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Cultured B.Cepacia

chipie12

New member
Well, it happen. My 12 year old son has cepacia. He has to go for a bronchoscope on Wednesday so the Dr. can see for sure. I just feel like one we get over one hurdle there is another one waiting. He already has MRSA and we are still dealing with the "blood in his urine" issue. That might be from a coagulation(sp?) problem. On top of all that, I lost my mother on the 14th and inherited my bipolar sister and her (not house broken) dog. I don't know what God has in store for my, but I don't know how much more I can take.

His dr. said that their cepacia patients are all about college age and here my little guy has to deal with this 10 years earlier. He's my life and this is killing me. He's so brave and doesn't deserve the hand he's been dealt. I'm sorry for venting, but I usually vent to my mom, but she's gone.
 

chipie12

New member
Well, it happen. My 12 year old son has cepacia. He has to go for a bronchoscope on Wednesday so the Dr. can see for sure. I just feel like one we get over one hurdle there is another one waiting. He already has MRSA and we are still dealing with the "blood in his urine" issue. That might be from a coagulation(sp?) problem. On top of all that, I lost my mother on the 14th and inherited my bipolar sister and her (not house broken) dog. I don't know what God has in store for my, but I don't know how much more I can take.

His dr. said that their cepacia patients are all about college age and here my little guy has to deal with this 10 years earlier. He's my life and this is killing me. He's so brave and doesn't deserve the hand he's been dealt. I'm sorry for venting, but I usually vent to my mom, but she's gone.
 

chipie12

New member
Well, it happen. My 12 year old son has cepacia. He has to go for a bronchoscope on Wednesday so the Dr. can see for sure. I just feel like one we get over one hurdle there is another one waiting. He already has MRSA and we are still dealing with the "blood in his urine" issue. That might be from a coagulation(sp?) problem. On top of all that, I lost my mother on the 14th and inherited my bipolar sister and her (not house broken) dog. I don't know what God has in store for my, but I don't know how much more I can take.

His dr. said that their cepacia patients are all about college age and here my little guy has to deal with this 10 years earlier. He's my life and this is killing me. He's so brave and doesn't deserve the hand he's been dealt. I'm sorry for venting, but I usually vent to my mom, but she's gone.
 

dasjsmum

New member
Hi


Glad to hear your venting. You seem to have a lot on your shoulders at the moment...sending some positive vibes and prayers your way...
 

dasjsmum

New member
Hi


Glad to hear your venting. You seem to have a lot on your shoulders at the moment...sending some positive vibes and prayers your way...
 

dasjsmum

New member
Hi


Glad to hear your venting. You seem to have a lot on your shoulders at the moment...sending some positive vibes and prayers your way...
 

fourkidsmom

New member
HI, I am sorry to hear this, but if it helps my now 6 yr old son cultured b. cepecia at the age of 4. (the worst strain- III) My thoughts were the same...... this is too early. BUT he has been doing fine, they have better ways of controling it now, so don't worry to much about it. You sound like a great mom and I hope things get better for you!!

Fourkidsmom
Step mom to 15 yr old girl no cf
Mom to 13 yr old boy, cf carrier
Mom to 6 yr old boy with cf, G-tube, Med port, cultures cepecia, peusdo, staph, numberous surgeries and hospitalizations.
Mom to 4 yr old girl no cf, but chromosome 9 q deletion 21.2 q 22.1, and just diagnosed with epilepsy on 5/3/07.
 

fourkidsmom

New member
HI, I am sorry to hear this, but if it helps my now 6 yr old son cultured b. cepecia at the age of 4. (the worst strain- III) My thoughts were the same...... this is too early. BUT he has been doing fine, they have better ways of controling it now, so don't worry to much about it. You sound like a great mom and I hope things get better for you!!

Fourkidsmom
Step mom to 15 yr old girl no cf
Mom to 13 yr old boy, cf carrier
Mom to 6 yr old boy with cf, G-tube, Med port, cultures cepecia, peusdo, staph, numberous surgeries and hospitalizations.
Mom to 4 yr old girl no cf, but chromosome 9 q deletion 21.2 q 22.1, and just diagnosed with epilepsy on 5/3/07.
 

fourkidsmom

New member
HI, I am sorry to hear this, but if it helps my now 6 yr old son cultured b. cepecia at the age of 4. (the worst strain- III) My thoughts were the same...... this is too early. BUT he has been doing fine, they have better ways of controling it now, so don't worry to much about it. You sound like a great mom and I hope things get better for you!!

Fourkidsmom
Step mom to 15 yr old girl no cf
Mom to 13 yr old boy, cf carrier
Mom to 6 yr old boy with cf, G-tube, Med port, cultures cepecia, peusdo, staph, numberous surgeries and hospitalizations.
Mom to 4 yr old girl no cf, but chromosome 9 q deletion 21.2 q 22.1, and just diagnosed with epilepsy on 5/3/07.
 

PACmommy

New member
Just wanted to mention that Doctors in London Ontario have made a remarkable discovery about a weakness in the cell membrane of B. Cepacial which may lead to a development of a vaccine. If I can find the link I will post it.
 

PACmommy

New member
Just wanted to mention that Doctors in London Ontario have made a remarkable discovery about a weakness in the cell membrane of B. Cepacial which may lead to a development of a vaccine. If I can find the link I will post it.
 

PACmommy

New member
Just wanted to mention that Doctors in London Ontario have made a remarkable discovery about a weakness in the cell membrane of B. Cepacial which may lead to a development of a vaccine. If I can find the link I will post it.
 

dramamama

New member
I am so sorry you are going through such a hard time right now. I know the diagnosis of cepacia must be just devastating....I felt that way when I was diagnosed with abscessus..another difficult bug.

I am sorry for your loss....I can't really offer anything other than saying I will be praying for you.

Here is the article on the breakthrough in Cepacia....There is hope....

Key found to kill cystic fibrosis superbug

London, ON -- Researchers from the Schulich School of Medicine & Dentistry at The University of Western Ontario , working with a group from Edinburgh, have discovered a way to kill the cystic fibrosis superbug, Burkholderia cenocepacia. These investigators, under the leadership of Dr. Miguel Valvano, Department of Microbiology and Immunology, have had their research published in the May issue of the Journal of Bacteriology, and highlighted in Nature Reviews/Microbiology.

B. cenocepacia is a multi-drug resistant microorganism that lives in damp or wet places and causes rot in plants such as onions. While it rarely causes infection in healthy people, it can be fatal for people with cystic fibrosis (CF), an inherited disease where the lungs become clogged with thick mucus, often leading to chronic respiratory infections.

The team of researchers has identified a weakness in the armour that protects the B. cenocepacia bacterium from the effects of antibiotics. They hypothesize that preventing the synthesis of a key sugar required for this armour, 4-amino-4-deoxy-L-arabinose (Ara4N), may lead to a susceptibility within the cell membrane to antibiotics.

"We are very excited with these findings, as they will let us come up with novel molecules to disrupt the making of Ara4N," says Valvano. "These molecules could then be tested as novel antibiotics." Valvano is a Professor and Chair of the Department of Microbiology and Immunology, a Canada Research Chair in Infectious Diseases and Microbial Pathogenesis, and leader of the Infectious Diseases Research Group at the Siebens-Drake Research Institute. He is available for interviews.

The research was funded through the Canadian Cystic Fibrosis Foundation and the Canadian Institutes of Health Research (CIHR). "We're delighted by this news," says Cathleen Morrison, CEO of the Canadian Cystic Fibrosis Foundation. "The possibility of a life-saving antibiotic to fight B. cenocepacia is tremendously encouraging to adults and children who have cystic fibrosis."

Dr. Bhagirath Singh, Scientific Director of the CIHR Institute of Infection and Immunity, says "This discovery provides new hope for the eradication of these bugs from cystic fibrosis patients and to improve their quality of life by developing new treatments."
 

dramamama

New member
I am so sorry you are going through such a hard time right now. I know the diagnosis of cepacia must be just devastating....I felt that way when I was diagnosed with abscessus..another difficult bug.

I am sorry for your loss....I can't really offer anything other than saying I will be praying for you.

Here is the article on the breakthrough in Cepacia....There is hope....

Key found to kill cystic fibrosis superbug

London, ON -- Researchers from the Schulich School of Medicine & Dentistry at The University of Western Ontario , working with a group from Edinburgh, have discovered a way to kill the cystic fibrosis superbug, Burkholderia cenocepacia. These investigators, under the leadership of Dr. Miguel Valvano, Department of Microbiology and Immunology, have had their research published in the May issue of the Journal of Bacteriology, and highlighted in Nature Reviews/Microbiology.

B. cenocepacia is a multi-drug resistant microorganism that lives in damp or wet places and causes rot in plants such as onions. While it rarely causes infection in healthy people, it can be fatal for people with cystic fibrosis (CF), an inherited disease where the lungs become clogged with thick mucus, often leading to chronic respiratory infections.

The team of researchers has identified a weakness in the armour that protects the B. cenocepacia bacterium from the effects of antibiotics. They hypothesize that preventing the synthesis of a key sugar required for this armour, 4-amino-4-deoxy-L-arabinose (Ara4N), may lead to a susceptibility within the cell membrane to antibiotics.

"We are very excited with these findings, as they will let us come up with novel molecules to disrupt the making of Ara4N," says Valvano. "These molecules could then be tested as novel antibiotics." Valvano is a Professor and Chair of the Department of Microbiology and Immunology, a Canada Research Chair in Infectious Diseases and Microbial Pathogenesis, and leader of the Infectious Diseases Research Group at the Siebens-Drake Research Institute. He is available for interviews.

The research was funded through the Canadian Cystic Fibrosis Foundation and the Canadian Institutes of Health Research (CIHR). "We're delighted by this news," says Cathleen Morrison, CEO of the Canadian Cystic Fibrosis Foundation. "The possibility of a life-saving antibiotic to fight B. cenocepacia is tremendously encouraging to adults and children who have cystic fibrosis."

Dr. Bhagirath Singh, Scientific Director of the CIHR Institute of Infection and Immunity, says "This discovery provides new hope for the eradication of these bugs from cystic fibrosis patients and to improve their quality of life by developing new treatments."
 

dramamama

New member
I am so sorry you are going through such a hard time right now. I know the diagnosis of cepacia must be just devastating....I felt that way when I was diagnosed with abscessus..another difficult bug.

I am sorry for your loss....I can't really offer anything other than saying I will be praying for you.

Here is the article on the breakthrough in Cepacia....There is hope....

Key found to kill cystic fibrosis superbug

London, ON -- Researchers from the Schulich School of Medicine & Dentistry at The University of Western Ontario , working with a group from Edinburgh, have discovered a way to kill the cystic fibrosis superbug, Burkholderia cenocepacia. These investigators, under the leadership of Dr. Miguel Valvano, Department of Microbiology and Immunology, have had their research published in the May issue of the Journal of Bacteriology, and highlighted in Nature Reviews/Microbiology.

B. cenocepacia is a multi-drug resistant microorganism that lives in damp or wet places and causes rot in plants such as onions. While it rarely causes infection in healthy people, it can be fatal for people with cystic fibrosis (CF), an inherited disease where the lungs become clogged with thick mucus, often leading to chronic respiratory infections.

The team of researchers has identified a weakness in the armour that protects the B. cenocepacia bacterium from the effects of antibiotics. They hypothesize that preventing the synthesis of a key sugar required for this armour, 4-amino-4-deoxy-L-arabinose (Ara4N), may lead to a susceptibility within the cell membrane to antibiotics.

"We are very excited with these findings, as they will let us come up with novel molecules to disrupt the making of Ara4N," says Valvano. "These molecules could then be tested as novel antibiotics." Valvano is a Professor and Chair of the Department of Microbiology and Immunology, a Canada Research Chair in Infectious Diseases and Microbial Pathogenesis, and leader of the Infectious Diseases Research Group at the Siebens-Drake Research Institute. He is available for interviews.

The research was funded through the Canadian Cystic Fibrosis Foundation and the Canadian Institutes of Health Research (CIHR). "We're delighted by this news," says Cathleen Morrison, CEO of the Canadian Cystic Fibrosis Foundation. "The possibility of a life-saving antibiotic to fight B. cenocepacia is tremendously encouraging to adults and children who have cystic fibrosis."

Dr. Bhagirath Singh, Scientific Director of the CIHR Institute of Infection and Immunity, says "This discovery provides new hope for the eradication of these bugs from cystic fibrosis patients and to improve their quality of life by developing new treatments."
 
T

tammykrumrey

Guest
I am sorry to hear that you are having such a difficult time right now. I will keep you in my prayers. I know how you feel about the cepacia. My nephew was 9 years old when he started culturing B. Cepacia. He will be 16 this summer<img src="i/expressions/face-icon-small-smile.gif" border="0"> There are different strains of cepacia, some more challenging than others. I am not sure how much damage the cepacia has caused him, because he cultures everything else possible! Literally, I don't think that there is anythig else the poor kid can get!

I will say that now that Dalton is a teenager, it has been more difficult mentally than physically. He feels completely isolated from the 'CF world', which he basically is. I urge him to try on-line groups like this one, but he just won't budge. At almost 16, he knows everything<img src="i/expressions/face-icon-small-wink.gif" border="0"> I am sure that it may be harder on him as far as feeling isolated than maybe others because of the fact that there are my girls with CF also. It really has affected our family. Christmas, Easter, Birthdays, whatever...we always have to take into account that my sister and I have to keep our kids apart from one another. My mom and dad really have a hard time with not having their family together for the holidays or even just simple dinners. Our lives changed A LOT because of the cepacia.

I am sorry to ramble. But I do know how you feel. And please let me know if you have any specific questions. My nephew is also a teenager<img src="i/expressions/face-icon-small-smile.gif" border="0"> going through the same thing. Keeping you in prayers...
 
T

tammykrumrey

Guest
I am sorry to hear that you are having such a difficult time right now. I will keep you in my prayers. I know how you feel about the cepacia. My nephew was 9 years old when he started culturing B. Cepacia. He will be 16 this summer<img src="i/expressions/face-icon-small-smile.gif" border="0"> There are different strains of cepacia, some more challenging than others. I am not sure how much damage the cepacia has caused him, because he cultures everything else possible! Literally, I don't think that there is anythig else the poor kid can get!

I will say that now that Dalton is a teenager, it has been more difficult mentally than physically. He feels completely isolated from the 'CF world', which he basically is. I urge him to try on-line groups like this one, but he just won't budge. At almost 16, he knows everything<img src="i/expressions/face-icon-small-wink.gif" border="0"> I am sure that it may be harder on him as far as feeling isolated than maybe others because of the fact that there are my girls with CF also. It really has affected our family. Christmas, Easter, Birthdays, whatever...we always have to take into account that my sister and I have to keep our kids apart from one another. My mom and dad really have a hard time with not having their family together for the holidays or even just simple dinners. Our lives changed A LOT because of the cepacia.

I am sorry to ramble. But I do know how you feel. And please let me know if you have any specific questions. My nephew is also a teenager<img src="i/expressions/face-icon-small-smile.gif" border="0"> going through the same thing. Keeping you in prayers...
 
T

tammykrumrey

Guest
I am sorry to hear that you are having such a difficult time right now. I will keep you in my prayers. I know how you feel about the cepacia. My nephew was 9 years old when he started culturing B. Cepacia. He will be 16 this summer<img src="i/expressions/face-icon-small-smile.gif" border="0"> There are different strains of cepacia, some more challenging than others. I am not sure how much damage the cepacia has caused him, because he cultures everything else possible! Literally, I don't think that there is anythig else the poor kid can get!

I will say that now that Dalton is a teenager, it has been more difficult mentally than physically. He feels completely isolated from the 'CF world', which he basically is. I urge him to try on-line groups like this one, but he just won't budge. At almost 16, he knows everything<img src="i/expressions/face-icon-small-wink.gif" border="0"> I am sure that it may be harder on him as far as feeling isolated than maybe others because of the fact that there are my girls with CF also. It really has affected our family. Christmas, Easter, Birthdays, whatever...we always have to take into account that my sister and I have to keep our kids apart from one another. My mom and dad really have a hard time with not having their family together for the holidays or even just simple dinners. Our lives changed A LOT because of the cepacia.

I am sorry to ramble. But I do know how you feel. And please let me know if you have any specific questions. My nephew is also a teenager<img src="i/expressions/face-icon-small-smile.gif" border="0"> going through the same thing. Keeping you in prayers...
 

chipie12

New member
Thank you everyone for your kind words, support and information. It helps to know much as possible. I guess we will find out which strain he has after the bronchoscopy.
 

chipie12

New member
Thank you everyone for your kind words, support and information. It helps to know much as possible. I guess we will find out which strain he has after the bronchoscopy.
 
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