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#41885 10-04-2007 07:57 PM
Joined: Feb 2007
Posts: 1,940
"OCF across the pond"
Patient Advocate (1000+ posts)
"OCF across the pond"
Patient Advocate (1000+ posts)

Joined: Feb 2007
Posts: 1,940
Thought you might like to read the latest update from the Mouth cancer foundation regarding their battle with the NHS over new treatment funding.

MEDIA ALERT


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
#41886 10-04-2007 11:45 PM
Joined: Nov 2002
Posts: 3,552
Patient Advocate (old timer, 2000 posts)
Patient Advocate (old timer, 2000 posts)

Joined: Nov 2002
Posts: 3,552
It's the same thing as Erbitux. We have had many discussions about it. There are still some clinical trials going on about its efficacy for OC and some here have gotten it as part of their protocol.

http://www.oralcancerfoundation.org/searchresults.htm?cx=015422755131303034108%3Ao3fylifwmag&cof=FORID%3A11&q=Erbitux


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
#41887 10-05-2007 01:10 AM
Joined: Apr 2007
Posts: 794
"Above & Beyond" Member (500+ posts)
"Above & Beyond" Member (500+ posts)

Joined: Apr 2007
Posts: 794
My mom just completed her tx's of imrt and Erbitux, following with brachytherapy. They believe she is now cancer free.


Donna
CG to Mom, dx 4/25/07 with tongue cancer,T3N0,tx began 7/6/07, 31 tx's of IMRT, 8 cycles of Erbitux. Brachytherapy, surgery, left neck dissection and temp trach placed all on 9/17/07, trach removed 10/17/07. ORN of jaw, late effect of radiation symptoms. **lost my beautiful mother on 5/5/11.
#41888 10-05-2007 07:25 AM
Joined: Feb 2007
Posts: 1,940
"OCF across the pond"
Patient Advocate (1000+ posts)
"OCF across the pond"
Patient Advocate (1000+ posts)

Joined: Feb 2007
Posts: 1,940
I realise it is Erbitux Gary but the point is it is not available to patients in this country on the NHS and the Mouth Cancer foundation have been lobbying for it to be funded over here.This is a major breakthrough for us and even though it is not proven it is another chance of hope for some.


Liz in the UK

Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007
Recurrence June/07 died July 29th/07.

Never take your eye off the ball, it may just smack you in the mouth.
#41889 10-05-2007 09:42 AM
Joined: Sep 2003
Posts: 1,244
Patient Advocate (1000+ posts)
Patient Advocate (1000+ posts)

Joined: Sep 2003
Posts: 1,244
I wonder if the people on the panel making decisions for NICE have families?
If they do they all must be healthy or we not have to fight for acess to all the banned treatments.
Sunshine.. love and hugs
Helen


SCC Base of tongue, (TISN0M0) laser surgery, 10/01 and 05/03 no clear margins. Radial free flap graft to tonsil pillar, partial glossectomy, left neck dissection 08/04
#41890 10-06-2007 02:26 PM
Joined: Nov 2002
Posts: 3,552
Patient Advocate (old timer, 2000 posts)
Patient Advocate (old timer, 2000 posts)

Joined: Nov 2002
Posts: 3,552
Amen to that Liz! It has proven effective for colorectal cancer so we will have to wait and see.


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)

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