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ThisIsMS.com :: View topic - Hi Everyone
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Hi Everyone

 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Under 25 with MS
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JenniMe123
Newbie
Newbie


Joined: Aug 12, 2004
Posts: 5
Location: Connecticut

PostPosted: Fri Aug 13, 2004 7:30 pm    Post subject: Hi Everyone Reply with quote

Hi everyone! My name is Jenni. I am 14 and I was diagnosed about two months ago. If anyone wants to chat I'm always up to metting new people. Hope to hear from you all soon.
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CCmom
Family Elder


Joined: Apr 26, 2004
Posts: 118

PostPosted: Sat Aug 14, 2004 12:55 pm    Post subject: Reply with quote

Hi, Jenni! So happy to see you here! I'm working on getting more people your age to the site, so if you find anyone in your internet adventures, please let them know about this board. I know your story, but I'm sure others who use this message board in it's entirety would like to hear more about you!

For those of you who don't know me, I have a 16 year old son who was diagnosed with MS 3 years ago, at age 13. And as soon as I can get him to sit still long enough, I will ask him to post his story here!

I am so thankful to Arron for adding this forum. Ever since my son was diagnosed, I've searched for other young people, and my hopes are to bring everyone together here, on this forum. We all need support and friends who understand where we are coming from, people we can count on to understand our ups and downs, and just to listen. And I've never believed young people with MS belong in a regular MS message board with the majority of the people posting there being older. I think the young people with early MS diagnosis' are looking at an entirely different future than some of the MSer's who waited years and years for a diagnosis. There is so much hope on the horizon for you!

I think you will enjoy utilizing this web site. I certainly have. It is truly user friendly, and full of important information that will provide optimism and hope for all who take the time to browse around and read a bit. I hope that you will also encourage your parents to use this site. I think it is important that we all learn all we can learn about the different treatment options, and about each other.

I will be the moderator for this forum, so if anyone has any questions or would like to get in touch with me directly, please send me a private message. I'm looking forward to hearing from you, and please help spread the word!

Kim
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Kim R.
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Arron
Site Admin
Site Admin


Joined: Feb 02, 2004
Posts: 863
Location: California, USA

PostPosted: Thu Aug 19, 2004 6:29 pm    Post subject: Reply with quote

Hi Jenni, welcome to our site. Your journal entry was great-- I hope you continue to find the community useful and please let us know if we can do something better.

Best,
-arron
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billmac
Newbie
Newbie


Joined: Dec 13, 2004
Posts: 4

PostPosted: Mon Dec 13, 2004 4:37 pm    Post subject: MS in Kids and Teens Reply with quote

Hi all...

I just posted a long response (to Kim) in the general discussion section before I noticed the 'under 25' forum below.

I linked to some resources for kids and teens with MS, including a link to the NMSS site where you can get the Parent Handbook "Kids Get MS Too" I don't want to cross post, so find my other comments there!

-bill
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bromley
Family Elder


Joined: Sep 11, 2004
Posts: 1838

PostPosted: Sat Nov 26, 2005 10:38 am    Post subject: Reply with quote

The Witters,

If you have some great info to share why not share it with everyone?

I've not e-mailed you but suspect that you are either (i) religious nutters (ii) salesmen (flogging crap drugs, crap books, or crap computers).

Or perhaps you have a cure for this horrid disease but don't want to let everyone know?
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bromley
Family Elder


Joined: Sep 11, 2004
Posts: 1838

PostPosted: Sat Nov 26, 2005 11:07 am    Post subject: Reply with quote

The Witters,

I went on the site and read the two MS stories - they remind me of so many of the sites flogging dodgy supplements etc etc. I couldn't see any price list but assume we get this when we call you.

If the product is so great -why do we not hear about it at neurology conferences etc. Why has it not been trialled?

Let's come clean - what are you asking us to buy and how much is it?

This site is for people with this disease to share their experiences / talk about future treatments etc. It is not intended for salesmen to prey on the desperation of those with chronic diseases in order to make a profit.

You are either selling a supplement, or a book telling us what to avoid, or you services (whatever they are).

I have notified the site administrator to have your post removed.
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Ellenem
Getting to Know You...


Joined: Nov 20, 2004
Posts: 10

PostPosted: Sun Nov 27, 2005 3:00 pm    Post subject: Reply with quote

I havent actually been to this messageboard for a while so was quite suprised to discover someone from here had sent me a PM.

Didnt know what to make of it but then I realised that it was pretty much identical to what had been said here.

Like Bromley I have no idea what the Witters agenda is but what worries me is that I suspect its highly unlikely I was the only person PM'd.

There are a lot of people out there willing to try and scam MSers and other people desperately searching for answers and so we all have to be so careful and question anything that seems too good to be true... because it most likely is
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Arron
Site Admin
Site Admin


Joined: Feb 02, 2004
Posts: 863
Location: California, USA

PostPosted: Mon Nov 28, 2005 10:28 am    Post subject: Reply with quote

James, the ad on the screen is paid for by you to Google in a section sanctioned for advertising.

This bulletin board is NOT and it is obviously unacceptable for you to come here and mine business in this fashion. I also do not appreciate you sending private messages to members attempting to sell your goods. I think you know very well that this is not OK-- the private messages are intended for personal communication of a non-commercial nature.

Your posts will be deleted. Thanks for your understanding.
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Disclaimer: Any information you find on this site should not be considered medical advice. All decisions should be made with the consent of your doctor, otherwise you are at your own risk.
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