Thursday, March 10, 2011
What if...
Appt update
Bad news is Michala is so impacted that she is going to have to be admitted 2-3 days (praying for 24 hours) for an ng tube (I will have nightmares about that one for sure) & golytely. She has some bleeding but for now we will take care of this & then deal with that. She said we may have to end up with a gtube to be able to control this.
She did say for us to go ahead with our trip & we will admit her when we get back. Just one more thing! My attitude has stunk lately & this is definitely not helping. Gonna put it behind me & deal with it when we are back.
Update
Michala has never seen GI. We are hoping for a direction with her stomach issues. We couldn't get Abe in for an appt until the end of the month. I think his gtube is too small & is what is causing so much irritation. We are hoping she will check him & measure him for a new one.
Friday night Mike & I had a date. Our dear friends have been wanting to come over to play with our babies while we went out. They kept asking when they could come. Finally they gave us dates & said ya'll are going. We had a wonderful night out. When we got back home the house was full of laughter & smiles. They even asked when they could do it again. What a blessing to have friends that want to spend time with our children. It meant a great deal to us that they would give of their time for us.
Other than that not much is happening in our world. Just the daily fun stuff. Mike has a conference coming up next week so we will be heading to Orlando. We are very excited for some sunshine & to see our wonderful Disney friends.
We are almost there so I will cut this short. Hope everyone has a wonderful day!
Sunday, February 27, 2011
Michala in Marlee Anne's desk chair
Monday, February 21, 2011
Peter Pan
I have a feeling my words will not convey the amazement of this show. It's in the white tent beside World of Coke. If you have the opportunity to go in Atlanta or anywhere please do. You will not be sorry!
We were seated on the front row in the wheelchair section. Even for Mike & I those seats were really below the stage so don't sit on the front row! Marlee Anne has the opportunity to move to the second row during the second act & that was much better she said. However she did say that dad's lap worked really well too.
The screen is 360 & the view is spectacular. As the narration started I began to cry. I have always loved this story. Well when Peter Pan, Tink (oh my!) & the Darling children flew through the air I wish I could have taken pictures of my children's expressions on their faces. No words!
Ok all the cast was amazing. Tinkerbell had an attitude that was priceless. At one point Tink is hurt. Peter tells us all to whisper we believe in fairies. As I look around to see people whispering my eyes lock on this precious little girl. She is seriously into making Tink fly again. When Tink flies this little girl is amazed! This little girl could have very well fought cancer or is fighting it now but at that moment that didn't matter because in her sweet little mind she just single handily gave Tinkerbell the power to fly. Priceless!!! Then when Peter Pan & Captain Hook were right beside her fighting she was in awe one minute & laughing the next.
No way Camp Sunshine or Peter Pan the show could have known that it would impact so many lives on those few hours today. Maybe they hope they would. Well they succeeded. At least with our family I know they did.
So again if you have the chance to go see it please do.
Afterwards we had big plans to go to the Cheesecake Factory. However some of our Camp Sunshine friends wanted us to go eat at Baha Fresh with them. It was a great way to end the day spending time with them. So wonderful to see everyone!!!
Ok if you made it this far & it's still Monday please say a special prayer for Michala. Well even if it's Tuesday but hopefully by then all will be well.
Wednesday, February 16, 2011
3 years ago
When Mike got to the hospital we took the walk into the nursery to say our good-byes. Very similar to the journey with Mary Elizabeth years before. Once again family & friends came to journey with us.
I would have much rather taken him home & played house. However looking back I know had that not happen in the nursery he wouldn't be with us today.
Those 5 weeks in the NiCU were so hard. However I know the dear friendship that was renewed in Marvel Anne, the new friendship made with Nancy, Kim, sweet little Bridget, our dear Terri's, our forever friend Rebekah who spoiled him & of course our ever faithful Mo. Can't forget the NICU knitters that taught me how to knit. None of that would have happened. Even though I hated the suffering I am thankful for what came from it.
As I hold him now helplessly as he struggles with seizures I am thankful God had other plans. Not the seizures of course but his life. I have learned so much in the 3 difficult years of his life. So thankful to be reminded that this is only a blink of an eye.
I have had trouble today just being able to breathe. I so hope that this is behind me & there are better days ahead. For some reason I wasn't prepared for this to hit me so hard this year.
Monday, February 14, 2011
From Abe's daddy
Happy Birthday Abe,
One thousand and ninety five days longer than I expected. Yes I remember it well, sometimes too well. The day you came into this world and the horror that followed. The mere thought of having to give you back right after you came was heartbreaking. Can't say that I blame you, if I saw what you were getting into, well I might have asked to be recalled if I had a choice. After Marlee Anne was born I thought your Mom and I had gotten it right. Turned out to be just more pain and suffering for an innocent child. You see Abe, Marlee Anne was not suppose to be the only one who would gain a playmate. Now mind you, I have never been partial to a child's gender. I would have been just as happy and proud to have raised four girls, but even so I had hopes and dreams of what the two of us could have done. The world would have not been able to contain us. Sadly I get to stand by and watch you suffer through another difficult day. I wish I could fix you and make things right. However, I am just a simple man, incapable of healing you, but forever able to love you. Your recent smiles and giggles have been such blessings and I believe that better things are to come. I can't help it Abe I am just that way. I believe in the glass half full. I just know that God has a purpose for everything, not just for your life or my life, but in everything. Abe I look forward to the days ahead. There will be challenges and difficult times for sure, but we can make it. Even in the valley of the shadow of death the Lord will be with us. You see Abe I know how the story ends. There will be an eternity of time for the realization of all of our hopes and dreams, but just not here on this Earth…… just not here.
Happy Birthday My Son!
I love you,
Dad
Happy Birthday Abe
Wednesday, January 05, 2011
Happy New Year
> Well let's see the Christmas cards never went out, I didn't get my traditional Christmas ham for the first year ever, & I am just now telling ya'll Happy New Year. Still life went on & God is still good!
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> Christmas Day we were blessed to have Michala's Aicardi sister come & stay with us until this past Monday while her parents & 9 year old sister went on a cruise. We miss her greatly. Ok maybe not my back.
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> Mike is busy as always being the best husband in the world & number 1 daddy while juggling work & still going to college.
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> Mary Elizabeth seemed to be doing so much better until yesterday when she started getting real cold. Trying to keep her warm is so challenging lately. She is struggling with her eating & drinking again. I cannot believe she is almost 18 & we have to apply for guardianship for her.
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> Michala finally got her ipad. What a patient little girl. The jewelry & craft orders I got around Christmas helped along with her birthday money. She really likes it too. I thought I didn't want one until I saw her's but they are really cool.
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> Marlee Anne is doing good. She is studying hard & had no problem doing school through the holidays even though the other kids were out of school.
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> Abe has been struggling with his screaming. Maybe he was trying to tell us this lovely weather was coming.
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> I am taking it slow to get my back better. Have lots of things on my to do list but for now those will wait. I have really been enjoying making my jewelry.
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> I do hope that everyone has a healthy & happy 2011!
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> Always thankful!!!
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Tuesday, December 21, 2010
Thankful!
Friday when I sat Mary Elizabeth up to give her her morning meds she gasped for air. I suctioned her & gave her a breathing treatment before giving her her meds. She struggled taking her meds & wouldn't drink. I put her in the van & headed for the peditricians office.
Once there they came running in the room working with her & called the ambulance. The EMT saw her & said we would have to go across the street to Rockdale until she was stable enough to take to Egleston. When he picked her up it must have dislodged something because she was breathing much easier. He put her on 8 liters of oxygen just to get her sats at a good level. He said we would head to Egleston but if she got in distress again we would have to go to the nearest hospital.
I was shocked on the way to Egleston at how many people didn't pull over to let us pass. The EMT driving said they deal with that all the time. So my request is next time you see any emergency vehicle with their lights & siren on please pull over & let them pass.
Once we got to Egleston & they started working on Mary Elizabeth the EMT told me he was very scared when he walked in Dr. Patonay's office & saw her. I was the most scared I have been in quite awhile.
After her xray we found out she had double pneumonia. She was put on Cpap 8 liters at 100%. She was admitted to the ICU.
Thankful for the prayers! The medical team was all laid out start to finish. From Dr. Patonay & her amazing staff, the awesome nurse that stuck her once & only once for the most beautiful IV you have ever seen, to the doctors & nurses that released her from ICU. They kicked us out because the hospital was so full of really bad stuff & they didn't want her to get something else. We were also at a point we could do all they were doing except the IV meds. Once again our sweet girl reminded me of what a mighty God we serve. He used her in a mighty way at the hospital witnessing to many.
So you see while my heart wishes for more my spirit is renewed & thankful for the true spirit of Christmas that fills our home tonight. Mary Elizabeth is still on oxygen, taking extra meds, breathing treatments & suctioning but we are home together. A family unit as Marlee Anne says.
We cannot thank everyone enough for stepping in & filling the void while she was in the hospital. From taking care of the kids & Mike, bringing me Starbucks since the coffee shop was closed, bringing my hospital bag that I ran out & forgot, doing my last minute shopping for me & just volunteering truly for whatever! Thanks so very much for the support & most of all the prayers! Please continue the prayers for healing for Mary Elizabeth's lungs. She is still a very sick little girl. Please pray for protection so that everyone else stays well.
Our Christmas cards have not gone out, things we usually do have not been done, but you know what, the most incredible time of year will still happen on Saturday morning. We will wake up in a warm home together & sing happy birthday to Jesus. Merry CHRISTmas ya'll!!!
With love & a thankful heart!
Friday, December 03, 2010
For a great cause
My friend made wonderful necklace, bracelet & earring sets & donated them to help the Magana family adopt Liliana. The set is $20 & would make a lovely Christmas gift. You can order from the website below. Thanks!The Magana family is adopting a beautiful special needs child named Liliana from China and as many of you know, international adoption is very expensive. I donated 100 snowflake glass tile necklaces to the Magana family to help with adoption fees. 100% of the purchase price goes toward bringing Liliana home this January! You can purchase a snowflake necklace as well as a matching bracelet and earring set that my sister donated on Liliana's blog. http://www.snowflakesoflove.blogspot.com/ I really want these to sell well for the Magana family! Thanks so much for looking!
Thursday, October 14, 2010
Appt update
Well he decrease Michala's VNS cycle. She is still having 2 seizures a day. Some are pretty violent & they last any where from 2-20 minutes. Once again we accept they fact that she is going to have them. It's about quality of life. She had gained 6 lbs in 3 months & Dr. Flamini was very pleased with that. It's that cheeseburger diet he put her on.
Ok so for our little complex buddy. He did not adjust his VNS because he didn't want to throw something else in the mix. He wants him to have a CAT scan to make sure there is nothing there putting pressure on his brain. We are going to try melatonin & then clonodine. In other words who knows?! At least we have options to try.
Our big excitement came when the fire alarm went off & Dr. Flamini about fell out of his chair. We had to be escorted down the elevator by security. We still don't know what happen. We were only told that it wasn't a drill.
I am tired & I know this email comes across as negative. I don't mean to be! I am thankful to have a doctor who cares about our children & mine & Mike's well being as well.
Thanks again for all the prayers!!!