Emily’s Smiles through Difficult Trials

Updates about the Emily Hollis Medulloblastoma Cancer Journey

Hoping for a better day!

Filed under: — sho at 11:04 am on Friday, February 23, 2007
Emily is still sleeping. I hope she wakes up in a better mood this morning.  Drs. have not been in yet.  I will update later today.  Just finished washing Emily,  A volunteer retired highschool teacher is here to read stories to Emily.  She came by last time we were in, and Emily has been asking about her this time.   I will keep in touch  Dawn

A little better today

Filed under: — sho at 10:13 pm on Thursday, February 22, 2007
Today Emily has been more alert.  She is still not feeling good but the meds are helping with the vomiting.  She has been very whiny today.  They have given her so many meds and pre-meds and antibiotics and fluids, I guess we would be whiny too.  More platelets were given.  We did manage to get her on the trike this morning, but that was short and she wanted to return to her bed and draw some.  The CT scan looked good, what a blessing.  The chest Xray was fine.  Dr. G said it is probably a combination of both a strep and viral infection.  Emily did not have any fevers today, and is continuing on antibiotics.  Dr. G said “she is one tough little girl”.  We don’t know  when Emily will be able to go to the apt.  She will have to still be on antibiotics at the apt.  Well I have to go Iam being called to snuggle.  Talk to you later, 
Dawn, Eddie and Emily 

P.S.  Eddie talked to Greg Mosher, Sr.  and he said Greg Jr. is doing better, and Lonnie Crawford, is taking his radiation treatments in Wilmington.  Still will do surgery after radiation.  Please remember these two families in prayer.

Still very sick/CT & more tests

Filed under: — sho at 8:08 pm on Wednesday, February 21, 2007
I don’t where to start.  The last 2 days, Emily has still been fighting the fevers. Vomiting alot and is on 3 different nausea meds.   Drs.  have put her on 3 antibiotics and the fever is only coming down for a little while when tylenol is given.  The cultures form the ER is positve for strep in her lines,  but they are doing a series of cultures because the fevers are not reacting to the antibiotics. Not sure if there are other types of infection, viral or both.   She had a chest xray earlier and it looks fine.  We just came back from doing a CT,   because she is having headaches and vomiting regularly.  I Pray it is not the ventricles in the brain building pressure, since the shunt was removed. Dr said it could be because of the high fever.    Emily feels very very bad.  She had another blood transfusion and platelets today.  She had her nose suctioned to rule out something.  else. Sleep is limited.  It is so busy in the room and Emily has to be soaked often in Povidone Iodine, oh she really likes that.  Physical Therapist came by this morning to check Emily’s legs and feet.  She has limited motion in both and can hardly flex feet and legs without pain.  We are making plans on what to do when Emily recovers from this stay. It can be the chemo treatment but it is also due to the very limited movement she said.  I have another Physical Therapist that will be coming to the Apartment as soon as we are back, to evaluate again.  Sometimes you have to go out on your own to find out info.  I am checking on Insurance also to see not only about now,  but I want to know what can happen after treatment, because she is going to need Occupational Therapy, which we started some during radiation, but she doesn’t have any good days for that now.  Physical Therapy plus speech has to be worked in there sometime.  I did inquire about Pitt Memorial in Greenville, which is an inpatient hospital. for rehab patients.  They say a patient on a schedule there needs 5 days a week 2x a day for each therapy treatment, more intensive therapy.  The physical therapy that is done here  in the hospital is the type, to get patients ready to be discharged, not the type of intensive therapy needed to help a patient long-term.   I am going to see if I can find out more info with my insurance company and what they may or may not pay.  Or they may not tell me any info without a Drs. order.   Eddie is on his way and will be here around 9:30 pm.   I will let you know more when we find out about the tests.   Thank You to everyone for your much needed prayers.  
Love,  Emily and Dawn 
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