Report on type 1 diabetes in TVE

A 30 -minute minidocumenal has just given on TVE2, about silent diseases.2 type 1 diabetics have come out and a woman with multiple sclerosis.

Link

Diabetics are represented by a young girl, who says she is doing very well, gives motivation talks to diabetic children and wants to be a nurse.And on the other hand, a very young child where above all looks how hard it is for parents.

Thanks for the link.

The only thing that I did not like the report is the nurse who takes care of the child in the cole.Look at the sugar and say we are going to see if you can eat or not.Very Taliban to be a child of about 4 years, right?

That report is nefarious.Poor kid.To continue believing at our dreams Link

diabolique said:
that report is disastrous.Poor kid.To continue believing in our dreams

The truth is, I am infinitely more interesting how to take it in daily life, than in a timely ascent to Tibet with the best bomb and measurement equipment and a team of specialist doctors from behind, supervising everything in real time.That they stay there for a few years alone, with nothing like that, if they are so brave.

That type of reports at the end are the ones that make us the most.

Then people think, if you can go up to Everest and do everything they don't need to help you or subsidize anything.If you are so well, we better dedicate research funds to other diseases.

You have not understood anything.Damage to you only.Better continue crying in the sofa taking sugar to see if it goes up instead of looking at Nacho del RM or Andreu Simón winner of the Transgrancanaria or Zverev number two of the ATP in the 22nd 22. brave and beings of overcoming that we are and daily.To each one his Everest, in effect yes.To live that are two days.

When I debuted with 25 years I also played adventure sports and all possible follies.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

Go for God, poor child, who send him to eat the fast sandwich PQ is in descent and do not prove the jelly beans.
If you give you a jelly before the sandwich, you will no longer have to eat it quickly ..
It is true that the diagnosis of a young child changes our lives, but that it does not absorb it ...
Father's mobile follow -up 24 hours .. pff

sherpa41 said:
When I debuted with 25 years I also did adventure sports and all possible crazy things.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

moñiño said:

sherpa41 said:
when I debuted with 25 years also did adventure sports and all possible crazy things.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

The story is not to have to be 100% always or have the pressure etc, it is not that DB adapts to you.We have that "obsession" for being at the levels closest to normal to try to avoid or minimize the dreaded DB complications, just for that, at least me.And when aone. They diagnose DB type 1 or already older from 60 or so, you know that you have less years of life ahead with db that you have already lived without it.But we start children and we have the 50s already, we have been in the DB for many years, in my case I do not know what it is not to have it PQ since childhood debut, so it is a sword of Damocles, we want to become old withThe least possible limitations and that is why our "obsession" for control is not the same to have debuted with 9 Q with 60 years.

If they offer you the sensor and you are not doing well you are always in time to say that you prefer the strips.And they will give it to another.The majority gives us life but there are people who take it badly and prefer their control by previous methods.

@"Moñiño" you can do whatever you want but outside the workplace.
Last week I had a PRL course for railways (occupational risk prevention) and they told me that mutualRepair tunnels.I don't get out of office but I didn't know, I thought they didn't put limitations.

ruthbia said:
@"moñiño" you can do what you want but outside the workplace.
Last week I had a PRL course for railways (occupational risk prevention) and they told me that mutualRepair tunnels.I don't get out of office but I didn't know, I thought they didn't put limitations.

I know how it goes, I work in the renewable sector and I have my formations and renovations of it every 2 years.And suitable with Nanai limitations.I perfectly throw me 8 hours hanging from a shovel or similar and that remains so.From the theory, as sometimes reads in the advice here, to practice ....... It is far.Moreover, what I found is that they would not renew me in a project for diabetic (obviously they did not tell me like that, but a partner indicated where the shots came, and that many other partners did not want to work by my side byIf something happened to me.As what matters is to make money, if you don't fit the machinery outside.That is what happened to me.I already say that what the endocrine asks me many times on paper is very easy, but real life puts other conditions.
The tips are very good (as well, do not drink that, do this and stop doing the other, as you can think of ...).But you have to take them to the practice and conditions of the life of each one.Salu2

meginer said:

moñiño said:

sherpa41 said:
sherpa41 said:
when I debuted with 25 years also did adventure sports andAll possible follies.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

The story is not to have to be 100% always or have the pressure etc, it is not that DB adapts to you.We have that "obsession" for being at the levels closest to normal to try to avoid or minimize the dreaded DB complications,Just for that, at least me.And when one is diagnosed with type 1 or lada already of greater from 60 or so, you know that you are less years old ahead with db that you have already lived without it.But we start children and we have the 50s already, we have been in the DB for many years, in my case I do not know what it is not to have it PQ since childhood debut, so it is a sword of Damocles, we want to become old withThe least possible limitations and that is why our "obsession" for control is not the same to have debuted with 9 Q with 60 years.

My sister debuted with 3 and does not want bombs.Si sensor, finish with him (the free that is not very much because there is a lot of difference almost always with the blood measure), but of bombs, so he has seen in each other says no.They have offered it several times to put a bomb.He is 50 years old, he does not remember his life without diabetes.
PD: My diabetic grandmother since 33 and with her discipline (there was not as much improvement as today) I reached 103 years with her diabetes.I do not see much reason to think that you have to affirm sharply that because it is diabetic you will live less, as you indicate.

moñiño said:

meginer said:

moñiño said:
moñiño said:

sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
When I debuted with 25 years I also played adventure sports and all possible follies.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

The story is not to have to be 100% always or have the pressure etc, it is not that DB adapts to you.We have that "obsession" for being at the levels closest to normal to try to avoid or minimizeThe dreaded DB complications, just for that, at least me.And when one is diagnosed with type 1 or lada already of greater from 60 or so, you know that you are less years old ahead with db that you have already lived without it.But we start children and we have the 50s already, we have been in the DB for many years, in my case I do not know what it is not to have it PQ since childhood debut, so it is a sword of Damocles, we want to become old withThe least possible limitations and that is why our "obsession" for control is not the same to have debuted with 9 Q with 60 years.

My sister debuted with 3 and does not want bombs.Si sensor, finish with him (the free that is not very much because there is a lot of difference almost always with the blood measure), but of bombs, so he has seen in each other says no.They have offered it several times to put a bomb.He is 50 years old, he does not remember his life without diabetes.
PD: My diabetic grandmother since 33 and with her discipline (there was not as much improvement as today) I reached 103 years with her diabetes.I do not see much reason to think that you have to affirm sharply that because it is diabetic you will live less, as you indicate.

I don't care to live less if I have an acceptable life.What I do not want is to have important limitations I carry with dB and I have an impote retinopathy, your grandmother was luckyFor a few years, glyds that do not go from 5.5, and with little glycemics variability and still ... of course it was not always the case and the first 10 years and adolescence played a bad pass.
I want to say with this that we debuted in the 80s we did not have the same fate (so to speak) that those who debut now, with much more information and means.That is why I become the victim, I still try to control my best but the reality is what it is.

meginer said:

moñiño said:

meginer said:
meginer said:

moñiño said:
moñiño said:
moñiño said:
moñiño said:

sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
When I debuted with 25 years I also did adventure sports and all possible crazy things.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

The story is not to have to be 100% always or have the pressure etc, it is not that DB adapts to you.We have that "obsession" for being at the levels closest to theNormality to try to avoid or minimize the dreaded DB complications, just for that reason, at least me.And when one is diagnosed with type 1 or lada already of greater from 60 or so, you know that you are less years old ahead with db that you have already lived without it.But we start children and we have the 50s already, we have been in the DB for many years, in my case I do not know what it is not to have it PQ since childhood debut, so it is a sword of Damocles, we want to become old withThe least possible limitations and that is why our "obsession" for control is not the same to have debuted with 9 Q with 60 years.

My sister debuted with 3 and does not want bombs.Si sensor, finish with him (the free that is not very much because there is a lot of difference almost always with the blood measure), but of bombs, so he has seen in each other says no.They have offered it several times to put a bomb.He is 50 years old, he does not remember his life without diabetes.
PD: My diabetic grandmother since 33 and with her discipline (there was not as much improvement as today) I reached 103 years with her diabetes.I do not see much reason to think that you have to affirm sharply that because it is diabetic you will live less, as you indicate.

I don't care to live less if I have an acceptable life.What I do not want is to have important limitations I carry with dB and I have an impote retinopathy, your grandmother was luckyFor a few years, glyds that do not go from 5.5, and with little glycemics variability and still ... of course it was not always the case and the first 10 years and adolescence played a bad pass.
I want to say with this that we debuted in the 80s we did not have the same fate (so to speak) that those who debut now, with much more information and means.That is why I become the victim, I still try to control my best but the reality is the one.

For my "living acceptably" is living life without being exclavo of diabetes.And no victim, but see where you put the focus, where you put your energy, what you feed ...... in limitations, to live less.Next to something negative there is the same way of saying it positively "I do not want to live with limitations" you could say as "I want to live, despite diabetes" acceptably and ldesfrutanco of what I feel like and outdating what I propose. "There are two ways of saying the same, but in that mental language, that way you speak in your mind, within you, that language with yourself, one will lead you to anxiety, depression and the other to action(Learn which are my limits with diabetes, which I can do consistently to my current situation, or when I can do it, or that I have to modify to achieve what I intend ... there are people without feet and without hands,that has focused on positive and achieve things that neither you nor I do.Well, the same as you and that I, but have not focused on that, have focused on adapting to have the life they want to have.As you want to see it).Half empty glass, or half full glass?.

moñiño said:

meginer said:

moñiño said:
moñiño said:

meginer said:
meginer said:
meginer said:
meginer said:

moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:

sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
When I debuted with 25 years I also did adventure sports and all possible follies.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

The story is not to have to be 100% always or have the pressure etc, it is not that DB adapts to you.We have that "obsession" for beingAt the levels closest to normal to try to avoid or minimize the dreaded DB complications, just for that, at least me.And when one is diagnosed with type 1 or lada already of greater from 60 or so, you know that you are less years old ahead with db that you have already lived without it.But we start children and we have the 50s already, we have been in the DB for many years, in my case I do not know what it is not to have it PQ since childhood debut, so it is a sword of Damocles, we want to become old withThe least possible limitations and that is why our "obsession" for control is not the same to have debuted with 9 Q with 60 years.

My sister debuted with 3 and does not want bombs.Si sensor, finish with him (the free that is not very much because there is a lot of difference almost always with the blood measure), but of bombs, so he has seen in each other says no.They have offered it several times to put a bomb.He is 50 years old, he does not remember his life without diabetes.
PD: My diabetic grandmother since 33 and with her discipline (there was not as much improvement as today) I reached 103 years with her diabetes.I do not see much reason to think that you have to affirm sharply that because it is diabetic you will live less, as you indicate.

I don't care to live less if I have an acceptable life.What I do not want is to have important limitations I carry with dB and I have an impote retinopathy, your grandmother was luckyFor a few years, glyds that do not go from 5.5, and with little glycemics variability and still ... of course it was not always the case and the first 10 years and adolescence played a bad pass.
I want to say with this that we debuted in the 80s we did not have the same fate (so to speak) that those who debut now, with much more information and means.That is why I become the victim, I still try to control my best but the reality is the one.

For my "living acceptably" is living life without being exclavo of diabetes.And no victim, but see where you put the focus, where you put your energy, what you feed ...... in limitations, to live less.Next to something negative there is the same way of saying it positively "I do not want to live with limitations" you could say as "I want to live, despite diabetes" acceptably and ldesfrutanco of what I feel like and outdating what I propose. "There are two ways of saying the same, but in that mental language, that way you speak in your mind, within you, that language with yourself, one will lead you to anxiety, depression and the other to action(Learn which are my limits with diabetes, which I can do consistently to my current situation, or when I can do it, or that I have to modify to achieve what I intend ... there are people without feet and without hands,that has focused on positive and achieve things that neither you nor I do.Well, the same as you and that I, but have not focused on that, have focused on adapting to have the life they want to have.As you want to see it).Half empty glass, or half full glass?.

It is that I do not speak of the future but of present, it is that I already have non -small limitations, it is that it is already happening to me and I am not greater, that is a matter, it is difficult to see the glass half full in these situations

moñiño said:

meginer said:

moñiño said:
moñiño said:

meginer said:
meginer said:
meginer said:
meginer said:

moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:
moñiño said:

sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
sherpa41 said:
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sherpa41 said:
sherpa41 said:
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sherpa41 said:
When I debuted with 25 years I also did adventure sports and all possible follies.

Until I realized that instead of thinking about what I was doing, there was all the most pending activity of sugar, the next meal or punctured and did not enjoy anything.I threw myself for a mountain or descended a river, and I did not realize for always thinking about the other.

If I had an equal sensor it would have been better but now with 50 years I already tell you that I am interested less than anything.And if I had 25 again, I think it's what I would least want to do again.Although of course with the best material and a team of doctors watching in real time, even the most fearful diabetic does.

The really hard thing is to be alone in a work daily downloading boxes (or similar) with few breaks to eat or click.With the right material and also fails from time to time.

My father, with 74 years they have put a sensor.He says they have taken his freedom.It only is pending all day of the same, of his beeps, and when not, to see why he does not whistle, to see now that I go out to his daily walk, to see how I am ..... instead of beingIn life.Since it was diabetic he gives his walks.Before without a sensor he enjoyed his walk and if he noticed something, he ate something or acted accordingly and ready.He says that they will forget about the true sensor, his body (the sensations of his body) and that he loses enjoy the bed (and other things), to see if he is going up, going down or doing the pine (things that before the sensor barelyThey worried him).They give sensors but do not prepare psychologically.In addition, he sees that he has the usual ups and downs, with or without a sensor.The only thing that corrects them before but they do not stop appearing from time to time and as he says, they will not stop appearing, but would not be diabetic.

I understand you perfectly.
There is a lot of pressure that put us endocrine, family, other diabetics ..... for having to be perfect.I am diabetic and I have to assume it.In diabetes 1+1 they are not always 2. That perfect control is impossible.If not it would not be diabetic.I have to accept it.I am diabetic and not obsess so much.Thus there are anxieties, depressions, anguish ... and all those things that are read in other posts.Sometimes I perceive an envelope that we get to have to be 100%.I think you have to adapt your diabetes to your life and not your life to diabetes.If you do so, you lose what your life was and that feeling of loss generates all that frustration.You are diabetic, it is the only thing that has changed in your life.AdaptateIf you adapt the diabetes to your life, as those athletes do, you will reach the top of your Everest, but most importantly, you will reach it without fear, without anguish, enjoying it (with or without diabetes you only live once. If those athletes can;And not everyone has great medical teams, many have more than their self -knowledge, I know several; you can also.
I refuse for diabetes to condition my life.I still jump in parachute, learning to pilot Ulms, to get the title of aquatic lifeguard, bike races, training and karate competitions or kick box .......... and doing a thousand things.We adapt, my diabetes and me, to the situation and enjoy this only life that I have.That when I am going to die, I do not have to regret all the things I wanted to enjoy and do and that I prefer myself.Salu2

The story is not to have to be 100% always or have the pressure etc, it is not that DB adapts to you.We have that "obsession" for beingAt the levels closest to normal to try to avoid or minimize the dreaded DB complications, just for that, at least me.And when one is diagnosed with type 1 or lada already of greater from 60 or so, you know that you are less years old ahead with db that you have already lived without it.But we start children and we have the 50s already, we have been in the DB for many years, in my case I do not know what it is not to have it PQ since childhood debut, so it is a sword of Damocles, we want to become old withThe least possible limitations and that is why our "obsession" for control is not the same to have debuted with 9 Q with 60 years.

My sister debuted with 3 and does not want bombs.Si sensor, finish with him (the free that is not very much because there is a lot of difference almost always with the blood measure), but of bombs, so he has seen in each other says no.They have offered it several times to put a bomb.He is 50 years old, he does not remember his life without diabetes.
PD: My diabetic grandmother since 33 and with her discipline (there was not as much improvement as today) I reached 103 years with her diabetes.I do not see much reason to think that you have to affirm sharply that because it is diabetic you will live less, as you indicate.

I don't care to live less if I have an acceptable life.What I do not want is to have important limitations I carry with dB and I have an impote retinopathy, your grandmother was luckyFor a few years, glyds that do not go from 5.5, and with little glycemics variability and still ... of course it was not always the case and the first 10 years and adolescence played a bad pass.
I want to say with this that we debuted in the 80s we did not have the same fate (so to speak) that those who debut now, with much more information and means.That is why I become the victim, I still try to control my best but the reality is the one.

For my "living acceptably" is living life without being exclavo of diabetes.And no victim, but see where you put the focus, where you put your energy, what you feed ...... in limitations, to live less.Next to something negative there is the same way of saying it positively "I do not want to live with limitations" you could say as "I want to live, despite diabetes" acceptably and ldesfrutanco of what I feel like and outdating what I propose. "There are two ways of saying the same, but in that mental language, that way you speak in your mind, within you, that language with yourself, one will lead you to anxiety, depression and the other to action(Learn which are my limits with diabetes, which I can do consistently to my current situation, or when I can do it, or that I have to modify to achieve what I intend ... there are people without feet and without hands,that has focused on positive and achieve things that neither you nor I do.Well, the same as you and that I, but have not focused on that, have focused on adapting to have the life they want to have.As you want to see it).Half empty glass, or half full glass?.

But yes, I am with you that the attitude is very important