Your courage amazes me... you are very positive about everything, as am I... I
learned when we were diagnosed that if you sit on it and become depressed about
it, you don't live... and my son will live a long and full life.... and so will
every child and adult with CF. Our dr. is confident in a cure in the near
future... science is magic, but prayer works too... If you keep this attitude,
you will be fine...

pjduncan <pjduncan@...> wrote:
Tianni,

If nothing else comes from this invistigation, at least I am much
more informed about CF than before. I have a pretty good science
background so I've been doing a lot of reading. One thing that I've
found is that there are a lot of variations of CF and no one can know
for sure what path things will take.

In the papers I've read I've seen that more and more kids are living
longer and healthier lives with CF, so hope is something you should
pull in from as many sources as you can. Then you can give that hope
to your son by giving tons of love and attention, which I'm sure
you're great at.

Whatever the outcome of my problems, I definitely stand with you in
hope that there will be a cure very soon.

Best wishes.

--- In cysticfibrosissupport@yahoogroups.com, Tianni Nicholson
<newmommy1202@y...> wrote:
> If your sweat test does come back positive... you are a miracle and
just gave this mother hope that her son will lead a normal, full
life!!! Thank you, you don't realize wha that means.... I wish you
luck in your endevors.... Tianni Rowley, 19 month old son with CF
>
> Lisa Lee <lisaannlee@c...> wrote:I think what I would do first is
just ask my general physician to do a simple sweat test. Given the
symptoms I don't see why he wouldn't order one. Or try a
pulmonologist, they will definitely order the test. Once you find out
if your positive or negative, you can seek out a specialist. My docs
love to order tests, but you'll need one to know for sure. Lisa 43wcf
> ----- Original Message -----
> From: pjduncan
> To: cysticfibrosissupport@yahoogroups.com
> Sent: Monday, August 02, 2004 7:03 PM
> Subject: [Cystic Fibrosis Support] Request for info on adult
onset CF
>
>
> I would appreciate comments from anybody with knowledge about
adult
> onset (or adult diagnosed) CF. I'm a 37 year old male. For a
full
> year now I've had several symptoms that have yet to have a
specific
> diagnosis. A year ago I went to a doctor with both abdominal
pain
> and chest discomfort/pain. It was the first time I had been to
him
> and was confronted with one of those forms to list all
> diseases/symptoms that one suffers from. On that form I included
> many things which were either intermittent or ongoing problems
such
> as sinusitis, fatigue, sleep problems and digestive dysfunction.
I
> guess I appear too healthy because he was very dismissive and
said he
> couldn't think of a single thing that might lead to such a wide
> variety of symptoms and then subjected me to a psychological
> questionnaire. After this wonderful encounter I ignored the
symptoms
> for about 6 months before the feelings of chest pain got worse.
> Using a new doctor I've now had chest X-Ray, Chest CT with some
sort
> of injection, heart stress test, TB test and asthma evaluation.
All
> of these were negative or normal. Every time I have a day where
the
> pain is most noticeable I tend to do a bit of poking around the
> internet to see if I can find some leads. This time I ran across
> references to adult onset CF. So here's the question. With the
> below listed symptoms/history is it possible that I could have a
> variant of CF that's gone undiagnosed to age 37? and if so is
there
> a doctor in S. Cal that might have experience with adult onset
CF,
> such that they wouldn't simply write hypochondriac in my chart?
>
> 1 year history of intermittent chest discomfort/pain. Slight
pain
> usually occurs with laughing, yawning, coughing or deep breaths.
> Sometimes I tend to cough but rarely is anything coughed up. In
> general breathing seems a bit more difficult than in the past.
>
> I have fairly bad sinusitis with congestion and post nasal drip.
> Pulmonologist that ruled out asthma seems to think chest pain is
> secondary symptom of sinus problems. I went to an allergist
years
> ago that said the only thing I'm allergic to is dust mites. My
> sinusitis problems seem to occur even when in environments
presumably
> relatively free of dust mites.
>
> I have had surgery for nasal polyps 6-8 years ago. I understand
> polyps are potentially correlated with CF.
>
> I had a gallstone at age 25. This is very rare in skinny, young
men
> which is why it went misdiagnosed for a full year. I now
understand
> that this is also correlated with CF.
>
> I have had intermittent digestive problems for a number of
years.
> Also, for a long time I have noticed that stools often are
covered
> with thick mucus.
>
> I have had lower abdominal pain that is hard to pinpoint and
doesn't
> seem to feel like intestinal pain/cramping.
>
> I've had several urinary tract infections (rare in guys my age)
and
> was told I had a slightly enlarged prostate by urologist.
>
> I have Hashimoto's syndrome thyroid disease. I take synthroid
and my
> levels are normal.
>
> Despite having drug controlled normal thyroid levels, I have now
> started to feel fatigued on a regular basis.
>
> Sometimes I seem to be heat sensitive, feeling hotter and
sweating
> more than would seem appropriate for ambient temperature.
>
>
> Yahoo! Groups Sponsor
> ADVERTISEMENT
>
>
>
>
>
> --------------------------------------------------------------------
----------
> Yahoo! Groups Links
>
> a.. To visit your group on the web, go to:
> http://groups.yahoo.com/group/cysticfibrosissupport/
>
> b.. To unsubscribe from this group, send an email to:
> cysticfibrosissupport-unsubscribe@yahoogroups.com
>
> c.. Your use of Yahoo! Groups is subject to the Yahoo! Terms of
Service.
>
>
>
>
> [Non-text portions of this message have been removed]
>
>
> Yahoo! Groups SponsorADVERTISEMENT
>
>
> ---------------------------------
> Yahoo! Groups Links
>
> To visit your group on the web, go to:
> http://groups.yahoo.com/group/cysticfibrosissupport/
>
> To unsubscribe from this group, send an email to:
> cysticfibrosissupport-unsubscribe@yahoogroups.com
>
> Your use of Yahoo! Groups is subject to the Yahoo! Terms of
Service.
>
>
>
>
> ---------------------------------
> Do you Yahoo!?
> New and Improved Yahoo! Mail - 100MB free storage!
>
> [Non-text portions of this message have been removed]


Yahoo! Groups SponsorADVERTISEMENT


---------------------------------
Yahoo! Groups Links

To visit your group on the web, go to:
http://groups.yahoo.com/group/cysticfibrosissupport/

To unsubscribe from this group, send an email to:
cysticfibrosissupport-unsubscribe@yahoogroups.com

Your use of Yahoo! Groups is subject to the Yahoo! Terms of Service.


---------------------------------
Do you Yahoo!?
Yahoo! Mail - 50x more storage than other providers!

[Non-text portions of this message have been removed]