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Posted
Hi doc

As the fount of all knowledge I really can spell you know I was a lecturer until this is it right that some lesions even if malignant still don tgrow' and reading your stories where one fellow had a lump under his tongue and was given radio but not surgery he seemed to be far better than people who have had surgery I dont want peoples personal details as I realise they are confidential but why that treatment and not surgery and will you please tell me if you can I know its rare but how long does a slow growing mucoid epidermoid in minor glands take to develop assuming person is in good hea;th I realise its like asking how long is piece of string but only want educated guest and you people up there seem to have or k=make a lotof time for your patients
 
Posts: 118 | Location: Caerphilly | Registered: 08 March 2003Reply With QuoteReport This Post
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Hello Eileen (isn't that a line from a song? Dexys Midnight etc.).

I think you're being just a little unfair dumping questions like that on Vinod.

In my very, indeed extremely, limited view of things I would have thought that each individuals response to such an invasive disease varies wildly.

Whilst you, yourself, may well think you're in the prime of health it may well be that there are things which, given the right set of circumstances, may prove you wrong.

There are, I'm sure, so many factors affecting the progress, or otherwise, of any disease that any satisfactory reply can only be a guess.

Listen to your body, and as with a doctor, view the result with scepictism (surely that spellings wrong).

However I await more knowledgeable replies.
 
Posts: 252 | Location: halifax | Registered: 23 May 2003Reply With QuoteReport This Post
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Hi

Cum cum. Its not beyond the wit of a doct like ours who sees loads of cases every year to make an eductated guess i only want to know couldit be 1 year or 6 years I will tell you the time scale in PM
 
Posts: 118 | Location: Caerphilly | Registered: 08 March 2003Reply With QuoteReport This Post
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Hi Blitz

Just kidding about the spelling. Hope no offence is taken. Me - I can only type with one finger! So it takes me a while to type a reply Big Grin .

I am not an expert on salivary gland tumours, I deal with the oral care, pre- & post-treatment, of my head and neck cancer patients. Through the RDOC website, I try to make it easy for patients to access information on mouth cancers. See Introduction and Background.

Mucoepidermoid carcinoma is the most common malignant minor salivary gland tumor representing 38% of malignant neoplasms. Mucoepidermoid carcinomas occur most commonly in the palate and can be divided into 3 grades: low, intermediate, and high. The clinical presentation and course of mucoepidermoid carcinoma correlates with the grade of the lesion. Low grade and intermediate grade lesions can be treated with wide-local excision and neck-dissection in clinically positive necks. High-grade lesions require wide-block surgical excision. Neck dissection and post-operative irradiation are also recommended. You may find your answer in MINOR SALIVARY GLAND TUMORS in the section about mucoepidermoid carcinoma.

Hope that helps. Smiler

Best wishes
Vinod :coffee:


Disclaimer: Please see your own dentist/doctor for a proper diagnosis as my words should not, in any circumstances, be taken as dental/medical advice.

"If you see what is small as it sees itself, and accept what is weak for what strength it has, and use what is dim for the light it gives, then all will go well. This is called Acting Naturally."
Lao-Tsu, Tao Teh King
 
Posts: 3342 | Location: St Luke's Hospital, Bradford and Pinderfields Hospital, Wakefield | Registered: 14 December 2002Reply With QuoteReport This Post
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HI ALL and to Dr Joshi, What has happened about having a chat room? is there anything we can do?

Paul
 
Posts: 799 | Location: London England | Registered: 06 March 2003Reply With QuoteReport This Post
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quote:
Originally posted by Paul:
[qb] HI ALL and to Dr Joshi, What has happened about having a chat room? is there anything we can do?

Paul [/qb]
Hi Paul :thinking:

I think a chat room would be a great idea in the future. However, it wouldn't be cost effective to install expensive :twocents: chat software on the RDOC site now because not enough people would use it to justify the expense.

Lets wait for this message board to emulate a "live chat room" before pursuing it. The message board first needs hundreds of members so that messages are posted straight after each other. The number of messages posted definitely needs to increase. The last thing we want is an empty chat room and new comers thinking that this is a dead site...

Also, if everyone starts chatting online now then nobody will be posting messages on the board for new-comers to read. The collection of conversations and discussions on this board, which is fully searchable, makes it worth joining. Live chat room discussions would not be catalogued and would not be searchable. So we have to make sure we have hundreds of members so that people use the message board and chat too.

:coffee: For now, I would suggest everyone organising "live chat" amongst yourselves using free AOL Instant Messenger or Yahoo Chat or MSN Messenger, etc.

This message board only started this January so we should really make the most of it first. :sigh: Maybe next year we'll have live chat, we'll see how busy this board gets...

Best wishes, Krishan Smiler


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Posts: 261 | Location: Surrey | Registered: 13 December 2002Reply With QuoteReport This Post
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Some of the lurkers who just read need to come out and comment and introduce themselves. It is not so frightening to comment on some aspect of the illness or a relative's illness that is bothering us.

I agree with you Krishan you need a lot more people actually commenting on aspects of the many variations of the problems that occur within the forum before a chat room is opened.

Sites do cost money to run and this is already providing a valuable service. What you need is a mass mailing to hospitals making them aware of the site. I was directed to the Bacup site by my oncologist and although it was OK what I really wanted/needed was a site specific to my cancer like this one is.

We should be thinking of ways to get this site message across to the community that deals with head and neck cancers and dental restoration.

Ideas please from the rest of you.....
 
Posts: 525 | Location: United Kingdom | Registered: 10 June 2003Reply With QuoteReport This Post
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Pauline, I do agree with your comments.

Talking openly about cancer, and ones hopes and fears is, I'm sure, quite difficult for most of us.

I still find hard to open my soul to strangers, but I keep trying.

I only wish I could come up with some positive ideas for attracting people, because this is certainly the best site for head and neck cases that I've found so far.
 
Posts: 252 | Location: halifax | Registered: 23 May 2003Reply With QuoteReport This Post
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quote:
Originally posted by Pauline Thomas:
[qb] We should be thinking of ways to get this site message across to the community that deals with head and neck cancers and dental restoration.

Ideas please from the rest of you..... [/qb]
Thanks Pauline. Well, hopefully this year's Mouth Cancer Awareness Week (in November) will provide us the opportunity to promote this new message board through the media. Cool


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http://www.mouthcancerfoundation.org
 
Posts: 261 | Location: Surrey | Registered: 13 December 2002Reply With QuoteReport This Post
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HI ALL Krishan,Pauline, Pikeman,I agree really it is too early to set up a chat room as the few who do post will stop posting and the site will look like a "desserted battle field " I think the last thing we need right now is to let people think we have givn up or all gone to the next world Smiler (not you Krishan). It is the best site I have found on neck and mouth Cancer and we should put our brains together and promote it as much as possible. As a long shot I am going to email This Morning programme and tell them of the Mouth & Neck Cancer week and see if they will give us at least a mention. The statistics I read are frightening and kills more people than breast Cancer and if I read it right 50% chance of living 5 years.

Paul
 
Posts: 799 | Location: London England | Registered: 06 March 2003Reply With QuoteReport This Post
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Hi

Nice to see my friend pikeman still putting in his opennyworth your a great characyer and this board would be the poorer without you. You kind sympathetic yet not afraid ro spell it out Im sure Paul would agreeb with me

Thanks
 
Posts: 118 | Location: Caerphilly | Registered: 08 March 2003Reply With QuoteReport This Post
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Paul, what a cracking idea tp try and get some media mention.

It might be an idea, a bit nearer the time, for all of contacted our local TV and radio suggesting they do something - even if it's only a mention. The more people who know about these forms of cancer, their probable causes, and just how lethal they can be compared to some of the "popular" cancers the better it must be for everybody.

Eileen, thanks for those kind words. Now I'll have to think back to try to remember what I wrote to warrant them.
 
Posts: 252 | Location: halifax | Registered: 23 May 2003Reply With QuoteReport This Post
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HI, Have contacted by email This Morning & GMTV and replied to a question "did the net save your life"? I will try anything. Roll Eyes
I will try the BBC but they are very prudish I think but have a go.

Bye for now guys

Paul
 
Posts: 799 | Location: London England | Registered: 06 March 2003Reply With QuoteReport This Post
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Well done that man!!!

But don't you think Paul that it would be better to leave approaches until nearer the time. Didn't Vinod say that the Awareness week was scheduled for November?

Comment?
 
Posts: 252 | Location: halifax | Registered: 23 May 2003Reply With QuoteReport This Post
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Hi Dont forget they plan ther programmes well in advance "strike while the irons hot" comes to mind Big Grin
 
Posts: 799 | Location: London England | Registered: 06 March 2003Reply With QuoteReport This Post
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