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rdrone
Member
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Posted: Thu Nov 19th, 2009 19:40 |
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Greetings to All,
My Thanks to Dr. Marshall and everyone supporting this effort.
I have completed my first month on the Minocyline 25mg. I must say that my experiences have happened exactly as they were described on the Marshall Protocol site. I had to take it slowly this past month. I had several IP experiences after I had taken the Minocycline. ( It is amazing that this minimal amount of antibiotic could make me feel this bad ) For the two days following, my MS symptoms were a little tougher. I experienced the flu like symptoms, weakness, fatigue, very heavy feeling legs, and the brain fog. So I increased my Benicar schedule as per the site's direction and spent a lot of time relaxing, sleeping, and reading. By the third day I was feeling better. I would take an extra day off and start back on the fourth day on the Minocycline. By the end of the month I have arrived at a place where I cant take the Mino. every other day with minimal problems. I am going to stay on that schedule for the next two weeks then I will raise my Mino. dose to 50mg. All is Well !!
Be Encouraged, I am,
Rdrone
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Diag. M.S. 1995,(Aug08)25D:18pg/ml 25D:19ng/ml Ph1Sept08 40mg Olmacip 4xDay, 75mg Minocyclyn every other day,
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Barney
Moderator
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Posted: Sun Nov 22nd, 2009 02:14 |
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Hello Rdrone,
Sounds like you have it all controlled and are doing well.
Welcome to MP and glad you are wise to do this.
You may want to review the guidelines for managing immunopathology:
http://AutoimmunityResearch.org/phase1.pdf
and
http://mpkb.org/doku.php/home:mp:managing_immunopathology
HANG IN THERE, WE WILL MAKE IT!!!!BARNEY
Last edited on Sun Nov 22nd, 2009 14:51 by
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Sarcoidosis diabetes asthma| loss r/kidney| hysterectomy osteoporosis| Start MP 1/1/05| My Story| ABC of MP| Bacteriality|
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rdrone
Member
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Posted: Sun Nov 22nd, 2009 07:33 |
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Thanks Barney,
Rdrone
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Diag. M.S. 1995,(Aug08)25D:18pg/ml 25D:19ng/ml Ph1Sept08 40mg Olmacip 4xDay, 75mg Minocyclyn every other day,
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paulalbert
Moderator
| Joined: | Fri Oct 26th, 2007 |
| Location: | |
| Posts: | 99 |
| Status: |
Offline
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Posted: Sun Nov 22nd, 2009 14:52 |
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Hi Barney,
Don't forget that the new address of the KB is mpkb.org – not mp-dev.com. 
Even so, if you put in the wrong address, it will forward you to the correct address.
thanks,
Paul
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Barney
Moderator
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Posted: Sun Nov 22nd, 2009 22:35 |
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Paul,
I will add it in also........next time.
HANG IN THERE, WE WILL MAKE IT!!!BARNEY
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Sarcoidosis diabetes asthma| loss r/kidney| hysterectomy osteoporosis| Start MP 1/1/05| My Story| ABC of MP| Bacteriality|
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eClaire
Member
| Joined: | Thu Oct 18th, 2007 |
| Location: | Virginia USA |
| Posts: | 375 |
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Offline
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Posted: Mon Nov 23rd, 2009 00:47 |
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Welcome to the site! I am most encouraged by your post. It seems we have few members with MS and it is always helpful to find other people with a similar diagnosis to discuss their experiences on the MP. (Despite the fact that much of our experience is alike regardless of the disease label we carry.) I hope other people with MS find you.
Claire
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42mo on MP; CFS FMS MCS COPD hypermob. IBS/GERD osteopor.; 125D48 25D<4;
NoIRs during most daylight outings;
Ph1.Dec06 * ModPh2.Jun07 * AbxBrk.Mar-May08 * Ph2.Oct-Nov08 * Ph1.Jan2009 * Olm.alone.Jun10
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