Tim Ferguson

Hi ladies and gents,
Anyone see Good News Week last night and find out that the comedian Tim Ferguson who used to be in the Doug Anthony AllStars with Paul McDermott and Richard Fidler has MS?? Those guys are just fantastic. He was diagnosed in 1995 and looks in fairly good shape considering his length of diagnosis although that is no indication of how he feels I know. Still a funny man.
Cheers,
Jodi.
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Please Note: Any advice given on OzMS must not be taken as medical advice, it's merely advice given by members from their own experiences of living with Multiple Sclerosis. Always check with your GP or Neurologist or other medical professionals, it's the smart thing to do and only logical! If you have something to contribute please do so, everybody has something to offer.


Comments
People Like That
I didn't see that Jodi, thank you for posting though as it is people like that who are still out there doing what they do with such great humour, that gives me inspiration to just keep on keeping on.
Smile, It Confuses People.....
Really surprised!
Hey JJ,
didn't know that, wish I had watched it. I know he has heaps of kids, thought that it was that that made him crazy!
Helen.
Tim on GNW/YouTube
Here is the clip from GNW that Jodi is referring to.
brilliant
Nothing wrong with his brain- well in an obvious way! Still witty and smart!
great,
thanks for posting.
Helen.
(Richard Fidler rocks!!!)
It's Tim with MS, not Richard
Hi all,
I think you're getting confused, it's actually Tim who has MS. That's Tim in the interview. It was Tim's diagnosis that really led to the breakup of the DAAS as he had been having some severe attacks prior to diagnosis.
Tim then disappeared for a while off the radar and then reappeared for a while.
I enjoyed watching this interview as I think he's very witty but the only thing I'll say is that he did paint the picture that 'MS is nothing to worry about', instead of maybe saying that he is lucky he's able to do certain things whereas others are not. He could have even said 'google it folks' to learn more about it, and I reckon google would have been hit big time with people having a look to read. Tim knows like all of us how severe the attacks can be, and what it does to lots of people, so he should try and somehow highlight that.
It's the people that are faces in the media who have MS, that are the ones crucial to educating people about MS and what an insidious disease it is, and why we need the general publics help in the way of donations towards a cure, and raise awareness for understanding and flexibility for people with MS.
In saying that though, Tim does a lot of work with the MS Society for different functions. I just wish more people like him that are in the spotlight would tell the 'true' picture of MS and why we need people to donate etc; It's messages like MS is nothing, that makes the general population think well MS can't be very bad at all. Maybe it just affects how you walk, how bad can that be...so we'll continue to donate to cancer council, or something else that seems like it needs more help than the MS Society.
comedian
He is very funny- I know nothing of the background as I am a new migrant, but he made me chuckle.
Not confused - in lust with Fidler
Hi Karen,
Not at all confused - I'm just voting for my favourite Allstar, Richard Fidler! Although it used to be Paul until I saw him live. Richard's on radio here in Brisvegas, saw him at a live broadcast a couple of months age and took lots of fawning pictures! Tim does not seem to have lost any wit or humour.
It struck me that 'celebrity' MSers usually don't 'comeout' until the illness becomes obvious, and I suppose that is logical because some fear dimunition of their careers.
I read the GNW forums, most posts related to Tim's admission and how people felt sorry that he has MS. Karen I take your point about educating about how aweful MS can be - but I am getting sick of hearing that I am sick and sick of the disabled label. Not all MSers get it bad, so it's hard to find a "generic" MSer - there isn't one. I went to the MS Society here today for my weekly exercise class. I see people who cannot move and am very grateful that I can - it's the diseases unpredictability and variability which makes it hard to apply a 'one size fits all approach' to educating about the illness.
Helen.
allways laughter!!!!
laughing its the best medicine`!!!
Well put helen!!! its so unpredictable alot of us suffer many different ways some more visable than others!!!!
It sure is
Laughter is indeed the best medicine and I go to comedy clubs a LOT. Best night out for a load of fun sitting down
"What lies behind us and what lies before us are tiny matters compared to what lies within us." - Ralph Waldo Emerson
The Weekly Review
Hiya
Just to add to this, Tim did an interview with The Weekly Review in June which was the first time he publicly acknowledged his MS since being diagnosed in 1995. So I don't quote it wrong I have posted the link to the article.
http://theweeklyreview.com.au/article-display/Allstar-To-Class-Act/2936
Everyone deals with is differently.
Smile, It Confuses People.....
Why?
Karen H,
I totally understand where you're coming from, but I think it is unfair to assume that just because Tim Ferguson has MS and that he is sometimes in the public eye, it is somehow his duty to educate the masses. I think that could possibly be why he kept it private for as long as he could - he says in the interview posted by Amber A that he does not want to be a flag bearer and I totally respect that.
Clearly everyone experiences MS in different ways. For him it may *be* nothing to worry about - perhaps he doesn't want people to worry about him which is why he played it down. He was diagnosed a number of years ago, maybe he's been very fortunate and this is his reality. I think it's great that he came out with his story, but beyond that I don't think he has a duty to any one of us to act in a certain way, or say certain things.
As I said, I get your point and in an ideal world we'd have a spokesperson to reach everyone and make them understand. But at the end of the day, he is just a man who has MS and is dealing with it in a way that is best for him. Criticising him for that seems unfair to me. I think people with MS have enough weight on their shoulders...doesn't sit well with me to expect him to take on more of a role than that, just because he's occasionally on the telly.
My opinion, anyway
Review ARticle
That is an excellent article Amber, thanks for posting it.
HElps to have a life that was and is based around humour.
Helen.
He's on a comedy show
Hello Karen,
I agree with both Helen and Stacey. It is not his job to educate the masses. Also, give the guy a break. He's on a COMEDY show for Christ's sake. It's his job to be funny, not be a wet blanket. Just be glad that he told the truth, that it's a revelation to lots of people and people will certainly be googling him I would say. They may even research the illness out of curiosity. It's still publicity.
Jodi.
"What lies behind us and what lies before us are tiny matters compared to what lies within us." - Ralph Waldo Emerson
Thanks Amber
Thanks Amber for posting that article link. This is the kind of thing I'm talking about that is extremely useful when a public figure can use the media in ways to educate people, and in a lot of ways he's done that with being so frank about his disease and attacks.
As far as the other comments in regards to my post, we are all entitled to our own opinions and I respect that. I also give praise where praise is due and stated that Tim does do a lot for MS through things he does with the MS Society. What I was making reference to was that a lot of people may have perceived that comment that MS is really nothing to be concerned about at all, when as we all know it is. He could have thrown something little at the end of that comment to denote that it's not all that funny really, but hey I'm doing the best I can. As I said a simple google it folks may have worked - just my thoughts. I truly hope that people may have done that anyway hearing him just mention MS, and thought hmmm I'll just google it.
I have nothing against Tim. I think he's brilliant and I was quite upset when he left the DAAS because he really is clever and had a real presence in the group. I'm happy for him that he still can incorporate the things he enjoys into his life. But what concerns me is that so many people aren't that lucky. Yes, we all know MS is unpredictible and we all want a cure now, but how are we going to get there and educate the public. The only way I see how is be using people who the general public know and can relate to to get that message out there.I mean look at Jane McGrath and Glenn and what they've done for breast cancer recognition etc;
The vast majority of people with MS are scared of the words 'MS' getting out there to our employers and the consequences of that, and the only reason we are worried about that is really because there is lack of education and understanding in the general public which leads to a lot of people losing their jobs. The only way to change that is to have people who can show that some people with MS can still do these things, but also point out that others are not so lucky. We need this picture to be clear and that it is unpredictible, therefore folks it's ever so important that we find a cure, but in the meantime it's important to support those around us that have MS so they can still work, play and enjoy a good quality of life...
Anyway, that's just my thoughts. If we want to be serious about being understood and about finding a cure, we need people with MS that the public recognise, to get out there and tell their stories. Not to be ashamed of it, or scared of it as that's the exact behaviour that a lot of people with MS have. I'm not saying that Tim has to do this at all. I think the interview he gave in the link Amber posted was fantastic! I totally understand it's a comedy show but just felt his comment on the show may have made people think MS is no big deal.
I remember Fiona O'Loughlin on an episode where she was openly talking about her rehab for drinking etc; she made light of it but also there was a very seriousness undertone. But the difference here is we all know that alcoholism is very serious. She is now narrating a show on ABC called Addiction (on right now on ABC 9.30pm). This is the very place she did her rehab. I think it's fantastic of her to stand up and publicly admit her problem and now is helping to educate others about the thruth of addiction and rehabilitation through this series. It's a really good series...makes you really see about the lives and why this happens to people.
I just wish that we could find a good advocate, a real prominent figure in our society that has MS, that would take that flag and bear it for us to get the message out there to take away the stigma of MS.
Majority of people are too scared to declare they have MS publicly through fear of being judged, instead of being understood. Some people say it's because they don't want sympathy, well in my opinion that may be so in some cases, but in most cases it's more about the fear of being judged. If it was sympathy we feared people would still probably hold jobs etc; but it's more fear based because people are scared they will lose their jobs and more if they come out and admit they have MS!!! This is the sort of thing we need to berid of.
We need people to just understand that our needs may be different. We are the same person but there may be periods of time where we need more flexibility in our work etc; because this disease is unpredictible.
Anyway, I think Tim does a great job and just wish I had his wit.
Well said Karen
It is so true that we don't talk about it because we fear losing our jobs.
Having had it happen to me when I was first diagnosed (after 24+ years with an employer I enjoyed working for) a "Commercial Decision" got around the Discrimination laws and that was it - see ya and we're a business not a charity!!!
But I believe not a lot is known about it (to be honest I didn't know much about it, I only saw Betty Cuthbert at the Opening Ceremony of the Olympic Games), even the Pharmacist Assistant asked what it was all about when I put in a repeat for the Betaferon.
Maybe a show GNW put the seeds of questioning in a lot of viewers heads and they can Google it. AT least that would be a help in gettiing acceptance NOT sympathy!!
Any way, that's my view.
Lisa
Rock, Paper, Scissors, Lizard, Spock
Tim Ferguson on The Circle
4 min 34 seconds is when the
4 min 34 seconds is when the MS discussion begins in the above
Good points
Yes thanks Amber for posting this. I agree that he did gloss over it a bit, but can understand he may not want to make a big issue.
I really feel it would be good to have some people, some with MS and perhaps medical people to talk more about some of the things etc we can have. Even provide feedback about how it affects their lifestyle and problems they have encountered, and of course it is not immediately the end of the world for people.
Belinda
Belinda
MS and being open
I admired the way he handled the question we all know how hard it is to talk about our MS because he is so well known with in th 35+ age group he may not of want to panic people by saying to much. but by mentioning it people will go wow and jump on the net and read about it.
Yes we should all help people understand MS and what we go thu day to day. i know im scared of how people will react. so i put my hands together to Tim for being brave enough to tell Australia on TV