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#41137     05-07-2007 09:25 AM      |       Joined:  Mar 2007  Posts: 179    Gold Member (100+ posts)   |           Gold Member (100+ posts)    Joined:  Mar 2007  Posts: 179  |    hi, dn't know if this is the correct  spot to post this but....  My husband just finished with 3 rounds of cysplatin Chemo, and 37 rad. he has head and neck cancer(nasal pharynx) sp. not the greatest.  This has been a long and brutal journey. with 11 out of 20 lymph nodes.  He is given a 4 week break now.  His dr. wants him to go on a chemo pump for 96 hrs. 1 week for the next 3 months.  He is very upset about this and wants to know if it makes a difference.  Has anyone done this?  thanks caregiver to Tom.        
CG to husband 53,39 rads. 3 rds cisplastin ended 6/2/07 Tonsils removed 1.10.07 11 of 20 nodes positive- lump removed on rt. side of neck 1/26/07 cancer of  nasal pharnyx TXN2MX  2nd rd. of chemo- carbo/taxol on 6/11/07
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#41138     05-07-2007 02:03 PM      |       Joined:  Mar 2007  Posts: 525    "Above & Beyond" Member (300+ posts)   |           "Above & Beyond" Member (300+ posts)    Joined:  Mar 2007  Posts: 525  |    Hello Ladyjoe Welcome to the Oral Cancer Foundation Forum. I can not answer that question but many here can and will. You have come to the right place. Most "newcomers" post in the wrong place the first time. It is no biggy. Go to the "forum home" page, select the "Introduce yourself" forum and put this information there. Also, read the faq at the top of the page. This will help you get familiar with navigating & using this site. Also, go to the "General Board" forum and open it. Scroll down to the topic "How to Get The Most Out Of This Forum". Open and read it for more "tips". We just were discussing how a newcomer has to learn on their own. We are trying to make it easier. Before you introduce yourself I suggest you do this: At the top of the page click on "my profile". Then click "edit profile". Scroll down to the signature box and type in your DX, Tx.(just like you wrote in this post) This will appear at the bottom of every post you make or respond to. See mine at the bottom of this post. You can change it anytime. It is not required but it saves you from explaining yourself every time you post. Sorry for the "letter" without an answer. Looking forward to your company on the forum. Good Luck! Petey       PS: GO STEELERS! Don't mind me, I'm just another confused DOLFAN???            
DX 3-21-07 L tongue,SCC Stage IV (T3N2MO) TX Slash/Burn/Poison Method. ***Rapid Aggressive Recurrence 8-4-07 with same DX/TX. Life does not cease to be funny when people die any more than it ceases to be serious when people laugh. Never Give Up!   ****UPDATE**** Our dear friend Petey passed away, RIP 9-2-07
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#41139     05-08-2007 07:50 AM      |       Joined:  Mar 2007  Posts: 179    Gold Member (100+ posts)   |           Gold Member (100+ posts)    Joined:  Mar 2007  Posts: 179  |        
CG to husband 53,39 rads. 3 rds cisplastin ended 6/2/07 Tonsils removed 1.10.07 11 of 20 nodes positive- lump removed on rt. side of neck 1/26/07 cancer of  nasal pharnyx TXN2MX  2nd rd. of chemo- carbo/taxol on 6/11/07
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