We're on earth, my parents call tito and is about to come, as we pack up and go to the exit. I am very dormidito rebuelo but I hear something, I had a very good flight and I have wanted to sleep in my crib. GO
is this, my mom is a little nervous, I do not need to get home and see all the people are all here and do not stop shouting and singing that finally everything is over and now we begin a new life.
This is the shirt that we all received, we had a poster with signatures and phrases for more me realize how it was my reception was very emotional, something my parents will never forget nor will I forget me.
We are home and now begins the hard, rehabilitation and expect no more crisis.
We have long been at home and no crisis but I'm getting a little unwell with a cold and occasionally I have a spasm. The doctor told us always that the most normal
is that when this bad, have a crisis, that the operation was very large because the malformation was great and there were parts that could not be causing me to play because it could damage worse.
We are in an important day, dad's birthday, we are in late October, I'm quite catarrito and mucus and start some cramping today, all but the medical care and had warned us that the important thing is to find proper medication and it was surgery, to return the disease treatable with medications.
These months have been adaptive and drug trials, we have performed a difficult few months such as winter, so occasionally I still have a crisis, but in the worst days I fail to 4 or more, Mommy says that compared with before it could reach 70, now live in glory. I've changed a lot, I argue when I pick up and I move fast, and I can turn around and put one upside down, and babble a lot and am able to coordinate my hands and take off his jacket to put my fingers and play with my little teeth.
I'm in the store, is a nursery school for special children and taught me many things, going to rehab every day and once a week pool I am with my children and many educators are very affectionate. Enter the store meant a lot because it was full, but the tenacity of mommy and daddy force have made many people have helped us to enter. From here on behalf of my parents and especially on my behalf I thank all those people, they know who they are, and fellow Heads Papi and the Pater S.
I'm very resourceful, but this is a long struggle and there are times when I have not a crisis for several days or weeks, but then I get the lesser evil and I have 2 or 3 for a few days, but can see my improvement. In December we had the first rebición and everything was as it had to go back in June to see how it goes ......
Well, this time we have taken too long to write this chapter in a short week will put some more pictures now, and since we will post a video, right now our life is very busy, Aimar looks like another child, his epilepsy is much better we have grown from 50 to 70 daily crises to have no or at most 2 to 4, when this unwell, as this year's winter was very cold here in the Canaries since every time a bad cough, but something we have to keep going until we can vaccinate small. Right now we are paying close attention also to the greater, because now it is more controlled Aimar have to try to do too much attention to Azael, as though he loves his brother always wants us all together. From here I want to apologize to all those who follow this blog for taking so long but now among children and work responsibilities have been very busy, We also expected a bit so that people saw the lottery ticket sold to help my child and came out winning. Commenter also that we are in the process of complaint against the insurance company because they do not always want the medical expenses of the operation of Aimar and in order to return the money they so kindly have "borrowed" all the good people who has known my little story. Thank you very much and will continue ......
Hoping it with less time between each entry.
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