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I so want to live so much, because I for whom ... My lovely bride gives me the strength to fight for that every day. The disease, however, fierce opponent, suffocating, steals your breath and with all the strength wants to steal my life. So I need help, just to be here, not for himself, but for Monica ...
At first glance, one might say that I'm the picture of health. So what does this disease attacks from within, often without giving any external symptoms. I look normal, but my organs digests mortal enemy, constrictor. Cystic fibrosis is associated with lung disease. Yes, unfortunately it is not. It attacks the whole body, especially the respiratory system, gastrointestinal tract, destroys the lungs, bronchi, pancreas. Fills them with mucus, which prevents respiration, digestion and absorption of food. The patient must perform daily inhalations and drainage, to get rid of mucus, often fed also by gavage.Every now and then attack him further infections - pneumonia, bronchitis ... This is a chronic disease does not attack again, but every day, destroying the joy of life. It is incurable, there is no cure.
Cystic Fibrosis I was diagnosed quite late. I was 9 years old, still sick. I came to the hospital in Rzeszow, where after one test immediately directed me to Warsaw for the Mother and Child Institute. The diagnosis was devastating. It meant that my life will always take place at the dictation of the fight against cystic fibrosis and the disease is likely to end them prematurely.
From diagnosis every day is a struggle for breath. I ended up a normal life. Fun, school, free time ... I did not know such a concept, for me were continuous inhalation, drainage, medicine, and instead of a holiday - stays in hospitals.
But I have a reason to fight the disease - my wonderful fiancee, who gives me the strength to get up every day. Every day with her is my weight in gold, and every moment - so incredibly beautiful. We are planning to get married, start a family ... I would love to be healthy and get rid of cystic fibrosis, but I know that this is not real.Every day I fight and I'm doing better, he supports me sweetheart. Every day, thanks for life and for being on my way appeared Monika, who is with me.
My treatment is unfortunately very expensive - medicines, rehabilitation equipment, trips to doctors (about 600 km in one direction, from near Sanok to Karpacz). In a few years it may be that I will need a lung transplant, which unfortunately also involves enormous costs. I pray not really much for me to count every penny. For you it's just a coin, 1 PLN, but for me it is brick, which gives me the strength and the means to fight the disease.
The average life expectancy of people with cystic fibrosis in Poland about 30 years ... But I'll do everything to stay here any longer, because I have to fight and I have to whom. I believe that through love I can conquer death. I do not want any material objects, I want only one thing - to be able to heal. Me and Monika you will appreciate any your help
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I so want to live so much, because I for whom ... My lovely bride gives me the strength to fight for that every day. The disease, however, fierce opponent, suffocating, steals your breath and with all the strength wants to steal my life. So I need help, just to be here, not for himself, but for Monica ...
At first glance, one might say that I'm the picture of health. So what does this disease attacks from within, often without giving any external symptoms. I look normal, but my organs digests mortal enemy, constrictor. Cystic fibrosis is associated with lung disease. Yes, unfortunately it is not. It attacks the whole body, especially the respiratory system, gastrointestinal tract, destroys the lungs, bronchi, pancreas. Fills them with mucus, which prevents respiration, digestion and absorption of food. The patient must perform daily inhalations and drainage, to get rid of mucus, often fed also by gavage.Every now and then attack him further infections - pneumonia, bronchitis ... This is a chronic disease does not attack again, but every day, destroying the joy of life. It is incurable, there is no cure.
Cystic Fibrosis I was diagnosed quite late. I was 9 years old, still sick. I came to the hospital in Rzeszow, where after one test immediately directed me to Warsaw for the Mother and Child Institute. The diagnosis was devastating. It meant that my life will always take place at the dictation of the fight against cystic fibrosis and the disease is likely to end them prematurely.
From diagnosis every day is a struggle for breath. I ended up a normal life. Fun, school, free time ... I did not know such a concept, for me were continuous inhalation, drainage, medicine, and instead of a holiday - stays in hospitals.
But I have a reason to fight the disease - my wonderful fiancee, who gives me the strength to get up every day. Every day with her is my weight in gold, and every moment - so incredibly beautiful. We are planning to get married, start a family ... I would love to be healthy and get rid of cystic fibrosis, but I know that this is not real.Every day I fight and I'm doing better, he supports me sweetheart. Every day, thanks for life and for being on my way appeared Monika, who is with me.
My treatment is unfortunately very expensive - medicines, rehabilitation equipment, trips to doctors (about 600 km in one direction, from near Sanok to Karpacz). In a few years it may be that I will need a lung transplant, which unfortunately also involves enormous costs. I pray not really much for me to count every penny. For you it's just a coin, 1 PLN, but for me it is brick, which gives me the strength and the means to fight the disease.
The average life expectancy of people with cystic fibrosis in Poland about 30 years ... But I'll do everything to stay here any longer, because I have to fight and I have to whom. I believe that through love I can conquer death. I do not want any material objects, I want only one thing - to be able to heal. Me and Monika you will appreciate any your help
