Oxygen Sensor, 2003 Yukon Xl

glasses!

Yes, from today, Ada also wears glasses. The commission Tuesday afternoon we just left the visit with the ophthalmologist and we went to pick up this afternoon. Appreciated the speed of optics!

The truth is that it was a hard blow for us, not because they have to wear glasses but mostly because Ada has proved to be very myopic . From 12 diopters in one eye and 11 in another, even in these early glasses Ophthalmology has a lowered diopters. When the laser was operated on 2 November 2009, already warned us that the ROP increased risk of myopia and strabismus and other complications, but never imagined that we could reach these levels. In our families there is a history of myopia magna genes and were not prepared for it. I particularly have conceded this much worse news than that of the hearing, perhaps because the evolution of Ada in the last six months has been nothing but positive and had begun to forget the possible consequences their extreme prematurity . Furthermore, I asked the doctor if myopia continue to grow and he replied that depended on each child, which in some cases corrected a bit in childhood and had another peak in adolescence, and in others was always more. This last possibility makes me very afraid because I know that beyond the use of headphones we have cochlear implants, but I think there is little (or no) room for maneuver before an eventual blindness. I run too much and probably are irrational fears of mother, as I understand people who said that alcohol could be much worse.

The fact is that Ada has released this afternoon glasses. They are orange with rimmed glasses and organic pasta, and have two holes in the rods to secure the fastening with a rubber neck. We have fun but also tried to thin and discreet ear headphones also have to sustain. The truth is that the reaction of our lioness in optics has been very positive and confirmed that her glasses were necessary: \u200b\u200bas soon as we left, started to look around her carefully and made a pair of laughter, and has become very serious when there have again removed to adjust the rubber. Returning home was turn his head 180 degrees to see everything that happened in the street, and even have the impression that crawl more speed and better handling objects and toys! Well, see Now if we detected and corrected (the important) deficit visiu encouraged to walk at once!

Some friends and acquaintances have asked how we noticed that the girl looked good there. To be honest, we do not suspect anything. When he was 5 months corrected came home from a cousin, Ada has the same age and I was very surprised that so excited watching her mother prepared a bottle for ten or twelve feet away. I remember at that time I told Andrea that Alberto would do a view of an eagle, but I attributed the lack of reaction to his Ada psychomotor retardation. A couple of weeks, the speech therapist told me that he felt he was approaching a few toys, but I did not give more importance, however had to review a few days ... Thus, myopia has detected an ophthalmologist for periodic checks many since leaving the hospital. A child born would have found out much later, with the consequent prejudice to their psychomotor development and visual acuity. As always, we thank our health system and professionals who monitor the Ada!

change the subject from today until Thursday and we enjoyed the company of Gaspare uncle, with whom we visited on Friday and Saturday for the first time in Valencia. The following Ada enjoyed much movement fish ' Oceanog Rafic , and we see how we get rid of the uncle playing with his niece. Besides being a survivor, had our little luck with her grandparents and uncles. It is the first grandchild and niece both sides and I guess that is why dear!

Pokemon Soul Silver Ds Komplettl�sung

lung disease in infants can prematuros better with a good nutrition

lung disease that develops the soil prematuros babies who require prolonged ventilation after its Birth mejorarse can with a proper nutrition, According to desprende a study at the University of Michigan.

The research, published today in the medical journal Pediatric Pulmonology, showing the relationship between children's lung growth and diet.

Thus, among the 18 infants with bronchopulmonary dysplasia (BPD) in underpinning the study, those who gained weight above the mean lung volumes were improved significantly.

BPD typically develops in premature infants who require prolonged ventilation or oxygen therapy after birth, leading to significant reductions in air flow when compared with children born in the space of nine months.

addition, babies who have lung disease are more likely to develop asthma in future.

The investigators caution that more research is needed to examine the effects of different nutritional regimens on lung growth, while acknowledging that even babies get better with a good diet, are not able to achieve lung volume of premature children.

is considered premature babies born before 37 weeks of pregnancy, and one of every eight children born in the United States is, according to data from the Centers for Disease Control and Prevention (CDC).

Source: http://www.google.com/hostednews/epa/article/ALeqM5hFVBDuhXDBlQA3tXg15otVgYE9tA?docId=1451131

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visiting the NICU

This afternoon we went to San Juan de Dios because they inject the penultimate dose palivizumab to Ada and we have used to greet our angels homes in the NICU. After living nearly 5 months, have become part of our family and we like to visit them regularly. We think it is the least we can do to show our (infinite) and we thank you and encourage them to continue with their work.
Working in a NICU should be harsh, despite the shift and rotation, it is inevitable that the team that serves newborns emotionally involved in their care. The stays are much longer and the suffering of children and parents is known. There is not always a happy ending, and when tragedy occurs, is devastating for everyone. So, I guess that has to be very satisfactory reunited children, Ada, despite having everything against them have been released, and they have gone quite well.
As expected, the flood and have been very much awake, she watched her children all smiles and distributed to everyone that dedicated attention. From the threshold
the door to the room where we waited and despair, I saw an early heat in a cradle located in the same place was Ada, and I considered it unbelievable that she has never been so small (and when he was a third born child of that !!!). I've seen so fragile, so helpless ... Every time I would talk to the NICU with all parents and reassure them, but the suffering is intimate by definition and no question. I know the nurses will take care of them tell the story of Ada and I hope this helps to imagine a bright future for their children during these times of darkness.
I remember those days as a nightmare with brief moments of lucidity. The time was stopped for us, yet we escaped on their hands, and I do not know where they went to stop those months ... When the children were born it was summer and it seemed impossible that the sun came out every day and that people could leave their homes and live life as if nothing. Friends and relatives knocking us but generally we had no desire to talk and we ended up appointing spokespersons. I hope we keep that anyone feels offended by rancor or have not received the attention and appreciation they deserved.
After the visit, we have the picnic in Ada (as always at the wrong time) in the lobby of the hospital and have bought the story and the Centella Blue Bird, that many times we read the wall of the corridor and that explains the NICU with great tenderness and imagination the story of a premature ending coming home. The store in our book of memories, for when our small to grow. Few children have documented his life so! I hope that Ada is not ashamed of his scars and takes so are wounds of war that he won.
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Questo pomeriggio siamo San andati John of God ad Ada affinchè inniettassero the penultimate dose Palivuzumab e abbiamo approfittato salutare to Go to our angels and personality della TIN. Dopo di convivienza a nearly 5 Mesi, sono become part of our family and we like to visit them regularly. We think that is the least we can do to show our (infinite) thanks and we believe that so animate them to continue their work. Working in
TIN must be very hard, despite the shifts and rotations, it is inevitable that staff takes care of babies is emotionally involved in their care. The trips are very long and the suffering of infants and parents is unknown. It is not always a happy ending, and when a tragedy happens, it is devastating for everyone. For this, I imagine to be a satisfaction to meet again with children who, like Ada, even though all have made it down, and I'm leaving quite well.
As was to be expected, have seen very grown up and very alert, she watched all her little smiles and distributed to all who devoted a little attention.
From the threshold of the entrance door to the room where we waited and desperate, I have seen a premature baby in a cradle located in the same place where the heat was Ada, and it seemed incredible that Ada had been so small (and when it was born a third part of that baby !!!). I've seen so fragile, so helpless ... Every time I go back to the NICU I would like to talk to all parents and reassure them, but the pain is by definition intimate and no one asks questions. I know that nurses are responsible to explain to parents the story of Ada and I hope this will help them to imagine a bright future for their children in these times of darkness.
I remember those days as a nightmare with brief moments of lucidity. Time stood still for us, but at the same time the day we ran out of the hands, and I do not know where those months are gone ... When our children were born it was summer and it seemed impossible that the sun came out every day and that people would go away on vacation and live their lives as if nothing had happened. Friends and family called us but, in general, we did not really want to talk and eventually we designate a spokesperson. I hope no one holds a grudge nor feel offended for not having received attention and the thanks he deserved.
At the end of the visit, we have a snack in Ada (as usual not the time for snack) at the hospital and we bought the story, "Centella and the bluebird, which many times we read on the wall TIN of the corridor and explained with great imagination and tenderness of the story was that it was premature to home territories. The store as our book of memories, for when our little one is great. Few children have their lives documented so! I hope that Ada is not ashamed of the scars that door and take them for what they are, the wounds of a war that has won.

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Finished good life

S'han acabat tamb les vacances for us and we again have the full schedule of visits: Yesterday, respiratory, speech therapist and nutritionist today and tomorrow audiometry and physical therapy ... Goodbye to the good life and times! We discuss the respiratory
we would like to enroll in Ada kindergarten this September and he wrinkled his nose a bit. She thinks it would be very beneficial to the psychomotor development of Ada and its sociability, but considers that it is still fragile from the respiratory standpoint. The lungs are fine and the girl has cooled only twice since he came home (we are now leaving the second), but we can not drop our guard. He says that back in June to discuss and, if finally at home, will prescribe Singulair to prevent possible bronchitis.
regard to the nutritionist, has not been high despite the growth of Ada is more than satisfactory. With 13 months (corrected) measured 79.5 cm and weighs 8.9 kg ... When he got home was below the third percentile in height and is now over 90, his curve has crossed the entire table! The weight is satisfactory but is not far from the end of 2010. Between mucus and coughing, Ada has eaten much less this week and this morning did not want breakfast. The visit was at 11:00 and just before entering the query has a macropipí, so the balance has scored less than 500 grams marked the day January 2: (
got the video camera because the speech therapist could see the progress of the graphic testimony of Ada. I knew that our chili silenced during the meeting, like always: D: D I am curious to
hear the opinion of the psychomotor therapist about the progress we made during the Christmas break. The Nonno's granddaughter-addicted and since a week ago, Ada does not touch down to earth (literally), so I do not know if we progress much: P But the truth is that it is a joy to see them together and happy and consent, although we know that they pay expensive from tomorrow, because the grandparents back in Italy Ada voldrà accept no els que s'han acabat Bracos a totes hores.
Desitgeu sort-nos.
------------------------------------------------- ---------------------------------------------- The holidays are
finished and we go back to having the full schedule of visits: Tuesday pulmonologist, nutritionist and speech therapist today, and tomorrow, audiometry, physiotherapy ... Farewell to the good life and good times!
We commented to the pulmonologist that in September we would like to include Ada kindergarten and turned up their noses. He understands that it would be very useful to the psychomotor development of Ada and its sociability, but considers that it is still fragile in terms of breathing. The lungs can be seen very well and has been cooled by two small times since returning home (we are now out of the second), but we can not lower our guard. He says that in June and we'll talk about that, if the end is kindergarten, the Singulair ricetterà possible to prevent bronchitis.
As for the nutritionist, did not give us the final OK in spite of the fact that the growth of Ada is more than satisfactory. With 13 months (correct) measure 79.5 cm and weighs 8.9 kg ... When we got home had a height below the third percentile and is now over 90, his curve has gone through the whole table! The weight is more than satisfactory, however, is far from the end of 2010. Between mucus and cough Ada ate much less than normal this week and did not want to have breakfast this morning. The visit was at 11:00 and just before going to the medical examination showed a macro-pee, so that the scale has reported 500 grams less than at January 2: (
I had to bring the camera to the speech therapist could have proof of the progress of Ada. I knew our dumb beast would do during the session, as he always does: D: D
I am curious to hear the opinion of the physiotherapist on psychomotor progress they made during the Christmas holidays. The grandfather was a nephew-dependent and is a week that Ada does not touch your feet on the ground (literally), so I do not know if he has improved: P But the truth is that it is a Insieme e gioia vederli Felici e glielo lasciamo fare, anche che sappiamo it is expensive to pagheremo departed da domani, and Grandparents tornano perché in Italia non e Ada Vorrat accettare Potro che gia non essere tutto il tempo taken in braccio.
Augurateci buon fortune.

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these four things well

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Tomato Juice Mrs And Mr T Can

drum, balance and gratitude

Yesterday I had a chance to stop this wonderful blog and I noticed that Ada is the very recently abandoned and just hang videos ... As the father of the baby does not seem to want to write, I try to amend it by making me more This from now.

The Ada has lived his second Christmas was very different from the first, we spent alone in a room of St. John of God Hospital very saturímetre pending. This year we enjoyed the company of our family (with the absence of my father, who died shortly before the arrival to the world of Ada) and closest friends. We played shit and we bought gifts strain again has a new cousin born and from 5 to 12 and have to nonnos home. Ada

This Christmas we are presented with their first ta-ta-ta and I think I speak for Alberto and me when I say that this has been a great thrill because of their deafness. It is certainly clear evidence that hearing aids and speech therapy work! Another good sign is that beginning to understand some words when I say that daddy smiles and comes crawling at full speed until the door of the room to receive it. About

motor, Ada still does not walk but instead goes on the couch with incredible ease. Moves across the floor crawling, and rises to reach the goals that you draw attention to misdeeds. I finally learned to clap! A couple of weeks before Christmas had begun to take a toy in each hand and struck each other, but that means that applauds their understanding of the world is advancing. Although it may seem ridiculous, it was a milestone for me in particular worried me greatly.

Another gratifying is that, for a month or so, Ada adults interested in food and even has taken a couple of cookies out of hand. When sick, eat with great appetite and is getting longer than a day without bread. Eat lentils without crushing, plant and Rissotto has dared even with chicken fingers! But far from doing so alone, and when you leave bits of food for the tasting is limited to playing with textures and just throwing everything on the floor.

On December 29 was fulfilled a year of arrival at the house of Ada and the outcome could not be more positive. The dependence of oxygen, the same analysis, the profound deafness, epilepsy, hyperactivity and autism fears are thankfully long gone, and you begin to imagine the possibility that our daughter goes to school one day normal. But, now is when I have insomnia!

I finish this my first post (I had until now limited to a translator) giving thanks to all those who accompanied us and helped us at this time. The evolution of Ada is largely due to Maria Jose, the physiotherapist CDIAP that accompanies CITY 11 months ago. It is a superb professional who has always empathize with me and my fears (which were not few!) And has managed to reassure me feet on the ground. Occasionally I thank you but so far he had not ever publicly and is a debt I had.

Our thanks also to the entire team CREDAV Jordi Perelló Sabadell, which follows Ada since confirmed his deafness and works as a day can develop normally despite his disability. Silvia, Pilar and Nuria, his speech therapist, are sweetest people who love their work and work with Ada at the same time showing him affection. The resume on 11 speech therapy sessions and try to explain exactly what are they.

I want to thank again all companies which participate in the forums, relatives, friends and friends of friends who were moved by the story of Ada and gave him strength to live and grow healthily.

And finally, thanks to the team of St John of God hospital that lives up to its motto and for us it is really friend. In these 17 months we have always felt treated with respect and understanding, and is a joy to return to the NICU and feel the warmth of becoming pediatricians and nurses who fought for the life of Ada although Alguna moment tots plegats haguéssim deixat creure de-hi.
GRÀCIES!

Penja tres fotos del dia de Reis

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Yesterday I went to end up randomness to this wonderful blog and I realized that what Ada was very recently abandoned and only publish videos ... As the father of the creature does not seem to like writing, try to correct the situation being more present from now.

Ada has lived her second Christmas and it was very different from the first, we spent alone in the room Hospital Sant Joan de Déu and very steep pulse oximeter. This year we were in the company of our family (with the absence of my father, who died before arrival to the world of Ada) and closest friends. We did "shit" the trunk (Catalan tradition) and we bought gifts again, a new little cousin was born and the day 5 to 12 we have grandparents in the house. Ada

This Christmas we got her first ta-ta-ta and I think I speak for myself and for Albert when I say that this event has generated a great emotion because of his deafness. Without doubt, it is clear evidence that hearing aids and speech therapy work! Another good clue is the fact that she begins to understand some words when I say that daddy arrives smiling and crawling at full speed toward the door of the hall to receive him.

As for the drive, in Ada, however, still does not walk on the couch and changing rooms with incredible ease. It moves into the apartment and crawl up to get the objects that attract their attention and make mischief. And finally, he learned to clap! A couple of weeks before Christmas had begun to take a toy in each hand and hit them, but applaud the fact that means that his knowledge of the world is progressing. Although it may seem ridiculous, it was a goal that worried me a lot.

Another reason for joy is that, for a month or so, to Ada are you interested in eating the large to the point steal a few cookies from the hands. When he is not sick, eat with a big appetite and is getting longer than a day without bread. Eat lentils without chopping, vegetable risotto and also had the courage to eat chicken fingers! But it is still light years from eating alone, and when we leave the pieces because they try to eat, play is limited to examining the consistency and then pull it all ends up on the ground.

On December 29 he did a year of arrival at the home of Ada and the budget can not be more positive. The dependence on oxygen, paralysis, profound deafness, the epilissia, hyperactivity and autism are fortunately fears have been in the past, and begin to imagine the possibility that our daughter one day to go to school normally.

I want to finish this my first post (so far I would just act as a translator) to thank all the people who accompanied us and helped us throughout this time. The evolution of Ada is mainly due to Maria Jose, the physiotherapist CDIAP Ripollet of that with us for 11 months. It 's a great professional who has always entered into sitnonia with me and my concerns (which were not few!) And has been able tranquillizarmi always down to earth. Every now and thank you so far but I had not ever made public and is an outstanding debt I had.

Our thanks also to the whole group of CREDAV Jordi Perelló of Sabadell, who follows Ada since it confirms the deafness and works one day will grow normally because their disabilities can mangrado. Silvia, Pilar and Núria, the speech therapist's, are very sweet people who love their profession and work with Ada at the same time showing her affection. On the 11th we start speech therapy sessions and will try to explain in that consist.

I want to thank again all the companions of the forums where I participate, relatives, friends, and friends of friends who were moved by the story of Ada and gave her the strength to live and grow up healthy.

And finally, thanks to the team of Sant Joan de Déu, a hospital that lives up to its motto for us is a true friend. In these 17 months we were always treated with respect and understanding, and is a joy to return to UCIN and hear every time the friendliness of pediatricians and nurses who have fought for the life of Ada though at times everyone had stopped believing.
THANKS!

I put three pictures of the Epiphany (here we celebrate the three kings)

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Speech of Making New Year