Magnesium Levels: Hi, All. I'm nearly... - Kidney Transplant

Kidney Transplant

3,688 members2,119 posts

Magnesium Levels

blackkat2 profile image
14 Replies

Hi, All. I'm nearly 7 years post-transplant. My magnesium levels are chronically low, despite heavy supplementation. I've tried all the various varieties (oxide, citrate, gluconate, etc.), as well as diet modifications. Nothing raises my levels. My transplant team is stumped. Anyone else have the same problem? Advice? Thanks.

Written by
blackkat2 profile image
blackkat2
To view profiles and participate in discussions please or .
Read more about...
14 Replies
YorkyinNorfolk profile image
YorkyinNorfolk

Hello, this is interesting as my GP (UK) recently mentioned my lower magnesium levels following some blood test results. I’ve had my transplant over 22 years. I’ve been taking some magnesium supplements as a result. Having quickly read up on it following your post there have been studies around magnesium levels in renal transplant patients as it’s been identified as quite a common issue. It appears to be related to our lower eGFR and possibly our medication following transplant but exact reasons are not known. My eGFR is around 50-53 now.

This article explains it quite well but it looks like there is a need for further research on the issue:

pmc.ncbi.nlm.nih.gov/articl....

blackkat2 profile image
blackkat2 in reply toYorkyinNorfolk

Thanks, YorkyinNorfolk!

meggy619 profile image
meggy619

I have tried supplements such as powders, but did not like them, I purchase Almond butter ( with crunchy bits) from the supermarket, this is high in Magnesium, 1 teaspoon daily worked for me, in fact my transplant team now recommend some patients try this, if they don't like powders, I also add a tablespoon of ground almonds and pumpkin seeds, 50 -50 % to my oats at breakfast time, pumpkin seeds also contain Magnesium and Nitric oxide, which is good for blood pressure and blood flow, It also helps improve gentlemen's problems with E .D Please Do Not Try This If You Are Allergic To Nuts

blackkat2 profile image
blackkat2

Thanks, meggy619!

Lady1984 profile image
Lady1984

good morning … i’ve noticed the solgar magnesium citrate works for me well .. any other brands i didn’t obsorb well .. after taking for 3 months continuestly did my bloods and it went back up to 7 from 5

blackkat2 profile image
blackkat2 in reply toLady1984

Thank you, Lady1984!

hope1419 profile image
hope1419

Low magnesium seems to be a recurring issue after transplant. I think our bodies were not used to good kidney function and now they flush all electrolytes. I started to have magnesium issues right after transplant; to the extent, that I ended up at the emergency room because I was having numbness in my face and arms, and they wanted to discard a stroke -- it was the low magnesium. Any way, my doctor gave me a list of foods high in magnesium combined with different suplements. I had to be out of the magnesium citrate because I had too.mich diarrhea. The doctor say it was counter productive because I was loosing all the electrolytes. I now have to use an over the counter one that works for me, (Magnesium- magnesium glycinate lysinate chelate 100 mg 4 pills X2/day) but I have to watch my levels constantly. They tend to be low anyway. I have to eat lots of beans and nuts.

blackkat2 profile image
blackkat2 in reply tohope1419

Thank you, hope1419!

meggy619 profile image
meggy619 in reply tohope1419

Because your kidney is not connected to the central nervous system, It is in effect a dumb filter, in simple terms, a kidney connected to the CNS is retaining things you need as well as discharging things you don't. Magnesium for instance is not retained, a doctor friend says you can not have too much magnesium, he is healthy but still consumes magnesium rich foods

Panda9122021 profile image
Panda9122021

My level was a little low on my last test. I'm 3 years post-transplant. I hadn't been eating as many nuts and pumpkin seeds as before. Hoping a few of those will help.

Tashikat profile image
Tashikat

Hi there ….I have had Afib since 2016, 7 years after my kidney transplant. I had 4 ablations & have taken medications fir it, & now my kidney is rejecting likely from the Flecanide. A friend told me about Dr Caroline Dean & her liquid ionized magnesium called ‘Remag’. I have been taking it for a year & my Afib is non-existent. Its truly the best magnesium on earth. Google it to order it. I also recommend her book ‘The Magnesium Miracle’…so much info!! Best wishes!!

blackkat2 profile image
blackkat2 in reply toTashikat

Thank you, Tashikat!

Merlin_Way profile image
Merlin_Way

How low is the mag level in your blood draws? Mine ranges from 1.4 to 2.0 mg/dL. I take 850 mg daily of Mag in pill form, plus granola-type foods. I don't sense that taking a high dose makes much difference.

blackkat2 profile image
blackkat2 in reply toMerlin_Way

Mine's usually around 1.6, just below the normal range. I take 1600mg but, as you say, it doesn't seem to make much difference!

Not what you're looking for?

You may also like...

Levels

Hey guys im 5 week post transplant.. it took a while for my kidney to kick in. In the last 2 weeks...
Bradybean profile image

varying tacrolimus levels - suggestions?

I’m 4 years, 7 months past transplant and still working with my Nephrologist to staboliza...
CoYogi profile image

Levels for kidney transplant

I am over 3 yrs transplant. Does anyone who has a few years still have Tac levels up and down, and...

creatinine levels

I’m 9 months out from my kidney transplant and all is going well except this month my bloods show...

Recent kidney transplant patient

Hi About 6 years ago I was diagnosed with Polycystic Kidney Disease a genetic disease which causes...
yahoo999uk profile image

Moderation team

See all
JessicaJ_NKF profile image
JessicaJ_NKFAdministrator
Cap21_NKF profile image
Cap21_NKFPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.