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RE: update on Caden

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Dear Krystena,

I am so very happy for you .I do believe you must accept for the moment

what they have said to you & do the best you can for your precious

one.......I wish you all the wonderful times in the world with your

precious family. Have a super holiday/

LOVE & HUGS, grandmomBEV

update on Caden

Hi all.

The pulmonologist told me yesterday that his report meant NO Cystic

Fibrosis. That is great. For now, that is all I can go on. I guess it

ispossible that he could have some rare unidentified mutations. Unless

the genetic counselor tells me other wise, I am going to once and for

all be satisfied and confident that he is in the clear.

However, it doesn't change the fact that he still needs immediate

attention to his sinuses and malabsorption. I guess we will take this up

with his metabolic dr Friday. Maybe it is related to his FOD. Who

knows..

Caden's eyes are so swollen and red underneath today.

I have done the nasal washes for two days now. Yesterday's was a

success. This morning. Nothing came out.

They are supposed to call me today with his blood allergy test and sinus

CT report.

I just wanted to thank you all so much for all of the support you have

given me.

As devestating as it was to think my son could have been afflicted with

not one but two life threatening diseases, I am thankful to have learned

all that I have about Cystic Fibrosis.

I wish you all a very Merry Christmas and you will always be in my

heart.

Love,

Krystena s

Caden 4 yrs Glutaric Aciduria type II

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