{'en': 'Parents of children with diabetes', 'es': 'Padres de niños con diabetes'} Image

Parents of children with diabetes

Velia's profile photo   04/28/2008 5:35 a.m.

Very good to the Papis.
I just have to greet me, that I have already left on the route a will on how Celia is going with the bomb and how happy we are.
I'm glad to see Maclaudi and Pumba here again.
Mamidejuan, who will have a great time in the snow, sure.In addition, Juan is very responsible.

Health to all

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DiabetesForo
01/23/2009 9:59 a.m.
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Hello everyone:
I greet me very quickly that we are going to school.
Here everything is quite well, with the storm above but at the moment nothing serious.
Maria has this weekend that comes her first Squash championship.It is very important for her to take this step and be able to do the same as her sister who has been in competition for a few years.
I'm afraid we will spend the week with nerves.I hope we don't shoot glycemia very much.
I'll tell you how the thing is going.
Mamidejuan, over time I hope Maria does the same as Juan and can go wherever she wants without depending on anyone.You will be uneasy while it is outside, but at the same time you should be relaxed and proud, your mission comes to a good end.
Greetings to all and to take care of yourself.

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DiabetesForo
01/26/2009 2:51 a.m.
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Good morning dads ....
Quiet weekend.Angela's friend at home since Friday, imagine the glycemia, it was already difficult to upload them ...
Jose, good luck for Mary on Saturday.The truth is that it is a joy that our children can make their dreams.
What's the rest of mamis and kids?We want you to be well .. Let's see if you have a hole and tell us how are you ...
Marcita, how is Noe?When do you return to Cáceres?
Kisses and good day for everyone.

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Velia
01/26/2009 4:08 a.m.

De los buenos tiempos, siempre quiero más...
Mamá de Ángela, ¡16 añitos, fiera!. Debut: octubre de 2003.
Bomba insulina Medtronic Paradigm Veo desde junio 2005
Última hemo 6.1

  

Good, fresh and windy days !!
What a desire that comes Julio !!!!!!!!!!!!!!!!
Jose, I'm glad to see you here again.The nerves will be inevitable for Mary before such an event.You will see how everything is going well.
Velia And Angela?The nerves wreak havoc.
Not something strange happened to Noe.Before dinner he had 79. He had dinner as always, we put the usual insulin and in the post he had 62. We did not leave the house throughout the afternoon and did not exercise.It recoured a ration and at 2 in the morning I had 248, I did not corrected and at 4 I already had 160 but it has risen with 41. I did not explain this roller coaster, come on, another file X.
Velia, Cáceres will go in March, but we are waiting for the appointment, I already tell you something.
Well, kisses for everyone and spend a good day.

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DiabetesForo
01/26/2009 4:53 a.m.
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Hello everyone!!.
Jose, I'm glad to see you here, and good luck for Mary in her first championship !!!You will tell us.
Well, the truth is that Juan's weekly in the snow will be a great step;As Alea says, it is true that Juan is responsible, but ... and diabetes?Is it responsible? As has happened to Noe tonight, what is that descent?, From Juan me, but of the diabetes no.
He has told me that this week will get less insulin because he prefers to be high, but I know that when it is measured and passes from 200 it scares ...
And, in addition, pending time ... wishing everything changes for next week: shock :.Can it be? ...
A hug

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DiabetesForo
01/26/2009 6:18 a.m.
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Mamidejuan, you are lucky that Juan detects the downs.I know it's hard to leave them.In fact I cannot leave Celia yet, and she is already mentalized not to go to the study trip, but I suppose that having Juan to his brother near will be a guarantee.
Of course, the concern is not removed by anyone.And the mobile bill, either.

Jose, to do Maria very well in the Squash.

Health to Papis.

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DiabetesForo
01/26/2009 6:23 a.m.
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Good, family.
Mommy, you will be of the nerves, you will see how good everything goes and what a great time for Juan.Someday you will have to let them fly alone, but how difficult it should be.
Well, Noe tonight, normal glycems and repair sleep.Let's see if it can be.

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DiabetesForo
01/28/2009 7:26 a.m.
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Mamidejuan, reading you I have remembered a joke that I like (that is, bad)

A man goes to the consultation of a psychiatrist, totally distressed.
- Calm down, what's wrong with you?
- Doctor is that sometimes I think the chickens think that I am a corn grain and that they are going to eat me, and I panic ...
- But see, good man, you know it's not a corn grain ...
- Yes, doctor, I know, but ... do chickens know?

hehehe, it's funny to me

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DiabetesForo
01/28/2009 11:50 a.m.
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Hahahaha, thanks Alea, a smile to start the day.
Sunday is Noe's diabetes-anniversary, two years old, my mother, how many punctures will have taken in these two years?Better or think about it and how he has become accustomed to living with diabetes, controlling his food and being aware of his controls and insulin ...: ((((
Anyway, sad day, with MEONA fog that covers the bones.Good morning and kisses to all.

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DiabetesForo
01/29/2009 4:15 a.m.
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Thank you all for your support I know that there are many people in my same situation that after a while sees things with more hope and clarity.The truth is that from my endo I do not get anything clear and they have not sent me to the educator, I have looked for my life, putting myself in contact with the association and reading a lot on the Internet and the forums.I have a question can you put a continuous measurement monitor to such a small child?Thanks again to everyone

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shandra
01/29/2009 3:44 p.m.
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Shandra, we are all on the same ship, so you have nothing to thank.

The meter is already more complicated, because social security does not yet finance it and I do not know if in such a small child it would be advisable.

What community are you from?I ask you why there are more generous autonomies than others to finance things.

Greetings

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DiabetesForo
01/29/2009 4:16 p.m.
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Shandra, we are all on the same ship, so you have nothing to thank.

The meter is already more complicated, because social security does not yet finance it and I do not know if in such a small child it would be advisable.

What community are you from?I ask you why there are more generous autonomies than others to finance things.

Greetings

Hello Alea, I am from La Rioja and here for what they told me they do not wantI could put a continuous meter would be willing to pay it.

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shandra
01/29/2009 5:06 p.m.
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Good morning, Papis ...
Welcome to the thread, Shandra .... The truth is that at this point the attitude of certain specialists about the new technologies applied to diabetes seems incomprehensible ... and the worst of all is that I imagine that it will be due to ignorance,Lack and lack of interest ... The demons take me!My daughter has been a bomb for 3 and a half years and of course I do not tire of saying that it is the best thing that has happened to us.I think that I have to go back to the injections and I get bad, so I give me that there are new methods and to my understanding much more effective for the control of diabetes, they allow the luxury of not wanting to hear about them.... this is incredible !!!!
The bomb is designed for all types of people and why not, even infants.Let's see which method is more reliable than one who can supply insulin dose of 0.01 at 0.01 units or stop insulin entry, etc.It is a highly recommended method to avoid hypoglycemia, not recommended in the littlethat measuring more often (that for nosostros was not a problem because I measured the same with the mixtures and with the lantus), the insertion of the catheter can be somewhat more annoying, but it is done every 3 or 4 days, any problem with the perfusionInYou decide you will have to work it, but I encourage you to keep informing you about it and that you think that to return to what you have there is always time ...
There is a section on bombs where there is a thread about the continuous meter (my daughter is wearing and my husband too), in case you want to read it.But I would recommend that you will first throw all your energy on the pump theme .... courage and here you have us for what you need.

Uffff, jolin, seems to be paid and tó ... hahaha, what a paragraph! .. Well, what about the missing? .... I hope they are all well.

Kisses and good day.

Velia's profile photo
Velia
01/30/2009 4:26 a.m.

De los buenos tiempos, siempre quiero más...
Mamá de Ángela, ¡16 añitos, fiera!. Debut: octubre de 2003.
Bomba insulina Medtronic Paradigm Veo desde junio 2005
Última hemo 6.1

  

Hello family,
How are everyone ????Every time I do more than begging me for so much vaguería, although I am not sin of being the only one, huh?
Nyah's birthday was fine and that the cachulinos came but they behaved, so good day at the end.We continue with luxury glycems (fear gives me) although it has had some file X that has forced me to go to school and another of visits to the pediatrician for urine infection and by work and miracle has disappeared without more.I continue with my ailments also of file and I don't do more precious every day ......... In short, life is beautiful.:)) Ja, ha, it seems that I have seen the announcement of the compresses of: I like to be a woman !!!:))
Well, bullshit apart, I hope that the sick are already fully recovered, everything, everything is missing.
A kiss to all and good weekend.

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Beky
01/30/2009 6:12 p.m.
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Goodaaaaaaaaaaas !!!!!

Beky, I'm glad to see you here, and above all you're well.
We have postponed the weekend getaway, last night noe with vomiting: ((, Pocha again, not to vary, we don't spend a good week:-/ When summer will come! And my maid, three quarters of the same,Let's see if I save myself: shock :.

Well, good weekend to all.Kisses.

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DiabetesForo
01/31/2009 4:58 a.m.
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Jolin, Marcita, Poor Poor Noe, tells many kisses on me, what a course that takes the poor, to see if he begins to do good and do not get so malitos.
Well, ask for forgiveness for not having welcomed Sandra, Leo but when I write the saint goes to heaven.Well, what has been said, welcome to this family because this forum for some is almost a family that in some cases helps more than their own.
I am Nayah's mother, debuted with 8 months and just turned 4, we have been with a bomb for 5 months and as all is the best that has happened to us since we started in this.We were with NPH with the same inconveniences as you, our previous endocrine did not want to hear anything of a bomb and we did not stop until we got it if, changing from city.
I do not know how you are putting the insulin fast whether with pen or syringe, but if it is with a pen for now I would try to speak with the endocrine to pass you to syringe of half unity to be able to better adjust the pattern and avoid those ups and downs.Also click after eating help enough if you have not told you.
Greetings and I give you a lot of encouragement, at first it is very hard but you have to miss the time ......
A kiss to allsssssss.

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Beky
02/01/2009 7 p.m.
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Good morning !!!! ... how are you going?I see Noe is Malina again.A little kiss for her and see if it improves soon.
Becky, how time passes, I still remember when I met you in the other forum ..., by the way, I'm glad that glycemia go like this ... well !!!They last what they last.
Angela unstable glycemic, it costs me the night, but we will continue trying ...
Well, daddies, a kiss and good day for everyone.
Kisses.

Velia's profile photo
Velia
02/02/2009 2:59 a.m.

De los buenos tiempos, siempre quiero más...
Mamá de Ángela, ¡16 añitos, fiera!. Debut: octubre de 2003.
Bomba insulina Medtronic Paradigm Veo desde junio 2005
Última hemo 6.1

  

Hello everyone:
Welcome Shandra, I assure you that in this forum you will discover and learn many more things that your stup-endo can inform you.
I see that for your community you are for mine (northwest zone), to us today, and we are going for 4 years on this issue, no one has spoken to us, nor insinuated, that insulin bombs exist.We have come to the conclusion that they do not want to complicate at all, you are looking for life to adjust the insulin differences well and already.They don't care that they have to put them 3-4-5 times insulin up to date.They are not flesh of their flesh.
On the other hand, you have to get little by little knowing the disease and studying your child's responses a lot to insulin doing methodical controls.Over time you will do less and you will have more security.That said we all go out and you will not be less.
The Internet is fine, but with caution, you can get to find erroneous information and many false hopes.There are uncontending that they want to do business with these issues.
Well, it's fine with roll, as Velia says, they seem to pay us.
Maria could not debut in competition, they canceled all competitions at the autonomous level for the storm, after Catalonia all caution is little.
Marcita, I encourage that winter is going on and summer is approaching, you know, sun, beach, vacations 8) 8)
I leave you, I had a week without writing and it happened to me.
Kisses to all and take care of you to take care of them:-/

DiabetesForo's profile photo
DiabetesForo
02/04/2009 2:51 a.m.
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Hello everyone again, I know that this disease is always complicated with unforeseen ups and downs but it boils my blood when I read that other children with the bomb go great and my endo does not want to hear about them.They are children for God, I make glycemia tests about 11 times minimum daily and I no longer have fingers to prick him.I will continue fighting for a bomb or at least for the continuous meter that would solve my life a lot.I have another six -year -old girl who already tells me that I spend the pending day of her brother and she feels a bit abandoned, and she is right there are times that I feel helpless to see that I cannot unfold to attend the two forThe same and that telling that my husband and I no longer have a respite for us and I cannot allow a hard to spend my community, it costs us to destroy my family harmony.The other day my son put himself in 500 for no apparent reason and after putting the fast one he lowered at an impressive speed, so he clicks to control him. I do not understand how between one visit and another with my endo they are three months only for thehappy proof.And during that time what?I look for my life. Well that now the one who lengthens too much is me.A kiss and that all who are malitos are improved.

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shandra
02/04/2009 3:51 a.m.
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Hello everyone.
Shandra, I'm afraid we sometimes have to fight the elements.
I have changed it 4 times of endocrine, until you find this team, which is wonderful.
You will touch you to fight, inform you of whether in your community there are more prone to put bombs than the one who touched you and, where appropriate, ask for the change.
If the problem is autonomy, apart from getting the colors because other poorest autonomies do finance the bomb and threaten them with the press, the only option you would have is to register temporarily in another in which they are granted.

Luck.
Health

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DiabetesForo
02/04/2009 10:24 a.m.
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