just got the news

LisaGreene

New member
Hi Jenifer,
I hope things are settling down a bit since you posted this a few weeks ago. The fact that your daughter has been doing so well for 9 years without meds is relly good news! I know she was sick on and off but it sounds like she has a mild case of CF (yes, there are mild and not-so-mild cases depending on many factors including your gene mutation).

But, it's still a hard thing to go through of course and your daughter (and you) will need lots of positive support and vibes around you to help you stay optimistic. Please, please find a copy of our book in your library or hospital to borrow because it will give you the parenting skills to handle this with your daughter and your MIL! There are many important things you need to know about how you respond to your daughter that can impact how she handles this.

Here is an article I recently posted that will help you understand what I am saying. Feel free to share this with your MIL! :)

Hugs to you and your daughter. Having CF is not an easy road but can bring unexpected blessings along the way if you let it.
Lisa G.
mom of 2 kids with CF

Never Give Up! Don't Let Statistics Rob Your Hope and Joy
by Foster Cline, MD and Lisa C. Greene

When a child is first diagnosed with a medical condition, especially a life-threatening one, the first question many parents understandably ask is, "How long does my child have to live?" Medical professionals respond by quoting the statistics.

Statistically, all illnesses have a somewhat predictable course or an "average life expectancy." But statistics based on the group norms may be very misleading and even disabling when applied to individual children. It's very hard to predict who will be among the many who "beat the odds."

In the past, medical professionals were known to advise parents of children with cystic fibrosis not to worry about saving for their children's college education. And parents have been known to lower their expectations concerning their children's performance in school, sports, or other important matters relating to the future and living a "normal" life.

This lowering of expectations, with its suggestion of a "What's the use?" attitude does a great disservice to children. It encourages them to become both entitled and to feel hopeless within themselves. Achievement and self-image both suffer.

The average life expectancy for many diseases is increasing at a fairly rapid rate due to medical advances. What might be an accurate statistic today probably won't be tomorrow. While it is important to understand the statistics, it is not helpful to be governed by them. The Nash family knew this to be true:

When Liz was diagnosed with cystic fibrosis in 1973, her parents were told not to expect her to graduate from high school. She did much more than that. Liz earned a PhD in molecular genetics, interned at Johns Hopkins University and went on to become a research scientist in CF. She also volunteered as a mentor to teens with CF, who struggled with thoughts about their future and medical compliance.

Liz was optimistic, enthusiastic, and passionate about her life's work and interests. She shunned the limitations imposed by CF. As captain of her college ski team she refused to give up the sport when oxygen became necessary. She simply skied with a backpack filled with portable oxygen tanks.

As an inspiring individual, Elizabeth Nash was selected to carry the 2002 Olympic Torch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time but her spirit lives on as her example and courage continue to bring hope to many.

With many medical conditions, there is a strong correlation between good self-care and longevity. Parents can use statistics to inspire hope and spark an "I can beat this" attitude. Parents who give off positive, "we can beat this" vibes generally raise kids with the same determined spirit. We have met many CF parents and their children who demonstrate this indomitable and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
. Emphasizing that significant medical progress is being made in almost all areas, and that health and longevity are increasing for almost all illnesses.
. Realizing that for all individuals, the future is unknown. Many lives are shortened by unexpected illness and traumatic events.
. Encouraging their children to believe that they have every chance of being one of those children "who fall on the high side of the bell curve because you take such good care of yourself."
. Understanding that the quality of a life is measured not by its length, but by the amount of love, accomplishment, and giving that fills it.
. Understanding that worrying about the future and chewing on the mistakes of yesterday rob both today and tomorrow. The resulting hopelessness, negativity, and worry can shorten lives and certainly diminish the quality of life.
. Believing that those who bravely face life's obstacles build a character that not only leads them to be more capable people and leaders, but sets an example that enhances the lives of all with whom they come in contact.

Answering a child's questions about the course of his or her illness can be difficult. How can parents answer their child's questions with hope if they have not come to a good place themselves? The child will almost always take the parent's cues. So don't let scary statistics rob your hope and joy!

***********************
From the book "Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Other Special Needs" by Foster Cline, M.D and Lisa C. Greene available online and bookstores. Dr. Cline is a well-known child psychiatrist, author, and co-founder of the popular Love and Logic parenting program. Lisa is the mother of two children with cystic fibrosis and a certified parent coach. For free audio, articles and other resources, visit <a target=_blank class=ftalternatingbarlinklarge href="http://www.ParentingChildrenWithHealthIssues.com.">http://www.ParentingChildrenWithHealthIssues.com.</a>

Copyright 2008 by Foster Cline MD and Lisa Greene. All rights reserved. Reprinted with permission.
 

LisaGreene

New member
Hi Jenifer,
I hope things are settling down a bit since you posted this a few weeks ago. The fact that your daughter has been doing so well for 9 years without meds is relly good news! I know she was sick on and off but it sounds like she has a mild case of CF (yes, there are mild and not-so-mild cases depending on many factors including your gene mutation).

But, it's still a hard thing to go through of course and your daughter (and you) will need lots of positive support and vibes around you to help you stay optimistic. Please, please find a copy of our book in your library or hospital to borrow because it will give you the parenting skills to handle this with your daughter and your MIL! There are many important things you need to know about how you respond to your daughter that can impact how she handles this.

Here is an article I recently posted that will help you understand what I am saying. Feel free to share this with your MIL! :)

Hugs to you and your daughter. Having CF is not an easy road but can bring unexpected blessings along the way if you let it.
Lisa G.
mom of 2 kids with CF

Never Give Up! Don't Let Statistics Rob Your Hope and Joy
by Foster Cline, MD and Lisa C. Greene

When a child is first diagnosed with a medical condition, especially a life-threatening one, the first question many parents understandably ask is, "How long does my child have to live?" Medical professionals respond by quoting the statistics.

Statistically, all illnesses have a somewhat predictable course or an "average life expectancy." But statistics based on the group norms may be very misleading and even disabling when applied to individual children. It's very hard to predict who will be among the many who "beat the odds."

In the past, medical professionals were known to advise parents of children with cystic fibrosis not to worry about saving for their children's college education. And parents have been known to lower their expectations concerning their children's performance in school, sports, or other important matters relating to the future and living a "normal" life.

This lowering of expectations, with its suggestion of a "What's the use?" attitude does a great disservice to children. It encourages them to become both entitled and to feel hopeless within themselves. Achievement and self-image both suffer.

The average life expectancy for many diseases is increasing at a fairly rapid rate due to medical advances. What might be an accurate statistic today probably won't be tomorrow. While it is important to understand the statistics, it is not helpful to be governed by them. The Nash family knew this to be true:

When Liz was diagnosed with cystic fibrosis in 1973, her parents were told not to expect her to graduate from high school. She did much more than that. Liz earned a PhD in molecular genetics, interned at Johns Hopkins University and went on to become a research scientist in CF. She also volunteered as a mentor to teens with CF, who struggled with thoughts about their future and medical compliance.

Liz was optimistic, enthusiastic, and passionate about her life's work and interests. She shunned the limitations imposed by CF. As captain of her college ski team she refused to give up the sport when oxygen became necessary. She simply skied with a backpack filled with portable oxygen tanks.

As an inspiring individual, Elizabeth Nash was selected to carry the 2002 Olympic Torch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time but her spirit lives on as her example and courage continue to bring hope to many.

With many medical conditions, there is a strong correlation between good self-care and longevity. Parents can use statistics to inspire hope and spark an "I can beat this" attitude. Parents who give off positive, "we can beat this" vibes generally raise kids with the same determined spirit. We have met many CF parents and their children who demonstrate this indomitable and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
. Emphasizing that significant medical progress is being made in almost all areas, and that health and longevity are increasing for almost all illnesses.
. Realizing that for all individuals, the future is unknown. Many lives are shortened by unexpected illness and traumatic events.
. Encouraging their children to believe that they have every chance of being one of those children "who fall on the high side of the bell curve because you take such good care of yourself."
. Understanding that the quality of a life is measured not by its length, but by the amount of love, accomplishment, and giving that fills it.
. Understanding that worrying about the future and chewing on the mistakes of yesterday rob both today and tomorrow. The resulting hopelessness, negativity, and worry can shorten lives and certainly diminish the quality of life.
. Believing that those who bravely face life's obstacles build a character that not only leads them to be more capable people and leaders, but sets an example that enhances the lives of all with whom they come in contact.

Answering a child's questions about the course of his or her illness can be difficult. How can parents answer their child's questions with hope if they have not come to a good place themselves? The child will almost always take the parent's cues. So don't let scary statistics rob your hope and joy!

***********************
From the book "Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Other Special Needs" by Foster Cline, M.D and Lisa C. Greene available online and bookstores. Dr. Cline is a well-known child psychiatrist, author, and co-founder of the popular Love and Logic parenting program. Lisa is the mother of two children with cystic fibrosis and a certified parent coach. For free audio, articles and other resources, visit <a target=_blank class=ftalternatingbarlinklarge href="http://www.ParentingChildrenWithHealthIssues.com.">http://www.ParentingChildrenWithHealthIssues.com.</a>

Copyright 2008 by Foster Cline MD and Lisa Greene. All rights reserved. Reprinted with permission.
 

LisaGreene

New member
Hi Jenifer,
I hope things are settling down a bit since you posted this a few weeks ago. The fact that your daughter has been doing so well for 9 years without meds is relly good news! I know she was sick on and off but it sounds like she has a mild case of CF (yes, there are mild and not-so-mild cases depending on many factors including your gene mutation).

But, it's still a hard thing to go through of course and your daughter (and you) will need lots of positive support and vibes around you to help you stay optimistic. Please, please find a copy of our book in your library or hospital to borrow because it will give you the parenting skills to handle this with your daughter and your MIL! There are many important things you need to know about how you respond to your daughter that can impact how she handles this.

Here is an article I recently posted that will help you understand what I am saying. Feel free to share this with your MIL! :)

Hugs to you and your daughter. Having CF is not an easy road but can bring unexpected blessings along the way if you let it.
Lisa G.
mom of 2 kids with CF

Never Give Up! Don't Let Statistics Rob Your Hope and Joy
by Foster Cline, MD and Lisa C. Greene

When a child is first diagnosed with a medical condition, especially a life-threatening one, the first question many parents understandably ask is, "How long does my child have to live?" Medical professionals respond by quoting the statistics.

Statistically, all illnesses have a somewhat predictable course or an "average life expectancy." But statistics based on the group norms may be very misleading and even disabling when applied to individual children. It's very hard to predict who will be among the many who "beat the odds."

In the past, medical professionals were known to advise parents of children with cystic fibrosis not to worry about saving for their children's college education. And parents have been known to lower their expectations concerning their children's performance in school, sports, or other important matters relating to the future and living a "normal" life.

This lowering of expectations, with its suggestion of a "What's the use?" attitude does a great disservice to children. It encourages them to become both entitled and to feel hopeless within themselves. Achievement and self-image both suffer.

The average life expectancy for many diseases is increasing at a fairly rapid rate due to medical advances. What might be an accurate statistic today probably won't be tomorrow. While it is important to understand the statistics, it is not helpful to be governed by them. The Nash family knew this to be true:

When Liz was diagnosed with cystic fibrosis in 1973, her parents were told not to expect her to graduate from high school. She did much more than that. Liz earned a PhD in molecular genetics, interned at Johns Hopkins University and went on to become a research scientist in CF. She also volunteered as a mentor to teens with CF, who struggled with thoughts about their future and medical compliance.

Liz was optimistic, enthusiastic, and passionate about her life's work and interests. She shunned the limitations imposed by CF. As captain of her college ski team she refused to give up the sport when oxygen became necessary. She simply skied with a backpack filled with portable oxygen tanks.

As an inspiring individual, Elizabeth Nash was selected to carry the 2002 Olympic Torch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time but her spirit lives on as her example and courage continue to bring hope to many.

With many medical conditions, there is a strong correlation between good self-care and longevity. Parents can use statistics to inspire hope and spark an "I can beat this" attitude. Parents who give off positive, "we can beat this" vibes generally raise kids with the same determined spirit. We have met many CF parents and their children who demonstrate this indomitable and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
. Emphasizing that significant medical progress is being made in almost all areas, and that health and longevity are increasing for almost all illnesses.
. Realizing that for all individuals, the future is unknown. Many lives are shortened by unexpected illness and traumatic events.
. Encouraging their children to believe that they have every chance of being one of those children "who fall on the high side of the bell curve because you take such good care of yourself."
. Understanding that the quality of a life is measured not by its length, but by the amount of love, accomplishment, and giving that fills it.
. Understanding that worrying about the future and chewing on the mistakes of yesterday rob both today and tomorrow. The resulting hopelessness, negativity, and worry can shorten lives and certainly diminish the quality of life.
. Believing that those who bravely face life's obstacles build a character that not only leads them to be more capable people and leaders, but sets an example that enhances the lives of all with whom they come in contact.

Answering a child's questions about the course of his or her illness can be difficult. How can parents answer their child's questions with hope if they have not come to a good place themselves? The child will almost always take the parent's cues. So don't let scary statistics rob your hope and joy!

***********************
From the book "Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Other Special Needs" by Foster Cline, M.D and Lisa C. Greene available online and bookstores. Dr. Cline is a well-known child psychiatrist, author, and co-founder of the popular Love and Logic parenting program. Lisa is the mother of two children with cystic fibrosis and a certified parent coach. For free audio, articles and other resources, visit <a target=_blank class=ftalternatingbarlinklarge href="http://www.ParentingChildrenWithHealthIssues.com.">http://www.ParentingChildrenWithHealthIssues.com.</a>

Copyright 2008 by Foster Cline MD and Lisa Greene. All rights reserved. Reprinted with permission.
 

LisaGreene

New member
Hi Jenifer,
I hope things are settling down a bit since you posted this a few weeks ago. The fact that your daughter has been doing so well for 9 years without meds is relly good news! I know she was sick on and off but it sounds like she has a mild case of CF (yes, there are mild and not-so-mild cases depending on many factors including your gene mutation).

But, it's still a hard thing to go through of course and your daughter (and you) will need lots of positive support and vibes around you to help you stay optimistic. Please, please find a copy of our book in your library or hospital to borrow because it will give you the parenting skills to handle this with your daughter and your MIL! There are many important things you need to know about how you respond to your daughter that can impact how she handles this.

Here is an article I recently posted that will help you understand what I am saying. Feel free to share this with your MIL! :)

Hugs to you and your daughter. Having CF is not an easy road but can bring unexpected blessings along the way if you let it.
Lisa G.
mom of 2 kids with CF

Never Give Up! Don't Let Statistics Rob Your Hope and Joy
by Foster Cline, MD and Lisa C. Greene

When a child is first diagnosed with a medical condition, especially a life-threatening one, the first question many parents understandably ask is, "How long does my child have to live?" Medical professionals respond by quoting the statistics.

Statistically, all illnesses have a somewhat predictable course or an "average life expectancy." But statistics based on the group norms may be very misleading and even disabling when applied to individual children. It's very hard to predict who will be among the many who "beat the odds."

In the past, medical professionals were known to advise parents of children with cystic fibrosis not to worry about saving for their children's college education. And parents have been known to lower their expectations concerning their children's performance in school, sports, or other important matters relating to the future and living a "normal" life.

This lowering of expectations, with its suggestion of a "What's the use?" attitude does a great disservice to children. It encourages them to become both entitled and to feel hopeless within themselves. Achievement and self-image both suffer.

The average life expectancy for many diseases is increasing at a fairly rapid rate due to medical advances. What might be an accurate statistic today probably won't be tomorrow. While it is important to understand the statistics, it is not helpful to be governed by them. The Nash family knew this to be true:

When Liz was diagnosed with cystic fibrosis in 1973, her parents were told not to expect her to graduate from high school. She did much more than that. Liz earned a PhD in molecular genetics, interned at Johns Hopkins University and went on to become a research scientist in CF. She also volunteered as a mentor to teens with CF, who struggled with thoughts about their future and medical compliance.

Liz was optimistic, enthusiastic, and passionate about her life's work and interests. She shunned the limitations imposed by CF. As captain of her college ski team she refused to give up the sport when oxygen became necessary. She simply skied with a backpack filled with portable oxygen tanks.

As an inspiring individual, Elizabeth Nash was selected to carry the 2002 Olympic Torch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time but her spirit lives on as her example and courage continue to bring hope to many.

With many medical conditions, there is a strong correlation between good self-care and longevity. Parents can use statistics to inspire hope and spark an "I can beat this" attitude. Parents who give off positive, "we can beat this" vibes generally raise kids with the same determined spirit. We have met many CF parents and their children who demonstrate this indomitable and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
. Emphasizing that significant medical progress is being made in almost all areas, and that health and longevity are increasing for almost all illnesses.
. Realizing that for all individuals, the future is unknown. Many lives are shortened by unexpected illness and traumatic events.
. Encouraging their children to believe that they have every chance of being one of those children "who fall on the high side of the bell curve because you take such good care of yourself."
. Understanding that the quality of a life is measured not by its length, but by the amount of love, accomplishment, and giving that fills it.
. Understanding that worrying about the future and chewing on the mistakes of yesterday rob both today and tomorrow. The resulting hopelessness, negativity, and worry can shorten lives and certainly diminish the quality of life.
. Believing that those who bravely face life's obstacles build a character that not only leads them to be more capable people and leaders, but sets an example that enhances the lives of all with whom they come in contact.

Answering a child's questions about the course of his or her illness can be difficult. How can parents answer their child's questions with hope if they have not come to a good place themselves? The child will almost always take the parent's cues. So don't let scary statistics rob your hope and joy!

***********************
From the book "Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Other Special Needs" by Foster Cline, M.D and Lisa C. Greene available online and bookstores. Dr. Cline is a well-known child psychiatrist, author, and co-founder of the popular Love and Logic parenting program. Lisa is the mother of two children with cystic fibrosis and a certified parent coach. For free audio, articles and other resources, visit <a target=_blank class=ftalternatingbarlinklarge href="http://www.ParentingChildrenWithHealthIssues.com.">http://www.ParentingChildrenWithHealthIssues.com.</a>

Copyright 2008 by Foster Cline MD and Lisa Greene. All rights reserved. Reprinted with permission.
 

LisaGreene

New member
Hi Jenifer,
<br />I hope things are settling down a bit since you posted this a few weeks ago. The fact that your daughter has been doing so well for 9 years without meds is relly good news! I know she was sick on and off but it sounds like she has a mild case of CF (yes, there are mild and not-so-mild cases depending on many factors including your gene mutation).
<br />
<br />But, it's still a hard thing to go through of course and your daughter (and you) will need lots of positive support and vibes around you to help you stay optimistic. Please, please find a copy of our book in your library or hospital to borrow because it will give you the parenting skills to handle this with your daughter and your MIL! There are many important things you need to know about how you respond to your daughter that can impact how she handles this.
<br />
<br />Here is an article I recently posted that will help you understand what I am saying. Feel free to share this with your MIL! :)
<br />
<br />Hugs to you and your daughter. Having CF is not an easy road but can bring unexpected blessings along the way if you let it.
<br />Lisa G.
<br />mom of 2 kids with CF
<br />
<br />Never Give Up! Don't Let Statistics Rob Your Hope and Joy
<br />by Foster Cline, MD and Lisa C. Greene
<br />
<br />When a child is first diagnosed with a medical condition, especially a life-threatening one, the first question many parents understandably ask is, "How long does my child have to live?" Medical professionals respond by quoting the statistics.
<br />
<br />Statistically, all illnesses have a somewhat predictable course or an "average life expectancy." But statistics based on the group norms may be very misleading and even disabling when applied to individual children. It's very hard to predict who will be among the many who "beat the odds."
<br />
<br />In the past, medical professionals were known to advise parents of children with cystic fibrosis not to worry about saving for their children's college education. And parents have been known to lower their expectations concerning their children's performance in school, sports, or other important matters relating to the future and living a "normal" life.
<br />
<br />This lowering of expectations, with its suggestion of a "What's the use?" attitude does a great disservice to children. It encourages them to become both entitled and to feel hopeless within themselves. Achievement and self-image both suffer.
<br />
<br />The average life expectancy for many diseases is increasing at a fairly rapid rate due to medical advances. What might be an accurate statistic today probably won't be tomorrow. While it is important to understand the statistics, it is not helpful to be governed by them. The Nash family knew this to be true:
<br />
<br />When Liz was diagnosed with cystic fibrosis in 1973, her parents were told not to expect her to graduate from high school. She did much more than that. Liz earned a PhD in molecular genetics, interned at Johns Hopkins University and went on to become a research scientist in CF. She also volunteered as a mentor to teens with CF, who struggled with thoughts about their future and medical compliance.
<br />
<br />Liz was optimistic, enthusiastic, and passionate about her life's work and interests. She shunned the limitations imposed by CF. As captain of her college ski team she refused to give up the sport when oxygen became necessary. She simply skied with a backpack filled with portable oxygen tanks.
<br />
<br />As an inspiring individual, Elizabeth Nash was selected to carry the 2002 Olympic Torch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time but her spirit lives on as her example and courage continue to bring hope to many.
<br />
<br />With many medical conditions, there is a strong correlation between good self-care and longevity. Parents can use statistics to inspire hope and spark an "I can beat this" attitude. Parents who give off positive, "we can beat this" vibes generally raise kids with the same determined spirit. We have met many CF parents and their children who demonstrate this indomitable and inspiring attitude.
<br />
<br />In summary, wise parents handle statistics and medical predictions by:
<br />. Emphasizing that significant medical progress is being made in almost all areas, and that health and longevity are increasing for almost all illnesses.
<br />. Realizing that for all individuals, the future is unknown. Many lives are shortened by unexpected illness and traumatic events.
<br />. Encouraging their children to believe that they have every chance of being one of those children "who fall on the high side of the bell curve because you take such good care of yourself."
<br />. Understanding that the quality of a life is measured not by its length, but by the amount of love, accomplishment, and giving that fills it.
<br />. Understanding that worrying about the future and chewing on the mistakes of yesterday rob both today and tomorrow. The resulting hopelessness, negativity, and worry can shorten lives and certainly diminish the quality of life.
<br />. Believing that those who bravely face life's obstacles build a character that not only leads them to be more capable people and leaders, but sets an example that enhances the lives of all with whom they come in contact.
<br />
<br />Answering a child's questions about the course of his or her illness can be difficult. How can parents answer their child's questions with hope if they have not come to a good place themselves? The child will almost always take the parent's cues. So don't let scary statistics rob your hope and joy!
<br />
<br /> ***********************
<br />From the book "Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Other Special Needs" by Foster Cline, M.D and Lisa C. Greene available online and bookstores. Dr. Cline is a well-known child psychiatrist, author, and co-founder of the popular Love and Logic parenting program. Lisa is the mother of two children with cystic fibrosis and a certified parent coach. For free audio, articles and other resources, visit <a target=_blank class=ftalternatingbarlinklarge href="http://www.ParentingChildrenWithHealthIssues.com.">http://www.ParentingChildrenWithHealthIssues.com.</a>
<br />
<br />Copyright 2008 by Foster Cline MD and Lisa Greene. All rights reserved. Reprinted with permission.
 

kelliannesmom

New member
We got the results for Brandon, my 5 year old son. He has the same 3 mutated genes as his older sister. He too get frequent pneumonia & has asthma, but he doesn't have the intestinal problems Kellianne has.
I have a lot of the same symptoms as Kellianne in that I get pneumonia easily when I get a cold & I have had digestive issues since as long as I can remember. I have had so many endoscopies & colonoscopies & they have labeled it idiopathic IBS. They give me cholesterol medication to bind me up so I don't have diarrhea. Without it I am running to the bathroom constantly. With it, I can't make it through a meal without having to use the bathroom. So my doctor ordered the DNA test for me as well. I have the same 3 mutated genes as both of my kids.
Kellianne has been on the digestive enzymes for a month & is feeling so much better. She still has some days with diarrhea, but most are without. She is also on AquaADEK & hasn't had a nose bleed since she started taking them. She went in for a recheck & she has gained 4 ounces, but grew almost an inch! I started the enzymes & the AquaADEK on Tuesday & am feeling great. I haven't had to take the cholesterol medicine in 3 days!!
The CF social worker at the doctor's office came in & talked to the kids & me on Tuesday. She explained that although we have 3 mutated CF genes we do not have Cystic Fibrosis, but a mutation CF with Cystic Fibrosis like symptoms. They expect us to live a long life, so that is great news. She also gave us Axcam cards to help cover the cost of the Ultrase MT & they will send us free AquaADEK every month. That is a huge help as our current prescription plan doesn't cover the vitamins.
The best news is I am actually healing. I fell 2 weeks ago & my knee hit a rock & tore the skin & muscle away from the bone. It was a bad injury. But I always seem to get infected, despite antibiotics. The ER have me on IV & oral antibiotics & I still got infected. I had a drain in & the drain was pulled 12 days ago & the hole hasn't closed. I have had a discharge with a draining pocket. When I changed the bandage today, there was very little draining & the hole is starting to close. I am guessing it is because I am finally able to digest the vitamins & minerals properly & my body is healing the wound.
 

kelliannesmom

New member
We got the results for Brandon, my 5 year old son. He has the same 3 mutated genes as his older sister. He too get frequent pneumonia & has asthma, but he doesn't have the intestinal problems Kellianne has.
I have a lot of the same symptoms as Kellianne in that I get pneumonia easily when I get a cold & I have had digestive issues since as long as I can remember. I have had so many endoscopies & colonoscopies & they have labeled it idiopathic IBS. They give me cholesterol medication to bind me up so I don't have diarrhea. Without it I am running to the bathroom constantly. With it, I can't make it through a meal without having to use the bathroom. So my doctor ordered the DNA test for me as well. I have the same 3 mutated genes as both of my kids.
Kellianne has been on the digestive enzymes for a month & is feeling so much better. She still has some days with diarrhea, but most are without. She is also on AquaADEK & hasn't had a nose bleed since she started taking them. She went in for a recheck & she has gained 4 ounces, but grew almost an inch! I started the enzymes & the AquaADEK on Tuesday & am feeling great. I haven't had to take the cholesterol medicine in 3 days!!
The CF social worker at the doctor's office came in & talked to the kids & me on Tuesday. She explained that although we have 3 mutated CF genes we do not have Cystic Fibrosis, but a mutation CF with Cystic Fibrosis like symptoms. They expect us to live a long life, so that is great news. She also gave us Axcam cards to help cover the cost of the Ultrase MT & they will send us free AquaADEK every month. That is a huge help as our current prescription plan doesn't cover the vitamins.
The best news is I am actually healing. I fell 2 weeks ago & my knee hit a rock & tore the skin & muscle away from the bone. It was a bad injury. But I always seem to get infected, despite antibiotics. The ER have me on IV & oral antibiotics & I still got infected. I had a drain in & the drain was pulled 12 days ago & the hole hasn't closed. I have had a discharge with a draining pocket. When I changed the bandage today, there was very little draining & the hole is starting to close. I am guessing it is because I am finally able to digest the vitamins & minerals properly & my body is healing the wound.
 

kelliannesmom

New member
We got the results for Brandon, my 5 year old son. He has the same 3 mutated genes as his older sister. He too get frequent pneumonia & has asthma, but he doesn't have the intestinal problems Kellianne has.
I have a lot of the same symptoms as Kellianne in that I get pneumonia easily when I get a cold & I have had digestive issues since as long as I can remember. I have had so many endoscopies & colonoscopies & they have labeled it idiopathic IBS. They give me cholesterol medication to bind me up so I don't have diarrhea. Without it I am running to the bathroom constantly. With it, I can't make it through a meal without having to use the bathroom. So my doctor ordered the DNA test for me as well. I have the same 3 mutated genes as both of my kids.
Kellianne has been on the digestive enzymes for a month & is feeling so much better. She still has some days with diarrhea, but most are without. She is also on AquaADEK & hasn't had a nose bleed since she started taking them. She went in for a recheck & she has gained 4 ounces, but grew almost an inch! I started the enzymes & the AquaADEK on Tuesday & am feeling great. I haven't had to take the cholesterol medicine in 3 days!!
The CF social worker at the doctor's office came in & talked to the kids & me on Tuesday. She explained that although we have 3 mutated CF genes we do not have Cystic Fibrosis, but a mutation CF with Cystic Fibrosis like symptoms. They expect us to live a long life, so that is great news. She also gave us Axcam cards to help cover the cost of the Ultrase MT & they will send us free AquaADEK every month. That is a huge help as our current prescription plan doesn't cover the vitamins.
The best news is I am actually healing. I fell 2 weeks ago & my knee hit a rock & tore the skin & muscle away from the bone. It was a bad injury. But I always seem to get infected, despite antibiotics. The ER have me on IV & oral antibiotics & I still got infected. I had a drain in & the drain was pulled 12 days ago & the hole hasn't closed. I have had a discharge with a draining pocket. When I changed the bandage today, there was very little draining & the hole is starting to close. I am guessing it is because I am finally able to digest the vitamins & minerals properly & my body is healing the wound.
 

kelliannesmom

New member
We got the results for Brandon, my 5 year old son. He has the same 3 mutated genes as his older sister. He too get frequent pneumonia & has asthma, but he doesn't have the intestinal problems Kellianne has.
I have a lot of the same symptoms as Kellianne in that I get pneumonia easily when I get a cold & I have had digestive issues since as long as I can remember. I have had so many endoscopies & colonoscopies & they have labeled it idiopathic IBS. They give me cholesterol medication to bind me up so I don't have diarrhea. Without it I am running to the bathroom constantly. With it, I can't make it through a meal without having to use the bathroom. So my doctor ordered the DNA test for me as well. I have the same 3 mutated genes as both of my kids.
Kellianne has been on the digestive enzymes for a month & is feeling so much better. She still has some days with diarrhea, but most are without. She is also on AquaADEK & hasn't had a nose bleed since she started taking them. She went in for a recheck & she has gained 4 ounces, but grew almost an inch! I started the enzymes & the AquaADEK on Tuesday & am feeling great. I haven't had to take the cholesterol medicine in 3 days!!
The CF social worker at the doctor's office came in & talked to the kids & me on Tuesday. She explained that although we have 3 mutated CF genes we do not have Cystic Fibrosis, but a mutation CF with Cystic Fibrosis like symptoms. They expect us to live a long life, so that is great news. She also gave us Axcam cards to help cover the cost of the Ultrase MT & they will send us free AquaADEK every month. That is a huge help as our current prescription plan doesn't cover the vitamins.
The best news is I am actually healing. I fell 2 weeks ago & my knee hit a rock & tore the skin & muscle away from the bone. It was a bad injury. But I always seem to get infected, despite antibiotics. The ER have me on IV & oral antibiotics & I still got infected. I had a drain in & the drain was pulled 12 days ago & the hole hasn't closed. I have had a discharge with a draining pocket. When I changed the bandage today, there was very little draining & the hole is starting to close. I am guessing it is because I am finally able to digest the vitamins & minerals properly & my body is healing the wound.
 

kelliannesmom

New member
We got the results for Brandon, my 5 year old son. He has the same 3 mutated genes as his older sister. He too get frequent pneumonia & has asthma, but he doesn't have the intestinal problems Kellianne has.
<br />I have a lot of the same symptoms as Kellianne in that I get pneumonia easily when I get a cold & I have had digestive issues since as long as I can remember. I have had so many endoscopies & colonoscopies & they have labeled it idiopathic IBS. They give me cholesterol medication to bind me up so I don't have diarrhea. Without it I am running to the bathroom constantly. With it, I can't make it through a meal without having to use the bathroom. So my doctor ordered the DNA test for me as well. I have the same 3 mutated genes as both of my kids.
<br />Kellianne has been on the digestive enzymes for a month & is feeling so much better. She still has some days with diarrhea, but most are without. She is also on AquaADEK & hasn't had a nose bleed since she started taking them. She went in for a recheck & she has gained 4 ounces, but grew almost an inch! I started the enzymes & the AquaADEK on Tuesday & am feeling great. I haven't had to take the cholesterol medicine in 3 days!!
<br />The CF social worker at the doctor's office came in & talked to the kids & me on Tuesday. She explained that although we have 3 mutated CF genes we do not have Cystic Fibrosis, but a mutation CF with Cystic Fibrosis like symptoms. They expect us to live a long life, so that is great news. She also gave us Axcam cards to help cover the cost of the Ultrase MT & they will send us free AquaADEK every month. That is a huge help as our current prescription plan doesn't cover the vitamins.
<br />The best news is I am actually healing. I fell 2 weeks ago & my knee hit a rock & tore the skin & muscle away from the bone. It was a bad injury. But I always seem to get infected, despite antibiotics. The ER have me on IV & oral antibiotics & I still got infected. I had a drain in & the drain was pulled 12 days ago & the hole hasn't closed. I have had a discharge with a draining pocket. When I changed the bandage today, there was very little draining & the hole is starting to close. I am guessing it is because I am finally able to digest the vitamins & minerals properly & my body is healing the wound.
 

laurenwinn

New member
Hi
I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?
 

laurenwinn

New member
Hi
I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?
 

laurenwinn

New member
Hi
I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?
 

laurenwinn

New member
Hi
I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?
 

laurenwinn

New member
Hi
<br />I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>laurenwinn</b></i>

Hi

I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?</end quote></div>


Find another doctor that is willing to do testing. If not just for Cystic Fibrosis....maybe Swachman Syndrom also. It has similiar characteristics of CF, but mainly digestive in nature.

We have quite a few members who had a "negative or borderling" sweat test, but genetic testing revealed CF. Dont EVER let a doctor make your feel absurd or guilty for additonal testing!!!

If you want to print some out to show it is possible we will find testimonials from the site for you!!
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>laurenwinn</b></i>

Hi

I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?</end quote></div>


Find another doctor that is willing to do testing. If not just for Cystic Fibrosis....maybe Swachman Syndrom also. It has similiar characteristics of CF, but mainly digestive in nature.

We have quite a few members who had a "negative or borderling" sweat test, but genetic testing revealed CF. Dont EVER let a doctor make your feel absurd or guilty for additonal testing!!!

If you want to print some out to show it is possible we will find testimonials from the site for you!!
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>laurenwinn</b></i>

Hi

I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?</end quote></div>


Find another doctor that is willing to do testing. If not just for Cystic Fibrosis....maybe Swachman Syndrom also. It has similiar characteristics of CF, but mainly digestive in nature.

We have quite a few members who had a "negative or borderling" sweat test, but genetic testing revealed CF. Dont EVER let a doctor make your feel absurd or guilty for additonal testing!!!

If you want to print some out to show it is possible we will find testimonials from the site for you!!
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>laurenwinn</b></i>

Hi

I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?</end quote>


Find another doctor that is willing to do testing. If not just for Cystic Fibrosis....maybe Swachman Syndrom also. It has similiar characteristics of CF, but mainly digestive in nature.

We have quite a few members who had a "negative or borderling" sweat test, but genetic testing revealed CF. Dont EVER let a doctor make your feel absurd or guilty for additonal testing!!!

If you want to print some out to show it is possible we will find testimonials from the site for you!!
 

JazzysMom

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>laurenwinn</b></i>
<br />
<br />Hi
<br />
<br />I am sorry to hear about your family's diagnosis but relieved to see it is atypical! I was wondering if you ever got your daughters sweat test number? My son has a lot of respiratory infections and CHRONIC digestive/constipation problems with a rectal prolapse, and a surgery corrected hydrocele. He took a sweat test and passed it with flying colors with a 7. He is 3 years old I should mention. Because of the passed sweat test we were forwarded to a gastroenterologist. This doctor seems to think its absurd to get a genetic test and made me feel guilty for even wanting any tests done to rule out digestive problems. The other day I came across an article on the American Academy of Pediatrics Website linking hydroceles in boys to Cystic Fibrosis, I don't know what to do?</end quote>
<br />
<br />
<br />Find another doctor that is willing to do testing. If not just for Cystic Fibrosis....maybe Swachman Syndrom also. It has similiar characteristics of CF, but mainly digestive in nature.
<br />
<br />We have quite a few members who had a "negative or borderling" sweat test, but genetic testing revealed CF. Dont EVER let a doctor make your feel absurd or guilty for additonal testing!!!
<br />
<br />If you want to print some out to show it is possible we will find testimonials from the site for you!!
 
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