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Old 12-14-2015, 10:01 AM
Sredna Sredna is offline
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Join Date: Nov 2015
Posts: 6
8 yr Member
Sredna Sredna is offline
Junior Member
 
Join Date: Nov 2015
Posts: 6
8 yr Member
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Quote:
Originally Posted by mrsD View Post
Sometimes, if numbness is present, when people start the nutrients to begin healing, the numbness is replaced by increased sensations as the nerves "wake up". This is temporary.

Also if one is really low in B12, beginning it may temporarily reduce potassium in the serum. This is because the B12 stimulates the bone marrow to make new blood cells which deplete potassium.

So eating potassium rich foods may help with this. Normally this is not a long lasting effect either, as the bone marrow will stop
when it senses enough blood cells have been manufactured.

Lyrica and gabapentin are strange, in that they cause rapid tolerance in some people. They do not work equally for everyone or predictably.
Thank you for the quick reply MrsD. She hasn't had any numbness, more pins and needles, burning, stinging, ache and painful stabbing. But once the symptoms went down they weren't replaced by a feeling of numbness. We also haven't gotten the B12 levels back (only got a note saying they were "normal" and as we all know that doesn't mean much unfortunately). So when we get those numbers I might increase to a higher B12 dose. In 2011 she had a B12 level of 250, so it might be more or less than that at the moment. But I doubt it's over 400 - the doctos have told her that she has issues absorbing B12. I haven't yet looked at Folate/Folic Acid. I want to get the B12 levels from the blood work before continuing with more supplements.

As for Lyrica resistance - it's not impossible. But since we have been ramping up the dosage about 25mg every three days I would think the resistance wouldn't be an issue yet. She's also at a relatively low level at the moment. Nour neuro says we should aim for 200mg (so thats about one more week of dosage uppings) and see how that works.

Tomorrow my wife will hopefully have a phone call with the neuro and discuss this unfortunate new development.

On a side note I'm a bit scared of introducing new supplements because I'm afraid it will cause more issues with the NP. Is this an ungrounded fear? I'm mostly thinking of Folate, ALC, Q10, Alpha Lipoic Acid and Benfotiamine as these are a bit more rare supplements here in Sweden so there's not much "official guidance".
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