Hi Family, has anyone had any experience with any B12 cream, ointment or any other lotion or crème to ease the numbness in hands?
I have been injecting 1ml, B12 SC weekly sometimes 2x a week, for year and a half, there has been improvements, tests are all in range Folic, vitamin D, etc.
The numbness has really just started, and has gotten worse, from this excellent forum I understand the numbness is probably the result of nerves coming alive. I took PPPI’s for a long time as prescribed by my Dr. Only to learn that PPI’s block B12 absorption, and resulted in all my B12 deficiency problems.
Also, I learned that amlodipine besylate for high blood pressure also blocks vitamin B12, all prescribed by my Dr.
By substituting and changing diet I am off all blood pressure medication, after B12 damage.
Sorry for the length of this post.
This forum has helped me and my Dr. TREMENDOUSLY!
MAY GOD BLESS AND HEAL US ALL
THANK YOU,
P.S. Does compression gloves help with easing the numbness?
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RisingOne
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hello, you might try increasing frequency of s.i. , or active sublingual b12 drops.
I used transdermal b12 spray but I believe its uptake by the body is small compared to injections and efficacy is probably after long term use However everone is different and it might suit you. Best wishes
I believe that the B12 molecule is too large to get through the skin . Injections are the most efficient way to get B12 . Oral or sub-lingual tablets might help if you don’t have P.A. Also sub-lingual and nasal sprays are a possibility. The skin in the nose and under the tongue will allow the passage of B12 in some people .
Hi RisingOne, I think at one point you were doing them more frequently?
Numbness while already injecting for some time is probably -not- a sign that the nerves are coming back alive, but quite the opposite.
If you are using cyano, you might want to try daily, if you can tolerate it. Methyl might also require more frequently (others who use it will know better).
Or do you mean the numbness is going away?
How are folate levels and are you taking any? B12 needs folate (folic acid, folinic, methylfolate, or folate from food) to do its job properly.
generally, symptoms can come back if you reduce frequency. when did you reduce the frequency? If it was recent, then the body might take some time to adjust to the new dose and then things will improve. Also, why were you unable to function at EOD frequency?
sounds strange. At least I have not heard of body pain after injection. Generally, the side-effects of a B12 injection include skin rashes, hives etc. Worsening symptoms may indicate some other issue, such as a viral infection, too hot a climate etc. that requires a higher dose temporarily.
I hurt for weeks after loading doses but stayed with it. I had to start Glutathione and Magnesium to help my body cope as well as electrolytes. It has been 5 weeks since I started loading doses and my body is not hurting as much. It almost felt like my body was tired and achy and sore and my general pain was high, but it was a different pain from the sharp stabbing nerve pains, and lightening bolt type pain, among other pains I was feeling from not getting enough B12.
B12 cannot be absorbed in a cream through skin.. you would be better to try eod injections making sure to take all cofactors daily of folic acid, b complex with no more than 10mg of b6, potassium rich foods and magnesium malate or glycinate..
You can tell how effective transdermal adsorption would be by looking for traffic in the other direction. Do you find your bodily fluids leaking out through your skin? 😛
What works for me is 1 Tablespoon Black Strap Molasses, once a day and Papaya Enzyme chewable Tablets available from Amazon by NaturesPlus with meals.
It was the PPIs, that wrecked my digestive system, and caused the B12 deficiency, GP failed to diagnose correctly, After much prayer and research I came across an article that described my situation perfectly, I than came upon this web site and educated my GP, who described B12 injections. I now SI EOD,
Long journey but much prayer got me through the GERD and B12 deficiency.
I had PA since the '80s but a few years ago developed hiatus hernia and was put on Zantac. When that got banned it was Emozul. I've had digestive issues for nearly forty years and took Creon until I got a severe allergic reaction and had to stop taking it. Since then I've used digestive enzymes and have tried most of them, including papaya. Molasses I've not tried but will give it a go.
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