5 days of doxy
-
- Family Elder
- Posts: 2209
- Joined: Thu Jun 17, 2004 2:00 pm
- Location: Bedfordshire UK
- Contact:

Last edited by SarahLonglands on Sun Dec 19, 2010 4:55 am, edited 2 times in total.
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.
Thanks Agatha i am in my fifth month now of antibiotics , that MRI really doesn't mean much, the two new lesions bother me but maybe they were formed before. There was nothing active at the time of the MRI. I have had certain things improve enough to keep me going on this so will see.
Hard to know.....
Hard to know.....
Had ms for 28 yrs,
8.5 EDSS
SPMS, 54 yrs old
Taking it day by day
8.5 EDSS
SPMS, 54 yrs old
Taking it day by day
-
- Family Elder
- Posts: 2209
- Joined: Thu Jun 17, 2004 2:00 pm
- Location: Bedfordshire UK
- Contact:
Sorry Robbie for above error but I like your sense of humour: Air borne toxic event!
Sarah
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.
It's funny how people react to you taking antiobiotics for treating MS. They think it's great that your trying but you can tell inside their thinking what the hell is he doing that for. There are so many symptoms of MS that people don't even relize you have,like earlier on in this disease if you were just sitting no one would know there was anything wrong with you even though you were a mess inside. Things that have improved for me are some of those hidden symptoms so to look at me you might think why is he taking that stuff but for me i just feel better. I don't know why or how but just glad i tried it. It could all come crashing down tomorrow but for now it is so much better than before.I still get pretty depressed sometimes, much much less.Since i have been on this site i never been one to value hope but i can see now how important it is. I need to walk again.
Had ms for 28 yrs,
8.5 EDSS
SPMS, 54 yrs old
Taking it day by day
8.5 EDSS
SPMS, 54 yrs old
Taking it day by day
-
- Family Elder
- Posts: 2209
- Joined: Thu Jun 17, 2004 2:00 pm
- Location: Bedfordshire UK
- Contact:
Yes, one lady we know sees that I am getting better then wonders why I say I can't come round for coffee in the middle of the day because I am busy painting. Her response was that she understands because I must want to get as much done before the disease hits me once more and I might not ever be able to paint again! She also thinks it "a nice hobby for me," not thinking that it is my profession.
Robbie, I am sure you will walk again because you are so determined.
Sarah
Robbie, I am sure you will walk again because you are so determined.
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.
I agree Robbie - though I've found it's usually health professionals of various kinds who are sceptical. This unfortunates includes many of my friends since I am a health professional myself! Like you many of my improvements are invisible - eg. I have stopped feeling cold and shivery after 20 years of being cold.
My MS nurse visited last week and after telling her how much better i felt since taking the abx she clearly thought it was nonsense. She is a very kind lady and I could see her hesitating over what to write in her notes and in the end i suggested she should just write what she was thinking ie 'the patient is bonkers'. Ha ha! She took it quite well.
Sarah - that must make you really mad!
Agatha
My MS nurse visited last week and after telling her how much better i felt since taking the abx she clearly thought it was nonsense. She is a very kind lady and I could see her hesitating over what to write in her notes and in the end i suggested she should just write what she was thinking ie 'the patient is bonkers'. Ha ha! She took it quite well.
Sarah - that must make you really mad!
Agatha
-
- Family Elder
- Posts: 2209
- Joined: Thu Jun 17, 2004 2:00 pm
- Location: Bedfordshire UK
- Contact:
From nov 19, 2010
Robbie, mri's apart, are you still getting better, strengthwise, walking wise and so on? I hope you are still exercising, even if you have given up abx. There are several people who keep their options open and use abx whilst having ccsvi treatment: the two aren't incompatible.
Sarah
From dec 07, 2010Went to my neurologist today and she did her tests and at the end of our 15 minute visit she said "you seem to be in a holding pattern" I was really glad to hear her say that.
I haven't had an mri since two years after starting treatment. Since I am obviously not getting worse, I see no point, but who knows, maybe by brain looks like a Swiss cheese by now!Got the results of my last MRI it showed two new lesions and two that had disappeared. This MRI is being compared to one I had in August, 2008 . I started the full antibiotic treatment in August, 2010 so it is hard to compare these two MRI's.I am going to continue with antibiotics and another MRI down the road which will be a little more telling.
Robbie, mri's apart, are you still getting better, strengthwise, walking wise and so on? I hope you are still exercising, even if you have given up abx. There are several people who keep their options open and use abx whilst having ccsvi treatment: the two aren't incompatible.
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.
Hi Sarah i had an MRI done at the beginning of the abx but it was being compared to one in 2008 and it showed some progression but that might have happened prior to starting abx so we did another to see if the abx had stopped any progression while on it but it had not so he stopped it,not sure why i felt so strong sometimes, must have been one hell of a placebo effect. Over the last couple months i knew things were going down hill but i kept up with the abx.Will keep up with the exercise as much as i can. I know the test for CCSV is being done at a hospital close by now so i thought i would grasp at that straw now, Glad i tried the abx it's the only real way to find if something works.
Had ms for 28 yrs,
8.5 EDSS
SPMS, 54 yrs old
Taking it day by day
8.5 EDSS
SPMS, 54 yrs old
Taking it day by day
-
- Family Elder
- Posts: 2209
- Joined: Thu Jun 17, 2004 2:00 pm
- Location: Bedfordshire UK
- Contact:
Robbie, yes, minocycline might even be slightly better but David prefers to use doxy because it has fewer side effects, so its better when you are not seeing someone all the time. You know, maybe if the new lesion is only small, it might vanish like the ones I had just before I started treatment. You were doing so well, this could well be the case.
Sarah
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.