Olivia Jane is doing great!

Since Olivia Jane's Christmas present to her mommy....(being off of everything) she has been put back on oxygen today. She is still not on a feeding tube, so she only eats by bottle. This is definite positive; however, it is tuckering Olivia out so much that she needs help via nasal cannula. This has really upset my sister, so please keep her in your prayers as well as Olivia Jane! Olivia has been given the 'ok' to eat however much she thinks that she can handle now. Please pray that Olivia just needs a little boost of oxygen and that she will come home soon....healthy and breathing on her own!

Thank you to everyone for donating...my sister should download the pics sooooon! As soon as she gets a second to do so, I will get the pics uploaded! The nurses were so excited and shocked that so many people donated!

I love you Olivia Jane! Stay strong and keep getting healthier everyday sweetie! I can't wait for you to come home!

~Aunt Jessie

Merry Christmas

Merry Christmas everyone!! Well Olivia did good through her surgery. It took about 45 minutes for the whole surgery. Dr. Pickett replaced her temporary shunt with a permanent shunt and made another incision in her belly to lead the tubing into her abdomen, where the fluid will flow. She came off her pain meds this morning and seems to be handling that well. They were not able to take her off the ventilator because she was still so medicated and was not wanting to breathe on her own. But now that the pain meds are off we are hoping she will be back on the nasal cannula tonight. I am really hoping they will restore her feedings today but we will see. The nurse said that the muscles and the digestive system is the last to wake up after surgery so they don't want to rush into feeding and her little belly not be ready, but i cannot wait to feed my baby again. Please continue to pray everyday for my baby. She still has a lot of obstacles to overcome before i can take her home. Thank you so much to everyone that has continued to pray for her.

Today is the day that the preemies of the NICU will get their Christmas present from Olivia Jane! I will post pictures of the precious moment as soon as I can! Thank you all so very much for your prayers and for any donations that you gave for this wonderful benefit!

Prayers Needed!!!

Dr. Pickett came in today to tap Olivia's head to drain some more fluid and as soon as he tapped it more filled in. He was able to get 25 cc's off but it is still full. So Olivia will be having her surgery to get her VP shunt tmrw. He told me that he would take the temporary shunt out and replace it with a permanent shunt that has a tube attached to it. The tube will be placed down the side of her neck and another incision will be made on her chest to guide the tube into her abdominal cavity, where the fluid will flow and be reabsorbed by the body. She will go back into intensive while she recovers through all of this and I pray that she recovers fast. Please pray for her that she does well with this surgery and that there are no complications with the surgery and she recovers quickly. I'm hoping that after she recovers she will start eating even better and gain more weight and i really hope this helps her get off the oxygen. She has been up and down with her oxygen the past couple days but i believe it is because of the fluid on her brain. So hopefully the shunt will fix all of that. Please pray extra hard the next few days for my angel. I love her so much and i want her home so bad i can't explain it. I know she is so strong and i know God has been by her side every step of the way. I prayed to God today as i held Liv to please take care of her and keep her strong and let her come home to me soon. Thank you so much for all your prayers. I am so blessed to have everyone care for her so much.

Olivia,

I love you so much babygirl. I am so proud of you and you have come so far. You are so strong and i know you will be ok. I never realized how much strength i had in me but you have definitely made that show through this. I have to be strong for you and i will always be that for you. You are so beautiful.You and your sissy are my whole world and i dont know what i would do without the two of you. Thank you so much for letting me be your momma. I feel that i am the luckiest woman in the world to have the honor of having two beautiful, amazing little girls. I love you more than anything in the whole world Olivia Jane.

~Mommy

And here comes another part of the roller coaster....

Ok, so we thought that Olivia Jane was doing so good that she may not need the permanent shunt; however, Melissa was told today that Olivia will need the shunt. The surgery will take place next week. She was doing so good, but she is swelling again. They drained fluid from her head today, and it soon began to collect fluid again. Melissa is very upset, so please keep her in your prayers as well as Olivia. Dr. Pickett was really hopeful, but it seems that God has other plans. Once again, I am trying not to ask why, but it is so hard when I see the pain that my sister goes through. I just pray that when she has the surgery, Olivia can come home very soon.

On a happier note, her eye test was performed today and it came back great! She still has premature eyes, but they are great right now. Thank you God! Thank you for your continued prayers, and please continue to pray for Olivia! Olivia Jane, I love you so much..please stay strong sweet angel! God, please protect my precious niece!

~Aunt Jessie

Olivia is a chunky monkey!!! :)

So Miss Olivia is now weighing 3 pounds and 10 ounces! I am so excited. She is finally getting up there. Her little cheeks are filling out and she is just adorable. She is taking her bottles very good still and is now up to three bottles a day. Over the weekend i was giving her a bottle and she finished the whole thing in 7 minutes. We were shocked. She must be getting the hang of this a bit more. :) I am so proud of my babygirl.

She was not feeling very well yesterday. She just seemed very tired and she looked kinda pale so today they are checking her blood to see if she is low on red blood cells. The nurse said she is showing symptoms that she is low so she will more than likely get another blood transfusion today. It should make her feel better and hopefully help her get off of the oxygen a bit better. Dr. Pickett is supposed to come in today to look at Olivia's head and take the stitches out. I hope he still thinks her head is doing good. Please pray with me that she will not have to have the permanent shunt placed. I just really don't want her to have to go through that. Please everyone pray that she will not have to have that done.

Santa will be visiting the NICU today. It is going to be so cute. He is taking pictures with all of the babies. Im so excited ........... Liv's first picture with Santa! That will definitly be going in the scrapbook.

Thank you to everyone who has donated for the wubbanubs! They are ordered and should be in any day now. I will post a picture of all of them when i get them in. I am so happy with the turnout and i can't thank yall enough for all of your donations to help make this come true.

I love you Olivia
~Mommy

Pictures of Olivia Jane

Olivia is doing so well with her bottles. She is now up to two bottles a day. Go Liv!!!! Mommy is so proud of you angel!

Olivia with her Wubbanubs....... She loves her little giraffe and caterpillar! :)

Olivia is so Beautiful. I love her so much!

Olivia is a STAR!!

Olivia was in her first commercial today. Amy and Chris George visited the NICU today to do the commercial for the Melissa George Neonatal Memorial hockey game. This is the game where the jerseys will be auctioned off to buy Giraffe Omni Beds for the NICU. They filmed Olivia while she was sleeping and while I was at her bedside. She looked so beautiful. I willl let everyone know when they are going to air the commercial so everyone can see Olivia in action!   :)

Olivia has gained a bit more weight and is now at 3lbs 5.6 oz. YAY Olivia!!! Im so excited I really hope it continues to go up. I was able to give her another bottle today and she did wonderful with it. It was such an amazing feeling when she was eating her bottle because she was just staring at me and it was like she was just telling me "I love you Mommy". I will never forget that moment. I fall more and more in love with her every day. She started to get a little tired at the end of the bottle but she managed to finish it. All that work tuckered her out though because she was snoozing after that. Dr. Pickett came in again today and said her head still looked really good, so that is very good to hear. Please continue to pray that she will not have to go through with the permanent shunt surgery. We still have not heard for sure but I am still praying throughout the day everyday that she will not have to have that surgery. Thank you all so much for your prayers for Miss Olivia. She is such an amazing, beautiful little girl. Please keep her in your prayers everyday.

I love you Olivia
~Mommy

Liv's First Bottle

I got to give Olivia her first bottle today! I was so excited. The nurse told me that we were just going to try the bottle and see how she did, but not to get dissappointed if she didn't take it because we just have to try. Well Olivia showed us because that little girl drank that whole bottle!! I was so proud of her. She did so good. The nurse was even shocked because she drank the whole bottle in 20 minutes. GO LIV!!! So now i get to give her a bottle once a day and we will gradually move her up to more bottles a day and finally get rid of the feeding tube. I am so excited.

On another note Amy George with the Melissa George NICU Foundation came by yesterday and asked if it would be ok if Olivia was in the commercial for the NICU Havoc game. Every year they hold a Havoc hockey game where the players where special pink and blue jerseys to be auctioned off to raise money for the NICU. The money have been used to purchase the Giraffe Omni beds. These beds are incredible and have saved many lives including my babygirl Olivia. The beds are not cheap by any means so the money is very much needed. I hope everyone that is reading this comes to the game. It will be held January 8, 2011 at the VBC. So come help support our Huntsville Havoc and support our babies at the NICU.

Please continue to pray for Olivia! I know everyone has been so amazing through all of this and i want to thank each and every one of you. It means so much to me. Olivia has came a long way and i know that God has heard all of our prayers so please don't stop whatever you do. Pleasse pray that Liv will not have to go through with the permanent shunt surgery. That would be absolutely amazing. I have prayed hard about that so please pray with me. I should know more about that later so i will keep everyone posted. Thank you again from the bottom of my heart for praying for my babygirl.

I love you Liv
~Mommy

Thank you GOD!!!!

Ok so i called up to the NICU this morning to check on my little angel and Jenny , her nurse, said that Dr. Pickett just left from visiting her. He said that her head looked good and the size has gone down so that is great news. He also said that her head looked so good that we may be able to take this temporary shunt out and not have to do the permanent one!!! OH MY GOODNESS!!! I could not believe what she said. This is the best news i have ever heard in my whole entire life! I know it is not 100% but oh gosh it felt so good to hear that. Olivia has not had any more seizures and her shunt is draining well so that is great news. I have prayed and prayed that God would heal Liv's lil brain and she would not have to have this permanent shunt. I truely believe God is listening and i am asking each and everyone of you to please pray that this comes true. Pray that she does not have to get this permanent shunt and all is well with her brain. I cannot get the smile off my face right now. To hear good news is just an incredibly, amazing feeling. I cannot express enough how much my girls mean to me. I live my life for my two girls. God please please please take care of Liv and be by her side. I pray constantly that Olivia will not have to have this permanent shunt put in God Please Hear Me !!!!!!

Thank you all so much for praying for my babygirl! Please continue to pray for her everyday and please pray hard that she does not have to get that permanent shunt. That would absolutely amazing!

I love you Liv
~Mommy

Kangaroo Care Makes Me Happy!!!

So today i woke up and was very down. I felt very depressed and could not get out of that mood. I missed Olivia so badly this morning. It is getting so hard to keep going on with this. I think just the fact that it has been almost 2 months and i still dont have my baby is really getting to me. I want Olivia to be home with me so bad i cant stand it. I recorded a book called "All the Ways I Love You" today and took it up to the NICU. So now the nurses can open the book up and i can read her a book even when I'm not there. I told the nurse  today how i was just missing her really bad today and she asked me if i wanted to do kangaroo care and of course i said YES!! i was so excited. It always makes me feel better when i get to do that . It is such a wonderful feeling. I cant wait until the day comes that i can hold her all day every day and believe me i am going to. She lost an ounce yesterday so today she was 3 lb and 3 ounces. I really wish she could hurry and gain some weight. I need her to gain weight for so many reasons.... she will start holding her temp on her own better, she will be hopefully eating her bottle by then, she will be getting this last surgery she will need before she can come home, and she will just be so darn cute with her little chubby cheeks. The doctor said her protein levels in her blood are still too high for her to get the permanent shunt because it would just end up clogging the tube if we tried now so we just have to wait. Everyone please, please. please continue to pray for Olivia to get stronger with each passing day and to come home soon. I love my daughter so much and all i want in this whole world is for her to come home safe and healthy.

I love you Olivia
~ Mommy

Mommy loves you Olivia Jane!!

Olivia has not had any more seizures. Thank you GOD!!! That seizure scared me so badly. The nurse was changing her diaper when she noticed that Olivia's eyes started going back and forth and then her head started to shake back and forth. She called the charge nurse and they rushed her back into the NICU from progressive. The doctor came in and performed a spinal tap and they got blood from her to send it off to test for infections. They were not sure at that point what was causing her seizures. I was able to hold her after her seizure it broke my heart because i was not able to stop all of this and more than anything in the world I just want all of this to stop and her come home where she is supposed to be. Dr. Davison and Dr. Pickett looked over Liv's CT scan and said the were concerned about the periventricular area of her brain because in his exact words "that area did not look pretty". That area of the brain can be responsible for seizures so more than likely that is why she had one and we should not be surprised if she has more to come. I pray to God that she doesn't but if she does they will start her on a daily seizure medicene. I was also told to be prepared for the possibility of Liv having Cerebral Palsey. I hate even thinking about that but no matter what Olivia will have the best life ever and i will make so sure of that. Olivia is such a beautiful little girl. I love her more than anything in this world. I am just blessed that God has granted me two of the most beautiful daughters in the world. Her cultures from the spinal fluid and blood have still not came back they will not be in until about saturday. On a good note though Liv has gained 60 grams and is now at 3lb 4 oz. YAY LIV!!! I'm so proud of you sweetie. Thank you to everyone for praying for her and please please keep praying for her to get stronger and to get healthy. I also want to send out a special thank you to all the people that have donated for the Wubbanubs. These babies will get to snuggle with their little Wubbanub this Christmas and its all because of people like you that have been so generous.

I love you Olivia Jane. Please keep staying strong and know that mommy is by your side everyday and I can't explain how much you mean to me and how much I love you and oh my goodness i cant wait for you to get home. Olivia, you have made me such a stronger person and so much more humble. You have taught me that life is too short to ever be angry with someone. No one is ever promised tommorrow and you have taught me that I am not in control of anything so just live life everyday and dont think twice about it. God has already planned out all of our days. God gave me you early because he knew I could handle all of this. I have to admit it is very hard but I would never ever give up not even for a minute. I love you so much Olivia Jane.

~ Mommy

PRAY PRAY PRAY!

Today is Melissa's birthday, and even with Olivia's seizure - we wanted to try and make my sister smile. So, we all went to Casa Ole' and every year, I try to embarrass her by getting them to sing. Well, after I had already put in my request to embarrass her, and to make her laugh, she warned me that I better not do it and that she was not in the mood. So, instead of helping; it would have made things worse.

I went to the front to tell the manager not to sing her "Happy Birthday" because her daughter is in the NICU, and today was not a good day. He patted me on the shoulder and said "ok". About 10 minutes later he came to Melissa with a rose made of aluminum foil and a dollar bill, and said to put it behind Olivia for good luck. He prayed for Olivia and then sung Happy Birthday to Melissa. Thank you Case Ole' for your prayers, and for anyone that goes there...tell the manager that wears glasses that we thank him again! He said that he has not seen his family in years, and I thought that he was going to cry! Bless him!

Again, I don't know anything more than I did this afternoon. All I know is that Olivia's nurse was doing her "care" for the day and saw that Olivia's eyes started to roll and move around and then her lil' head started to shake back and forth. They have done a cat scan, and we should get those results tomorrow. They have also done a spinal tap and blood work but we will not know those results until at least Friday. Please pray for Olivia that this is something that can be fixed! God, I love my niece so much that my heart burns for her! Please protect her, heal her! I love you God, and I have faith in you that you can heal her, no matter what the doctors say her outcome may be....God, you can heal her! I praise you Lord!

~HAPPY BIRTHDAY SISSY~

Thank you for your prayers, and Olivia Jane - I love you so very much baby girl!

~Aunt Jessie

PLEASE PRAY FOR OLIVIA JANE!

Olivia Jane has had a seizure and needs your PRAYERS! We do not know anything yet, but tests are being done as I type this! Please PRAY! As soon as I know more, I will let you guys know! Olivia, please stay strong; don't give up! You are a fighter and I know that you can get through this! I love you angel!

~Aunt Jessie

Thank you for the donations!

You know, when my sister asked me about getting a letter together and mailing it to people, asking them for donations....I thought of the blog. When I got the message out here, I thought that maybe we would get $50.00, but NO! You guys have came through and made promised donations, and because of you and your wonderful generosity...the NICU babies are going to have a fulfilled "Wabbanub" Christmas! It is not much to most people, but when you are in this situation and a nurse tells you that a Wabbanub could help your precious preemie's sucking reflex and eye coordination happen, you are going to try it. But, we thought of the other preemies and want them to have that chance too. The NICU does so much for these precious little babies. We know that we can't ever afford to donate enough for a ventilator or a bed, but a Wabbanub can help the smaller things! So, thank you so much for your help and I will be sure to post pictures of the special Christmas Day!

On  Olivia Jane note, she has done SO wonderful after her subgaleal ventricular shunt (temporary shunt),  she has been moved to the "big girl" Progressive Care Unit! Thank you again for your prayers! Because of your prayers, she has progressed so well after surgery and I can only continue to pray that she does well in the future! The doctors told Melissa that it is a long-shot, but that it has been known for the preemie to get ready for the permanent shunt, and then before surgery - everything is fine and NO shunt was needed! Please pray that this happens and Olivia is healed by God. The power of prayer can get us there! Please continue to pray; if everything goes ok, she will just need to gain some more weight, regulate her own temp, drink from her own bottle, and come home! Olivia weighs 3 pounds 2.4 ounces! Wooohooo! I love you so much Olivia Jane!

~Aunt Jessie

Between God and His Angel....This is a MUST READ!

Did you ever wonder how mothers of premature babies are chosen?
Somehow, I visualize God hovering over Earth,
selecting his instruments for propagation
with great care and deliberation.

As he observes, he instructs his angels to take notes in a giant ledger.

Finally, he passes a name to an angel and smiles. "Give her a preemie."

The angel is curious. "Why this one, God? She's so happy."
"Exactly," smiles God. "Could I give a premature baby a mother who
knows no laughter? That would be cruel."

"But does she have the patience?" asks the angel.
"I don't want her to have too much patience, or she'll drown
in a sea of self-pity and despair.
Once the shock and resentment wear off she'll handle it.
"I watched her today. She has that sense of self and independence
so rare and so necessary in a mother.
You see, the child I'm going to give her has a world of its own.
She has to make it live in her world, and that's not going to be easy."

"But Lord, I don't think she even believes in you."
God smiles.

"No matter, I can fix that. This one is perfect.
She has just the right amount of selfishness."
The angel gasps, "Selfishness? Is that a virtue?"

God nods.

"If she can't separate herself from the child occasionally, she will never survive.
Yes, here is a woman whom I will bless with a child less than perfect.

She doesn't know it yet, but she is to be envied.
She will never take for granted a spoken word.
She will never consider a step ordinary.
When her child says momma for the first time,
she will be witness to a miracle and know it.
I will permit her to see clearly the things I see--
ignorance, cruelty, prejudice--
and allow her to rise above them.
She will never be alone.
I will be at her side every minute of every day of her life
because she is doing my work as surely as she is here by my side."

Olivia is PRECIOUS!

I just want to say THANK YOU to my wonderful sissy for inviting me back to see my beautiful niece! I got to go back and see Olivia in the NICU and she once again, melted my heart. Her little button nose is my absolute favorite. She has the most beautiful little eyes, and the sweetest lil' feet. I thank you God for my niece and I pray to you, that she gets stronger with each passing day. Her little hands were curled up under her chest as if she were cocooned up. She had a ventilator put in for surgery and because of the pain meds, she needed the ventilator too. While on pain meds, she would stop breathing on her own. But since Sunday, they have stopped the meds unless they were desperately needed. She was breathing over the ventilator on her own, so Monday morning about 3am, the ventilator was removed! YAY! Thank you God!

On another note, my sister bought Olivia a "Wubbanub", which is pacifier attached to a little stuffed animal. This stimulates hand and eye coordination for preemies, but also helps them keep their pacifiers in their mouths. The NICU loves them as well, but does not have the money to furnish them for every baby. Also, the parents of the preemies can't always afford them, so that is where my request comes in. They are about $10.00 a piece. My sister wants to try and raise enough money to buy each of the NICU babies a Wabbunub for Christmas. You can google them to get for information, but please consider it. The NICU has done so much for my precious niece and this feels like the least that we can try and do. If you are interested in helping give these preemies a lil' Christmas gift, email Melissa at mfoster128@gmail.com. Thank you so much for your prayers for Olivia Jane! Please continue to pray for her and that she continues to gain weight, and hopefully come home soon! I love you so much Olivia Jane!

~Aunt Jessie

Prayer is powerful

Prayer is the answer to every problem in life. It puts us in tune with divine wisdom which knows how to adjust everything perfectly. So often we do not pray in certain situations, because from our standpoint the outlook is hopeless. But nothing is impossible with God. Nothing is so entangled that it cannot be remedied. No human relationship is too strained for God to bring about reconciliation and understanding. No habit so deep rooted that it cannot be overcome. No one is so weak that he cannot be strong. No one so ill that he cannot be healed. No mind is so dull that it cannot be made brilliant. Whatever we need, if we trust God, He will supply it. If anything is causing worry and anxiety, let us stop rehearsing the difficulty and trust God for healing, love, and power.

One of the nurses from the NICU brought this in and i wanted to share it with everyone. I love this and truely believe in God's power. Olivia is living proof that God is so amazing. Thank you God for my precious angel and Thank you God for keeping her strong. I can't wait to bring my baby home.

Olivia..... you are so strong baby

Olivia has done wonderful through this surgery. She had alot of swelling saturday the day after her surgery from all the fluid. She had gained a little over 200 grams just from all the fluids. She is back to 3 pounds and 1 ounce though. Now we just need to focus on getting her to gain some more weight. She will have to have another surgery after she gets around 4 pounds. This one will be to put the permanent shunt in that will drain the CSF into her abdomen. She will most likely have this shunt for the rest of her life. It is very scary to think that but it will be saving her life and that is what is so important. She is eating good too. They actually started her feeds back the day after surgery which surprised me because i didnt think they would until today. Needless to say i was very excited about that tho i didnt want her to go without eating. Olivia's primary nurse is a wonderful lady by the name of Melissa and she is so sweet. She took a picture of my baby at 3 o' clock this morning when she took her off the vent. I was so excited to see her little face without all those crazy tubes up her nose. So thank you Melissa you made my day! Well thank you all for all your prayers. Prayer has been such an amazing thing through this whole long process. I believe God can hear all prayers and if we pray and trust in God that he will answer our prayers, then he will. Please continue to pray for my sweet angel. We need to pray for her to stay strong, gain weight and get and stay healthy. 

I love you my Liv,

~Mommy

Olivia did great!..Thank you GOD!

Olivia pulled through surgery great! Dr. Pickett was able to take off 8ml of fluid from Olivia's head, and more will be taken off soon. She has a small patch on the top-side area of her little head. The temporary shunt will be in place until she is big enough for the permanent shunt. THANK YOU EVERYONE FOR ALL OF YOUR PRAYERS!! Prayers and faith in God is what got Olivia through this! For now, she has been taken off of her feedings but should start back in a couple of days. Please pray that Olivia recovers great, and that this is the beginning to the road home! Now, Olivia just needs to gain about 2-3 pounds, get the permanent shunt, and come home! PLEASE PRAY that is all we have left! She is such a tiny little angel to have been though so much. I will know more tomorrow about her condition and will update you all! Again, thank you! thank you! I love you my sweet Olivia Jane!

~Aunt Jessie

More information on the surgery...

Olivia is going to have a subgaleal ventricular shunt, which is a temporary bypass of the normal cerebrospinal fluid (CSF) pathways. This will be used until she is big enough for a normal shunt. Please pray that everything goes wonderfully! We were at first told that she was going to have surgery first thing in the morning, but we have recently been told that she would not have surgery until tomorrow afternoon. Melissa is really upset because we were hoping that Olivia would be able to have the surgery in the morning. This means that Olivia will not get to eat from midnight tonight until Monday or Tuesday of next week.

The upside of the surgery is that after all is said and done, Olivia should breath better on her own without assistance from the nasal cannula and should eat even better along with weight gain. She has also been moved back to the Neonatal Intensive Care from the Progressive Care. It will depend on how well Olivia does after surgery on when she can move back to Progressive. Please pray that Olivia pulls through the surgery! Dr. Pickett is doing the surgery so please pray for him too! Thank you for all of your prayers, and I will keep you updated tomorrow as I know things as well. We are praying for you sweet Olivia Jane! I love you!

~Aunt Jessie

Another surgery!

Well, the doctors have told Melissa that lil Olivia Jane will have surgery early in the wee hours tomorrow for a temporary shunt. It sounds awful but I am looking at it as an answered prayer. We prayed for Olivia to be ok, and this will allow that in a way. It is not the permanent one because she is still too small. They estimated weight that she would be is around 4 pounds for the permanent one, and she is only around 2 pounds 12 ounces. The temporary pump will be a bag that will collect the fluid from her brain, and I am assuming that they can empty it? They will put her to sleep for the procedure, but unfortunately she will not be able to eat for at least 2-3 days after. We all know that she can't afford to lose any weight! Other than that, I am not sure on the details, but I will know more later.

I just wanted to get this out so that you guys can start praying that everything goes great and God answers our prayers once again! Thank you to our cousin Tracy for your comments! A big thank you to Charlie too! To everyone else that sends this website around, thank you too! That is the only way to get it out there about Olivia - is through church, Facebook, and just by mouth! If someone stops me in the store or says hi, I say hi back but ask for a prayer for my niece! I know it sounds silly, but she is my niece...my angel! I love my nieces like I love my children! My heart breaks to see her in the NICU this long, but I know that she is in the best place right now and that is what keeps all of us going!

Thank you again to everyone for your prayers! They are going to get Olivia Jane home; I just know this! PLEASE keep praying! I love you Olivia Jane!

~Aunt Jessie

Olivia still needs your prayers!

Please continue to pray for Olivia Jane! Her head is still swelling, but she did not get sick today! After she ate, Olivia kept it down. The nurses are feeding her slower per feeding and that has seemed to help too. Instead just breast milk, the nurses have put Olivia on "preemie" formula to help her gain weight. If she can gain some weight, hopefully she can have the shunt put in sooner rather than later! The faster they can put the shunt in, the quicker she will be on the road to recovery.

However, prayer is so important! Melissa talked to a NICU nurse and she told Melissa that there have been instances where the preemie will be in Olivia's position, get ready to go into surgery and then the fluid is gone and the preemie's ventricles in the back of the brain are fine! That is called a miracle and God can do that, so please pray! Olivia needs every prayer imaginable! I know that it can be done, I have faith that it can be done! PLEASE PRAY! God, please heal Olivia's brain and remove the fluid!

Melissa also got to do "kangaroo care" again today, which she LOVED! She got some really good pictures of that, so I will get them up as soon as I can. Please tell everyone about this beautiful little gift from God! Please tell them to pray. I ran into a friend of mine from high school today at the mall with my sister, and I couldn't help but tell her immediately about Olivia and asked for prayer and gave her this website! Thank Emilea for your prayers! ;) The more prayers we have the better Olivia's chances are at a miraculous recovery!

I love you Olivia Jane! Stay strong sweet angel!

~Aunt Jessie