Who is “Keeping” Who – Kevin and Maggie Bell – The Church at Cahaba Bend
Growing up with a special needs sibling hasn’t always been easy. You learn a lot about yourself and you learn a lot about others. I always thought that Matt would most likely become my responsibility someday. And when I knew that Kevin was going to be the man God had chosen for me, this became his responsibility as well. He never once questioned that this was part of a “package deal”.
Whenever
people have asked about Matt’s personality, the best way I can describe him is
that he loves everyone. We should all
aspire to be more like him. He doesn’t
see race, nationality, gender, economic status- basically, if you show him any
attention, you are one of his favorite people on the planet.
Now, don’t
get me wrong, there are some really tough days.
He can be very stubborn (it runs in the family), and he has some severe
obstacles to overcome that many of us take for granted. But I think it is very fair to say that the
good far outweighs the bad.
Four years
ago, my parents, as hard as it was, accepted the fact that taking care of Matt
had become too hard for them. We made
the decision to place him in a nursing home so that he can have around the
clock care. At the time, Kevin, the boys
and I didn’t have a home that could accommodate Matt’s day to day needs as well
as my and Matt’s brother lives away in Maryland and has a severely autistic
child of his own.
Matt was
doing fairly well at the nursing home but was incredibly lonely. He is a very social person, and loves to talk
to everyone. Unfortunately, when the
COVID pandemic began, he was placed in a difficult situation of having to stay
in his room almost all of the time, and worst of all, none of his family could
visit. Our last visit with him before
the nursing home closed the doors to visitors was March 6th, 2020.
On April 28th,
we were notified that Matt was COVID positive.
His nursing home had been overrun with positive cases. Although Matt’s symptoms were thankfully
minimal, he was sent to UAB hospital for roughly a week, then to a step-down
nursing facility for another two weeks, and finally back to his nursing home.
If you know anything about those with intellectual disabilities, you know that
they do not adapt to change well, especially when you aren’t able to see those
you love the most. Matt became
frustrated at the nursing home. And on June 2nd, we received a call
that we either had to pick him up or they were sending him to the UAB
psychiatric floor.
So there it
was, Matt was coming to live with us. We
had no time to plan and at that moment our family dynamic quickly changed. I
knew Matt wouldn’t be able to go back to my parent’s home. Their health was not great and there was no
way they could take care of him and themselves on a daily basis. Everything happened so quickly, I’m not even
sure we had a sit down conversation with our boys (Matthew-16, Jake-14, and
Tucker-12) to tell them what all was happening; however, we adapted and did
what a family does.
Prior to Matt coming to live with
us, Kevin and I had shared with our SS class about the difficult time Matt was having
being away from us. We also shared the worry I was shouldering knowing how hard
it was on him mentally being unable to see any of us. Our church family
prayed with us often and lifted us up. During
this time of adjustment, it was solely through prayer and action from our CCB
family that helped take the burden of uncertainty off our shoulders. Our
church is full of "doers" and once the "doers" had a task
they were all over it. Steve Collins and Scott Mitchell as well as the
Community Outreach group spearheaded the operation to convert some space in our
home into two bedrooms. Other people helped purchase items for Matt that
he needed. All of this took a major burden off us so that we could get to
work on the paperwork side of bringing Matt into our home.
God always has a plan
and while we may not always see it when it is happening, we know He is working
all things to His good. The Covid-19 pandemic has brought a strain to
many people. However, being a schoolteacher and having schools closed
allowed me the flexibility to accomplish much needed, and exhausting, paperwork
to have Matt's insurance and waivers updated and formalized.
During this time, God gave us many small wins that helped us know that this was His plan and that Matt and our family would be ok.
Soon, some
of the tasks began to overwhelm Kevin and myself. While we were trying to be there for
everyone, there were still so many obstacles to overcome. Kevin and the boys loved Matt but had never
lived with him. There are some strategies that work and don’t work. It became a boot-camp, so to speak, for them
on how to handle certain situations. We
knew that we would have to make some big arrangements to accommodate Matt’s
needs.
One morning
while on a Zoom call with our Sunday School class, everyone was asking how we
were all doing. Kevin and I both feeling
overwhelmed from the new responsibilities placed before us, broke down. We knew Matt needed his own room and needed
other accommodations but financially weren’t sure how to make that happen. Our church family jumped in and made it
happen. Within a couple of hours a plan
was set into place that would build out a room for our boys so that Matt could
have a bedroom on the main floor.
In the
meantime, I had joined an online financial bible study with people from all
over the US. One day while talking about
our recent changes, Matt walked into the zoom call. When the leader saw and met Matt, she said,
“Maggie I literally felt the Holy Spirit moving through him”. Throughout that
study, one particular bible verse stood out to me and when I read it to Kevin,
he said, “Well now we know we are doing the right thing.” The verse was 1 Timothy
5:8, NIV: "Anyone
who does not provide for their relatives, and especially for their own
household, has denied the faith and is worse than an unbeliever." From
that moment on we never questioned what God’s plan was for us and Matt.
Soon
after moving in with us, we discovered that Matt’s arterial stenosis, a
lifelong condition manageable up to this point, had become severe, and he would
have to have open heart surgery. He had
never had surgery before, not to mention one so taxing. In August, Matt had his surgery. His recovery went very smoothly, at
first. However, in September, while
visiting the doctor for his surgical follow-up, we discovered that Matt was
becoming septic. The events leading to
this discovery were major in keeping him alive, and I know it was nothing short
of the hand of God that Matt is still here.
Matt has had other setbacks, including infection developing in his bone,
however after many weeks of IV antibiotic infusions, he is back to his happy,
sometimes stubborn, and obstinate self.
Some
days his care is overwhelming, and to be completely honest, frustrating. On one particularly exhausting night while
giving him a bath, I was washing his feet.
I was reminded of the time when Jesus washed his disciples’ feet, “I,
your Lord and Teacher, have washed your feet, so you also should wash one
another’s feet. I have given you an
example. You should do as I have done
for you,” John 13:14-15. I immediately felt humbled and in the presence of
God. Who am I to complain and be
frustrated when God has given us so many blessings, including being responsible
for such a wonderful gift as Matt.
Our
children have had to grow up a lot, but it has been fascinating to watch them
grow and mature into amazing young men.
They have become more empathetic and loving and don’t hesitate to help
when we need them.
Matt
loves going to church, he loves being around people. And I can’t help but think that God put him
here for a purpose. He brings people
together. He loves unconditionally. His heart has been broken and he has had
people that he loves disappoint and leave him, but he forgives and loves just
as Jesus called us to do. He is such a
reminder that we should all aspire to be more like Jesus.
People
often say that Kevin and I are such great people for taking Matt into our home. I’m always appreciative, but I also can’t
help but think, isn’t this what family does. And not just family but those that are like
our family. Matt is the one that we
should all be thanking. He makes us all
want to be better people.
I have a tendency to overthink and worry, but I've found a verse in the past year that has helped sustain me. I think I have heard it a million times, but one day while walking through a store by myself, I found this quote based on scripture from Daniel 3:17-18, "And if not, He is still good." While things are hard, and we pray for certain answers and guidance, I know that my God will sustain me. Even if it isn't how I want Him to. He knows far more about our circumstances, than we ever could. For example, I feel I can confidently say that had Matt not come to live with us when he did, we never would have known how severe his arterial stenosis had become and he may not be here with us now. And again, the day we discovered Matt's sepsis, he was refusing to get out of bed. But I called on friends and co-workers to pray for him to get up so we wouldn't have to reschedule, not knowing how sick he already was. Another day of waiting to be seen, and I'm not sure he would still be here. Isn't God amazing?
**One final note, Matt is unable to verbalize clearly his wants, needs, etc. His tongue is partially paralyzed due to his disability. And so, while he has never professed verbally his love for Jesus, I found one day while cleaning out his room at my parent’s house, his declaration of his faith. Signed “Matthew Melton, January 19, 2008.”
Comments
Post a Comment