Never Give Up!

LisaGreene

New member
I am sending some articles out for a newsletter and thought you'd especially like this one. It's one of my favorites cause it's so inspiring and hopeful. I hope you find it to be so, too.
Lisa (mom of 2 kids with CF and author)

<b>Don't Give Up! The Trouble with Statistics...</b> by Foster Cline, MD and Lisa C. Greene

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.

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."

Historically, medical professionals have been 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, Liz was selected to carry the 2002 OlympicTorch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time. Her example and indomitable spirit continues to bring hope to families with CF.

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 courageous and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
<UL>. 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. </UL>
Excerpt taken from the book <i>Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Special Healthcare Needs</i> by Foster W. Cline MD and Lisa C. Greene available in bookstores nationwide and online booksellers including www.amazon.com and www.loveandlogic.com.

Visit www.ParentingChildrenWithHealthIssues.com for the free stuff. :)
 

LisaGreene

New member
I am sending some articles out for a newsletter and thought you'd especially like this one. It's one of my favorites cause it's so inspiring and hopeful. I hope you find it to be so, too.
Lisa (mom of 2 kids with CF and author)

<b>Don't Give Up! The Trouble with Statistics...</b> by Foster Cline, MD and Lisa C. Greene

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.

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."

Historically, medical professionals have been 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, Liz was selected to carry the 2002 OlympicTorch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time. Her example and indomitable spirit continues to bring hope to families with CF.

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 courageous and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
<UL>. 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. </UL>
Excerpt taken from the book <i>Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Special Healthcare Needs</i> by Foster W. Cline MD and Lisa C. Greene available in bookstores nationwide and online booksellers including www.amazon.com and www.loveandlogic.com.

Visit www.ParentingChildrenWithHealthIssues.com for the free stuff. :)
 

LisaGreene

New member
I am sending some articles out for a newsletter and thought you'd especially like this one. It's one of my favorites cause it's so inspiring and hopeful. I hope you find it to be so, too.
Lisa (mom of 2 kids with CF and author)

<b>Don't Give Up! The Trouble with Statistics...</b> by Foster Cline, MD and Lisa C. Greene

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.

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."

Historically, medical professionals have been 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, Liz was selected to carry the 2002 OlympicTorch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time. Her example and indomitable spirit continues to bring hope to families with CF.

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 courageous and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
<UL>. 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. </UL>
Excerpt taken from the book <i>Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Special Healthcare Needs</i> by Foster W. Cline MD and Lisa C. Greene available in bookstores nationwide and online booksellers including www.amazon.com and www.loveandlogic.com.

Visit www.ParentingChildrenWithHealthIssues.com for the free stuff. :)
 

LisaGreene

New member
I am sending some articles out for a newsletter and thought you'd especially like this one. It's one of my favorites cause it's so inspiring and hopeful. I hope you find it to be so, too.
Lisa (mom of 2 kids with CF and author)

<b>Don't Give Up! The Trouble with Statistics...</b> by Foster Cline, MD and Lisa C. Greene

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.

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."

Historically, medical professionals have been 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, Liz was selected to carry the 2002 OlympicTorch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time. Her example and indomitable spirit continues to bring hope to families with CF.

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 courageous and inspiring attitude.

In summary, wise parents handle statistics and medical predictions by:
<UL>. 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. </UL>
Excerpt taken from the book <i>Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Special Healthcare Needs</i> by Foster W. Cline MD and Lisa C. Greene available in bookstores nationwide and online booksellers including www.amazon.com and www.loveandlogic.com.

Visit www.ParentingChildrenWithHealthIssues.com for the free stuff. :)
 

LisaGreene

New member
I am sending some articles out for a newsletter and thought you'd especially like this one. It's one of my favorites cause it's so inspiring and hopeful. I hope you find it to be so, too.
<br />Lisa (mom of 2 kids with CF and author)
<br />
<br /><b>Don't Give Up! The Trouble with Statistics...</b> by Foster Cline, MD and Lisa C. Greene
<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.
<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 />Historically, medical professionals have been 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, Liz was selected to carry the 2002 OlympicTorch through Union Square in San Francisco. Liz died at nearly 33, well past her "statistical average" at the time. Her example and indomitable spirit continues to bring hope to families with CF.
<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 courageous and inspiring attitude.
<br />
<br />In summary, wise parents handle statistics and medical predictions by:
<br /><UL>. 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. </UL>
<br />Excerpt taken from the book <i>Parenting Children with Health Issues: Essential Tools, Tips and Tactics for Raising Kids with Chronic Illness, Medical Conditions and Special Healthcare Needs</i> by Foster W. Cline MD and Lisa C. Greene available in bookstores nationwide and online booksellers including www.amazon.com and www.loveandlogic.com.
<br />
<br />Visit www.ParentingChildrenWithHealthIssues.com for the free stuff. :)
 

holmfamily1992

New member
I loved this article!! At first, when this all started for my family we couldnt even look at our son without crying. I couldnt even read the statics because they were so depressing. I didnt know anything about CF so of course I did all the research possible. After we had time to process what was goin on and knowing that more of our children could have this disease we developed the attitude "we can beat this!" I as a mother of 8 refuse to just lay down and let it take ahold of my family. If there isnt a cure then we can be apart of finding one! We will continue to encourage our children to play sports, run and play, and just act like normal kids. I never want to set limitation on my kids and if we run across something that they struggle with then we will just modify it so they CAN do it.

Thank you, Tina
 

holmfamily1992

New member
I loved this article!! At first, when this all started for my family we couldnt even look at our son without crying. I couldnt even read the statics because they were so depressing. I didnt know anything about CF so of course I did all the research possible. After we had time to process what was goin on and knowing that more of our children could have this disease we developed the attitude "we can beat this!" I as a mother of 8 refuse to just lay down and let it take ahold of my family. If there isnt a cure then we can be apart of finding one! We will continue to encourage our children to play sports, run and play, and just act like normal kids. I never want to set limitation on my kids and if we run across something that they struggle with then we will just modify it so they CAN do it.

Thank you, Tina
 

holmfamily1992

New member
I loved this article!! At first, when this all started for my family we couldnt even look at our son without crying. I couldnt even read the statics because they were so depressing. I didnt know anything about CF so of course I did all the research possible. After we had time to process what was goin on and knowing that more of our children could have this disease we developed the attitude "we can beat this!" I as a mother of 8 refuse to just lay down and let it take ahold of my family. If there isnt a cure then we can be apart of finding one! We will continue to encourage our children to play sports, run and play, and just act like normal kids. I never want to set limitation on my kids and if we run across something that they struggle with then we will just modify it so they CAN do it.

Thank you, Tina
 

holmfamily1992

New member
I loved this article!! At first, when this all started for my family we couldnt even look at our son without crying. I couldnt even read the statics because they were so depressing. I didnt know anything about CF so of course I did all the research possible. After we had time to process what was goin on and knowing that more of our children could have this disease we developed the attitude "we can beat this!" I as a mother of 8 refuse to just lay down and let it take ahold of my family. If there isnt a cure then we can be apart of finding one! We will continue to encourage our children to play sports, run and play, and just act like normal kids. I never want to set limitation on my kids and if we run across something that they struggle with then we will just modify it so they CAN do it.

Thank you, Tina
 

holmfamily1992

New member
I loved this article!! At first, when this all started for my family we couldnt even look at our son without crying. I couldnt even read the statics because they were so depressing. I didnt know anything about CF so of course I did all the research possible. After we had time to process what was goin on and knowing that more of our children could have this disease we developed the attitude "we can beat this!" I as a mother of 8 refuse to just lay down and let it take ahold of my family. If there isnt a cure then we can be apart of finding one! We will continue to encourage our children to play sports, run and play, and just act like normal kids. I never want to set limitation on my kids and if we run across something that they struggle with then we will just modify it so they CAN do it.
<br />
<br />Thank you, Tina
 

BonnieD

New member
I am amazed at all the new developments, test and treatments today. It is great. Maybe all our years of fund raising did loads of good.

My two children were diagnosed at near birth or just over a year. Raising children with a chronic, often terminal illness, was very difficult. We did our best to have them live normal lives and they did. They played some sports, some musical instruments, visited friends in other states, went to CF camps, etc., etc.

I always felt lucky to have known that my children were seriously ill and understand that life is precious and often short. We did everything we ever wanted to with them and had no regrets for things not done. Other children get hit by cars or freak accidents and their parents have loads of regrets for things not done.

Don't get me wrong, I love and miss my children every day and am sorry for not being with them today, but I was given the precious gift of almost 27 and 30 years with each of them. Also the most extraordinary gift of a 19 year old granddaughter. It is not easy, but do your best to enjoy.
 

BonnieD

New member
I am amazed at all the new developments, test and treatments today. It is great. Maybe all our years of fund raising did loads of good.

My two children were diagnosed at near birth or just over a year. Raising children with a chronic, often terminal illness, was very difficult. We did our best to have them live normal lives and they did. They played some sports, some musical instruments, visited friends in other states, went to CF camps, etc., etc.

I always felt lucky to have known that my children were seriously ill and understand that life is precious and often short. We did everything we ever wanted to with them and had no regrets for things not done. Other children get hit by cars or freak accidents and their parents have loads of regrets for things not done.

Don't get me wrong, I love and miss my children every day and am sorry for not being with them today, but I was given the precious gift of almost 27 and 30 years with each of them. Also the most extraordinary gift of a 19 year old granddaughter. It is not easy, but do your best to enjoy.
 

BonnieD

New member
I am amazed at all the new developments, test and treatments today. It is great. Maybe all our years of fund raising did loads of good.

My two children were diagnosed at near birth or just over a year. Raising children with a chronic, often terminal illness, was very difficult. We did our best to have them live normal lives and they did. They played some sports, some musical instruments, visited friends in other states, went to CF camps, etc., etc.

I always felt lucky to have known that my children were seriously ill and understand that life is precious and often short. We did everything we ever wanted to with them and had no regrets for things not done. Other children get hit by cars or freak accidents and their parents have loads of regrets for things not done.

Don't get me wrong, I love and miss my children every day and am sorry for not being with them today, but I was given the precious gift of almost 27 and 30 years with each of them. Also the most extraordinary gift of a 19 year old granddaughter. It is not easy, but do your best to enjoy.
 

BonnieD

New member
I am amazed at all the new developments, test and treatments today. It is great. Maybe all our years of fund raising did loads of good.

My two children were diagnosed at near birth or just over a year. Raising children with a chronic, often terminal illness, was very difficult. We did our best to have them live normal lives and they did. They played some sports, some musical instruments, visited friends in other states, went to CF camps, etc., etc.

I always felt lucky to have known that my children were seriously ill and understand that life is precious and often short. We did everything we ever wanted to with them and had no regrets for things not done. Other children get hit by cars or freak accidents and their parents have loads of regrets for things not done.

Don't get me wrong, I love and miss my children every day and am sorry for not being with them today, but I was given the precious gift of almost 27 and 30 years with each of them. Also the most extraordinary gift of a 19 year old granddaughter. It is not easy, but do your best to enjoy.
 

BonnieD

New member
I am amazed at all the new developments, test and treatments today. It is great. Maybe all our years of fund raising did loads of good.
<br />
<br />My two children were diagnosed at near birth or just over a year. Raising children with a chronic, often terminal illness, was very difficult. We did our best to have them live normal lives and they did. They played some sports, some musical instruments, visited friends in other states, went to CF camps, etc., etc.
<br />
<br />I always felt lucky to have known that my children were seriously ill and understand that life is precious and often short. We did everything we ever wanted to with them and had no regrets for things not done. Other children get hit by cars or freak accidents and their parents have loads of regrets for things not done.
<br />
<br />Don't get me wrong, I love and miss my children every day and am sorry for not being with them today, but I was given the precious gift of almost 27 and 30 years with each of them. Also the most extraordinary gift of a 19 year old granddaughter. It is not easy, but do your best to enjoy.
 

LisaGreene

New member
Way to go Tina! It sounds like you are an amazing mom. 8 kids? Wow!

When our son was first dx'd, the stats (lower at the time) threw me into a major funk. It took awhile to come out of it but I am so glad that I found inspiring, encouraging books by others that gave me hope. That is what motivated me to co-write this book and I hope that it does the same for others.

One of the best gifts we can give our kids is a normal life. There is so much hope...

Take care,
Lisa
 

LisaGreene

New member
Way to go Tina! It sounds like you are an amazing mom. 8 kids? Wow!

When our son was first dx'd, the stats (lower at the time) threw me into a major funk. It took awhile to come out of it but I am so glad that I found inspiring, encouraging books by others that gave me hope. That is what motivated me to co-write this book and I hope that it does the same for others.

One of the best gifts we can give our kids is a normal life. There is so much hope...

Take care,
Lisa
 

LisaGreene

New member
Way to go Tina! It sounds like you are an amazing mom. 8 kids? Wow!

When our son was first dx'd, the stats (lower at the time) threw me into a major funk. It took awhile to come out of it but I am so glad that I found inspiring, encouraging books by others that gave me hope. That is what motivated me to co-write this book and I hope that it does the same for others.

One of the best gifts we can give our kids is a normal life. There is so much hope...

Take care,
Lisa
 

LisaGreene

New member
Way to go Tina! It sounds like you are an amazing mom. 8 kids? Wow!

When our son was first dx'd, the stats (lower at the time) threw me into a major funk. It took awhile to come out of it but I am so glad that I found inspiring, encouraging books by others that gave me hope. That is what motivated me to co-write this book and I hope that it does the same for others.

One of the best gifts we can give our kids is a normal life. There is so much hope...

Take care,
Lisa
 

LisaGreene

New member
Way to go Tina! It sounds like you are an amazing mom. 8 kids? Wow!
<br />
<br />When our son was first dx'd, the stats (lower at the time) threw me into a major funk. It took awhile to come out of it but I am so glad that I found inspiring, encouraging books by others that gave me hope. That is what motivated me to co-write this book and I hope that it does the same for others.
<br />
<br />One of the best gifts we can give our kids is a normal life. There is so much hope...
<br />
<br />Take care,
<br />Lisa
 
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