My son was diagnosed at 6 months old. The information that I have read discussed how this is a progressive condition. The more you stay on top of your treatments and care, the easier it is to manage symptoms. I think that before your sister moves forward from this, she should be evaluated by a CF specialist to plan a course of action....then return to her missionary work. I realize this is being written about a month after your posting so I am sure everything I say her has already been said. This is what I appreciate about the forums.
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Mild CF - no need for treatment?
- Thread starter NancyLKF
- Start date
My son was diagnosed at 6 months old. The information that I have read discussed how this is a progressive condition. The more you stay on top of your treatments and care, the easier it is to manage symptoms. I think that before your sister moves forward from this, she should be evaluated by a CF specialist to plan a course of action....then return to her missionary work. I realize this is being written about a month after your posting so I am sure everything I say her has already been said. This is what I appreciate about the forums.
My son was diagnosed at 6 months old. The information that I have read discussed how this is a progressive condition. The more you stay on top of your treatments and care, the easier it is to manage symptoms. I think that before your sister moves forward from this, she should be evaluated by a CF specialist to plan a course of action....then return to her missionary work. I realize this is being written about a month after your posting so I am sure everything I say her has already been said. This is what I appreciate about the forums.
My son was diagnosed at 6 months old. The information that I have read discussed how this is a progressive condition. The more you stay on top of your treatments and care, the easier it is to manage symptoms. I think that before your sister moves forward from this, she should be evaluated by a CF specialist to plan a course of action....then return to her missionary work. I realize this is being written about a month after your posting so I am sure everything I say her has already been said. This is what I appreciate about the forums.
My son was diagnosed at 6 months old. The information that I have read discussed how this is a progressive condition. The more you stay on top of your treatments and care, the easier it is to manage symptoms. I think that before your sister moves forward from this, she should be evaluated by a CF specialist to plan a course of action....then return to her missionary work. I realize this is being written about a month after your posting so I am sure everything I say her has already been said. This is what I appreciate about the forums.
JennyCoulon
New member
Treatment really should start now. Both my 4 year old and almost 10 year old have mild lung disease mostly digestive but we are proactive rather than reactive.
JennyCoulon
New member
Treatment really should start now. Both my 4 year old and almost 10 year old have mild lung disease mostly digestive but we are proactive rather than reactive.
JennyCoulon
New member
Treatment really should start now. Both my 4 year old and almost 10 year old have mild lung disease mostly digestive but we are proactive rather than reactive.
JennyCoulon
New member
Treatment really should start now. Both my 4 year old and almost 10 year old have mild lung disease mostly digestive but we are proactive rather than reactive.
JennyCoulon
New member
Treatment really should start now. Both my 4 year old and almost 10 year old have mild lung disease mostly digestive but we are proactive rather than reactive.