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Ilena

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Hi Cheryl, how wonderful that you are both doing well...I imagine it

was very difficult though right after surgery. I appreciate your

input on work..I really have not been up to it, but I felt as though

my doctors were pushing me. I feel relatively normal now (things

seem to have settled down in May) and at the end of September I will

begin part-time. It is good to hear that someone was advised to

stay home a year if possible - that way I dont feel as if I've been

lazy. I agree, you really do need to take your time, and go through

the whole process, emotionally and physically.And you are doing well

too? Does your husband feel guilty about your donation, I

do...though maybe this goes away in time?

Daily, I take 2000mg cellcept, 3 mg prograf, 3mg rapamune, 10mg

prednisone along with a whole bunch of other things, but those are

my immunosuppressants - hopefully they will get reduced soon, but I

have other autoimmune issues as well.

Thanks again

Ilena

> Dear Ilena,

>

> Congrats on your transplant. I was my husband's donor in 12/99

and he is

> doing just wonderful. We were advised by the tx team if we could

afford it to

> let him mend for a year before going back to work. I know right

after tx

> everyone seems to have all this energy and think they can do

anything. I guess

> after being sick for so long, you do feel just wonderful. I know

Randy continued

> to get better and better each month and we saw him hit sort of a

plateau at 6

> months and another one at 9 months. He decided to go back to work

part time

> (2 days/week) during the 11th month post tx. I can honestly say

his recovery

> has been one with very few and minor hiccups. We strongly believe

it was

> because we allowed him to heal. For the next 6 months after

going back to work,

> he went to 3 days/week, then 4days and finally full time. He has

never looked

> back since then. He loves what he does and sometimes I just have

to tell him

> to slow down. Often he goes to work at 6am and gets off at

4:30pm. I made

> a deal with him... he can go in as early as he wants but please be

home for

> supper and time in the evening with the family. He is an

electronics engineer

> and designs new technology stuff. He is like a kid in a candy

store at

> work--lol.

>

> He was fortunate that they were able to stablize his medications

early on and

> by 8 weeks post tx his meds havent changed. He takes 1/mg

prograf twice a

> day, 5mg prednisone once a day, magnesium because of the prograf,

a

> multivitamin, calcium because of the prednisone and bactrim 3times

a week. He takes

> morning meds with breakfast and evening meds with dinner. The tx

is almost an

> afterthought for us. We have both done very well. We chose

living donor because

> we wanted to get on with our lives and also get Randy tx'd before

he got too

> emanciated. The healthier you are going into the surgery, the

quicker and

> healthier you are after it.

>

> Let us know how you are doing and welcome to the group!

>

> Cheryl & Randy

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