Jump to content
Forums are under active construction. ×

Neuroblastoma Childhood Cancer please read.


Guest nachomuncher

Recommended Posts

Guest nachomuncher

:kane Hi everyone just wanted to say some of you may be aware that my daughter Briony 3yrs old was mentioned in a discussion a while back i think it was one entitled the worst thing you heard today or something like that. I have to confess i dont use this site much these days cause im way too busy so i hope this wont sound cheeky.(here goes)

 

Briony lost her fight aged just 3years 3months and 3 days on the 19th march this year she thought a disease that only affects around 100 children in the U.K. each year so its vry rare the survival rate is very low. If a child is cleared of the disease it can still come back within 5 years and sadly there is no cure once it returns then it can be treated but not cured.

 

Im asking for anyone who can help please go to http://www.nsoc.co.uk and when i say help i dont mean putting there hands in there pockets i want more and more people to be aware of this disease I live in barnsley South Yorkshire and my daughter was treated first at leeds general infirmary then moved to jimmy`s before we moved to Sheffield Childrens Hospital and in the last two years me and my wife have known (not including Briony) 4 cases of this horrid disease and two have now passed on one thankfully was caught really early and is cleared but still needs regular checkups scans and x-rays and the other child is in junior years around six or seven and its come back and like i said before it can be treated but as yet not cured. So please all i am asking if possible please visit http://www.nsoc.co.uk for more info on the disease and lets all try and raise more awareness for a disease thats so rare its almost forgotten about. :kane

Link to comment
Share on other sites


Guest FreeSpirit

I am extremely sorry to hear you lost your daughter through this terrible disease. nachomuncher, it must have been an extremely traumatic experience for you and your family, and my thoughts are with you.

 

I will be gladly read through the website in the hope it makes me more aware of neuroblastoma.

Link to comment
Share on other sites

Guest Nemesis Enforcer
Very sorry to here this Nachomuncher, my best wishes go out to you and your family and I hope that this thread raises awareness of the plight of children and their families suffering from this terrible disease
Link to comment
Share on other sites

Guest nachomuncher
:kane From myself and my wife and two sons thanks so far to all of you who have sent there regards/condolences and well wishes and to all those who read this in the future thanks. :kane
Link to comment
Share on other sites

Guest nachomuncher
My friend Tom died from Neuroblastoma in 2003, had the disease since he was little.
:kaneMy friend im sorry to hear that you out of most people must know now the pain and hurt this disease does to familys im certainly not a religious man but nor do i make fun or snub anyone who is but i do believe no one really leaves us. take care dude. :kane
Link to comment
Share on other sites

Can't even begin to understand how you're feeling now, as a father myself.

 

Sorry doesn't cut it, but I am sorry to hear that :(

Link to comment
Share on other sites

Guest MojoPogo
Sincerest sympathies to you and yours mate, i cant pretend that i understand what you must be feeling, but i can empathise. We're here for you if you need us.
Link to comment
Share on other sites

I can't even begin to imagine the pain you and your family have gone through and are still going through. Sending much love to you all.

 

I have heard a bit about this type of cancer but I will encourage others to have a look at the site.

Link to comment
Share on other sites

Guest Kanenite
I'm really sorry for your loss. People have already said but it really is unimaginable to experience what you must be feeling. My thoughts are with you and your family.
Link to comment
Share on other sites

  • 2 weeks later...
Guest nachomuncher
:kane To all of you out there who sent thoughts to me and my family i thank you all so much and hope that some day there will be a cure for this disease thats taking the lives of innoccent little children some may notice my new avater just thought folks would like to see my precious little angel. Always smiling. Again thanks to you all for your kind words and keeping me strong/sane. :kane
Link to comment
Share on other sites

Guest Al Stevens
I am so sorry to hear of the tragic lose you and your family have suffered Nachomuncher (I would have replied alot sooner, however there some family problems going on right now). I just want to extend something in a way of words to try and help heal the pain you and your family is going through this rough time of your life.
Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Unfortunately, your content contains terms that we do not allow. Please edit your content to remove the highlighted words below.
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.



  • Active Fan Clubs

×
×
  • Create New...