night when you're wondering if your child is crying because she's in pain from a stomach flu, teething, cancer or pancreatitis.  It's hard to wake up and do your hair and put on make-up when you wonder if you'll just end up crying it all off because your daughter bit you and had a meltdown.  It's hard to pick up the phone and call your sister because, when your child hears your voice in "talking on the phone" tone, she comes into the room and immediately demands your attention by yelling and whining, and then proceeds to throw herself against the wall, bang her head on the floor, and bite her hands.  
It's just plain old hard.
So, while cancer seems to always get everyone's attention with WAGR, when our kids are diagnosed with Wilms Tumor and our world suddenly becomes filled with people who want to help, want to bring food, want to send you a gift card, want to watch your kid so you can do some laundry (don't get me wrong, we DO appreciate these things)...we could really use those people to surround us on a daily basis in between the meltdowns and specialists; to celebrate the first step at age 3 or the first time they used the potty at age 5.  We could really use the friends calling us to say, "I know you're busy, but I was hoping we could all take the kids to the park and have a picnic."  We could really use people who want to learn more, want to help support us, want to come with us to a WAGR Weekend so they can meet other families with WAGR, or want to read our newsletters so they can get a  better glimpse into our WAGR World.

The best fly repellent for us; the rarely understood, is love, compassion, and inclusion.

Wednesday, November 5, 2014

When the Heart Hurts ~ WAGR Wednesday

Photo by Erin Moore Photography
Yes, my daughter is legally blind.  Yes, she is a cancer survivor.  Yes, she has high blood pressure and the possibility of kidney failure down the road.  Yes, she is developmentally delayed. But what do I fear the most?

Her heart being hurt.

I was picked on as a kid, and I know how much it made my heart hurt.  I don't want to see her go through that.  But here she is, a ten year old who still sucks her thumb.  A ten year old who is scared to lock a bathroom stall door for fear of being locked in.  A ten year old who, when the rules of the "game" change, or when someone doesn't WANT to play it her way, will break down into tears and not listen to reason. 

I feared it a "little" when we lived in WI, but that started to wane as we were becoming more and more woven into the fabric of the community.  I saw how the kids loved her, her good parts and her not-so-good.  I saw how they just kind of attributed some of her quirks to "that's Evie."  So, when we decided to follow God's plan to take us 1800 miles away to Nevada, it was the social changes that made my heart hurt the most. 

School work, we can deal with. New doctors, we can work through.  Getting new medicaid coverage, just a matter of time and mountains of paperwork.  But, friends...friends?  How do you establish the same types of friendships that took nearly a decade to create?

Last week, the ugly beast of Evie's anxiety reared it's ugly head.  Her amazing group of girlfriends were at recess with her, and they had planned to play school (just like Evie loves to do), but then some decided that they DIDN'T want to play school.  I guess that didn't go over well, and there were tears from Evie...and, if you've ever seen the tears and reaction to "plans changing" for her, well...it can get pretty dramatic.  The teachers took care of the situation, and that was great.  I didn't really think anything of it, because it didn't seem to bother Evie all that much, so I thought, "no big deal." 

Until Monday...

I'm used to seeing the girls surround Evie and just kind of absorb her into the flock when I drop her off in the morning.  They USUALLY give me a big hug, and start chatting about their weekend, while Evie is, not-so-subtly, trying to get me to leave.  But, on Monday, there was an odd silence when we approached the spot where her class lines up.  The girls were already involved in their own conversations, they looked up at us and smiled, but Evie didn't get sucked into the circle like she usually does. 

I saw the blank look on Evie's face, like there were gears turning, but she didn't quite know what to think. She just stood there, staring at the circle of girls.

"How about if I stay and we can chat?" I asked.

"No." said Evie, not removing her eyes from the circle.

A girlfriend strolled by and said, "Hi, Evie, how was your weekend?"

"Good," Evie replied with a smile.

"I'm going to go get in line," said the friend, excusing herself.

Evie turned around and went to the back of the line of backpacks that held the students' places on the ground.  Still the circle of girls didn't break up, or open, or invite.

Why did this feel so tense to me?

A boy walked up to Evie and started talking with her, so I carried Evie's "big book bag" over to her (it holds her assigned reading which is enlarged so she can read it with her low-vision).  I set it down and gave Evie a kiss.

"I love you, Peanut and I'm excited to see you after school, and then tomorrow is a no school day, and we can spend the whole day together!"  I said, adding the last part as a comfort, more so for me than for her.

On  my way out of the playground, I tried to hold back the tears.  Thankfully, my sunglasses helped mask my blinking eyes.  I started to recall the story of the playground drama from Thursday (we had Friday off of school)...and I realized that the awkwardness and tension may have been coming from that.

Oh no...my worst fear!  They had seen a meltdown and now things were weird.  To use my Minnesota-Girl vernacular, "Crap."

I had a lot of other things on my mind that day too:  The medicaid paperwork was due and I hadn't had a callback yet from my two messages I left with questions on how to fill it out; I still didn't have access to Evie's chart at her new medical specialist's office, so I didn't have a way to get them some necessary documents; and I was trying to figure out how to prove to medicaid that Evie doesn't qualify for SSI when a parent can't sign a child up for SSI on-line, so you have to go to an office and do it in person, and yet I only had a week to get the papers back to the Las Vegas office. 

I became a complete emotional wreck. 

This is when the heart REALLY hurts.  When all the weight of WAGR piles on and you don't know how to fix ONE let alone ALL of the problems. 

Evie's SPED teacher phoned me in response to a distraught e-mail I sent her.  We agreed that this is a difficult situation.  That the kids need to learn not to take this type of thing personally; that it's Evie's inability to cope with change well, and that it's okay to not let her get her way.  I wanted to let the teachers to know that I don't expect kids to play with Evie if she's being difficult; that we can give her a choice to play cooperatively or to have some alone time, but that demanding everyone do everything her way is not an option.  I'm so thankful for her teachers who are so eager to help Evie "fit in" and yet teach her the right way to socialize.

Thankfully, we had yesterday off of school, so I was able to protect my bird the way a momma bird does.  Today when I dropped Evie off, it seemed like things were back to normal for the most part.  Her friends were enthusiastic and welcoming and warm. 

Maybe I had over-reacted.  Maybe I had let me own  past hurts affect how I saw this situation.  Maybe there were a bunch of other reasons why Monday morning felt different.  I'll never know.  But I do know that I wanted to share the heart-ache that we feel as parents of kids who are "different".  That sometimes, the medical fears play second fiddle to the socialization fears. 

That sometimes the heart.
                                       just.
                                             hurts.

Wednesday, October 29, 2014

Patience as Patients ~ WAGR Wednesday

Photo of Janet (Ms. Jackson, if you're nasty) couresty of http://welove3t.weebly.com/uploads/4/3/9/1/4391192/207730_orig.jpg
As I sit here, my bright pink ear piece plugged into my right ear and the microphone/mouth-piece curved down along my jaw line (go ahead, picture Janet Jackson, I'm okay with that), I am listening to broken, fuzzy, pointless music and waiting (25 estimated minutes) for my call to be connected to someone at the Division of Health and Human Welfare somewhere, in some building, in some city here in the great state of Nevada.

I thought I'd take the time to write a little bit about the patience that we have to demonstrate as we meander the rocky river of life with WAGR.

I knew that moving to a different state would mean re-applying for all of Miss E's services.  I knew that we'd be going through an onslaught of "first" appointments in which we may or may not meet people who give a flying fig about a disease as rare as WAGR.  I knew that I'd be applying for a substitute teaching license and would be basically unemployed as we met our annual deductible for our health insurance and paid the bulk of our medical costs out of pocket (Thank God for HSAs!). 

I forgot, however, how much PATIENCE it takes.  

I have patience with little classmates of Miss E who are trying to learn about the syndrome that their new classmate has...can I not have patience with the doctors who are treading into new territory as well? 

I have patience with the social worker who exchanges pleasant conversation with me as she learns about WAGR in our home...can I not have patience with the person who sits in the office and has to take angered call after angered call from people who need their help just as much, if not more, than my family does?

I have patience with the pharmacy that knew us well because they had been in the trenches of medication after medication for blood pressure and glaucoma and constipation from chemo...can I not give a little of that patience to the new pharmacy here who never seems to have a correct co-pay total for me even months into this process?  A lot of information runs through a pharmacy each day.  

"Patience," I must tell myself, "You are here and teaching new people about WAGR.  Someday, when they will hear the term again, they will say, 'Oh, I remember doing this for someone with WAGR before' and that will bring comfort to another family who is diving in to the rocky river for the first time.

Well, I'm down to 10 more minutes of my (estimated) wait time.  Yay, I've used this time wisely!  Had I closed my eyes to listen to the "tin can" music, I likely would have drifted off to sleep and missed the opportunity to talk once it was my turn.  

 I'm not sure if you are aware, but I try to blog often about WAGR/11p Deletion Syndrome, and share my point of view as a mother of a child with it.  There are a lot of intricacies that accompany this genetic disorder, and they are worth laying out on the table so parents and guardians can discuss them with doctors, therapists, teacher, and even friends and family.  

To read more of my WAGR Wednesday posts, just follow this link!  

And, for the record, I just got off my call...it was 56 minutes and 43 seconds long...I had a truly nice chat with Phyllis, who was sweet as could be, and she will get my message to the worker assigned to our case...she requests 48 hours to return calls...

Patience...

Wednesday, October 22, 2014

Devoted to Doing Good ~ Guest Blogging Day

Photo Courtesy of Gualberto 107/freedigitalphotos.net
Do everything you can to help Zenas the lawyer and Apollos on their way and see that they have everything they need. Our people must learn to devote themselves to doing what is good, in order to provide for urgent needs and not live unproductive lives.  Titus 3:13-14

This week we embark on a new adventure.  For 10 years we were seeing the same doctors in Madison, WI.  They had seen us through good times and bad.  They had delivered us both exciting news and devastating news.  They had become trusted, loyal, and steadfast companions in our WAGR Syndrome journey.  

But that chapter comes to a close and we now turn our eyes to the medical professionals in California.  They don't know us.  

Read more at http://www.comfortinthemidstofchaos.com/2014/10/devoted-to-doing-good.html ...

Friday, October 10, 2014

What's a Parent to Do? ~ Guest Blogging Day

Photo Courtesy of ImageryMajestic/freedigitalphotos.net
Remind the people to be subject to rulers and authorities, to be obedient, to be ready to do whatever is good, to slander no one, to be peaceable and considerate, and always to be gentle toward everyone.  Titus 3:1-2 NIV

I've decided that God likes to humble me weekly as a means by which to give me my next "blog" topic.  At least, that's the way it's felt lately.  Just this past week, I can name two distinct times when I did NOT do as Paul had instructed here in Titus 3.
 
Continue reading on Comfort in the Midst of Chaos...

Wednesday, October 8, 2014

My Kingdom For An Epi-Pen...~WAGR Wednesday

Emerald Bay on Lake Tahoe
The never ending excitement of having a child with a rare disease...

Most of the time, in spite of all of Evie's numerous diagnoses, we live a tranquil life.  However, on Thursday of last week, we experienced another "bump in the road."  

I got a message on my phone from Jeff saying that Evie had been stung by a bee at school.  He said he was going to take Benedryl over to the school.  I suggested he get the non-drowsy since we'd never really had an issue with bee stings, so a major dose was probably over-kill. 

As it turned out, that was everything EXCEPT for over-kill.  When Jeff was still on his way there, he got a voice mail from school saying that they were going to administer the Epi-pen because Evie was swelling dramatically and turning blotchy red and white. 

Evie has been stung by bees before, and we have never seen an allergic reaction.  This time, however, had the nurse at school not made the decision to administer epinephrine, I shudder to think of what I would be sitting here writing right now.  

It was our first trip to the ER here in Nevada.  Evie was transported by ambulance to the hospital, and I met her and Jeff there.  Evie, in her character said upon my arrival..."I have a question for you...for ALL of you..."  We paused and awaited this important, tear-filled question:  "Can I still give my book talk tomorrow at school?" 

Tough.as.nails, these kids with WAGR are. 

After being released from the ER, we dropped off our Epi-Pen RX at Walmart and headed to get some frozen yogurt while the meds were being filled.  I then drove Jeff and Evie back to school as Jeff's car was there (he had ridden in the ambulance with Evie to the ER.)  

When I returned to Walmart to pick up the RXs, I was told that they couldn't fill the Epi-Pen RX as it was written for a Junior Epi-Pen and Evie needed an adult due to weight.  When I said, "Well, there must be something we can do" the pharmacist told me that they had already called the doctor and he had left for the day and we'd have to wait for him to call back.  

Here's me...

"I just found out that my daughter has a life threatening allergy...I will NOT leave this store until I have an Epi-Pen in my hand."

"What do you expect us to do?" 

"There IS a way to get around this.  I'm certain that the doctors and nurses who observed Evie today would NOT want us to be without an Epi-Pen.  What number did you call?  I will call them and get this cleared up."

The pharmacist, pursed lips, doubtfully furrowed eye brows, turned the computer screen to show me the ER's phone number.  

I called and explained who I was and what I needed.  The receptionist informed me that I could call another number, which she gave me, and ask for an ER doctor to re-write the RX.  I then gave the pharmacist tech the new number and he called and got the re-write taken care of.  About 30 minutes later, I was on my way home with our precious Epi-Pen.

In all the things that we have been through; cancer, heart surgery, recurrent infections...I don't know that we have ever been at the precipice of a life-threatening situation such as this.  Had our WONDERFUL school nurse NOT administered the Epi-Pen...I quail at the thought. 

Did you know that the epinephrine administered through the pen is done so to prevent the HEART FROM STOPPING, and to keep the blood pumping to all parts fo the body.  I didn't realize how disastrous an allergic reaction could be.  Her HEART could have STOPPED.  This wasn't just a throat swelling, or eyes puffing up, or an itchy rash.  This was her HEART!.

So, I have learned many things from this experience, and one of them is to NEVER MAKE LIGHT of an allergy...the other is SCHOOL NURSES are LIFESAVERS...and finally GOD HAD US IN THE RIGHT PLACE AT THE RIGHT TIME.  

What would have happened if Evie had been stung when she was just with our family and we didn't KNOW she had this allergy?  What would have happened if she would have been on a field trip?  What would have happened?  What would have happened?  We were in good hands (in my life, I'd say we were in God's hands), and we are thankful to be enjoying the week we are just one week after such a harrowing experience. 

...and finally, I will not go ANYWHERE without our Epi-Pen...