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Hi, I just received a letter back from my GP after sending him information from David's website. He says that his theory seems to be very much a one-man theory and that I should seek neurological treatment options. I told him that I wanted to do an Elispot test offered by ArminLabs (i know it's not 100%) that I would finance. He has offered to take the blood but will not prescribe the antibiotics without a Neurologist's opinion frown

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Ah, you have the same problem as one of my friends up north!  Presumably Kent will sort out the messaging soon here, otherwise, where else can I contact you:  Facebook or Instagram?

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

hi Sarah, i've emailed you again :)

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.

Oh, this is silly because I didn't get it this time!!

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

I’ve messaged you on Facebook!

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.

Thank you, I will send you my reply in an hour or so!

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

I have just messaged you on Facebook, but I still can't find anything here!

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.