I love
blogging about Aaron the way that I’ve been able to do over this past year and
two months. Sharing Aaron with all of
you, and our life with Aaron, is a joy and a privilege. I sometimes wonder who is reading, and I
wonder if the blogs are a blessing, or do they ever come across as same-old,
same-old……….or shallow……….or silly……….or making light of a serious
situation. I know that many parents of
children with special needs really don’t have many reasons to laugh or even
smile. Their lives are full of the daily
care of children or adult children who need lots of care. Days are exhausting and nights are too
short. There is rarely any humor such as
we have with Aaron. Aaron happens to be
very verbal and at times, very funny.
Yet there are many seasons of frustration and tiredness for us as well.
My main
purpose for blogging is to share with all of you that even in the midst of
cares and burdens, and the heartache of having a child with special needs – we
can choose to see the good, or the humorous, and to take the time to learn the
lessons that God wants to teach us. I am
blessed beyond measure to share these thoughts and lessons with each of you.
Last week I
was very touched and very encouraged to hear from a special friend via
Facebook. Doretha Weyant and her husband
Brad crossed Gary’s and my path many years ago at Piedmont Bible College. We have reconnected through Facebook and have
enjoyed getting to know one another again.
Doretha and Brad have been a sweet testimony to me, and have given me
permission to share their story. We have
communicated a lot on Facebook for a long time, but last week I got this inbox
message from Doretha………..and it just blessed my heart to pieces. She said:
Patty, I thought of you and Aaron
yesterday at the doctor's office. I had gotten on the elevator to go to 2nd
floor and a mom with her 2 kids was on there. One looked maybe 8; the other a
teenager. The oldest boy said some strange thing very loudly and then went over
and hugged his mom. She looked at me and I just smiled at her. We got off the
elevator and they were coming to my dr. as well. They sat right behind me in
the waiting room, so I couldn't see them but could hear them. The oldest boy
was very loud and kept saying hey mom, hey mom, over and over til she would
respond. Then he would tell her all kinds of things from his day, doing so in a
rather loud voice. I sat there wondering if he had the same disability as
Aaron. Then I went in to see my knee dr. While in there I found out he had Down
Syndrome. I thought of your blogs about Aaron and I wish I could have
encouraged the mom, but didn't see them anymore. Just know that Brad and I
think of your family quite often and pray God will give you His grace to carry
on with your many trials in life. Aaron is a special guy and God has a
wonderful purpose for him here on this earth. Love ya. Doretha
The thing is……….Doretha wrote me
this note on the day that marked the one year anniversary of her own son’s
passing to heaven. This made her
encouragement to me even more poignant and meaningful. Let me allow Doretha to tell you about their
precious Ben:
Ben had Duchenne Muscular Dystrophy
which is an incurable genetic muscle disease. He had a mutation on his
dystrophin gene, a very large piece of the genetic exons were missing.
Dystrophin is the protein that basically keeps the muscles from falling apart.
He was diagnosed at 7 yrs old and we were told that he would be in a wheelchair
very soon and life span was no more than late teens to mid 20's. But when you are
dealing on a daily basis, as you know with Aaron, you don't think much about
the future.
Ben Wyant |
Ben had a
very loving set of parents in Brad and Doretha, and his siblings as well. He had many friends and a wonderful extended
family, as well as church family. He was
blessed, but I’m sure that he WAS a blessing as well – a huge blessing from all
the comments and the pictures that I have seen.
Doretha continues:
October
3, 2011 at 12:55 in the afternoon, as Brad and I sat next to Ben, the angels
came and carried him from his earthly home to his Heavenly one. This past year
has been the most difficult year of our entire lives and I have shed more tears
than I thought possible. We never realized how hard it was going to be to lose
our child. We knew since Ben was 7 yrs old that he would not live past his
20's. But, knowing it and experiencing it is two different things. Brad and I
have been blessed with 4 wonderful children, 2 in Heaven, 2 on earth. Thank you
Father for our blessing of Ben and the Godly life that he showed to all around
him. We know we will see him and Christina very soon!!
I cannot imagine the pain of that
moment, and the pain of the days following during this past year. And did you notice that Doretha mentioned yet
another child in heaven as well? Again,
here is Doretha:
Christina is the identical twin
sister of our daughter Katie. In 1983, when I was pregnant with them, the
medical field was just beginning to know about the problem I had with them. But
they didn't know how yet to fix it. It is called Twin to Twin Transfusion
Syndrome. You can look it up if you are interested in knowing more about it,
but it's when one baby becomes more of a host baby and the other becomes the
donor of food and nutrients and blood supply. The one baby gets bigger and
bigger, while the donor baby does not grow after a certain time. This is pretty
rare, but at least they know how to go in and fix it so that the babies have a
better chance of survival. So, we knew we were having twins. They were due on
March 25. We found out by mid January that Christina had died. Katie and she
came a month early on Feb. 28. Since Christina was so small the body starts to
absorb the dead tissue. Our doctor advised us that we did not want to have that
in our memory. So, we donated her body to the research department at Bowman
Grey School of Med. They were doing research on this very thing, so we thought
that was best. We have never seen our
precious Christina. But since they were identical twins then she looks just
like Katie.
Again, when I read
Doretha’s words I realize that this precious child, Christina, was bone of her
bone and flesh of her flesh. She and
Brad had such loss at this time………and then later to have loved Ben for all
those years, and have to let him go when God called him to heaven. Are Brad and Doretha bitter? Are they angry at God? Are they jealous of others who still have all
their children, or even of me as I write about our daily life with Aaron? You decide as you read what else Doretha told
me:
Do you ever wonder why God gave
Aaron to you and Gary? We have often wondered why God allowed us to have these
strange diseases in our family. Guess we may never know. But, I'm glad that the
Lord knows and gives us the strength to endure all these things. Keep up the
blogs. I really like reading them!!
Two things stand
out to me in Doretha’s words: First, the
Lord knows. Yes, He does indeed know
about our special children. He knows why
they were allowed to be like they are, as fearfully and wonderfully made as any
others. God is sovereign and even when
He doesn’t bend down and tell us the whys of His doings, we can trust that all
these things are somehow for our good and for His glory. I believe that often our special children are
here to draw us to God in a way that no other person or situation can. What an honor and a calling!
Secondly, Doretha
said that God gives us the strength to endure all these things. Oh, is that ever true! How could we ever do it on our own? “For His strength is made perfect in
weakness!” We don’t know how weak we are
until we are at our end and we fall into His arms, and let Him take over. Complete trust………..complete relief.
Thank you, Brad
and Doretha, for letting me share a part of your story and a part of your
heart. Thank you for being a strong
testimony of God’s faithfulness in your lives.
Thank you for allowing your pain to bless us. I look forward to meeting Christina and Ben
in heaven some day!
Brad, Doretha, and Ben |
And I will
continue to write as God leads and pray that He will direct my words to bring
honor to Him and encouragement to weary, questioning parents.
Patty,
ReplyDeleteThank you for this precious post. I remember when Dorthea and Brad posted that Ben had been called home to be with the Lord and my heart cried for their loss. Reading now about Christina makes their testimony even more amazing!
I read your blog and love it. Please don't stop writing. John and I were not blessed with children of our own so we have extra capacity for loving family and friend's children. Perhaps our arms are empty in order to hug someone who is hurting. So you see, when I read your blog about Aaron, sometimes I want to send a hug to Aaron for making me smile or to you and Gary when you have difficult days. Tonight, Hugs and prayers go out to our friends from PBC Brad and Dorthea. You are all a blessing to many of us and the Lord is working through you daily.
Kathryn, thank you for also sharing your heart. God has put you and John where you are for a reason, also, and I'm sure your heart has gone through many hurts as well. Thanks for your tenderness toward others. I see your sweet spirit in your writing and your words every day. I really appreciate your encouragement to me about the blog. Thank you so much for that!
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