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, 157 guest(s) and 1 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 - Introduction and a question about mechanism of action
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


Introduction and a question about mechanism of action
Goto page Previous  1, 2
 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Regimens
View previous topic :: View next topic  
Author Message
mormiles
Family Member


Joined: Mar 08, 2006
Posts: 79
Location: 75098

PostPosted: Sun Jan 07, 2007 10:01 pm    Post subject: Antivirals Reply with quote

Hi Frank, My husband is on several medications. The only side-effects he has experienced from any of them are: 1) one day only of dizziness and slight nausea on starting LDN---no side effects after that first day, and 2) a short period of mild depression following his first pulse of flagyl (metronidazole)---now he takes St. John's Wort for several days following his flagyl pulses, and the depression has not recurred. Because so many different medications and supplements were started within the same period, we cannot say that this one or that one had this or that effect when assessing all of these medications. Here are the exceptions: die-off reactions to starting and doubling doxycycline, less definitive die-off reactions to starting azithromycin, die-off reactions to flagyl pulses followed by clear improvements, urogenital improvements within a few weeks after starting LDN, less fatigue immediately after starting Lunesta (a sleep aid).

Frank, you are only just now immersing your mind in the subject of treatment with antibiotics, and you have much reading to do. I've told you that my husband is receiving comprehensive treatment, and he needs the full complement of what that entails. I consider the combined antibiotic protocol to be the most critical aspect of his treatment program. Please learn more about the antibiotics before splintering your focus.

That being said, I'll tell you that my husband is on two anti-virals: valtrex and amantadine. I don't know how much they cost yet because, by the time he started them last year, his medical costs had already exceeded the limit of expenses that we had to pay out of our own pockets before our insurance began to pay 100%, so they were free to us last year. Now a new "insurance" year has started, and we will soon find out how much they cost. After you have learned more from reading on Dr. Wheldon's site and CPn Help, then would be a good time to read what I have written about my husband's comprehensive treatment. Trying to learn everything about everything at one time has the result of not having learned very much about anything.

My husband/s treatment was begun in August 2006, and these are his improvements to date: much less fatigue, brain fogginess is gone, no more restless legs and feet, better balance, slightly better gait, improved vision. The fatigue, balance, gait, and vision are all improved, but still need more improvement. At this point, it is still unclear to what extent his remaining symptoms are due to current inflammation from infection or to "permanent" neurological damage. His short term memory still stinks, but we expect improvement in that area as well. We expect the antibiotic aspect of treatment to last 1-1/2 to 2 years before he switches to intermittent therapy. If his MS symptoms were more severe, we would expect a longer treatment, as that might indicate more extensive infections.
Back to top
View user's profile Send private message
CureOrBust
Family Elder


Joined: Jul 28, 2005
Posts: 1129
Location: Sydney, Australia

PostPosted: Sun Jan 07, 2007 10:54 pm    Post subject: Reply with quote

Frank wrote:
Do you actually have relapse when catching a flu (you said you wold have - maybe I just understand that english sentence wrong?)
Are these events really relapses (visible lesions on MRI?) or do you just feel temporary worse in the time of flu/cold - that would be quite usual.

For me, the only trigger for a relapse has been a cold/flu (10+yrs). The relapse usually occurs about 8 days after I notice I have a cold/flu, so it is usually gone by the time the relapse starts. Its not feeling bad because of the cold, i get new or worsening of MS symptoms that stick around much longer than the flu.

I have only had 2 MRI's spaced 2years apart so it would be difficult to attribute visible lesions to individual relapses.
Back to top
View user's profile Send private message
Frank
Family Elder


Joined: Jan 04, 2007
Posts: 270
Location: Germany

PostPosted: Wed Jan 10, 2007 12:38 pm    Post subject: Reply with quote

I've been offline for the last two days, because I switched my PC to the new Windows Vista operating system...

Thanks all for your kind explanations Smile !
I'll be reading a lot in the next days and weeks. I'll talk to my health insurance, whether they would compensate my expenses for ABX.
I'll also ask my neurologist and GP about their thougths on ABX.
Back to top
View user's profile Send private message
Anecdote
Family Elder


Joined: Jun 18, 2004
Posts: 1459
Location: Bedfordshire UK

PostPosted: Wed Jan 10, 2007 1:14 pm    Post subject: Reply with quote

Frank, send me your email and I will forward you some useful papers to show your neurologist and GP. That'll give you even more reading! Smile
You can get my email by clicking on the profile button.

Sarah
_________________
An Itinerary in Light and Shadow
Completed Stratton/Wheldon antibiotic regime for aggressive secondary progressive MS in June 2007, after four years. Still slowly improving with no exacerbation since starting. EDSS was 7, now 2 or often less.
Back to top
View user's profile Send private message Send e-mail Visit poster's website
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Regimens All times are GMT - 6 Hours
Goto page Previous  1, 2
Page 2 of 2

 
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





Personal Stories about millions of life experience--including multiple sclerosis support, lupus support, depression support . Built by the This is MS team.

Anonymous Confessions | Dream Dictionary
Site Map

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


Visit our sister site dedicated to Inflammatory Bowel Disease: This is IBD


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 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: 0.31 Seconds