The best treatment?
The best treatment?
Hello
I have not tried many treatments for MS and I'm getting so confused with all the information on here and mixed experiences so I thought maybe a poll that would show us all the most successful treatment on average would be helpful. I don't know how to change it so that you can vote more then once so I guess if you're using more then one just put the one you feel is helping you the most. (If I've left something out that you think I should add please let me know)
Moderators: I'm not sure if this is the right place, please feel free to move it if I got it wrong
I have not tried many treatments for MS and I'm getting so confused with all the information on here and mixed experiences so I thought maybe a poll that would show us all the most successful treatment on average would be helpful. I don't know how to change it so that you can vote more then once so I guess if you're using more then one just put the one you feel is helping you the most. (If I've left something out that you think I should add please let me know)
Moderators: I'm not sure if this is the right place, please feel free to move it if I got it wrong
- CureOrBust
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- gibbledygook
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Re: The best treatment?
Hi Courts,
By the way, I haven't been tested/treated for CCSVI yet, but they'll have to pry my fish oil from my cold, dead hands.
NHE
I had no problem viewing the poll and adding the two options. I'm not sure why it didn't show up for you. Did you scroll the page down? I know it seems obvious, but I just thought that I would check.Courts wrote:Thanks for the replies everyone. I tried to add the CCSVI yesterday but for some reason it didn't add it and now the poll doesn't even show up when I try to edit the original post, anyone know how I can change it?
By the way, I haven't been tested/treated for CCSVI yet, but they'll have to pry my fish oil from my cold, dead hands.
NHE
Thanks NHE, it showed up last night when I was trying to edit but not today for some reason oh well, thanks for fixing it for me
Fish oil you say? I've thought about getting some of that. I asked my neuro about it yesterday but he just shook his head. He doesn't believe in anything that hasn't been proven with clinical studies
Fish oil you say? I've thought about getting some of that. I asked my neuro about it yesterday but he just shook his head. He doesn't believe in anything that hasn't been proven with clinical studies
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Dont know how to delete this post!
Last edited by kathryn6112 on Tue Jun 22, 2010 7:12 pm, edited 1 time in total.
- kathryn6112
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Re: The Best Treatment
After I was diagnosed, I began to run into an plethora of anecdotal recommendations to take fish oil. There were personal recommendations from other people and recommendations in books and so on, but none had any references. I'm a "show me the data" type of person so I finally got on PubMed and did a little research of my own. The paper below was one of the first that I ran into that convinced me to give fish oil a try due to its anti-inflammatory effect. Early in my supplement regimen I would sometimes forget to take my supplements for a few days. I would notice that I was feeling really tired and run down. This tiredness would go away within a day of starting back up on my supplements. I now take 6 g/day of fish oil which provides 1800 mg/day of DHA & EPA omega-3 fatty acids.Courts wrote:Fish oil you say? I've thought about getting some of that. I asked my neuro about it yesterday but he just shook his head. He doesn't believe in anything that hasn't been proven with clinical studies
Cytokine secretion and eicosanoid production in the peripheral blood mononuclear cells of MS patients undergoing dietary supplementation with n-3 polyunsaturated fatty acids.
J Neuroimmunol. 1995 Feb;56(2):143-53.
- To demonstrate the influence of n-3 PUFA supplementation on cytokine and eicosanoid production in peripheral blood mononuclear cells (PBMCs) of MS patients (MSP), we investigated the impact of a 6-month dietary supplementation with these fatty acids on the levels of interleukin-1 beta (IL-1 beta), IL-2, interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) in the supernatants of stimulated PBMCs and serum soluble IL-2 receptors in a group of 20 relapsing-remitting (R-R) MSP and a group of 15 age-matched control individuals (CI). The production of PGE2 and LTB4 in the stimulated PBMCs was also assessed in patient and control groups supplemented with n-3 PUFAs. In both groups, n-3 PUFA supplementation led to a significant decrease in the levels of IL-1 beta and TNF-alpha, and this reduction was more pronounced in the 3rd and 6th month of supplementation. An analogous decrease was observed in the levels of IL-2 and IFN-gamma produced by stimulated PBMCs, and in the levels of serum soluble IL-2 receptors. n-3 PUFA supplementation also appeared to significantly affect prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) production in PBMCs, both in MSP and the control group. The reduced production of these proinflammatory eicosanoids, and the decrease of some cytokines with an immunohenancing effect as a consequence of n-3 PUFA supplementation, could modulate some immune functions which have been demonstrated to be altered in MSP.
- Quest56
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Courts,
Good question. Exercise is tops on my list. I'm now a Copaxone user, former LDN user, had the CCSVI stent treatment last September, former Betaseron user, and have used oral and intravenous steroids to treat exacerbations and slow progression several times.
Exercise is it. CCSVI and LDN are in second place, I feel each in turn helped me to continue exercising (I no longer take LDN, the CCSVI treatment took its place).
--Tracy
Good question. Exercise is tops on my list. I'm now a Copaxone user, former LDN user, had the CCSVI stent treatment last September, former Betaseron user, and have used oral and intravenous steroids to treat exacerbations and slow progression several times.
Exercise is it. CCSVI and LDN are in second place, I feel each in turn helped me to continue exercising (I no longer take LDN, the CCSVI treatment took its place).
--Tracy
CCSVI Procedure 9/16/2009 at Stanford
Stent in left and right IJVs
SPMS
Copaxone
Former Ampyra User
Regular Botox Bladder Injections
300mg d-Biotin / day
Stent in left and right IJVs
SPMS
Copaxone
Former Ampyra User
Regular Botox Bladder Injections
300mg d-Biotin / day
- CureOrBust
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I am on the highest available, 80mg. I take 40mg in the morning and the other half at night. I am lucky because my liver appears to be made of stainless steelkathryn6112 wrote:Cure or Bust, may I ask? What dosage do you take? I just do 20mg for high cholesterol but have thought about trying a higher dose.
I also find Steroids great and am on a monthly pulse cycle (3 days); but understand its not good for everyday use.
Then definitely give it a go! It didn't work for me, but others have reported great results. Good luck.kathryn6112 wrote:My family doc is on board to try anything even LDN - she is cool!
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