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I almost had everything ready. The idea of knowing that the next day I would be in paradise filled my mind with wonderful images from previous years. I had missed the latest issues due to various respiratory infections requiring intravenous antibiotic treatment. Now it was only hours …
That night, during dinner, my mother kept asking me things: Have you prepared all the medication? Have you taken enough clothes? Will someone from the Respiralia organization pick you up at the Port of La Savina? … As if I was 15 years old! My parents have always watched over me. I was diagnosed with Cystic Fibrosis at birth, and since then care has been continuous because relapses are important. With my respiratory limitations, I value more each laugh, each moment, each breath. Wouldn’t you?
“I’m going to check everything for the last time: sprays, nebulizers, medicines, masks… I start to think that I’m forgetting something, but what. I know that it is a very important device for people who have Cystic Fibrosis, especially when we do respiratory physiotherapy and inhaled therapy. In fact, I know that I should use it for a long time and not just for this treatment, but I don’t remember its name. I think you can find it on this same website. There are manuals published and surely you can find it in one of them. When you find this keyword, you will be able to access next chapter writing the password “keyword-Vertex” at https://www.respiralia.org/en/margos-holidays-part2/
In case you can’t find the key, here are two clues.
Clue 1: Send an email to firstname.lastname@example.org
Clue 2: Send an email to email@example.com
You will receive an automatic reply with the clue. Pay attention to your spam tray if you don’t receive it right away.