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 1:24 am


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 99 posts ]  Go to page Previous  1, 2, 3, 4, 5, 6, 7  Next
Author Message
PostPosted: Sun Oct 21, 2012 9:10 am 
Offline
Family Elder

Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2037
Location: Bedfordshire UK
Strange, because it doesn't on my computer: I must get out David's laptop and try that. :?

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.


Top
 Profile  
 
PostPosted: Sun Oct 21, 2012 9:15 am 
Offline
Family Elder

Joined: Sat Sep 24, 2005 3:00 pm
Posts: 449
Location: Chicago area
For the heck of it, I clicked on both of Sarah's references to cpn help. Neither works for me. I get the 'internet explorer cannot display...' message on each of them.

What's funny is, CPn Help is solely an informational site, doesn't accept any commercial messages and is self-supporting. It complements, but does not displace, what ThisIsMS does. JimK (the site owner) simply established it as a place to centralize all things related to chlamydia pneumoniae and its treatment.

_________________
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi


Top
 Profile  
 
PostPosted: Sun Oct 21, 2012 9:22 am 
Offline
Family Elder
User avatar

Joined: Mon Jul 11, 2005 3:00 pm
Posts: 264
Location: North Carolina USA
And my click was rewarded with basically the same, but asked if I wanted www.CPn Help.org.

Rica

_________________
2010 5 years 4 months Now on Amoxicillin, Doxy, Rifampin, Azith, and caffeine in addition to  flagyl. 90% normal good days-50% normal bad days. That is a good thing.


Top
 Profile  
 
PostPosted: Sun Oct 21, 2012 10:07 am 
Offline
Family Elder

Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2037
Location: Bedfordshire UK
So I'm not going mad, then?

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.


Top
 Profile  
 
PostPosted: Sun Oct 21, 2012 10:31 am 
Offline
Family Elder

Joined: Sat Sep 24, 2005 3:00 pm
Posts: 449
Location: Chicago area
No. at least not in the way you might have, if you hadn't done the antibiotic treatment! I was losing short-term memory rapidly when I began abx. It was one of the first improvements I saw. How wondrous, to be able to recall an entire telephone number without prompting from someone else.

_________________
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi


Top
 Profile  
 
PostPosted: Tue Oct 23, 2012 6:31 pm 
Offline
Family Member

Joined: Mon Sep 17, 2012 3:18 am
Posts: 28
MHP wrote:
Dear jimmy6
thank you so much for sharing your info. I am in the process too of talking to my GP and following Dr Wheldon treatment. As you mentioned there are not many people sharing how the treatment is doing for them that is why people like you are so valuable. I am intending to also share my experience and I have the conviction that Dr Wheldon findings are in the right path!
take care and keep us updated.
MHP

Have you started yet? Mick


Top
 Profile  
 
PostPosted: Mon Oct 29, 2012 1:25 am 
Offline
Family Member

Joined: Mon Sep 17, 2012 3:18 am
Posts: 28
Anecdote wrote:
Hi Mick, you really need you keep the doctor on your side so I should go along with the amoxicillin since it is just for seven days. It is compatible with the treatment and used to be used before NAC. Some people take it even now, even if they are taking NAC. It is often used for urine infections and they can often be silent.

Hello to Trish!!

Sarah

Hi Sarah Day 65 and Tricia has developed intermittent sharp paint in left arm and shoulder. I think that happened to you and your web site said that it lasted for three days? So treatment is working ? All went well with Amoxil treatment, bladder infection cleared up. Mick


Top
 Profile  
 
PostPosted: Mon Oct 29, 2012 2:37 am 
Offline
Family Elder
User avatar

Joined: Wed Jul 27, 2005 3:00 pm
Posts: 2732
Location: Sydney, Australia
Anecdote wrote:
So I'm not going mad, then?
Some people are already at their designated destination. :razz:


Top
 Profile  
 
PostPosted: Mon Oct 29, 2012 5:03 am 
Offline
Family Elder

Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2037
Location: Bedfordshire UK
To Cureo: Cheeky sod!! 8O

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.


Top
 Profile  
 
PostPosted: Mon Oct 29, 2012 5:12 am 
Offline
Family Elder

Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2037
Location: Bedfordshire UK
Mick, if it is the same sort of pain did, it did happen to me but lasted about three weeks. It was so bad I sometimes ended up in tears. It tended to move around, I would think it was going then it would reappear somewhere else. It happened just after my third pulse of metronidazole.

Sarah

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.


Top
 Profile  
 
PostPosted: Thu Nov 08, 2012 4:57 pm 
Offline
Family Member

Joined: Mon Sep 17, 2012 3:18 am
Posts: 28
Anecdote wrote:
Mick, if it is the same sort of pain did, it did happen to me but lasted about three weeks. It was so bad I sometimes ended up in tears. It tended to move around, I would think it was going then it would reappear somewhere else. It happened just after my third pulse of metronidazole.

Sarah

Hi Sarah Mick & Tricia here. Well Tricia has had a pretty bad time over the last 10 days . The pain in both her arms and shoulders has been very bad and it starts to happen a couple of hours after she takes the antibiotics.I gave her panadol for the pain but this had a good and bad reaction. Her face swelled up and became very red, her body became hot 38.6, her feet were very cold. I am going to DR today to talk about it as well as pick up third antibiotics. Tricia has lost some of the early gains that she made. Her arms dont move as well as before ,she is starting to slur slightly again. I have read the Relapse and Pseudo- relapse as well as Peripheral Nerve Inflammation and Central Pain in ms index and this sounds like what is happening to Tricia except that Tricia pain has gone on for about ten days and she has got slightly worse.Just come back from the Dr and he has recommended Nurofen for pain as well as given THE FIRST Metronidazole ,which Tricia will try to take in 10 days. Its funny that Tricia did not a bad reaction till 70 days into treatment. I can now understand why some people give up on the treatment after watching the pain on Tricia,s face . But she is not giving up. Mick


Top
 Profile  
 
PostPosted: Thu Nov 08, 2012 5:13 pm 
Offline
Family Elder

Joined: Sat Sep 24, 2005 3:00 pm
Posts: 449
Location: Chicago area
Mick, When the infection is being worked on by the abx, inflammation is the result. Inflammation causes most of our MS symptoms, so, of course, Tricia is experiencing the same 'symptoms' she did before. Pain can be the result of constant inflammation, as well.

While it stinks that she has to experience this, it's a good indication that the medication is doing exactly what it's supposed to do - killing the disease. I had a similar response, a few months into treatment, when a lower back injury site suddenly 'flared up', causing me a couple of weeks of pain and a real need to stay in bed as much as possible to avoid painful movement and difficulty walking. When it subsided, my back felt better than it had in decades and I have NEVER had a relapse of those particular symptoms again. It was worth it, to go through that pain, when the outcome was such a good one!

_________________
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi


Top
 Profile  
 
PostPosted: Fri Nov 09, 2012 6:49 am 
Offline
Family Elder

Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2037
Location: Bedfordshire UK
Mick, my pain, the only real pain I have ever had, lasted about three weeks, so ten days is nothing. You will tend to revisit all the old symptoms, as Mack said, but at least eventually that should be it.

Regards to Tricia!

_________________
An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.


Top
 Profile  
 
PostPosted: Fri Nov 09, 2012 4:38 pm 
Offline
Family Member

Joined: Mon Sep 17, 2012 3:18 am
Posts: 28
Hi Sarah and Mack Thank you for advice. Having both of you there a great comfort .We know now that we are on the right track and i have now altered . stopped Tricia,s doing her morning exercise and to stay in bed till pain has gone .Thank You Mick & Tricia


Top
 Profile  
 
PostPosted: Thu Nov 15, 2012 3:45 am 
Offline
Family Member

Joined: Mon Sep 17, 2012 3:18 am
Posts: 28
Anecdote wrote:
Mick, my pain, the only real pain I have ever had, lasted about three weeks, so ten days is nothing. You will tend to revisit all the old symptoms, as Mack said, but at least eventually that should be it.

Regards to Tricia!

Hi Sarah Mick here with more problems Tricia got sicker so Dr order blood tests and when the test returned it showed that there was something wrong with her liver so called ambulance and sent her to hospital for u-sound it and more blood tests.The ultra sound showed that the liver on the out side was okay as well as her other organs okay but the blood test as explained to me by the Dr at the hospital say that Tricia liver should operate at 100 but was 400 thats how he explained it to me in lay mens terms. He was not against the antibiotic treatment he just said that Tricia liver is not handling it and that she could have liver failure if Tricia were were to do this long term. He said it was a hard call to make for Tricia to make, he also said to call anytime for any advice . A report will be sent to our Dr and we will talk to him Your thoughts on this would be greatly appreciated


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 99 posts ]  Go to page Previous  1, 2, 3, 4, 5, 6, 7  Next

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. Antibiotics for Treating MS in Canada

mandamurr81

5

684

Fri Apr 12, 2013 7:07 pm

marcopolo View the latest post

There are no new unread posts for this topic. Antibiotics for ccsvi in Australia

Anecdote

11

1618

Thu Jan 19, 2012 7:41 am

Anecdote View the latest post

There are no new unread posts for this topic. Someone treating MS as an infection.

[ Go to pageGo to page: 1, 2 ]

Anecdote

23

6175

Sun Mar 24, 2013 1:11 pm

HealthyGirl1004 View the latest post

There are no new unread posts for this topic. CPn research from Australia

bromley

10

2991

Fri Feb 15, 2008 4:25 pm

Anecdote View the latest post

There are no new unread posts for this topic. Anyone on CPN or ABX in Australia? Need to chat :-) please

Liisa

4

1852

Tue Apr 01, 2008 7:55 pm

MacKintosh View the latest post

 


Who is online

Users browsing this forum: evans


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