Forum Discussion
Tri
1 year agoMember
Peripheral neuropathy, aches and vitamin supplements- caution about B6
Good morning I know a few of us have peripheral neuropathy and aches in our joints and may be taking magnesium and other vitamins to manage side effects.
Here’s an article of interest about checking your cumulative intake of B6 through any supplements.
If vitamin B6 consumption is inadvertently consumed above recommended levels it can be harmful - and to my surprise our bodies don’t excrete surplus amounts (apparently).
Here’s an article of interest about checking your cumulative intake of B6 through any supplements.
If vitamin B6 consumption is inadvertently consumed above recommended levels it can be harmful - and to my surprise our bodies don’t excrete surplus amounts (apparently).
15 Replies
- TriMemberHi @Afraser and @iserbrown agree with your good points. For me the article was good for raising awareness; just to discuss with our GP and have our levels checked (if we are taking vitamins and if we’re experiencing neuropathy already) and to know it’s not uncommon for Vitamin B6 to be added into other vitamins. The biggest surprise was reading Vitamin B6 is unusual- we don’t excrete the amount if it’s surplus to our needs.
- iserbrownMemberCertainly a confusing topic!
Early days I had all sorts of aches and pains and questioned my GP about supplements, Magnesium, Multi vitamins et cetera He calmed me down by going through my latest blood tests. All levels good!
Once in this bubble a heightened awareness of self and health dominates and we search for how did this happen, why did this happen, will it return et cetera
Eventually the body and thoughts settle!
Best wishes to all
Take care - AfraserMemberJust clarifying - I was told that Vitamin B ( a multi B was recommended) may help PN symptoms, not specifically B6. Most people get all the B6 they need in their diet. I don’t know anyone who
has been specifically recommended to take B6 for anything. - GorgySMemberI will check with my Oncologist. Hopefully he will advise me what would be the correct dose although it was my GP who suggested taking vitamin B for PN. Thank you, Arpie.
- arpieMember@GorgyS - it is interesting that one of the links suggests (as @Fraser said) that PN may be caused by a lack of Vit B6 .... and it well may be.
But as with any meds, taking the correct dose is critical - and it looks like the overdoses are all accidental thru not knowing what's in the tablets/supplements that they're taking ... even a Doctor who has had quite debilitating side effects from accidentally taking too much.
Even arsenic (in tiny amounts) was used as a beauty aid back in the 1800s (it made the skin beautiful & pale & translucent ...) But take too much - and you're dead!! - GorgySMemberjust found the information from Mez-BCNA and will go through these resources
Peripheral neuropathy | My Journey
Understanding Peripheral Neuropathy
Thank you Mez_BCNA and all for your support - TriMemberHi @GorgyS
I feel for you if you’re already experiencing neuropathy and it’s becoming more difficult for you. As @arpie suggested it could be very insightful for you to get a blood test to identify your Vit B levels and see whether or not that’s could be contributing to a problem (or not).
Regarding treatment for neuropathy, I discussed the option to take Lyrica for the nerve pain in my feet with my oncologist especially as it was waking me at night. In the end I decided not to, I took Panadol or Nuromol instead. At the time I also took magnesium tablets on and off as I thought they would help with the ankle and feet aches (not the electric shock type neuropathy pain). But I have stopped taking this now.The only supplement I have now is Vitamin D with calcium for osteopenia (again on the recommendation of my Oncologist) and occasionally a Hydralyte if I have an upset stomach.I’m beginning to appreciate how important a “whole” picture is for my GP and to remember to include any vitamins and supplements. Also, I am also appreciating that I need to record, file and store away carefully for future reference my health records! - arpieMember@Fraser ... I have Vit B12 injections every 3 months due to low levels, but as I don't take supplements or weight loss stuff, I should be OK & safe from doubling up (and it is a different one to B6.)
It seems that there are a lot of supplements that have Vit B6 in them (the problem one, if taken to excess) but it is not always obvious in the labeling (sometimes only seen in the small print.)
Those taking numerous supplements (any of them) with Vit B6 are the ones to keep an eye on, as cumulatively, the combined dosage may cause an accidental overdose ... which may even 'appear to be' neuropathy symptoms, with people taking even more again, as it is seen to be a possibly solution to 'reduce' the symptoms!
Personally, I'd be getting a blood test if you've been on Vit B6 for a long time ... particularly if you're taking other supplements as well. Take care - arpieMember@GorgyS - next time you see your GP, ask for a blood test including Vit B6 levels - and if you are continuing with B6 supplements (or magnesium or other supplements mentioned in the info from @tri & my post - have them checked every time you have blood tests, to be sure, to be sure.
I believe the tingling & numbness are consistent symptoms of neuropathy .... so it is well worth being aware of this.
As with any medication - different people react differently .... so it is important to monitor your levels of ALL Vitamins & particularly other 'over the counter' meds. Some are actually counter productive to some BC treatments - so always check with your medical team if there are any 'contraindications/problems' with anything that is not prescribed. Even taking Fish Oil capsules can affect your blood thinning ... so if you are put ON TO blood thinners, you are usually asked to NOT take Fish Oil Capsules as well!
take care - GorgySMemberAn interesting discussion: my neuropathy has started to become a real nuisance. I am taking a Vitamin B complex. How could I know if it is causing damage, as the symptoms—tingling, numbness, and the potential for permanent nerve damage—are the same as those of neuropathy. I will check with my doctor next time. Is anyone currently taking medication for neuropathy?