Brian Robert & LCH: PRAISE!!!!

Thursday, June 7, 2012

PRAISE!!!!

We want to thank everyone for praying for our family, especially little Brian Robert.

We got a call today that the sensitivities came back and Brian's drugs are being changed. He will no longer have an infusion of Vancomycin every eight hours but will have Rocephin every 12 hours. He will be finished on Sunday and we were told that he is able to leave for his Make a Wish trip on Monday. WE ARE THRILLED.

Thank you for your continued prayers. Please pray that the infection is completely gone from the port and that Brian will not have to have it removed. We will probably know the answer to this in a few weeks when he goes back in for his next chemo week. Or if he gets a fever between now and then.

We are assuming this is a different bacteria b/c the infection we were dealing with four weeks ago was resistant to Rocephin. This bacteria requires Rocephin. This makes us hesitant to leave Brian accessed for the entire week of chemo. Brian had been on treatment for two and a half years and has never had an infection in his port. The two weeks that we have left him accessed for the entire week, he has gotten infections in his port. We are a bit concerned.

1 comment:

nancygrayce said...: Wonderful news! Have a great time!; June 7, 2012 at 10:28 AM

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Brian, BB or "B-ber"

Brian is our seven year old boy. He is the third of four children, all born in just four years. Sept 2009 Brian was diagnosed with Langerhans Cell Histiocytosis. He spent seven months on Chemo and steriods. In April 2010 we had his port removed and celebrated "no more chemo!". His treatment from May forward was oral medicine on the weekends and scans/bloodwork every three months. Brian's firt set of scans/follow up with the oncologist in July were wonderful. We didn't quite make it to his second set of scans three months later in October. In late July/ early August we started noticing suspicious bumps on his scalp and a rash on his private area. On Sept 15, 2010 we took Brian to his oncologist. That appointment revealed the possibilty of more chemo. September 21 we had a biopsy that two days later revealed that Brian's LCH was back. We immediately had surgery to implant a port and in Oct 2010 started a second journey through chemotherapy and steroids for our little Brian. In March 2011 Brian's chemo drugs were changed around as his new protocal was not working. Brian was still presenting symptoms. We went back to the original combination of drugs but this time instead of being on them six months the plan was for twelve months. Brian completed his second round of chemo March 8, 2012. Even though Brian was completing treatment, we started noticing symptoms of Diabetes Insipidus in March 2012. He was diagnosed with D.I. March 22, 2012. His new diagnosis was considered a relapse for his LCH. Brian's third round (or fourth protocol depending on how you look at it) of chemo and a totally different protocol began April 2012. He had chemo five days in a row followed by a three week break for 12 months. He completed that protocol the first week of April 2013. In July of 2013 Brian had his port removed and we were over the moon excited about NO MORE CHEMO. In October of 2013 Brian had a recurrence of symptoms. He took six months of oral chemo. In April of 2014 he had another MRI. It was decided that Brian could stop treatment. By August-September 2014 he started showing symptoms again. October 2014 we are back in Houston to see what the next step will be for treatment of Brian's LCH.