Emily’s Smiles through Difficult Trials

Updates about the Emily Hollis Medulloblastoma Cancer Journey

Hives during the night

Filed under: — sho at 3:07 am on Friday, January 26, 2007
Emily is now sleeping. We had another breakout of  hives  tonight and know its the   Vancomycin, and not the Zofran.    Vancomycin is every 8 hours  along with Rifamphin  2 times a day (think that’s the right way to say that).   Its a strong antibiotic that  increases the antibiotic Vancomycin’s ability to attack this type of Staph.  Emily has been taking Benedryl  for pre-med   throughout the day  and  afternoon , and she still  broke out in hives. She was maxed on Benedryl already for   pre- meds,  so we tried to give her 12 MLS of Aterax by mouth but it was so thick and way to much for her to try to hold down,  and of course it didn’t,  but she tried so hard.  We had 8 MLS (syringe) down, but that is a far as it got.  She did hold down the tylenol!!  Its hard on the nurses when orders have to be written for meds to be given through her lines, and they’re not alreadywritten,  It Takes so long to get them from pharmacy,  and you try to do what will work fast, especially when they are reacting to a med.    It really gets our BP up when we have to see her do these unnecessary large dosages that cause all that deep vomiting especially when she has to have all these platelets to keep the area in the brain from bleeding. All that heavy vomiting is not a good situation plus orders for Zofran were stopped  early because they thought this may be causing  the hives, and nothing was written in its place,  and she has not been on any nausea med today  other than benedryl (which was for  pre-med precautions), not her regular nausea med., we did not know this.  She said  “Well mommy at least I held down the tylenol”. She just tries so hard.    But on a great note, this afternoon (Thursday)  Emily  made progress,  Colored in her big Scooby Coloring book,  and was more alert.  We are just sooooooo amazed by her determination and strength!   The CT scan showed only small amont of blood in the ventricles.  Platelet count looks good as of today.   OK,  GOD IS SO GOOD!  He was right by Emily’s  side the  whole time.    A neurosurgeon,  just came in to check on her surgery sites,  was  able to ask if there could be any problems with all the vomiting, and  he said her platelet counts are fine,  and that tubing  they placed in surgery  will  drain any pressure buildup.  God just sent the answers  needed to be able to  get some  sleep .  Good thing God never sleeps!  He knew we were so worried,   He sent the neurosurgeon,  in at 2:30 am , so questions could be asked.  We are so greatful  He loves us so much.  
Dawn & Eddie

No Comments

No comments yet.

RSS feed for comments on this post.

Sorry, the comment form is closed at this time.