Wednesday, December 31, 2014

Humble Pie :)

I can honestly say, I hope no one uses me as a role model.  I pray my children model after Christ, their perfect Savior, and not their very imperfect mother.  I have been very convicted today by my attitude regarding insurance.  I let frustration get the best of me instead of focusing on the blessing that abounds in my life.  God has always supplied our every need.  William has never gone without medical treatment, medication, or equipment.  Sherrod has never gone without medical treatment, medication, or equipment.  I've never had to watch my child struggle to live because we couldn't meet their needs or get them medical treatment.  None of our children have ever wanted for food, clothing, or shelter.  Even when things were hard, God has always made a way.  It's the reason we chose not to go with SSI to begin with...because we wanted to fully rely on Him.  Others may have made a different decision and that's okay.  This one was ours.  And He's NEVER let us down.  And He never will.  I know that.  We don't trust in Michael's job or our insurance or money itself.  We trust in Someone much bigger than all of that.  Someone Who controls it all.  He never promised it would be easy.  He never promised we would be able to do whatever we wanted, whenever we wanted.  He never promised we wouldn't have to work or sacrifice.  But He did promise to supply all our need according to His riches in glory through Christ Jesus.  And THAT I can rest in.

May the Lord continue to grow me in strength of faith and character in the coming year.

Tuesday, December 30, 2014


So...I kind of dropped off of my posting here because so many of my family and friends are on FB.  It was easier to just post everything there because I always post from my mobile.  But, as you can tell, I've gone back to the blog.  After William's most recent scary episode, Michael felt it would be better to keep everything about William here on his blog (and some tidbits about our family).  So here I am again! :)  That said, for those of you who are friends with me on FB, you know the frustration we've had with our insurance over Sherrod's insulin.  Grrr... We've often fought with them over William's needs, too.  It seems that our insurance company views my children as lab rats.  Experiment to see what works so they don't have to pay out the money we've already paid in if they can keep from it.  Why am I so frustrated about this today, you might ask?  Well, William's nebulizer quit today.  In my panic to get another one before his next treatment, Michael and I ran to the pharmacy and, you guessed it, the pharmacist informed us that our insurance does not cover his nebulizer.  Of course, we got it for him anyway.  The same as we did with his Vest.  AND with his Cough Assist.  AND with assistive walking devices.  I'm wondering if they aren't trying to force us into Government controlled healthcare? We've never taken SSI/disability for William for SEVERAL reasons.  Would private insurance try to force us into this?  Anyone have any experience or thoughts?

Anyway, William got his new nebulizer.  His last one was a plain ol' grey, drab nebulizer.  This one is a cool kangaroo one and he was pretty excited!

The pouch holds the neb cup when not in use.  Pretty cool, huh? :)

Monday, December 29, 2014

3 week x-ray

Well, today was the day.  The 3 week mark.  The day for William's x-ray.  I really expected it to be clear, as he is doing so much better.  But it wasn't.  There is still one small spot in that right lobe.  Ugh!  A new medicine and 3 more weeks.  The good news is that the homebound restriction is technically lifted.  The bad news is a new illness could be really, really bad, so we still have to be very careful.  So....3 more weeks.  Sigh.

Tuesday, December 23, 2014

Anyway Love

Okay, so I admitted yesterday that I've been struggling.  Wondering if my faith is as strong as I believed it was.  Today, I was looking over William's blog and I noticed several "draft" posts that never got posted.  The one that follows was in there from February 2010.  I don't remember it and it's especially strange because I see no reason why I would post it on William's blog.  I don't know where it came from or I would cite the author...

On Valentine's Day, Meg went all out, giving her husband, Peter, his favorite candy and tickets to a hockey game. Later that night, she wrapped herself in a special outfit purchased just for the occasion.
Peter got her a card.
At the grocery store.
That he purchased on the way home from work.
He didn't add anything to it, either. He just signed it, "Peter."
A couple of days later, Meg tried to explain that she felt a little taken for granted. Apparently, Peter misunderstood her intent because two months later, when they celebrated their anniversary, Peter didn't get Meg anything.
"How could you not get me anything for our anniversary?" she asked Peter the next day. "Especially after our conversation about Valentine's Day."
"Well, I thought about getting you something, but it didn't work out," he replied. "And then I knew not to get you a card because you said you didn't like that last time."
"It's not that I didn't like the card. It's that the card alone seemed a little sparse. But even that is better than nothing ..."
Several months later, Meg had a birthday. This time, Peter got her a present – a kitchen tool set. Several weeks before, Meg had asked to borrow Peter's tape measure and screwdriver. Peter figured that Meg should have her own small set of kitchen tools so she didn't have to borrow his.
Meg recounted all this and then explained how she had tried to get her husband to read several how-to books on loving your spouse. He would read the first few pages, lose interest and never pick the book up again.
"I've realized this is never going to change," she confessed. "But I love him anyway."
That last statement of Meg's, "but I love him anyway," is one of the most profound theological statements on marriage I've ever heard. Most of us base love on because, not on anyway. I love you because you're good to me. I love you because you're kind, because you're considerate, because you keep the romance alive.
But in Luke 6:32-36, Jesus says we shouldn't love because. We should love anyway. If we love someone because that person is good to us, or gives back to us, or is kind to us, we're acting no better than anyone else. In essence, Jesus is saying you don't need the Holy Spirit to love a man who remembers every anniversary – not just the anniversary of your marriage, but the anniversary of your first date and your first kiss. Any woman could love a man like that. Or if you love a wife who lavishes you with sports gifts, who goes out of her way to make you comfortable when you get home from work and who wants sex anytime you do – well, you're doing what any man would do. There's no special credit in that!
But if you love a spouse who disappoints you, who can be a little self-absorbed – now you're loving anyway. In doing that, you're following the model of the heavenly Father, who loves the ungrateful and the wicked.
... Or Anyway
Will you love only because? Or are you willing to love anyway? Will you love a man or woman who doesn't appreciate your sacrifice? Will you love a husband or wife who takes you for granted? Will you love a spouse who isn't nearly as kind to you as you are to him or her?
Just about every faithless marriage is based on because love. Christians are called to anyway love. That's what makes us different. That's what gives glory to God. That's what helps us appreciate God's love for us, because God loves us anyway. He gives and gives and gives – and we take Him for granted. He is eager to meet with us, and we get too busy to notice Him. He is good to us, and we accuse Him mercilessly when something doesn't go just the way we planned it.
But God loves us anyway. To love anyway is to love like God – and to learn about God's love for us.
That's love, the way God intended it.

This really made me think of God's love and my love for Him.  Do I love HIM anyway?  It's easy to love Him because...because He blesses me, because He takes care of my needs, because He protects me, because my life is easy.  The hard part comes on the anyway.  When times are hard, do I love Him anyway?  When I don't understand, do I love Him anyway?  When I am angry and hurt and broken, do I love Him anyway?  Do I understand that He is in control of all things AND that He works all things together for the good of those who love Him and who are called according to His purpose?  Do I trust His plan?
Yesterday, I was speaking with a friend and sharing my doubts of myself with her.  She lovingly reminded me that no one is able to bear hard things well, except for the grace of God.  God gives grace as it's needed.  Right now there are certain graces I don't need, but there are many that I DO need.  God gives me the graces I need in the time I need it.  (Thanks, Tanya!)  I do feel reassured.  I'm still struggling with my sleep, but I am praying through that, as well.  Fear still grips my heart at times, but I'll keep praying through that, too.  God's grace.  God's timing.  Perseverance.

I'll end with this song that has become a favorite of mine.  A friend sent it to me when I was in my 38-hour labor with Titus.  :)  By the grace of God, may I always be able to say, though He slay me...

P.S. Until today, I had only heard the song, not the message from Piper.  God is good all the time.  I feel as though He is bringing things together to reassure me.  Praises to Him.

Monday, December 22, 2014

Hard Things

So, I've never been a person to be gripped by fear.  Fear has never controlled my life or driven my thoughts.  I've never been a "what-if" person who is plagued by thoughts of dred.  Yet, I find myself in new territory.  I've been questioning if my faith is as strong as I once believed it to be.  Ever since I saw my little boy lying in that bed, helpless and limp, breathing on the ventilator.  I remember crying out to God, but all I could think of is that I'm not strong enough to walk this road.  I have friends who have walked hard roads in life who are a vision of strength in the Lord.  Who never waver.  Who praise Him faithfully in all things.  Who say, without hesitation, "The Lord gives and the Lord takes away.  Blessed be the name of the Lord."  Is this me?  Can I be so unwavering?  I don't know.  I honestly don't know.  I don't think anybody really does until you're in it.  I'd like to think my faith is that strong.  But I truly don't know.
Ever since William got out of the hospital this last time, I've been plagued with nightmares.  I'm not sleeping well.  In fact, I don't even like to go to sleep.  All I can see when I close my eyes is William lying in that hospital bed, appearing lifeless.  And my vision will shift between him and Riley until I can't tell the difference between the two.  It's weird and it haunts me.
Riley is my nephew.  I can't even describe how much he and William were alike.  Many of the same issues.  Much of the same heart, sweetness, and orneriness.  Riley stopped breathing 7 years ago and he never returned to us.  He was 6 years old at the time and he would have been 14 today.  William was 4 days old and he never knew his cousin.  That is truly a loss.  They would have enjoyed each other immensely.
Riley 2006, his brother, Kash 2013
My sister is a woman of strength.  She continues her life.  I admire her.  She did not let this great loss defeat her, make her into something she is not, define who she is.  Could I do the same?  I don't know,  but I pray I never find out.
It bothers me that I know that William's condition will likely shorten his lifespan.  It bothers me that there is little I can do for him.  It bothers me to not be in control of all things.  It is a daily struggle to give my cares to the Lord and not worry.  He had a whole year with no illness and I really fooled myself into thinking the worst was behind us, that he was strong, that the worry was over.  Now it's back with a vengeance.  How do I let go? How do I let him be a regular little boy and not fret over everything he does? Over every person he comes into contact with?  How do I not drive myself crazy trying to keep him healthy?  I know the answer lies only in my trust in the Lord.  That is my struggle.  Daily faith.  Constant trust.  True belief.  Lord, I believe, please help my unbelief.

Friday, December 19, 2014


Oh, this boy! He just melts my heart!

Last night when I finished singing, he leaned over and said, "I just love you.  ALL of you!" LOL! I'm not sure if that was a reference to my singing ability (or lack thereof) or not, but I sure know that it made me smile!  He does that often!  Out of the clear blue he'll just lean over and tell me he loves me.    He is such a blessing!  My heart overfloweth!

Wednesday, December 17, 2014

Home Bound

William asks me everyday when he gets to go somewhere.  When he gets to see his friends.  When he gets to see his friend, Matthew.  When he gets to ride his horse.  But he's still pretty weak.  His doctor appointment Monday went well, but it was like a covert operation.  I left him in the car with Sherrod while I went to the receptionist's window to check him in.  She opened the back door so he wouldn't have to wait in the waiting room, but go straight in to a room.  We washed and sanitized and got all OCD about cleanliness and germs.  Yet, this morning he awoke with a cough.  Ugh.  Two weeks until we go for his X-ray.  I think we'll all be a little stir crazy by then.  We aren't allowing any of the younger children (10 and down) to go anywhere.  The adults are all careful about where they go, except Michael, who has to work, but he's fanatical about cleanliness and changing his clothes.  We've not been allowing visitors over, either (that's a real bummer).  We are praying he gets the all-clear in 2 weeks.  Two more Sundays.  12 days.  I miss date nights with my husband (yes, even that's gone by the wayside for now)!  I miss our Church fellowship.  I miss the fellowship of our homeschool group.  I kind of feel like I live in a cave, but it's all worth it for a healthy boy!

Monday, December 15, 2014

Respiratory Therapy

William's home therapy station...
Suction machine (top left)
Nebulizer (top right)
Cough Assist (bottom left)
Vest Airway Clearance (bottom right)

He's been back to 4x daily for all 4 machines since he left the hospital.  He goes in for a recheck today.  I think he's sounding pretty good.  He's still really weak, though.  He isn't really crawling around much, but prefers to be carried.  Sometimes he wants to walk but it's usually about 20 steps or so, then he's spent.  I don't really know how much to push him and I'm kind of waiting until he gets the all-clear to push too hard.

As a side note...William really likes his hair to be cut short (he especially wants it to be cut like his friend, Christian's).  He was after me at the hospital about it being too long, as he really needed a haircut before he was admitted and 3 weeks later he was looking a little grizzly. :) Anyway, the day he got home I cut his hair.  He doesn't typically like for me to cut it because my clippers vibrate too much and I take too long.  :) However, since he's homebound, I told him he couldn't go to the salon for a haircut, so he tolerated mine.  I cut his hair while he was lying down.  Now, what hairstylist would do that? Well, as you can tell, there's a s slight diagonal to the front of his hair, but he was done and I didn't push it.  Unfortunately, the OCD part of me is really struggling with this...

Tuesday, December 9, 2014

Home Update

William is doing well at home, though still very weak. He is homebound for the next 6 weeks while he continues to heal. There is still a spot in his right middle lobe that must come out. We go to the doctor in 3 weeks to recheck it. If it's still there, he will have a change in medication then another 3 weeks. If it's still there after the 2nd X-ray (6 week mark), he'll have to go back into the hospital for a bronchioscopy to get a look at it. If the doctor can clean it out then, he will. If not, it will require surgery. Thank you for your continued prayers on William's behalf.

Sunday, December 7, 2014


AND...we're outta here! 3 weeks felt like forever! (Still with a long road ahead.)

Everyone is so happy to be together again! 

Saturday, December 6, 2014


William is the talk of the floor. He's been walking around, playing his harmonica today. He's had other parents and nurses from the other section coming up to ask him to play for them. So cute!

Thursday, December 4, 2014


Getting better all the time! If X-ray looks clear tomorrow and he continues to improve, we might get to go home Sunday! Whew! 3 weeks is a long time!

Wednesday, December 3, 2014

Special Visit

Look who came to visit William...

Monday, December 1, 2014


William made it through the entire night with no supplemental oxygen! Dr says he's doing very well but we're still looking at a few days to clear out that lung more. If we don't get it cleared completely there's a risk of secondary issues requiring surgery, so we definitely want to get it cleared up! William's blood pressure is elevated again, which could be a side effect of his medication. Just something to watch. I cannot express our love and gratitude enough to all of you who have been praying so diligently for him and caring for our family! Love to you all...