#37313 05-02-2004 04:23 PM | Joined: Apr 2004 Posts: 3 Member | OP Member Joined: Apr 2004 Posts: 3 | I had a partial glossectomy & lymph node removal in December. I really have no problems with my speech, but I was wondering if the chemo & radiation treatments (which I start tomorrow) will affect my speech any?
Partial gossectomy & lymph node removal 12-03, Oropharynx, Stage IV
| | |
#37314 05-02-2004 05:33 PM | Joined: Mar 2002 Posts: 1,140 Likes: 1 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Mar 2002 Posts: 1,140 Likes: 1 | I would guess that any change in your speech will be only temporary due to sores in your mouth caused by the radiation. At the end of my rad/chemo, just when I was ready to celebrate, I lost my voice, which happens to some people, and was reduced to a very soft whisper for about two weeks. There are many posts here on how to survive the rigors of radiation, and you can ask questions as you go along. Here is one tip. Before I lost my sense of taste all together, the chemo gave me an annoying metallic taste in my mouth which I found was relieved by sucking on honey lemon cough drops. Radiation is no picnic, but you can get through it. I am convinced that while I had great surgeons, it was the rad that saved my life and I would do it again in a minute. Keep that thought in mind and it may help you, as it did me. And let us know how you are faring. There are lots of us here to help you. | | |
#37315 05-03-2004 03:40 AM | Joined: Mar 2004 Posts: 164 Gold Member (100+ posts) | Gold Member (100+ posts) Joined: Mar 2004 Posts: 164 | I had a near total glossectomy in November and radiation didn't affect my speech just my swallowing. Just curious, why so long between surgery and radiation/chemo?
Lynn
Stage 3, N0, M0 oral tongue cancer survivor, 85-90% of tongue removed, neck disection, left tonsil removed, chemo/radiation treatments, surgery 11/03, raditation ended 1/04, lung mets discovered 4/04,
| | |
#37316 05-03-2004 12:20 PM | Joined: Apr 2004 Posts: 3 Member | OP Member Joined: Apr 2004 Posts: 3 | After my surgery, everything (all margins) came back negative. I felt fine for almost 3 months, then noticed a small lump on my jaw, which was biopsied & came back positive. That's when the ENT recommended radiation & chemo to treat the recurrence. After my first day, I feel OK so far. I am wearing a chemo pump to infuse my 5FU over the next 4 days and getting Cisplatin daily. Guess in hind site, I should have done radiation right after surgery....
Partial gossectomy & lymph node removal 12-03, Oropharynx, Stage IV
| | |
#37317 05-03-2004 01:39 PM | 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 | We always joked that we knew what the FU stood for but only because of the nasty reactions I had. I hope your experience is much better than mind. Best wishes for a tolerable treatment and fast recovery!
Ed
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
| | |
#37318 05-04-2004 10:26 AM | Joined: Oct 2016 Posts: 284 Gold Member (200+ posts) | Gold Member (200+ posts) Joined: Oct 2016 Posts: 284 | My mom lost her voice after the third week of radiation and then it came back about two weeks after she finished radiation. Her speech actually sounds better now than it did before she got the radiation.
You can't let the what you should have dones get you down. My moms experience was very similar. Her ENT's theory is save radiation for a recurrance I guess because going through radiation is very tough. Now eight weeks after radiation she is feeling more and more like her old self everyday.
Danielle
Originally joined OCF on 12/12/03 as DaniO or Danijams Dani-Mom SCC BOT & floor of mouth surgery-recur then surgery/rads & chemo completed 3/04 surgery 11/06 to remove dead bone & replace jaw w/ leg bone & titanium plate
| | |
#37319 05-04-2004 02:20 PM | 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 | For what it's worth, my doctor told me that in the last five years he has changed his view from neck dissection, radiation/chemo always to radiation/chemo first, neck dissection as a last resort for recurrence. He mentioned to me that he would give me everything he could the first round and go for the cure. He then told me if it comes back there is nothing to do but a neck dissection and would most likely only remove the discomfort.
Ed
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
| | |
#37320 05-04-2004 04:19 PM | Joined: Nov 2002 Posts: 541 "Above & Beyond" Member (500+ posts) | "Above & Beyond" Member (500+ posts) Joined: Nov 2002 Posts: 541 | My oncologist also holds similar belief as Ed's doctor. I had full dose of radiation/chemo to ensure a complete cure. If there is a recurrence, surgery is the only resort. When I further asked him if surgery can really do the job if cancer recurs in my case, he just stopped me by saying don't worry about things that may not happen. The team of doctors will deal with it and take care of me. So I learn not to think much about my illness these days.
Karen.
Karen stage 4B (T3N3M0)tonsil cancer diagnosed in 9/2001.Concurrent chemo-radiation treatment ( XRT x 48 /Cisplatin x 4) ended in 12/01. Have been in remission ever since.
| | |
#37321 05-05-2004 12:41 AM | Joined: Mar 2004 Posts: 164 Gold Member (100+ posts) | Gold Member (100+ posts) Joined: Mar 2004 Posts: 164 | I hope your treatment is going well. I hope that the 5FU doesn't get you down. I had a reoccurance 5 months after my initial cancer was discovered. The first cancer was so small they passed on radiation too. I just keep looking forward instead of backward.
God Bless! Lynn
Stage 3, N0, M0 oral tongue cancer survivor, 85-90% of tongue removed, neck disection, left tonsil removed, chemo/radiation treatments, surgery 11/03, raditation ended 1/04, lung mets discovered 4/04,
| | |
#37322 05-06-2004 03:46 PM | Joined: Jul 2003 Posts: 1,163 Patient Advocate (1000+ posts) | Patient Advocate (1000+ posts) Joined: Jul 2003 Posts: 1,163 | Hello Texas Teacher,
I had surgery followed by IMRT radiation. I had no side effects from the radiation. I was lucky in that regard. I had no Chemo. What type of radiation are you having?
My speech was messed up from my surgery. I can speak but It's diffucult to get out certin letters. D's, and B's are the worst for me. Wouldn't you know my name is Dan Bogan. In sales I do better in person than on the phone.
I wish you the best of luck as you continue your treatment. Remember one thing "It will get better"
Dan
Daniel Bogan DX 7/16/03 Right tonsil,SCC T4NOMO. right side neck disection, IMRT Radiation x 33.
Recurrance in June 05 in right tonsil area. Now receiving palliative chemo (Erbitux) starting 3/9/06
Our good friend and loved member of the forum has passed away RIP Dannyboy 7-16-2006
| | |
Forums23 Topics18,246 Posts197,130 Members13,317 | Most Online1,788 Jan 23rd, 2025 | | | |