Very interested in all this new MS info. Collecting bits of info for my MD
to see. Hoping that it won't be too long until we can all get releif from MS.
Have been dealing with RRMS for more than 20yrs & remained in remission for almost 10. Bladder functions normally now, can walk easily with a cane & found alternative methods to sleep better than I had ever hoped I would.
No pain at all.
As a fall project I have taken some time to write everything down on a
website, because it all works. Involves diet, exercise & several
supplements. Only one drug which costs less than $20.00/month.
alternative MS mgmt for now
A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
Return to “Chronic Cerebrospinal Venous Insufficiency (CCSVI)”
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- Multiple Sclerosis
- ↳ General Discussion
- ↳ Introductions
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- ↳ Undiagnosed
- ↳ MS Etiology and Pathogenesis
- Treatments
- ↳ Chronic Cerebrospinal Venous Insufficiency (CCSVI)
- ↳ Low Dose Naltrexone
- ↳ Tysabri (Antegren, Natalizumab)
- ↳ Copaxone
- ↳ Glatopa
- ↳ Avonex
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- ↳ Betaseron
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- ↳ Novantrone
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- ↳ Diet
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- ↳ Biotin (Qizenday, Cerenday, MD1003)
- ↳ Coimbra High-Dose Vitamin D Protocol
- ↳ Statins
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- ↳ Revimmune (Cyclophosphamide, Cytoxan)
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- ↳ Rituxan (Rituximab)
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- ↳ General Medications
- ↳ Tecfidera (BG-12, Dimethyl fumarate)
- ↳ Vumerity (Diroximel fumarate)
- ↳ Bafiertam (Monomethyl fumarate)
- ↳ Gilenya
- ↳ Aubagio (Teriflunomide)
- ↳ Mayzent (Siponimod)
- ↳ Zeposia (Ozanimod)
- ↳ Ponvory (Ponesimod)
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- ↳ Ampyra (Dalfampridine)
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