| Joined: Sep 2011 Posts: 19 Member | OP Member Joined: Sep 2011 Posts: 19 | hi! I am new to this. My mom in bangalore, india was diagnosed with scc right side of tongue stageII/III in feb. went through surgery, removed right lymph nodes and salivary gland and then went through 71/2 weeks of radiation. It finished in june. After 2 months she started getting pain in her left side and her left ear and left side of tonsil/lymphnode started selling. Dr. said tonsil infection and gave her 2weeks of antibiotics. Nothing helped. In the night times the pain is more. she went to her oncologist. He found a small lump like thing on her left side of tongue and prescribed higher dose of antibiotics for another 2 weeks. after 2 weeks he found that lump has decreased and told her to come after 2 weeks. That was yesterday. Yesterday he said that the lump is still there, but small so he needs to do biopsy. I am so scared. As she already went through radiation on her right side and it was very hard, I am scared for her chances.
She is a nonsmoker, non-drinker, no tobacco. She is 68 years old.
Please help, anybody, please.
sincerely, swati. | | | | Joined: Jan 2009 Posts: 1,844 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Jan 2009 Posts: 1,844 | Swati,
First breath, don't let fear overcome you as that helps with nothing. We have a saying on these boards that its NOT cancer until a biopsy says it is so we have to wait for the results. Until the results come get mentally and emotionally prepared to support your mom if it is a recurrence and take every opportunity to let her know how much you care.
None of us are guaranteed our next breath so be sure to enjoy every moment without letting fear and worry steal whatever joy you have in the time you are blessed with. One step at a time, that's the only way to move forward.
Keep your chin up
Eric
Last edited by ChristineB; 09-27-2011 10:26 AM. Reason: removed info about starting post
Young Frack, SCC T4N2M0, Cisplatin,35+ rads,ND, RT Mandiblectomy w fibular free flap, facial paralysis, "He who has a "why" to live can bear with almost any "how"." -Nietzche "WARNING" PG-13 due to Sarcasm & WAY too much attitude, interact at your own risk.
| | | | Joined: Dec 2010 Posts: 5,264 Likes: 5 "OCF Canuck" Patient Advocate (old timer, 2000 posts) | "OCF Canuck" Patient Advocate (old timer, 2000 posts) Joined: Dec 2010 Posts: 5,264 Likes: 5 | Agreed, if it's still there it needs to be biopsied. Did she have a CT scan? MRI? I'm assuming so. This cancer can sometimes jump sides. They should scan her as well. I know she's been through a lot. They can still operate to remove the spot. Some of it could also be related to the radiation. There is a spray radius despite the fact that it is focused, it's not always confined to the focus area. My hair thinned out all the way up to my crown on one side. despite the fact that the radiation was aimed at my tongue and neck! Also The affects of the radiation can last a long time. I have had tender spots on my tongue on the good side all along. They get better they get worse. They are not solid lumps more like areas of irritation related to the radiation. They are easing now, and I'm almost 6 months out. Good luck - I hope it's nothing.
Cheryl : Irritation - 2004 BX: 6/2008 : Inflam. BX: 12/10, DX: 12/10 : SCC - LS tongue well dif. T2N1M0. 2/11 hemigloss + recon. : PND - 40 nodes - 39 clear. 3/11 - 5/11 IMRT 33 + cis x2, PEG 3/28/11 - 5/19/11 3 head, 2 chest scans - clear(fingers crossed) HPV-, No smoke, drink, or drugs, Vegan
| | | | Joined: May 2011 Posts: 287 Gold Member (200+ posts) | Gold Member (200+ posts) Joined: May 2011 Posts: 287 | Hi Swati, I would agree with Cheryl and Eric. My father had developed a sore on his right tongue 3 months after radiotherapy (for his left tongue) and it was bothering us. We consulted the doctor and he adviced Biopsy but I was reluctant for another biopsy and asked for PET/CT first and if required, follow up it with biopsy if something suspicious comes up. Thankfully, it came all clear. Father; 67 yrs; RIP: 2012/05/26
TX:SCC pT2N1M0G2;Glossectomy+SND+CCRT(59.3Gy+6xCis.)[2009] TX:Nodal Mets; 3xDCF[2011/05/05] TX: RND + PMMC Flap[2011/07/11] DX:SCC PNI+ECE TX:Re-RT 60Gy[2011/09/21] TX:Gefitinib 250mg[2011/12/18]
| | | | Joined: Sep 2011 Posts: 19 Member | OP Member Joined: Sep 2011 Posts: 19 | Hi!
I got the biopsy report today. They say it is cancer again. I am very scared. Does she have any chances?
Please advise.
sincerely, swati | | | | Joined: Sep 2009 Posts: 618 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Sep 2009 Posts: 618 | Swat,
I am currently starting treatment for a second time. They say I have a chance and you will find a number of people in this site who have battled this disease more than once and survived.
Given that her second occurance looks small I would think they could treat her succesfully. We will all be praying for you here and best of luck.
Remeber to take this one day at a time. there is always hope and medical science has come a long way in treatin recurrance of oral cancer so keep your chin up.
Kelly Male 48, SCC (Soft Palet) Rt., Stage 1, T3n0m0, Dx, 8-09, Start IMRT 35 9-2-09 end 10-21-09 04-20-10 NED 8-11 recurrence, node rt. neck N2b 10-11 33 IMRT w/chemo wkly 3-12-12 PET - residual cancer 4-12 5 treatments with Cyberknife & Erbitux 6-19-12 Pet scan CLEAR 12-3-12 PET - CLEAR
| | | | Joined: Sep 2011 Posts: 19 Member | OP Member Joined: Sep 2011 Posts: 19 | Hi Kelly,
Thanks. It's just that she is in India and I am in U.S. I am begging her to come here, but with no insurance, my parents don't want to come. I know I just have to keep hope, but kind of getting hopeless. the new one, it's only few cells, it seems, came after just 21/2 months of radiation. Is total tongue removal only choice
please advise, swati
| | | | Joined: Jun 2007 Posts: 10,507 Likes: 7 Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) | Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) Joined: Jun 2007 Posts: 10,507 Likes: 7 | I am very sorry to read of your mother's recurrence. Of course she still has a chance. I am not very familiar with health care options in other countries. I can only tell you that a recurrence needs to be handled quickly and with the best medical professionals. I know here in the US there are many top doctors and cancer centers where she could get treated.
I have had oral cancer 3 times and luckily gotten thru it. Do NOT give up hope. Did the doctors suggest your mother needing a total removal of her tongue? Many times with surgeries a doctor will determine things like that when he is in there and taking frozen sections to view clean margins.
Please reread what Eric wrote about letting cancer steal away your time. Stay positive!!! When people get upset its difficult to think clearly.
Best wishes to your mother! ChristineSCC 6/15/07 L chk & by L molar both Stag I, age44 2x cispltn-35 IMRT end 9/27/07 -65 lbs in 2 mo, no caregvr Clear PET 1/08 4/4/08 recur L chk Stag I surg 4/16/08 clr marg 215 HBO dives 3/09 teeth out, trismus 7/2/09 recur, Stg IV 8/24/09 trach, ND, mandiblctmy 3wks medicly inducd coma 2 mo xtended hospital stay, ICU & burn unit PICC line IV antibx 8 mo 10/4/10, 2/14/11 reconst surg OC 3x in 3 years very happy to be alive | | | | Joined: Sep 2011 Posts: 19 Member | OP Member Joined: Sep 2011 Posts: 19 | Dear all,
Thank you all so much for all the support. Right now they are going to remove her teeth as the radiation damaged the gums. The problem in India is that we can't tell the doctors anything. They do what they want. I am telling my father to get a CAt scan done, but the oncologist says it's not necessary. I have not able to sleep in nights. Can't get leave from job to see mom as I went in may/june. So feel guilty and upset all th times. Thanks to you guys, I can vent my feeling out.
Yhanks again
swati
| | | | Joined: Jun 2007 Posts: 10,507 Likes: 7 Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) | Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) Joined: Jun 2007 Posts: 10,507 Likes: 7 | There is something called FMLA which would grant you time off to care for a sick family member. You are allowed up to 12 weeks per year. The only stipulation is that you have worked a full time job and have been with the employer for at least 1 year. If you have 11 months and 29 days, you dont qualify. Thats how strict it is. So if you used FMLA in May and June for 8 weeks, you still have at least another 4 weeks left. This is a nationwide law so you really could go as they cannot deny you and must hold your job. ChristineSCC 6/15/07 L chk & by L molar both Stag I, age44 2x cispltn-35 IMRT end 9/27/07 -65 lbs in 2 mo, no caregvr Clear PET 1/08 4/4/08 recur L chk Stag I surg 4/16/08 clr marg 215 HBO dives 3/09 teeth out, trismus 7/2/09 recur, Stg IV 8/24/09 trach, ND, mandiblctmy 3wks medicly inducd coma 2 mo xtended hospital stay, ICU & burn unit PICC line IV antibx 8 mo 10/4/10, 2/14/11 reconst surg OC 3x in 3 years very happy to be alive | | |
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