← Return to MTHFR: Anyone else have C677T Polymorphism & allergic to Cobalt?

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@colleenyoung

Hi @lilli64, welcome. I'm tagging a few other members who have MTHFR with the C667T variant, like @ronniekep @msfxit @hodagwi @tamikay @andyinaustin @gldnrtrvrlvr @bet @monk1015 to see if they know if they are allergic to cobalt. You can read more stories in this related discussion:
- Hyperhomocysteinemia with MTHFR C677T mutations. Does anyone have this? https://connect.mayoclinic.org/discussion/hyperhomocysteinemia-with-mthfr-c677t-mutations-does-anyone-have-this/

Lilli, How long have you known that you have this genetic mutation? How did you discover that you're allergic to cobalt?

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Replies to "Hi @lilli64, welcome. I'm tagging a few other members who have MTHFR with the C667T variant,..."

Thank you for connecting my post to other members. I found out last April, when my Therapist was testing me for medications through Genesight, But; I wasn't familure with genetics that much, since then I've been getting sicker and been learning quit a alot. I found out about the Cobalt through patch testing. When trying to figure out why I was having burning mouth syndrome. Unfortunately it is in B12, to my understanding that is what I need to get Methylmalonic acid levels down?. I live in Nebraska not getting alot of help with our broken system here, so trying to figure this out to know what direction I need to take for this.