Get it off your chest CF …
we’re back again!.. in hospital that is.
At the start of last week Stanley’s cough seemed to make an appearance again, we had only been back down to one lot of physio a day and down to prophylactic antibiotics for just a few days, but within a few days he seemed to be sounding rather noisy! It’s like we tempt fate every time we get down to just one lot of physio the dreaded cough returns!
month 3 already wow.. we’re now 12 weeks after diagnosis.
Stanley will be 15 weeks old next week and the past few weeks (touch wood) things have been pretty good!
After our two week stay in the hospital for IV’s Continue reading “3 month update. “
Just a quick post to keep people updated!
So yesterday we had both boys sweat tests as mentioned on the previous post..
The test took around an hour or so to complete, we were greeted by a lovely lady who was a biomedical scientist who explained the test.. Continue reading “sweating it out. “
So we realise we’ve been a bit quiet on the blog lately… sorry!
It’s been safe to say the past few weeks have been eventful! People may remember on Stanley’s 1 month update we had explained that after his last clinic appointment a cough had returned within a few days and he was then put on two more weeks worth of antibiotics Continue reading “2 month update. “
When we started this blog one of the things we said we would be is honest, each time you write a blog post write it like no one is going to see it. Ive had part of this blog written for a week or so now, but it has took me a while longer to put out there than our previous posts, I hadn’t got round to finishing it.. Continue reading “living up to the name and getting it off my chest. “
We will update the blog in between , but we have decided each month to give an update on Stanley, not only about his CF but his milestones and development as well!
We realise we’ve been updating the blog quite a lot.. This is just to get it started and so people can see what it is we are going to start fundraising shortly for!, we have been asked a lot of questions about Stanley and we will try and answer as many as we can within the blog! ( people are welcome to message us with questions or ask questions on the blog by commenting and we will try to include answers within the posts we put up ).
Sophie and I want to give you an insight into our life when we take a step back and look upon our family living with Cystic Fibrosis from our own points of view as parents – So here goes with my view on events…
We have had a few people asking what Cystic Fibrosis is and what it affects so here we have tried to explain the basics..
