@jldiazdel because it is very likely that you are right and that I have to put the batteries, thanks equally: wink:
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@Laureta What a bad luck!But surely they will lead you to another hospital.The bad, the usual, the waiting times.But well, you'll tell us to see what they tell you!Good luck!
T1 diagnosticada a los 24, tengo 32.
Además soy celiaca y con muchas alergias e intolerancias alimentarias, entre ellas profilina. Recientemente diagnosticada con hipotiroidismo también.
In Cuenca they only grant 3 a year.It took me 5 years since the request and must be for some well justified cause.In those 5 years I had to go through protocols before reaching the endocrine already say, that there is no other than the bomb,
In my case, at night, at dawn, also more or less on the same time, about 130/140 in twenty minutes up at 450/500, which the injected insulin (several brands, guidelines ...)I did not correct me (I had been lowering those values for hours), or diets ,,,, Estc (the unfitting protocol) that ended up leading me to a neuropathy (which neither my worst enemy recommends).And exhausted the protocol, in the end and the pump.But so, not good at first.And this is because of the high cost of all the replaceI spend every 2 months and it is a grassland that I could barely allowed;
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xiquillo71 said:
Hello everyone, I am new in the forum and I would like to know how I could get an insulin bomb, because I see that here all the people speak .... everyone andThank you for sharing your experiences, which helps us optimize our sweet lives.
I have put the glucomen bomb 3 weeks ago, St Pau Barcelona hospital.But I don't know if it's me, my diabetes and my life, but what everyone says it is going so well to wear a bomb, because I feel very frustrated and tired.I had never had so many hyper and hypos so many days in a row .. I can't sleep or make life !!
I am thinking of returning to the Bolis.Try the pump and you have to see how.
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