This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Wed Jun 19, 2013 7:38 pm


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 7 posts ] 
Author Message
PostPosted: Mon May 30, 2011 11:52 am 
Offline
Family Elder
User avatar

Joined: Fri Dec 31, 2010 4:00 pm
Posts: 163
Location: Texas
Hello, my friends,

For my next clinical trial, I am looking for MS patients who are in their teens to twenties...

Is there anyone out there on this forum who knows of the younger folks?

This study involves NO TRAVEL, and is a retrospective look at growth (prior to 16 months or so of age, obviously before any diagnosis was made).

Pediatricians have been good about taking these growth measurements in the last 20-25 years, but not prior to that. This is why I'm trying to locate the younger MS patients who may be able to find these records.

Can anyone help me? Interestingly, this study ties into CCSVI!

I would be eternally grateful for your help. And as usual, this is a study that I do not get paid to do, and of course, doesn't cost the participant anything, either.

We are on a mission! (Or my favorite battle cry, "This is SPARTA!").

:lol: Dr. Diana

_________________
Dr. Diana

Special interest in "brain drains" and how they affect numerous conditions, including MS, Ehlers-Danlos, Parkinson's, Alzheimer's, etc. I am a therapeutic optometrist on professional disability with EDS, POTS, CCSVI, mast cell disea


Top
 Profile  
 
 Post subject:
PostPosted: Mon May 30, 2011 12:22 pm 
Offline
Family Elder
User avatar

Joined: Wed Jun 02, 2004 3:00 pm
Posts: 201
Location: georgia
Dr. Diana,
Don't know if this will be any help to you but my now 23 year old daughter had postpartum optic neuritis (blurred vision in right eye) about 1and1/2 years ago. Same way my MS started and then 14 years of no symptoms and slow progression until 2009 Sister with pseudo tumor cerebri years ago. Is there a relationship I don't know. I did have CCSVI surgery. It helped with energy but not balance and walking. I hope my daughter can avoid my fate. According to Dr. Flanagan's book they don't know what MS is or what causes it but seem to be all to willing to treat it as an autoimmune disorder. Where's the proof of that?


Top
 Profile  
 
 Post subject: ccsvi
PostPosted: Mon May 30, 2011 4:37 pm 
Offline
Family Elder
User avatar

Joined: Thu Dec 03, 2009 4:00 pm
Posts: 1247
Location: south western pa.
hi dr. diana, are you in touch with dr. hubbard? their son devin i think is in his 20's.


Top
 Profile  
 
 Post subject:
PostPosted: Mon May 30, 2011 6:42 pm 
Offline
Family Elder
User avatar

Joined: Fri Dec 31, 2010 4:00 pm
Posts: 163
Location: Texas
Hi Coach,

Do you or your daughter have her head circumference, weight and length measurements from approximately birth to approximately 15 months of age? (or if not, would her pediatrician still be around to help with that?).

That would be of enormous help in this study. I'll be wrapping up the details this week and can shoot it over to you (or, actually, I guess I'll be announcing it. Doy).

Thank you so much! I am also FASCINATED by your sister having pseudo-tumor cerebri. How is she doing now?

Thank you!

_________________
Dr. Diana

Special interest in "brain drains" and how they affect numerous conditions, including MS, Ehlers-Danlos, Parkinson's, Alzheimer's, etc. I am a therapeutic optometrist on professional disability with EDS, POTS, CCSVI, mast cell disea


Top
 Profile  
 
 Post subject:
PostPosted: Thu Jun 02, 2011 9:12 pm 
Offline
Family Elder

Joined: Mon Aug 23, 2010 3:00 pm
Posts: 600
Sorry, I'm in early geezerhood so I'm well beyond the age bracket you're looking for. But I like the idea of studies being done by individuals who have a personal interest in finding answers. I think real success is more likely to come from such individuals than from pharmaceutical companies whose primary interest is the bottom line.


Top
 Profile  
 
 Post subject:
PostPosted: Fri Jun 03, 2011 8:53 am 
Offline
Family Elder
User avatar

Joined: Fri Dec 31, 2010 4:00 pm
Posts: 163
Location: Texas
Ha! Well thank you for considering it, David! (And be careful who you're calling a geezer - as I stare 54 in the face). 8O

I'm sure you are right - individuals rather than drug companies.
FOR SURE.
Thanks....

_________________
Dr. Diana

Special interest in "brain drains" and how they affect numerous conditions, including MS, Ehlers-Danlos, Parkinson's, Alzheimer's, etc. I am a therapeutic optometrist on professional disability with EDS, POTS, CCSVI, mast cell disea


Top
 Profile  
 
 Post subject:
PostPosted: Sat Jun 04, 2011 12:29 pm 
Offline
Family Elder

Joined: Mon Aug 23, 2010 3:00 pm
Posts: 600
DrDiana wrote:
Ha! Well thank you for considering it, David! (And be careful who you're calling a geezer - as I stare 54 in the face). 8O

I'm sure you are right - individuals rather than drug companies.
FOR SURE.
Thanks....


Don't worry. At 57 you're a long way from geezerhood. Anyway I only apply that term to myself. Just like you, I have a somewhat bizzare sense of humor. :wink:


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 7 posts ] 

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. Re: Clinical trial at Stanford

William57

1

860

Wed Mar 31, 2010 11:52 am

annad View the latest post

This topic is locked, you cannot edit posts or make further replies. The need for a double blind clinical trial

[ Go to pageGo to page: 1, 2, 3 ]

Direct-MS

34

2984

Sun Dec 05, 2010 6:43 pm

jimmylegs View the latest post

There are no new unread posts for this topic. NEW: Clinical Trial in Texas w/Dr. Diana

[ Go to pageGo to page: 1, 2 ]

cheerleader

29

2926

Thu Jun 02, 2011 6:14 pm

DrDiana View the latest post

There are no new unread posts for this topic. New York Albany clinical trial - when?

Ernst

7

580

Mon Jan 16, 2012 12:51 pm

PointsNorth View the latest post

There are no new unread posts for this topic. UK Stem Cell Clinical Trial for MS

vw35qrt

4

463

Sat Dec 29, 2012 5:01 pm

vw35qrt View the latest post

 


Who is online

Users browsing this forum: No registered users


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

Search for:
Jump to:  


News News Site map Site map SitemapIndex SitemapIndex RSS Feed RSS Feed Channel list Channel list
Read hundreds of personal Multiple Sclerosis stories on Experience Project. Experience Project is an anonymous community where people connect through their life experiences, made by the same people who built This is MS. With over 30 million personal stories about every possible life experience, you can quickly find people like you!


Interesting: Secret Confessions | Dream Meanings | Ask Questions, Get Answers

Advertise on the premier multiple sclerosis forum