After all we went through and are still going through I would like to announce we are pregnant. This was not planned and I'm very much in denial but I"m pregant with another precious child.
Went to the ob today I'm just barely 7 weeks so my due date is 4/4/2013 .
Sad that I'm not further along for sickness but good because Shane will
be a couple weeks older now. I haven't been nearly as sick with Shane
though but usually sickest in morning and could take naps all day
long!:) I just pray every night that I will have strength to take care
of Shane. So that's the news with us.
Love,
Emily
Ps. I heard the babies heart beat today and they will do a specialist at 24 weeks.
Wednesday, August 8, 2012
Wednesday, July 18, 2012
ENT and Helmet fitting
We took our journey once again to Primary's today and met once again with our Ent (ears,nose,throat) doctor to check up on Shane's Paralyzed left vocal chord and swollen larynx. He scoped Shane which he did not like and I don't blame him. He said that his left vocal chord is still not 100 % which shocked me because Shane is a TON louder than the kitten of a sound he used to make after his open heart. So this makes me wonder how loud would he be with all of his vocal chords non paralyzed! lol Our doctor said it may never come back but will keep checking up on him. As far as his reflux he will continue to take that medicine because our doctor still see the need and they will evaluate Shane in 3 months. Our Ent also mentioned once again about Shane's "floopy airway" because shane is a noisy breather, he used the analogy of opening and closing your index finger and middle finger together and Shane's airway only opens as if only his index finger opened and shut. If that makes sense. He says that as long as his sats are always good and dosen't turn blue than he should be fine with that.
After the Ent we went to go get Shane's head fitted for a helmet. They
put shane on a laser machine to scan his head.We should get the helmet
on the 30th of July and he will need to wear it 3 + months. Its nice
that our visits to Primary's are getting farther and farther apart. It
will be nice to when its once a year!
Wednesday, July 11, 2012
Heart doctor appointment
Just got back from seeing shane's heart doctor. He was 18lbs 9 oz and 28inches long. They did an Echo and EKG all came back with normal heart function. The doctor said that his left ventricle that wasn't pumping well was pumping as normal as the other good ventricle. Our doctor said " YOu weren't on the transplant list right? because if you are we need to take you off!" lol I said no were weren't but close to it! Shane is now off his medicines and I continue to feel my Heavenly fathers glorious hand in blessing my little ones heart. I'm so blessed and grateful for his love for our little family! I know this has not come with out the many fasts and prayers of everyone! Thank you all!
Wednesday, June 20, 2012
shane scare
After a
crazy scary day i have finally emerged from being up till 4am. Shane had
a high fever yesterday and was puking his food took him to pediatrician
and they said it could be several things his throat was sore his inner
ears were red and on his x ray showed slight fluid in lungs. So to be
safe they wanted us to go get blood work done at Mckay dee. When they
got blood work back it was showing signs of an infection. Due to Shanes
past of course they wanted to be safe ad we went to primarys.@ Primary's
they did more blood work, an iv, x -rays, checked his urine. All came
back good no pneumonia and the blood work actually had fewer signs of
infection not to mention his fever went down. So they said they were
thinking of keeping us for the night when they got the first blood wk
but Shane with the
help of a lords blessing and many prayers came home as exhausted as
his parents, with no fever and less signs of infection. They have
Shane's blood cultures to that they will get back today and I will
follow up with pediatrician.Thank you everyone for your concerns!!!
Sunday, May 27, 2012
Feeding Tube
As of May 26th Shane no longer has a feeding tube! He had consistent full bottles in a row for a couple days. So I decided it was time to take it out! The only downer is its not as easy to give him his medicine now! :) I will figure it out! His cry and voice also seems like its getting a little louder so I think his new medicine is helping! Yay!
Thursday, May 17, 2012
Swallow study/ Ent visit
Today we made our journey to Primary's for two appointments. Ears nose throat specialists then swallow study.
First We met with an ears nose throat specialists for concerns over Shane's quiet cry, noisy breathing and possible sleep apnea. They put a tube camera down to look at his vocal chords. They saw that he has a swollen larynx or Larynx Malaysia "floppy airway" that gets irritated by stomach acid and his feeding tube. So they gave him reflux medicine to see if that will help, this all causes the noisy breathing, gasping when sleeps snoring exe.. They also saw that one of his vocal chords is paralyzed on his left side which is causing the quiet cry and that is a chord that is wrapped around the aorta so his surgeries had big impact on that chord . they say it can come back after time hopefully by the time they are a year old. If it does not come back then he will just have quiet voice but won't affect his pronunciation of words but there is a surgery to fix it if it is needed. So all of those things were nice to know.
Second we did the swallow study to test Shane's swallow and to see if we can take his tube out. He did not aspirate on thin formula but we will need to increase the amount he eats orally slowly to what we give him total (7) ounces before we can take tube out. This is awesome news Give it a week or so and he will have it out! Oh and Shane weighed 18 lbs 4 ounces! He will be 5 months on the 19th.No wonder my arms have been tired! :) once again Shane is a strong little bugger making is way finally into "normalcy".
Thursday, May 3, 2012
Shane day a million update :)
Just wanted to share some good news ! Today our in home health
occupational therapist came by to check on Shane's neck/ head and his
eating to see the progress from last week. She was very impressed with
the improvement of his sitting up ability his head movement/ leaning
too much to one side and the shape of his head has improved she is
thinking if that continues the helmet is out of the picture! This is
good news because we called the helmet people and our insurance will
cover 90% of the helmet if we have been doing head stretches for 3
months when we have only been doing them since surgery. Otherwise it's
$2000! So now I won't have to stress about waiting another month to get
him evaluated for a helmet if she is noticing a difference in just a
week. I
also have been taking her advice and pacing Shane when he does eat the
tiny bit he can that has also been helping. She gave us good compliments
on keeping up with stretches because not all parents do! We were happy
and all the hard work is paying off! Thank you everyone for your
continued prayers!
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