#9371 03-24-2007 05:00 AM | Joined: Apr 2005 Posts: 2,219 Patient Advocate (old timer, 2000 posts) |  Patient Advocate (old timer, 2000 posts)
Joined: Apr 2005 Posts: 2,219 | Just bringing this thread back up to the top.
I want to thank everyone that has sent me a check so far. For those that haven't, the address is above in this thread and it's not too late to help support the OCF financially.
Brian needs YOUR help and if you want this website to keep going, now is the time to give. It doesn't have to be a lot. Every little bit helps. If every member gave just $10, think about how much money could be raised. Think about how much you and your loved ones receive from the OCF in the form of support, information and just having a place to vent. Money is also needed to help keep Brian traveling and fighting for funding for oral cancer research, recognition of the needs of oral cancer survivors and the need for Early Detection.
I hate to seem like a broken record, but it takes a great deal of money to keep this website and Brian running. How lost would you feel, if it wasn't here? I know I would be devastated.
Jerry
Jerry
Retired Dentist, 59 years old at diagnosis. SCC of the left lateral border of the tongue (Stage I). Partial glossectomy and 30 nodes removed, 4/6/05. Nodes all clear. No chemo no radiation 18 year survivor.
"Whatever doesn't kill me, makes me stronger"
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#9372 03-28-2007 04:53 AM | Joined: Dec 2006 Posts: 32 Contributing Member (25+ posts) | | Contributing Member (25+ posts)
Joined: Dec 2006 Posts: 32 | I'm new to this site. My husband was treated for SCC 2 yrs. ago. Had chemo, radiation (6 wks.) & surgery. So far so good. He goes for scans every 3 months but now it will be every 6 months. Unfortunately, he was just diagnosed with an acoustic neuroma (4mm) as he was having hearing problems. We are thankful that it was found while it is still small and we have time to consider options.
I am reading about the walk in Chicago and wonder when and where it will be held. We are from Schaumbug, IL.
Thanks for all the info here.
Linda K. (husband Ken)
Dx 06/2004 - SCC of left tonsil - resection of growth on neck, 6 weeks IMRT, 4 treatments chemo (Cisplatin). | | |
#9373 03-28-2007 09:12 AM | Joined: Jan 2004 Posts: 1,116 Patient Advocate (1000+ posts) | | Patient Advocate (1000+ posts)
Joined: Jan 2004 Posts: 1,116 | Hi Jerry, please PM or email me with your address so I can send you a check...Thanks, Carol
p.s. Thanks so much for participating!
Diagnosed May 2002 with Stage IV tongue cancer, two lymph nodes positive. Surgery to remove 1/2 tongue, neck dissection, 35 radiation treatments. 11/2007, diagnosed with cancer of soft palate, surgery 12/14/07, jaw split. 3/24/10, cancer on tongue behind flap, need petscan, surgery scheduled 4/16/10
---update passed away 8-27-11---
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#9374 03-28-2007 04:14 PM | Joined: Apr 2005 Posts: 2,219 Patient Advocate (old timer, 2000 posts) | | Patient Advocate (old timer, 2000 posts)
Joined: Apr 2005 Posts: 2,219 | Hi Linda,
Sorry to hear about Ken's new problem. I wish him and you as much success as you have had with the scc.
The June walk in Chicago has been postponed until September. It is not definite yet, but it was not going to work out for June. Keep checking back to see what is happening.
Carol, I sent you an email with my address and thanks for sponsoring me again this year.
Jerry
Jerry
Retired Dentist, 59 years old at diagnosis. SCC of the left lateral border of the tongue (Stage I). Partial glossectomy and 30 nodes removed, 4/6/05. Nodes all clear. No chemo no radiation 18 year survivor.
"Whatever doesn't kill me, makes me stronger"
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#9375 04-06-2007 05:19 PM | Joined: Oct 2006 Posts: 209 Gold Member (200+ posts) | | Gold Member (200+ posts)
Joined: Oct 2006 Posts: 209 | Dr Jerry Wilck has just announced his 2 year anniversary for being cancer clear in the Survivor Forum! What better way to celebrate with him and honor him as well, then to contribute to his 2nd annual New York Oral Cancer Awareness Walk which is being held this Saturday 04/14/07? It's not too late! 7 days to go! There are no minimums, anything you can send will help. Let's get a big push for his grand send- off and make him proud of all he has done for us! Send to: The Oral Cancer Foundation C/O Dr. Jerold B. Wilck KWH Dental Assoc. Suite 201 680 Middletown Blvd. Langhorne, PA 19047 or Make a donation on line on this site, just put in the notes or PO section of the donation that its for Jerry's New York walk.
Ginny, spouse of MikeG. SSC BOT T2N1M0 Stage III, Dx 06/27/06 at age 52, Tx 07/31/06 through 09/28/06 Chemo Cisplatin & 5FU x2, Radiation x42. Cancer free and doing well.
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#9376 04-07-2007 01:31 AM | Joined: Jan 2004 Posts: 1,116 Patient Advocate (1000+ posts) | | Patient Advocate (1000+ posts)
Joined: Jan 2004 Posts: 1,116 | Mike that is a wonderful idea!!!! Thanks for bring it to our attention!!!!!Carol
Diagnosed May 2002 with Stage IV tongue cancer, two lymph nodes positive. Surgery to remove 1/2 tongue, neck dissection, 35 radiation treatments. 11/2007, diagnosed with cancer of soft palate, surgery 12/14/07, jaw split. 3/24/10, cancer on tongue behind flap, need petscan, surgery scheduled 4/16/10
---update passed away 8-27-11---
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#9377 04-07-2007 01:21 PM | Joined: Mar 2002 Posts: 4,916 Likes: 63 OCF Founder Patient Advocate (old timer, 2000 posts) | | OCF Founder Patient Advocate (old timer, 2000 posts)
Joined: Mar 2002 Posts: 4,916 Likes: 63 | If you go to the webstore there actually is a link to NYU stuff. You can make a donation there vs the regular donation section and it will be earmarked as NYU. (It is a bit less flexible than the regular donation section which works in increments of 5 dollars.) Then as Mike said put in the comments block Jerry's name.
Brian, stage 4 oral cancer survivor. OCF Founder and Director. The first responsibility of a leader is to define reality. The last is to say thank you. In between, the leader is a servant.
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