chantelfox
New member
I don't know how many of you have MSN as your homepage, but
yesterday and today there is a video clip in the "Video
Highlights" section about a girl, Emily Schriver, age 13, who
has CF. Apparently she was diagnosed with it at age 9 and a
week after the diagnosis she decided to begin this fundraiser to
raise money for the CFF. She swims 100 laps and people donate money
per lap. It really is an inspirational story. I always admire
people like Emily. <br>
<br>
I am ashamed to admit that growing up I was no where near as
courageous as this young lady. I never told anyone about my CF
(unless they were a best friend and it took about a year before I
could manage tell them) and often told people the reason I
coughed was because of my "asthma". To this day I still
don't know why I felt compelled to keep it a secret (and still do).
I guess I just didn't want people to think I was "sick"
and treat me different. Has anyone had this issue? I really wish
that I could have gotten over it, because I would love to be
someone who helps in the fight against this disease and make people
more aware of it. From what I have experienced, people can
have the tendency to get really scared when I manage to get out the
words "cystic fibrosis". Most people have immediately
responded with "are you going to die?". Really it is the
people who have been getting close to you for a period of time
(friends, significant others) that get scared because they hear it
and don't know much about it, except that it can be terminal, but
LIFE is terminal! I just wish people knew more about it and
the fact that it's no longer a "childhood terminal
illness", like it was 50 years ago. I dated a guy for a
month about 4 years ago who stopped returning my phone
calls the very next day after I told him. After that happened
I managed to tell a friend who began to REALLY pressure me to tell
the whole College Group Bible Study of about 50 people at the
church I was going to. She made it seem like I was lying if I did
not tell a bunch of strangers about my CF. It got to the point that
I felt like I was a Lepper. I began to get really frustrated and
depressed, because I didn't feel like it was anyone's business but
mine and those who I chose to tell. Right before I left that church
I asked myself, "If it were diabetes that I had and not CF,
would I have to stand up and confess that to the whole
congregation?". I didn't se the big deal about telling a bunch
of people I hardly knew and hardly talked to.<br>
<br>
Has anyone had issues with telling people about your CF or am I a
total freak??? <img src=""> I really admire you people who get out there
and don't care about letting the whole world know about this
condition and I want to thank you from the bottom of my heart,
because it's your courage that helps people understand this thing
and not be so frightened of this condition.<br>
<br>
Take care all and Happy 4th of JULY!!!!!!!!!<br>
<br>
Chantel
yesterday and today there is a video clip in the "Video
Highlights" section about a girl, Emily Schriver, age 13, who
has CF. Apparently she was diagnosed with it at age 9 and a
week after the diagnosis she decided to begin this fundraiser to
raise money for the CFF. She swims 100 laps and people donate money
per lap. It really is an inspirational story. I always admire
people like Emily. <br>
<br>
I am ashamed to admit that growing up I was no where near as
courageous as this young lady. I never told anyone about my CF
(unless they were a best friend and it took about a year before I
could manage tell them) and often told people the reason I
coughed was because of my "asthma". To this day I still
don't know why I felt compelled to keep it a secret (and still do).
I guess I just didn't want people to think I was "sick"
and treat me different. Has anyone had this issue? I really wish
that I could have gotten over it, because I would love to be
someone who helps in the fight against this disease and make people
more aware of it. From what I have experienced, people can
have the tendency to get really scared when I manage to get out the
words "cystic fibrosis". Most people have immediately
responded with "are you going to die?". Really it is the
people who have been getting close to you for a period of time
(friends, significant others) that get scared because they hear it
and don't know much about it, except that it can be terminal, but
LIFE is terminal! I just wish people knew more about it and
the fact that it's no longer a "childhood terminal
illness", like it was 50 years ago. I dated a guy for a
month about 4 years ago who stopped returning my phone
calls the very next day after I told him. After that happened
I managed to tell a friend who began to REALLY pressure me to tell
the whole College Group Bible Study of about 50 people at the
church I was going to. She made it seem like I was lying if I did
not tell a bunch of strangers about my CF. It got to the point that
I felt like I was a Lepper. I began to get really frustrated and
depressed, because I didn't feel like it was anyone's business but
mine and those who I chose to tell. Right before I left that church
I asked myself, "If it were diabetes that I had and not CF,
would I have to stand up and confess that to the whole
congregation?". I didn't se the big deal about telling a bunch
of people I hardly knew and hardly talked to.<br>
<br>
Has anyone had issues with telling people about your CF or am I a
total freak??? <img src=""> I really admire you people who get out there
and don't care about letting the whole world know about this
condition and I want to thank you from the bottom of my heart,
because it's your courage that helps people understand this thing
and not be so frightened of this condition.<br>
<br>
Take care all and Happy 4th of JULY!!!!!!!!!<br>
<br>
Chantel