Diagnosed at 23

abnormal

New member
 Hi, I'm pretty new on this site... I received the results of my sweat test on my 23rd birthday in 1998 via telephone from the hospital that preformed the test and that was after putting the test off 3 years after my little sister was diagnosed with CF because I was 99.9% sure I had it as well. Not to mention the fact that I had to DEMAND to be tested because the stupid primary physician who missed diagnosed me for years with allergies, asthma and bronchitis,etc. thought there was NO way I could have CF because I had a son, even with the family history and the symptoms. IDOIT! Well after that, I went to a CF center and had my genetic test done. That came back with   delta508 and 3849+10kb C>t... It seems I have a some what "mild" case of CF I wish the same could of been said for my little sister, she passed away 5 years ago... <img src="i/expressions/face-icon-small-sad.gif" border="0">  Well... 13 years later I've been able to muddle through life with CF and I'm on to bigger and better things like a brain tumor....<div><br></div><div>Always abnormal...</div>
 

abnormal

New member
Hi, I'm pretty new on this site... I received the results of my sweat test on my 23rd birthday in 1998 via telephone from the hospital that preformed the test and that was after putting the test off 3 years after my little sister was diagnosed with CF because I was 99.9% sure I had it as well. Not to mention the fact that I had to DEMAND to be tested because the stupid primary physician who missed diagnosed me for years with allergies, asthma and bronchitis,etc. thought there was NO way I could have CF because I had a son, even with the family history and the symptoms. IDOIT! Well after that, I went to a CF center and had my genetic test done. That came back with delta508 and 3849+10kb C>t... It seems I have a some what "mild" case of CF I wish the same could of been said for my little sister, she passed away 5 years ago... <img src="i/expressions/face-icon-small-sad.gif" border="0"> Well... 13 years later I've been able to muddle through life with CF and I'm on to bigger and better things like a brain tumor....<br>Always abnormal...
 

abnormal

New member
Hi, I'm pretty new on this site... I received the results of my sweat test on my 23rd birthday in 1998 via telephone from the hospital that preformed the test and that was after putting the test off 3 years after my little sister was diagnosed with CF because I was 99.9% sure I had it as well. Not to mention the fact that I had to DEMAND to be tested because the stupid primary physician who missed diagnosed me for years with allergies, asthma and bronchitis,etc. thought there was NO way I could have CF because I had a son, even with the family history and the symptoms. IDOIT! Well after that, I went to a CF center and had my genetic test done. That came back with delta508 and 3849+10kb C>t... It seems I have a some what "mild" case of CF I wish the same could of been said for my little sister, she passed away 5 years ago... <img src="i/expressions/face-icon-small-sad.gif" border="0"> Well... 13 years later I've been able to muddle through life with CF and I'm on to bigger and better things like a brain tumor....<br>Always abnormal...
 

ymikhale

New member
welcome to this site, sorry to hear you were misdiagnosed for so many years, sometimes i am amazed how incompetent certain doctors are! Me are lucky to have neonatal screening, otherwise I am sure my dd would have never been diagnosed.BTW she has the same mutations as you.
 

ymikhale

New member
welcome to this site, sorry to hear you were misdiagnosed for so many years, sometimes i am amazed how incompetent certain doctors are! Me are lucky to have neonatal screening, otherwise I am sure my dd would have never been diagnosed.BTW she has the same mutations as you.
 

ymikhale

New member
welcome to this site, sorry to hear you were misdiagnosed for so many years, sometimes i am amazed how incompetent certain doctors are! Me are lucky to have neonatal screening, otherwise I am sure my dd would have never been diagnosed.BTW she has the same mutations as you.
 

Daverog75

New member
My story is the same, I was diagnosed at 22 after years of misdiagnoses, and I too had to ask to see a specialist.

Dave, 37 w/cf
 

Daverog75

New member
My story is the same, I was diagnosed at 22 after years of misdiagnoses, and I too had to ask to see a specialist.

Dave, 37 w/cf
 

Printer

Active member
There is a thread here, FORUM/ADULT - CFers over 50. You guys are younger but it is still a good read.

Bill
 

Printer

Active member
There is a thread here, FORUM/ADULT - CFers over 50. You guys are younger but it is still a good read.

Bill
 

MichaelL

New member
Welcome to the site. I was diagnosed at 34 with the same mutations you have. I've been told that our mutations are not fully understood by doctors and that they find us quite interesting.
 

MichaelL

New member
Welcome to the site. I was diagnosed at 34 with the same mutations you have. I've been told that our mutations are not fully understood by doctors and that they find us quite interesting.
 

towanda440

New member
so sorry to hear about your diagnosis, sister and brain tumor...way too much for a person to go through! I hope you are doing well.
My sister passed away from CF at age 30. I do not have it, but have witnessedthat it isso very hard to deal with and manage. I will keep your health in my thoughts and prayers.

Dawn
 

towanda440

New member
so sorry to hear about your diagnosis, sister and brain tumor...way too much for a person to go through! I hope you are doing well.
My sister passed away from CF at age 30. I do not have it, but have witnessedthat it isso very hard to deal with and manage. I will keep your health in my thoughts and prayers.

Dawn
 
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