neuroblastoma

Skip the page content navigation if you do not require links to content sections within this page.

Page Content Navigation

| Email Page | Help | | Site Map

Skip the main banner if you do not want to read it as the next section.


Page Banner


Skip the primary navigation if you do not want to read it as the next section.


Primary navigation

Skip the main content if you do not want to read it as the next section.


Main Content: neuroblastoma

 

To comment first login or register.

Forum Control Bar


Original topic post: neuroblastoma

written by: SarahBuckley
posted: 07.12.2011

message: My son aged 4 has been diagnosed with Neuroblastoma. He has a tumour in his tummy and secondaries in his bones and bone marrow. Is there anyone with experience of this disease, who would like to share their stories? He has started chemo and is on the high risk pathway, having chemo every 10 days for 80 days. We are struggloing at the mo, since he as at home, managing feeds through his NG and the enormity of it all. Just as you have a few days at home as a family he has to go back into hospital for more chemo for a couple of days. We feel we have supportive friends, but no one realy understands the process and adjustments this diagnosis has had on our lives.



CLIC Sargent is not responsible for the content of external sites.


The following page sections include static unchanging site components such as the page banner, useful links and copyright information. Return to the top of page if you want to start again.


Page Extras

End of page. You can return to the page content navigation from here.