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Just wanted to let you know that JD was released from Childrens Medical

Center Dallas yesterday to the care of his mother and I and to his home nurses.

JD

is doing somewhat better but is still having symptoms related to his RSV

illness. These symptoms can persist for some time. JD is doing better though

and

breathing under his own power and he seems happier now that he is at home.

One thing that I am struggling with is that JD has had to be placed back on the

ventilator. It is not giving him any breaths just support. He has tracheal

malaysia and his airway is collapsing some and Dr. Gelfand is not comfortable

with him being completely off the vent yet especially since he has been sick

twice now with hospital visits in less than a months time. We have not yet

discovered why the tracheal malaysia is showing up now but Dr. Gelfand will be

doing some tests in the future to determine exactly what is going on. JD may

need more time to grow for his airway to firm up or JD may have to face another

major surgery to make his airway better besides the one already scheduled this

spring for his nose. I can say is at peace with him being back on the

vent but I am really struggling with this. I know that there is nothing in

my power that I can do but place this in the hands of God. I just so hope and

pray that JD doesnt have to spend his entire life on the vent or trached. We

were so happy months ago when he successfully came off the vent and was doing

so well. We just dont want any bumps in the road but there really is nothing

that we can do to control it since we are not in control of this situation but

we do know God is.

At this time and possibly for quite a while, Dr. Gelfand is not comfortable

with JD having visitors. It is a situation of germs being brought in from the

outside and we dont want JD developing RSV again. It is such a nasty and

possible deadly viral infection. Olivia too is still battling RSV as she has

had

to be put on nebulized breathing treatments similar to JD. It is suspected

that both of our children have asthma and will battle this and be faced with

these types of breathing treatments for most of their childhood and teenage

years. Because of their prematurity, they cannot be exposed to noxious aerosols

or

noxious substances. There premature lungs just cant handle it.

We ask for your continued thoughts and prayers for JD. We are hoping that we

do not experience him getting sick again this winter and the helicopter

ambulance rides that he has been taking cease for awhile.

May the grace, peace, glory, and mercy of our Lord Jesus Christ be with each

of you.

In His Hands and still holding onto that rope,

, , Olivia (15 months) and JD (cHArgEd 15 months)

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and ,

thanks for the update. All the best to you in regard to the health in your

house!! It is a hard thing keeping " bugs " out when you have such vulnerable

little ones. Hopefully, they can be protected enough to get you all through

this.

pam

JD UPdate

Just wanted to let you know that JD was released from Childrens Medical

Center Dallas yesterday to the care of his mother and I and to his home nurses.

JD

is doing somewhat better but is still having symptoms related to his RSV

illness. These symptoms can persist for some time. JD is doing better though

and

breathing under his own power and he seems happier now that he is at home.

One thing that I am struggling with is that JD has had to be placed back on the

ventilator. It is not giving him any breaths just support. He has tracheal

malaysia and his airway is collapsing some and Dr. Gelfand is not comfortable

with him being completely off the vent yet especially since he has been sick

twice now with hospital visits in less than a months time. We have not yet

discovered why the tracheal malaysia is showing up now but Dr. Gelfand will be

doing some tests in the future to determine exactly what is going on. JD may

need more time to grow for his airway to firm up or JD may have to face another

major surgery to make his airway better besides the one already scheduled this

spring for his nose. I can say is at peace with him being back on the

vent but I am really struggling with this. I know that there is nothing in

my power that I can do but place this in the hands of God. I just so hope and

pray that JD doesnt have to spend his entire life on the vent or trached. We

were so happy months ago when he successfully came off the vent and was doing

so well. We just dont want any bumps in the road but there really is nothing

that we can do to control it since we are not in control of this situation but

we do know God is.

At this time and possibly for quite a while, Dr. Gelfand is not comfortable

with JD having visitors. It is a situation of germs being brought in from the

outside and we dont want JD developing RSV again. It is such a nasty and

possible deadly viral infection. Olivia too is still battling RSV as she has

had

to be put on nebulized breathing treatments similar to JD. It is suspected

that both of our children have asthma and will battle this and be faced with

these types of breathing treatments for most of their childhood and teenage

years. Because of their prematurity, they cannot be exposed to noxious aerosols

or

noxious substances. There premature lungs just cant handle it.

We ask for your continued thoughts and prayers for JD. We are hoping that we

do not experience him getting sick again this winter and the helicopter

ambulance rides that he has been taking cease for awhile.

May the grace, peace, glory, and mercy of our Lord Jesus Christ be with each

of you.

In His Hands and still holding onto that rope,

, , Olivia (15 months) and JD (cHArgEd 15 months)

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all the chargers go through this not just u hugs

>

> and ,

> thanks for the update. All the best to you in regard to the health in your

> house!! It is a hard thing keeping " bugs " out when you have such vulnerable

> little ones. Hopefully, they can be protected enough to get you all through

> this.

>

> pam

>

> JD UPdate

>

> Just wanted to let you know that JD was released from Childrens Medical

> Center Dallas yesterday to the care of his mother and I and to his home

> nurses. JD

> is doing somewhat better but is still having symptoms related to his RSV

> illness. These symptoms can persist for some time. JD is doing better

> though and

> breathing under his own power and he seems happier now that he is at home.

>

> One thing that I am struggling with is that JD has had to be placed back

> on the

> ventilator. It is not giving him any breaths just support. He has tracheal

>

> malaysia and his airway is collapsing some and Dr. Gelfand is not

> comfortable

> with him being completely off the vent yet especially since he has been

> sick

> twice now with hospital visits in less than a months time. We have not yet

>

> discovered why the tracheal malaysia is showing up now but Dr. Gelfand

> will be

> doing some tests in the future to determine exactly what is going on. JD

> may

> need more time to grow for his airway to firm up or JD may have to face

> another

> major surgery to make his airway better besides the one already scheduled

> this

> spring for his nose. I can say is at peace with him being back on

> the

> vent but I am really struggling with this. I know that there is nothing in

>

> my power that I can do but place this in the hands of God. I just so hope

> and

> pray that JD doesnt have to spend his entire life on the vent or trached.

> We

> were so happy months ago when he successfully came off the vent and was

> doing

> so well. We just dont want any bumps in the road but there really is

> nothing

> that we can do to control it since we are not in control of this situation

> but

> we do know God is.

>

> At this time and possibly for quite a while, Dr. Gelfand is not

> comfortable

> with JD having visitors. It is a situation of germs being brought in from

> the

> outside and we dont want JD developing RSV again. It is such a nasty and

> possible deadly viral infection. Olivia too is still battling RSV as she

> has had

> to be put on nebulized breathing treatments similar to JD. It is suspected

>

> that both of our children have asthma and will battle this and be faced

> with

> these types of breathing treatments for most of their childhood and

> teenage

> years. Because of their prematurity, they cannot be exposed to noxious

> aerosols or

> noxious substances. There premature lungs just cant handle it.

>

> We ask for your continued thoughts and prayers for JD. We are hoping that

> we

> do not experience him getting sick again this winter and the helicopter

> ambulance rides that he has been taking cease for awhile.

>

> May the grace, peace, glory, and mercy of our Lord Jesus Christ be with

> each

> of you.

>

> In His Hands and still holding onto that rope,

>

> , , Olivia (15 months) and JD (cHArgEd 15 months)

>

>

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My daughter (12 months) also was on and off the vent so many, many

times. She is breathing on her own now and did not have to have a

trach, but we don't know what tomorrow holds. You are right it all is

in God's hands. Celebrate the good times and hold onto hope. Congrats

on JD coming home. Don't worry about keeping visitors away. Until these

little ones can handle it, it is best to keep them protected from all

these germs (my daughter is a 26 week preemie and seems to catch every

ugly bug that comes near her). God Bless. You are in our prayers.

- M.

mother of Anabelle (12 months)

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