The Ivers Fam: Counting Counting Counting

Friday, February 4, 2011

Counting Counting Counting

I am SO sick of counting food seriously I already had to count three kids protein every flippin day and now that I have been counting my carbs for the last couple months I am done seriously it is RIDICULOUS I give up I am throwing in the towel. And don't let Shane fool you he doesn't count crap really like NEVER if the girls are hungry he asks me what to feed them if I am gone he will call or text me and ask me what they can have.If they go to grandmas or anywhere else I have to send food and have it counted or else they will not eat. I am looking forward to a few days of no counting yes while I am in the hospital which is pretty pathetic I really need a vacation. Sorry just had to throw this out there I feel better already!

11 days not that I am counting or anything

How much do you think she will weigh? I am gonna say 9lbs 3 oz.

1 comment:

Matt. Tara. Addi. Roslyn. said...: I'm sorry Jennifer!! That really does suck and I would feel the same way and throw in the towell. You guys needa go on a vacation after little Hadley is born! Good luck! :); February 6, 2011 at 12:37 PM

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My Girls Genetic Disorder Tyrosinemia Type 2

Type II tyrosinemia is caused by a deficiency of the enzyme tyrosine aminotransferase encoded by the gene TAT. Tyrosine aminotransferase is the first in a series of five enzymes that converts tyrosine to smaller molecules, which are excreted by the kidneys or used in reactions that produce energy. This form of the disorder can affect the eyes, skin, and mental development. Symptoms often begin in early childhood and include excessive tearing, abnormal sensitivity to light (photophobia), eye pain and redness, and painful skin lesions on the palms and soles. About half of individuals with type II tyrosinemia are also mentally retarded. Type II tyrosinemia occurs in fewer than 1 in 250,000 individuals.
Dr Longo informed us that there are less that 100 cases of tyrosinemia type 2 reported worldwide. I have four of them.. I am so thankful that Presley was diagnosed when she was (at 13months) and that Sam, Dylann and Hadley were diagnosed at birth. They are on a low-protein diet and are doing great!!