tag:blogger.com,1999:blog-407693481428535204.post8304270730258212150..comments2023-10-12T00:50:51.247-07:00Comments on Taming Symptoms of Multiple Sclerosis Blog: Reversing Multiple Sclerosis Neuropathy or MS Nerve Damage Using Vitamin B12?http://tamingmultiplescelorisis.blogspot.comhttp://www.blogger.com/profile/13019372302830483630noreply@blogger.comBlogger4125tag:blogger.com,1999:blog-407693481428535204.post-53075333688855095212011-06-06T06:31:14.544-07:002011-06-06T06:31:14.544-07:00As far as spasticity goes, reducing spasticity has...As far as spasticity goes, reducing spasticity has been a problem for me too in the past. What I found that works much better is taking calcium and magnesium together. Usually, people take twice as much Calcium as Magnesium, but since spasticity is often a result of a more severe Magnesium deficiency, it helps to relieve the spasticity by taking equal amounts of calcium to magnesium. Taking extra magnesium, along with the calcium helps to greatly reduce the spasticity in Multiple Sclerosis, at least that is what I have found to work for me. I hope this helps you to find more relief from the spasticity.http://tamingmultiplescelorisis.blogspot.comhttps://www.blogger.com/profile/13019372302830483630noreply@blogger.comtag:blogger.com,1999:blog-407693481428535204.post-87038972899749841852011-06-05T22:38:44.971-07:002011-06-05T22:38:44.971-07:00Also, I don't take iron now, since many people...Also, I don't take iron now, since many people with the MS, who have the CCSVI condition may have much higher levels of iron in the brain. My doctor does regular blood tests for iron and if I do come up low in iron, then he will tell me that I need to take iron. Not all people with MS have the CCSVI condition, and I am not sure if I do or not, but so far I don't seem to need to take iron, as a supplement.http://tamingmultiplescelorisis.blogspot.comhttps://www.blogger.com/profile/13019372302830483630noreply@blogger.comtag:blogger.com,1999:blog-407693481428535204.post-30885351929394082592011-06-05T22:36:15.917-07:002011-06-05T22:36:15.917-07:00I take large amounts of vitamin D and that helps a...I take large amounts of vitamin D and that helps a lot in reducing the MS attacks. I started taking the higher doses of B12 about a month ago, so I am not sure yet that the B12 can reverse more extreme nerve damage from MS yet, but I have found that taking the higher doses of B12 has been helping give me more energy, reducing the fatigue and it does help my nerves to function better than they have for a very long time. I did find that I couldn't tolerate taking vitamin B12, when I was first diagnosed with MS, since my mercury level was very high and mercury reacts with B12 to form the methyl form of mercury, which is much more toxic and causes much more nerve damage than any other form of mercury. Now that my mercury level is much lower than it was at first, I am finally able to tolerate taking vitamin B12. Also most people diagnosed with Multiple Sclerosis do have lower levels of B12 and need to take it if they can tolerate it. The methyl B12 absorbs much better than other forms of B12, since people with MS also have absorption problems when it comes to vitamin B12.http://tamingmultiplescelorisis.blogspot.comhttps://www.blogger.com/profile/13019372302830483630noreply@blogger.comtag:blogger.com,1999:blog-407693481428535204.post-6088004444384377282011-05-28T21:19:23.374-07:002011-05-28T21:19:23.374-07:00i take an incredible amount of B-12, and D too.......i take an incredible amount of B-12, and D too.... <br /><br />my neuro started me on both of those immediately... oh and iron too..<br /><br />the iron helps with spasticity, B-12 with neuropathy and energy, D for slowing progression....<br /><br />i don't know if it really is working or not but i can say that when i run out my supplements i don't feel as good... so something must be going on there...Sherrihttps://www.blogger.com/profile/11844785407011196401noreply@blogger.com