| Joined: Jan 2011 Posts: 168 Senior Member (100+ posts) | OP Senior Member (100+ posts) Joined: Jan 2011 Posts: 168 | I am wondering something, wondering if I am alone in this, but I have to admit that Michael Douglas coming out the way he did with the HPV connection has been unsettling for me. Since my DX and TX two years ago, I have often spoken about my cancer by relating it to what Michael Douglas had. He never went public with the HPV connection (until now), and, frankly, except for some close friends, I have not either. I am not a prude, but I have felt uncomfortable "coming out" as HPV+, as if I somehow brought this cancer on myself. I know, I know, it's silly on an intellectual level. And I tell myself all the time that millions of people walk around with the virus but few will develop cancer and that an HPV+ tumor responds better to treatment, etc. etc. Intellectually, I am good, but emotionally... I get stopped in my tracks. I struggle with it, I do. And now I feel like Michael blew my cover, sort to speak. Is it just me? Can anyone relate? Can I get a witness? LOL
SCC left tonsil, stage IV, HPV+, metastatic to one lymph node. Biopsy 12/23/10; tonsillectomy 1/13/11; DX 1/25/11; Peg in 1/28/11. Peg out 6/29. TX 1/31/11-3/21/11: 35 IMRT plus 3 Cisplatin. Pet-Scan 6/20/11 = CLEAR! Three years out, learning to live with the long-term side effects of radiation while reminding myself to feel blessed.
| | | | Joined: Jul 2012 Posts: 3,267 Likes: 4 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Jul 2012 Posts: 3,267 Likes: 4 | I hear ya, Michelle. Not difficult for them to put two and two together. I never experienced any bad feedback, but my social life is near 0 now. Many who knew me from the gym, work, know better to be insultive to me, and know I would not not take it lightly, in my past life lol, but I'm still no Charlie Brown to be picked on. I don't care what others think, and who are they to judge, and where were they the past 3.5 years when I needed help, and basically went through treatments, testing, dr visits, biopsy, consultations by myself, not even family, and could they do the treatments we went through, without crying, I doubt it, and you have the strength to stand up for yourself. Btw, I was never tested for HPV, but it's more likely it was. I think someone may have posted what to say to family, co-workers, friends, acquaintances, strangers, if you want to. Not all need to know everything, and info and be on a need to know basis, limited to what your comfortable with. Everyone knew at work since I was hospitalized for 6 months, many came to see me, and about 50 made a contribution to give me, and sent cards. That was three years ago, and still some are asking closer work friends how I'm doing, even yesterday. I miss work. Many cancer patients, have guilt, they may even say they deserved it from bad actions in life, and it's karma, and activities that may have caused it like drinking, smoking, intimate relations. I guess it's like any loss, first its shock, denial, blame or guilt, and acceptance that you go through. Cancer is a life altering event. Good topic. | | | | Joined: Nov 2009 Posts: 493 Platinum Member (300+ posts) | Platinum Member (300+ posts) Joined: Nov 2009 Posts: 493 | Michelle, I was negative for HPV and I never smoked. I was a light social drinker, but that was it. I sometimes feel guilty that I must have done something to bring on this horrible disease. I guess my feelings about MD are that at least he is getting people to talk about it and that's not so bad. I understand your feelings, but does it really matter how you got it? Years ago, in my grandmother's generation, any cancer was considered something to hide under the rug, and obviously that has changed. I also remember some of the comments Betty Ford got when she had breast cancer. Before that, nobody really talked about breast cancer publicly. I saw my ENT this week and he reiterated what OCF has been saying for a long time. HPV is the fastest growing cause of oral cancer, particularly in younger people.
Female, nonsmoker, 70, diag. 5/09 after tongue biopsy: stage IV. Left hemi-gloss. and left selec. neck disec. 30 lymph nodes removed May 20. Over 7 weeks daily rads. with three chemo. PEG removed 12/4/09 Am eating mostly soft foods. Back to work 11/09 Retired 4/1/11. 7 clear scans! Port out 9/11. 2/13. It's back: base of tongue, very invasive surgery involving lifestyle changes. 2/14: Now speaking w/Passey-Muir valve. Considering a swallow study. Grateful to be alive.
| | | | Joined: Jul 2011 Posts: 945 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Jul 2011 Posts: 945 | I didn't share the source of my husband's cancer ... unless someone asked directly "where could it have come from?". There I would answer truthfully, and would get one of three reactions: shock, scorn or relief (this, from my medical friends). Then I would go into the vaccine spiel. I have a LOT of sympathy for MD and his wife on this: I am not in the spotlight, and they are.
CG to husband - SCC Tonsil T1N2M0 HPV+ Never Smoker First symptoms 7/2010, DX 12/2010 TX 40 IRMT (1.8 gy) + 10 Cetuximab PET Scans 6/2011 + 3/2012 clear, 5 year physical exam clear; chest CT's clear of cancer. On thyroid pills. Life is good.
| | | | Joined: Mar 2002 Posts: 4,918 Likes: 65 OCF Founder Patient Advocate (old timer, 2000 posts) | OCF Founder Patient Advocate (old timer, 2000 posts) Joined: Mar 2002 Posts: 4,918 Likes: 65 | Just remember that the CDC says that almost every American that is sexually active will have and HPV infection at some point in their lives. So it's a big club. Most people who get the infection since it has no obvious signs, will never know they had it and cleared it. It is the most common sexually transferred infection there is. Anyone that gives you crap should know that they too likely belong to the HPV club, their just got cleared by an immune system that recognized it, and they compose 99% of those ever infected. 1% end up with this bad luck of the gene pool draw.
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. | | | | Joined: Oct 2008 Posts: 247 Likes: 1 Gold Member (200+ posts) | Gold Member (200+ posts) Joined: Oct 2008 Posts: 247 Likes: 1 | Michelle, You are not alone. You have a witness. I also find this MD fascination unsettling. Although a good thing for oral cancer awareness, on a personal level it is uncomfortable. I feel that we are now singled out and thought of as perhaps promiscuous. I have been honest about the oral cancer/ HPV+ link, depending on who asked me about causation. Actually, my husband's tumor was not tested, but it certainly fits the profile. I guess that talking about it honestly on my own terms is different than being talked about....
CG to husband, dx @ age 65, nonsmoker/social drinker. Dx 5/08 SCC Stage IV, BOT T1N2aM0. 33 IMRT - completed 9/12/08. Induction Chemo (Cisplatin, Taxotere & 5FU), plus concurrent Cisplatin. 1/09 PEG removed; 5/09 neg PET/CT; 5/10 PET/CT NED Dental extraction & HBOT 2013; ORN 2014; Debridement/Tissue Transfer & HBOT 2016
| | | | Joined: Oct 2012 Posts: 1,275 Likes: 7 Assistant Admin Patient Advocate (1000+ posts) | Assistant Admin Patient Advocate (1000+ posts) Joined: Oct 2012 Posts: 1,275 Likes: 7 | I just think it is odd that it is okay for one to admit to smoking and drinking but not oral sex.
Gloria She stood in the storm, and when the wind did not blow her way, she adjusted her sails... Elizabeth Edwards
Wife to John,dx 10/2012, BOT, HPV+, T3N2MO, RAD 70 gy,Cisplatinx2 , PEG in Dec 6, 2012, dx dvt in both legs after second chemo session, Apr 03/13 NED, July 2013 met to lungs, Phase 1 immunotherapy trial Jan 18/14 to July/14. Taxol/carboplatin July/14. Esophagus re-opened Oct 14. PEG out April 8, 2015. Phase 2 trial of Selinexor April to July 2015. At peace Jan 15, 2016. | | | | Joined: Mar 2013 Posts: 421 Likes: 1 Platinum Member (300+ posts) | Platinum Member (300+ posts) Joined: Mar 2013 Posts: 421 Likes: 1 | Hi Michelle, There's a stigma attached to HPV much the same as HSV type 1 and 2. People are just funny about it. Having had HSV most of my adult life, I was surprised when they didn't find HPV initially. However, they found it with the 2nd set of biopsies and removal of the cancerous lymph nodes. I was a smoker and drinker most of my adult life as well so it was kind of a double whammy in me getting SCC H&N. I was never so relieved to have been exposed to another STD at some point in my life  It doesn't phase me in the least as 90% of the population has been exposed or has HPV or HSV 1 or 2 or a combination of two or all. I find it amusing when someone poo poos me for telling them that cold sore is herpes
57 Cardiac bypass 11/07 Cardiac stents 10/2012 Dx'd 11/30/2012 Tx N2b MO Stage IV HPV+ Palatine Tonsillectomy/Biopsies 12-21-12 Selective Neck Dissection/Lingual Tonsillectomy/biopsies TORS 2/7/13 Emergency Surgery/Bleeding 2/18/13 3/13/2013 30rads/6chemo Finished Tx 4/24/13 NED Since
| | | | Joined: May 2013 Posts: 42 Contributing Member (25+ posts) | Contributing Member (25+ posts) Joined: May 2013 Posts: 42 | [quote=Brian Hill]Just remember that the CDC says that almost every American that is sexually active will have and HPV infection at some point in their lives. So it's a big club. Most people who get the infection since it has no obvious signs, will never know they had it and cleared it. It is the most common sexually transferred infection there is. Anyone that gives you crap should know that they too likely belong to the HPV club, their just got cleared by an immune system that recognized it, and they compose 99% of those ever infected. 1% end up with this bad luck of the gene pool draw.[/quote] And this is exactly why the whole MD thing bothers me too... There are also so many unknowns to this virus as well . Wished he would have reflected more on his recent performance... He had a great opportunity, I feel he blew it. Guess its up to the rest of us to clarify, support and educate!
Colleen Wife/advocate for husband. 52 yo nonsmoker ISSC tonsil stage IVa. HPV + Enlarged node & tonsil, CT 2/13 Bx lt tonsil 3/8, PET 3/16 Tx started 4/9/2013 Cisplatin x3 and IMRT x 7 wk Tx end 5/29 GT 5/24-7/17 Officially in Recovery Phase! : ) CT scan 8/13-NED ! CT scan 7/14-NED 5/2018- 5 year anniversary -NED
| | | | Joined: Dec 2003 Posts: 2,606 Likes: 2 Patient Advocate (old timer, 2000 posts) | Patient Advocate (old timer, 2000 posts) Joined: Dec 2003 Posts: 2,606 Likes: 2 | MD opened the door for discussion but we all have to generate the discussion locally first, in my opinion.
SCC Stage IV, BOT, T2N2bM0 Cisplatin/5FU x 3, 40 days radiation Diagnosis 07/21/03 tx completed 10/08/03 Post Radiation Lower Motor Neuron Syndrome 3/08. Cervical Spinal Stenosis 01/11 Cervical Myelitis 09/12 Thoracic Paraplegia 10/12 Dysautonomia 11/12 Hospice care 09/12-01/13. COPD 01/14 Intermittent CHF 6/15 Feeding tube NPO 03/16 VFI 12/2016 ORN 12/2017 Cardiac Event 06/2018 Bilateral VFI 01/2021 Thoracotomy Bilobectomy 01/2022 Bilateral VFI 05/2022 Total Laryngectomy 01/2023
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