Uno
Senior Member
- Messages
- 157
- Location
- Brighton, United Kingdom
Hi folks
Under my charity Neuroimmune Alliance, I am trying to arrange labs in the UK to offer a methylation pathways panel as recommended by Rich Van K.
Currently not one lab or doctor runs this test so I am trying to use existing labs to offer a service.
The Doctors Laboratory are saying that Homocystine needs to be frozen, does anyone know how correct this is?
It seems ridiculous that we have to send our bloods all the way to the USA to get tested!
If anyone has had any success with any labs please let me know!
Under my charity Neuroimmune Alliance, I am trying to arrange labs in the UK to offer a methylation pathways panel as recommended by Rich Van K.
Currently not one lab or doctor runs this test so I am trying to use existing labs to offer a service.
The Doctors Laboratory are saying that Homocystine needs to be frozen, does anyone know how correct this is?
It seems ridiculous that we have to send our bloods all the way to the USA to get tested!
If anyone has had any success with any labs please let me know!