Beeturia and Hemochromatosis.
Posted , 3 users are following.
Greetings.
Waiting on my DNA results for Hemochromatosis.
I have always found red beets to easy stomach pain, don't know why.
However I do experience a harmless side effect called Beeturia. Red/pink urine and fecal matter after eating beets.
I have heard there may be a connection between this condition and Hemochromatosis.
Curious, anyone else notice this harmless side effect from eating beets ?
Thanks
Robert
0 likes, 6 replies
sheryl37154 robert71867
Posted
I have never heard that there is a connection with Beeturia and hemochromatosis at all, and I read a lot about hemochromatosis - medical research. Is Beeturia harmful to you? If not, I would not worry about it. If anything, beetroots are high in sugar which is not good, and iron, but iron in vegetables is not harmful.
robert71867 sheryl37154
Posted
sheryl37154 robert71867
Posted
Even children with (non active) HH are more inclined to be anaemic and need iron rich food to grow. And anaemia as you say causes beeturia.
In my position as an advocate for a HH organisation, I have spoken to probably a couple of hundred people about their symptoms, and not once was your symptom mentioned. Some people has porphyria (of their hands) which is not necessarily a sign of HH. But if taken to a dr, it brings attention to something out of order.
Do you have beautiful skin? - beetroot is supposed to be good for the skin and it has some wonderful antioxidants.
We will see if this forum exposes a commonality.
stacie32 robert71867
Posted
I have porphyria cutanea tarda, this causes red/purple urine no matter what I eat and is also linked to iron loading/haemochromatosis. That's the only link to red urine/ haemochromatosis I've read of and I've scoured the internet on the subject for 3 years thinking I was going mad! 😁
sheryl37154 stacie32
Posted
stacie32 sheryl37154
Posted
A little Sheryl, I had to have a camera in my bladder to check for cancer which was uncomfortable. Even though it was a lovely strawberry red there was only ever blood detected on a dipstick twice(gp totally puzzled,opening new packs of dipstick and looking at me like I've two heads!😁. Even after this and being told I was imagining it/it's not possible by the urology nurses doing the tests, nobody ever mentioned porphyria but I had already started my own research, all my symptoms fit! Aswell as the urine ive got blisters,scarring,skin fragility, hairy face and arms etc. It was when they started mentioning kidney biopsies(I knew they were fine) that i kicked up a stink and pushed for testing until they took me seriously. I basically had to diagnose myself, still waiting to see haemotologist for proper info (gp knows very little) and treatment, 18 week wait... the sun is upon us soon and I have to try and avoid it 😣. Could be worse, it is the most treatable type. Xxx