The lowest my B12 ever showed was 408 (211-911) back in September 2012 but I had been using supplements, just form Tesco, as I was not clued in on the PA issue. I have since moved on to use Thorne B complex and use 1000 sublingual B12. I stopped all B's for 4 months for an active B12 test but it came back high in range. I've just paid for a homocysteine and IF.
I have Graves’/Hashi’s, thyroid removed.
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TSH 0.02 (0.55-4.78)
FT4 22 (9-23)
FT3 5(3.50-6.5)
Homocysteine 12 (10-15) AT RISK
IF 1.4 (0-10) Just paid for both of these tests last week for myself.
B12 777 (211-911) with supplementing
Active B12 119 (25-165) done in Jan 2012 after 4 months of not supplementing.
Folate 10.3 >3.40
Ferritin 89 (20-291)
IRON 23.2 umol/L 6.6 - 26.0
T.I.B.C * 81 umol/L 41 - 77
TRANSFERRIN SATURATION 29 % 20 - 55
Vit D 101 >50 replete
HbA1c 35 (20-41)
RBC
Haemoglobin 123 (115-165)
MCV 92 (77-99)
MCH 32.5 (27-32) HIGH
Haematocrit 0.349 (0.37-0.47) LOW
RBC 3.79 (4.20-5.40) LOW
MCHC 35.2 (30-37)
WBC
WBC 3.9 (4-11) LOW
Neutrophil 2 (2-7.5)
Lymphocyte 1.5 (1.5-4.5)
Monocyte 0.3 (0.2-1.12)
Eosinophil `0.1 (0.10-0.60)
Basophil 0.0 (0.0-0.20)
I have gene mutations for B12, B6, folate. Both the MTHFR C677T and MTHFR A1298C. FUT2 rs602662 is the gene that had a decreased ability to absorb B12. FUT2 is the gene for reduced amount of B6.
Based on these result could someone tell me if I should take it to the GP?
I should mention that my endo said to had odd shaped blood cells but said no more. Is any of this PA?
Sorry for the long post :0(