Hello. My name is Jason and i'm writing on my wifes behalf.
My wife has been feeling the effects of graves( almost all of them) since the birth of our
first child one year ago. We ignored the symptoms attributing them to postpartem hormones. A
week ago she mentioned one eye looked slightly bulged and I told her I thought that could be
thyroid. She went to have blood drawn and was diagnosed with Graves. She went to see the
local endo a few days ago and he confirmed diagnosis but ordered more tests. We received
those yesterday in a fax from endo's office.
I am scrambling to inform myself and came across this website. I wanted to
give some bloodwork results and the doctors recommendations. i would greatly appreciate your
thoughts on this matter.
1st bloodtest....all was normal except:
T3 %uptake H 42 (24-39) %
T4 H 15.8 (4.5-12.0) ug/dl
TSH L 0.01 (0.20-4.20) uIU/ML
CBC/NO DIFF
MCV L 78.4 (81-101) fl
MCH L 25.6 (26.0-34.0) pg
Differential
LYMPH H 43 (20-40)
the endo ordered a second set of tests as follows: thyroxine (T4) free, direct; TSH ;
triiodothyronine, free, serum ; thyroid perioxidase (TPO) Ab ; antithyroglobulin Ab. We
received only partial results so far......
T4 free direct H 3.87 (0.61-1.76) ng/dl
TSH L 0.005 (.35-5.5) uIU/ml
triiodothyronine,free,serum H 12.8 (2.3-4.2) pg/ml
*other results will follow
The endo said this was a severe case of G.D. that required 250mg PTU 3 times daily. My
wife refused the medicine because of breastfeeding.
Upon the 2nd blood test results he faxed a suggestion of 50mg twice daily.
My wife is still breastfeeding our one year old approx 8 times a day. In light of the
news she is reluctantly beginning a weaning process as speedy as possible while trying to
keep the baby and her stress about the weaning to a minimum.
are these suggestions in line with the test results?
what are risks in waiting a month or so before treatment untill baby weaned?
is there T3 (or anything else)getting in the breastmilk now? if so is this worse that
the PTU?
I am in the infancy of trying to understand this disease. I am trying to arm myself with
as much info as fast as possible because the endo is coming across like we gotta do
something right now. What little i've learned suggests educating yourself and making
informed decisions are a crucial part, but the doctor is making us feel like with the blood
results our research time is limited.
I can't express how important your time and thoughts would be to my family. i would
appreciate any thought or suggestions you have on this matter.
what would be your course of treatment in this case?
is the condition as serious as the endo suggests?