Nervous

what, if anything, do you know about mthfr polymorphism? my phone will not let me capitalize too much so this wont be the best blog post ever. but im worried and sharing . my cousin has mthfr and it caused her to clot at 11 weeks and lose her baby. when i told the nurse that it was in my family history (just the one cousin though) she turned white as a sheet and explained it a little bit. if i were to have it i would never relax. id be on bed rest blood thinners, etc. and have a chortened life span.

silly to worry about stuff that chances are, i dont have. but i do. its my job. i cant find anything on dr. google. so share any knowledge you have.

as for me, i got to see the monster today. baby fishy monster was doing some cartwheels and his heart was going a mile a minute. it was just a nurses visit so i didnt expect to see him, but when she heard we had a family history of twins, she pulled out an ultrasound maachine from the 90's and check him out. we just got one picture and since she couldnt zoom in its not very good, but since he was so little, he almost looked like a starfish. a cute one! anywho every 5 seconds my phone is now popping up with an alert about losing the page data and i dont want to retype this so i think i better post quick.

hopefully all remains well. only 29 weeks and 1 day left!