Welcome to This Is MS!

     Modules
· Home
· Content
· Downloads
· Encyclopedia
· FAQ
· Feedback
· Forums
· Journal
· Private Messages
· Recommend Us
· Search
· Site_Map
· Stories Archive
· Submit News
· Surveys
· Top 10
· Topics
· Web Links
· Your Account

     Google
Google
Web
This is MS
These ads help pay for the upkeep of our site. They are automatically served by Google and are not affiliated with This is MS.

     Languages
Select Interface Language:


     Who's Online
There are currently, 69 guest(s) and 15 member(s) that are online.

You are Anonymous user. You can register for free by clicking here

     Next Step

From the creators of This is MS comes Experience Project

EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at Experience Project.

Get started by sharing your Multiple Sclerosis story.


     Donations

To remain unbiased, This is MS does not accept corporate sponsorships.

Therefore, we must rely on our users to help support us. Please donate to our upkeep if you have the means. Thank you!


ThisIsMS.com :: View topic - Greetings from Tokyo
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


Greetings from Tokyo

 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Introductions
View previous topic :: View next topic  
Author Message
chalam
Getting to Know You...


Joined: Apr 21, 2005
Posts: 10
Location: Tokyo, Japan

PostPosted: Thu Apr 21, 2005 4:34 am    Post subject: Greetings from Tokyo Reply with quote

My 15-year-old daughter was recently diagnosed with MS. This was understandably heartbreaking for our family. She has started on Betaferon at the suggestion of our neurologist.

Let me point out that a) we are American and don't speak Japanese b) Betaferon is the only disease modifying drug on the market in Japan c) Japan doesn't have much MS. For these reasons, I am especially grateful for the information I am finding on your site. I realize that it is pretty much up to me to stay on top of what is going on in the MS world.

We see the neurololgist later this week and I will try asking about LDN, antibiotic therapy and statins. I don't expect him to know much about any of these therapies, but you never know.

Is anyone out there the parent of an MS teen?
thanks
Back to top
View user's profile Send private message
bromley
Family Elder


Joined: Sep 11, 2004
Posts: 1847

PostPosted: Thu Apr 21, 2005 7:21 am    Post subject: Reply with quote

Chalam,

My heart goes out to your daughter and your family. If you go to forums there is a section for under 25s with MS. CCMom is a mother whose son was diagnosed in his early teens - I'm sure she would be happy to share her experience with you.

The US national MS site (NMSS) has a section on teens with MS and a magazine for teens.

Best wishes.

Bromley
Back to top
View user's profile Send private message
Arron
Site Admin
Site Admin


Joined: Feb 02, 2004
Posts: 864
Location: California, USA

PostPosted: Thu Apr 21, 2005 12:12 pm    Post subject: Reply with quote

Hi and welcome!

As luck would have it, we recently added a section about parenting teens with MS:

http://www.thisisms.com/modules.php?name=Forums&file=viewforum&f=34

George Peabody is our volunteer moderator, and maintains a website specifically for this subgroup of MS'ers:

http://www.familieswithms.org/

I hope this is helpful, and we're very happy that you've found that our site has been a good resource for your difficult situation.
_________________
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.
Back to top
View user's profile Send private message
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Introductions All times are GMT - 6 Hours
Page 1 of 1

 
Jump to:  
You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum
You cannot vote in polls in this forum





We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project. Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS, on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!

Experience Project: I have Multiple Sclerosis


Anonymous Confessions | Free Dream Interpretations | Ask Any Question
Site Map

This site does not offer medical advice. All treatment decisions should always be made with the full consent of your physician.


All logos and trademarks in this site are property of their respective owners. The comments are property of their posters, quoted articles are © referenced source, all the rest © 2002-8 by thisisMS.com.
PHP-Nuke Copyright © 2005 by Francisco Burzi. This is free software, and you may redistribute it under the GPL. PHP-Nuke comes with absolutely no warranty, for details, see the license.
Page Generation: 0.10 Seconds