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Seriously?! – Dear FDA,… comment reply

August 16, 2009 – 10:36 pm

I started to reply to this comment within my last post Seriously?! – Dear FDA,… but I after I got going I figured it would be best if I address the comments with a new post…
Here’s the comment:
Dear Salty:
I think you’re being a little unfair to the FDA. They made a decision the CF community didn’t [...]

By Salty | Posted in Challenges, Cystic Fibrosis, treatments | Comments (4)

Seriously?! – Dear FDA,…

August 14, 2009 – 6:24 pm

Seriously?!
Dear FDA,
This is getting absolutely ridiculous.  For almost 8 months now I have been part of an Expanded Access Program, which has been going on for two full years now, for the clinical study of the drug Aztreonam delivered via a nebulizer.  To explain a little about this study, Aztreonam is an antibiotic which has [...]

By Salty | Posted in Challenges, Cystic Fibrosis, treatments | Comments (3)

I need this treatment. Please help tell the FDA.

November 21, 2008 – 5:15 pm

I find this extremely important.  I received this email (see below) and excuse me for just copy and pasting, but the Cystic Fibrosis Foundation, and myself, and others with CF, need your help.
Personally, I am waiting with baited breath for this treatment to hit the market.  Inhaled Aztreonam, AZLI, was expected to be available this [...]

By Salty | Posted in Challenges, Cystic Fibrosis, Support | Comments (2)