Mini Cabin Septic System Design

Nerea, of Valencia, was 20 when, in February 2010, he was diagnosed with Acute Promyelocytic Leukemia . He is currently studying 4 th of Medicine ("I went from course despite the emitters and my income," he says.)

For her and for all other patients with leukemia and other hematologic malignancies, it is important the cooperation of all to continue research with a single objective: that leukemia is, someday, a curable disease in all cases.

Become a member of the cure leukemia, become a member of the José Carreras Foundation.

We invite you to view a video that Neil has made to show everyone that in this, SE SALE!

Also check out the video of Neil and many more on Youtube Channel Foundation Josep Carreras, HERE

What Is Initiation For Phi Delta Epsilon Like?

CHRISTMAS LAUNCH CAMPAIGN 2010: With 5 and on wheels! VICTOR

CHRISTMAS CAMPAIGN 2010: November 22 / December 15

What
€ 5 mean to you?

The € 5 banknote, the smallest of all. Obviously has an economic value but he comes to pay a lunch menu or a full breakfast, or phone bill ...

however, with 5 € yes you can buy a bicycle ... HOW?

With a donation of 5 € you can help us make this Christmas leukemia patients recovering host in our apartments have a stationary bike to stay fit.

This Christmas, through the campaign "With 5 and on wheels "bikes we provide the host 6 floors for patients with hematological malignancies and their families . By this action, the patient severely debilitated by the chemotherapy and / or transplantation which have undergone may do gentle exercise each day. Our challenge is to get € 1,700 this Christmas to buy the 6 bikes. The Foundation DIR adds to this project and are preparing a manual of exercises for patients and families can enjoy bike and take full advantage.

DONATE HERE and NOW and help to make this Christmas gift for our host floors. If many people participate with 5 € we can make this project a reality.

Family Dollar Tech Decks

PLAN, FORMER PATIENT OF IMMUNODEFICIENCY SEVERE COMBINED

"It was just after receiving the first vaccine for three months, when Victor began to show signs of something was wrong came the coughing, fever and vomiting, the doctor did what he could, he was still happy, always so happy, and hungry, always been so greedy, but did not improve.

One Sunday evening, we took him to the emergency room at Mother and Child Hospital Sant Joan de Déu in Barcelona, \u200b\u200bwhere he was born with her brothers triplets, and I left, his skin showed signs red throughout the body, the fever down, the cough was persistent, and physical decline was significant. Testing began, first diagnosis, immunocompromised, had to spend more than a month to get the final diagnosis: "Severe Combined Immunodeficiency with increased B lymphocytes." We will never forget the moment, a room with seven doctors, all very serious, we did not understand what We talked, told us that the only solution was a t rasplante bone marrow, we still do not understand that we speak, only I had a question: is the only option? Yes.

We talked about the fate of siblings in these cases, analytical, insulation, cameras, many hundreds of probabilities, chemotherapy , ..., we room alone, saying nothing, we went walking to a nearby park, sat on a bench and cried, long time in silence, we still do not understand what we were talking.

The isolated in a room, there were no cameras at the hospital, while waiting for the results of tests to determine who was supported by his brothers, or us. While continuing to deteriorate, the results were negative, there was no support, was when we discussed the Josep Carreras Foundation and bank bone marrow donors. A case of meningitis in the hospital and hopes of finding a donor alerted to doctors could not continue without being isolated. He was taken to Hospital Vall d'Hebron Barcelona. plant in isolation chambers with their condition and appearance improved, but still did not appear a suitable donor, it was then that Dr. Ortega and Dr. Olive told us about stem cells, but had not tried before was the only possibility was 1995 and then did not know the potential of umbilical cords , time was running out, they would take stem cells from the bone of the father and trasplantarían Victor, confident that if there was no rejection, these cells create new marrow, hopefully fingers crossed.

On 7 July, San Fermin, the chupinazo entered through the veins of Victor, and started waiting, waiting a long time, so long! While repeated rejection episodes and increased doses of immunosuppressants, a toxic megacolon attacked mercilessly and it seemed that everything was going down, but not Victor's smile went out, had love for all nurses.

could not speak, but made himself understood perfectly, the nurse Rafa danced ... "there is a shark, shark, do not stop, go go" .. If asked How far are the nurses? will put his hands on his head and escaped her naughty smile.

He decided the order of drugs was taken orally, without question and always to arm or hand what they were going to spin if the port-a-cath, VENOCATH or catheter shift did not work, a good patient only one year.

One day, the number of rejections and immunosuppressive doses began to reverse, it seemed that everything was fine, I just had to gain weight, and on the street!. was released on August 15, 1996, 10 days shy of two years, not build defenses but accepted the bone, face the world, with all the dangers of a being that has been 14 months isolated in a sterile environment was his new challenge, but his smile was our hope, blindly trusted him.

outside the hospital were refusals, diarrhea and weight loss until it rejoined in January, malnourished and dehydrated. With the weather seemed to improve, is fed by vein, but his skin could not take any catheter until a rejection of a VENOCATH filled his lungs of fluid to be supplied as food. He was saved by a nurse, during a boring night, he went to play with, why Victor's smile was still in love, found it almost faded, scarcely breathing and purple complexion. He would have died that night had it not been for the nurse. Admitted to the ICU emergency, spent a week connected to two pumps that slowly, we subtracted the fluid in the lungs, was the only time he lost his smile. returned to the plant, with a catheter well connected and has since started to climb, with great dedication by all health personnel, until he left the hospital never to return!

learned to put a nasogastric tube and feeding with a pump, until they are turned off forever. At the age of three gave us all their first cell created by him, slowly but surely, recovery was already a fact, was the first successful vaccines, started going to school, ate everything, talked, ran, fell and got up again just ... Today, aged 16, is a normal kid, without sequelae, with only a few scars from multiple port-a-cath, VENOCATH and catheters needed, and most importantly, does not remember anything!

Victor's plan is to com artistic and removed the bachelor of fine arts career, to devote to education, and lend a hand Oleguer his brother, who is currently out of the same disease, but that is another story. "

Basketball Songs 2010

THE DAY THAT CHANGED MY LIFE!

currently Javier

May 30, 2008 .... . That was the day that changed my life. I'll make a brief summary to date. Had worked for ten years in a petrochemical company without unsubscribe and never check-ups every six months. So I went to work like any other day (just the day before had donated blood), I became the analytical and went to my job. Just before leaving, they called me telling me that Medical Services had some strange results and would have to repeat it (thought it was a lab error and the error was mine so I thought). The new results sent me straight to hospital for more tests. I asked what was happening, but I said nothing. Seeing that the thing was becoming rare, I asked them to take me to the hospital in Spain (where I live there and had a whole family). In the ambulance was the only time I cried.

In Cadiz, directly to Hematology (I have only gratitude for the plant staff and especially Dr. Mari Carmen). That night I knew my wife and I sensed it. After several days of testing, I was told I had acute myelogenous leukemia L5. Nothing to throw noses! I spent a month in hospital, after a week of chemo and expected side effects pero siempre con una sonrisa o una broma que gastar.

Después una semanita en casa, qué alegría, pero ya no era como antes, mi mujer (como es natural), con mucho miedo y poniéndome una sonrisa que no tenía y yo, sin esas fuerzas que antes tenía. A la semana, más de lo mismo, otra tanda de quimio y a esperar por donde salía la cosa. En el hospital no se aprende de los médicos, se aprende de los compañeros que están como tú y de sus familiares. Y me dí cuenta de una cosa, la medicina ayuda, pero la curación está en tu cabeza. Por eso os digo a los que estáis malitos, que tenéis que ser positivos y pensar que es un curing bad cold.

While my brothers were given the compatibility test. My brother had hepatitis, so only option left was my sister .... That day I played the original, I hope everyone will pass this!

As in Cadiz do transplant, I was sent to the Hospital de Jerez (thank you very much everyone and especially Dr. Garzón). It was a September 26, 2008 when I transplanted. The two months I was there not too well spent. He did not eat because I threw up everything and I got out of bed because I had a spinal tap which left me sore head strong calming only to lie down. I also had fever, aches number, etc ... typical, I go, but always very positive. When I left I was all crap, but very happy. From his hospital bed to bed in my house. I still would be many visits to the hospital for checkups and blood transfusions. Rejection? I did have and still I have a little. Of what? After all, rejection, liver, metabolic, dermatology, and I do not know what else ... But gradually being overcome everything. When I saw it with strength, I asked my doctor if I could play sports and I said, listen to your body! And what if I heard it!

The January 1, 2010 at 9:00 am, begins a purpose for me. That day I ran 5 minutes. On September 26, 2010 (the day just two years before my transplant), I finished my first half marathon (1:49:56).

As many know, the road is very difficult, but as a coach used to say Barcelona, \u200b\u200b always positive, never negative!

Everything is of course I have to thank my sister, who donated his bone me, my family was always there, my daughter Paula to just thinking would cry if I was not, gave me the strength to endure what I cast, and especially my wife Maria Angeles, that without it he could. Many times I cheated on a good face and a smile inside and cried like a cupcake. By the way, she is marrow donor.

always remember those who have left and I hope they are better, like me, and those who have not been able to do this, just hope that their families be strong and think they never stopped fighting, everyone has been very brave.

I've been lucky, you might also have. Let's go look!

Greetings to all,

Javier.

If you want information about bone marrow donation, click HERE .

becoming a member of the José Carreras Foundation, click HERE.