No keeping this girl down!

No keeping this girl down!

Today Leah is medically more or less in the same place as yesterday.
The samples that were taken from her lungs on Thursday and were sent to the laboratory haven’t grown anything, so this confuses the PCP diagnosis a little bit and has led some of the docs to suspect that Leah may have pneumonitis, another complication of transplant.
It’s not one I fully understand but I think it could be a type of GVHD (graft vs host disease) or some other kind of auto immune condition triggered by the transplant process.
I have been told that the only way to prove/disprove the diagnosis would be to do a bronchoscopy and a lavage which at present they are reluctant to do, as Leah is so ill.
In the meantime they will continue treating her for everything that they can think of treating her for, including PCP, and wait to see what happens.
Leah is less sedated today, she’s sucking on a Polly Pineapple ice pop, but typed that she would prefer a coke float – no chance!
She also typed “what about maths exam 10th Jan” and I said “Leah you won’t be doing this exam”.
Then she typed “maybe God wants me to go back a year but maybe I could still have lunch & break with my form class Mr M lets them go down town” – going back a year is something that Leah has fought hard against since her diagnosis, but here she is trying to make the best of her situation – no keeping this girl down 
Diagnosis of PCP

Diagnosis of PCP

Written in the Cancer Centre.
Leah’s chest infection has been confirmed as PCP – a type of pneumonia that only occurs in people who are immunocompromised.
 She’s on continuos oxygen and is on intravenous antibiotics and is back on steroids and is being regularly reviewed by her own Dr and by the ICU Dr in case she needs more intensive support.
If her condition stabilises our Dr hopes to be able to transfer Leah to Altnagelvin, our local hospital, early in the week.
This hospital we are in is approximately 70 miles from home.
Tuesday is Leah’s 16th birthday and the 1st anniversary of when this journey started – it was on her 15th birthday that Leah visited her GP and had a blood test taken which resulted in her being referred to a haematologist.
This led to 3 months of investigations & eventually we received a phone call in April telling us that Leah had paediatric myelodysplasia with monosomy 7 & needed a bone marrow transplant!
Prayer would be much appreciated for Leah’s speedy recovery please.