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Abigail7 progress
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Abigail7
Member in Phase 3


Joined: Wed Sep 13th, 2006
Location: Woodbine, Maryland USA
Posts: 35
Status:  Offline
 Posted: Thu Jan 11th, 2007 03:58

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In January of 2005 I was diagnosed with FUO (6months) anemia, CFS, Fibromyalgia, night sweats, muscle and joint pain, headaches, etc. After a hospital stay of one month, and many specialists unable to make a definitive diagnosis, I was released from the hospital on prednisone. This provided only temporary relief of my symptoms. I was then treated by Dr Ritchie Shoemaker. After initial testing he diagnosed my condition as Exposure to mold and began treatment with Cholestyramine. After much initial relief but never a complete cure of my symptoms I started on the MP in Oct. of 2006. My doctor started my initial dose of Benicar at 50mgs which was increased to 100mgs about 2 weeks later. The results of my D Metabolites were 1,25-D+57pg/mL and 25D=23ng/mL taken before starting MP. My herxing has been difficult but tolerable. Sometimes lasting for 2 days with severe pain in my arms, legs, shoulders and back. I have been using the Noir sunglasses both indoors and outdoors as my eyes have been extremely sensitive. My Cardio CRP result was 18.9 which I feel explains my low level of energy. I have been trying to avoid all sources of Vit D and Omega 3 (with occasional mishaps) and also trying to stick to a low carb diet (with occasional mishaps). I will try to "hang in there" with these difficult herxes and hope the end result will finally be a life without pain and suffering.



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CFS, FUO, FM, anemia, 1,25D57, 10/06 MP, avoiding light & D, Noirs, Ph3 7/07, D,25 06/09=12ng/mL

Aussie Barb
Member in Phase 3


Joined: Thu Jul 22nd, 2004
Location: Australia
Posts: 19553
Status:  Offline
 Posted: Thu Jan 11th, 2007 04:08

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Abigail
Thank you for posting..

"My doctor started my initial dose of Benicar at 50mgs which was increased to 100mgs about 2 weeks later." "My herxing has been difficult but tolerable"

Do you mind clarifying your meds dosing and schedules for us please..

Each time you post,  it is helpful if you will please list your MP meds in an index format at the beginning of your message.

Posting an Index of your MP meds dosing and schedule etc at the top of your post is helpful to Staff for replying and for other Members for reading and understanding .. and for your own reference at any time.

Your details enable us to assist you. You may like to look how some are doing it..   thank you...


Please check all precautions / instructions in the Phase One Guideline with your Dr. Some have it printed to check with regularly. It is very important that you and your Dr know to follow the essential aspects and guidelines as written for safety and efficacy of treatment..

If you would like your D tests interpreted see What to include in your preliminary test result reports.

Checklist when Starting MP

Thanks,  Barb ....

W
hen you can, please fill your signature line to help Staff and others reading and replying < see this link for details to include. Your details enable us to assist you. Thank You ..



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Barb: Dx Inflammatory Disease Endocrine Imbalance 2003| Depression| 24+ years not Dx| MP Aug04| ABC of MP| MP Search|
Abigail7
Member in Phase 3


Joined: Wed Sep 13th, 2006
Location: Woodbine, Maryland USA
Posts: 35
Status:  Offline
 Posted: Wed Jan 24th, 2007 00:49

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Dx 2005 6 months FUO/anemia/mold/CFS/Fibromyalgia=meds-prednisone, iron,2005 cholestyramine 2005/ Oct 19, 2006 started phase 1/D tests 1,25=57 pg/mL & 25 D=23 ng/mL crp 18.9/ Avoiding light and D/ Noirs/Beni 40 mgs evy 8 hrs 10/19- added 50 mgs of Mino every other day 12/25- 100mgs every other day 1/10/07.

Have already noticed an improvement in energy levels. Nausea, headaches are much diminished. Still dealing with joint pain in arms and legs. Episodes of lightheadedness especially in the morning. Pain meds needed less often. Some herxes intense.



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CFS, FUO, FM, anemia, 1,25D57, 10/06 MP, avoiding light & D, Noirs, Ph3 7/07, D,25 06/09=12ng/mL


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