Friday 25 August 2017

Part four.

CF, the gift that never stops giving....Results we've had back this week; 

His bone density scans came back as low. Meaning he is more at risk of osteoporosis and general breakages. This despite being on the maximum vitamin and calcium supplements he can be. We need to increase weight bearing exercises. 

His lung function has dropped. But this isn't altogether surprising, this early on IV's. 

Still waiting for blood and sputum lab results. I'm worried about these. 

Some concern has been raised about how many good veins he might have left, given the number of long/PICC lines he has had in the past, and a portacath been mentioned again. These are permanent implanted IV devices that are inserted into the chest (or arm) in surgery, that should last many years, and can be easily accessed every time he needs IV's. We've been pretty lucky to last without one all this time, purely because he is very good at having lines inserted and has no fear of needles (mostly due to his love of laughing gas - did I ever tell you, Isaac means 'laughing one' - so apt!). There are only so many places on a body they can site ports, before they run out of veins they can use too, so in some ways, the longer he can put this off for, the better, but it may be happening sooner rather than later at this rate. 

Today I have been at home with the girly ones, watching Flicka movies and making slime (their latest fads). Isaac is in good spirits still. I miss our family all being together under one roof, but I'm thankful that my boy is still smiling, to be here for now, and that everything is going well. Thank you for all the lovely messages x