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I will be doing my third shot tonight for the Hep C treatment. So

far, so good, as you all know. I went to my family doctor yesterday

for a check up. She is watching me locally, while my transplant

coordinator watches me from there. My family doctor was amazed at

how well treatment has been going for me so far. She was dreading

seeing me because she thought I would be sick with fever, chills,

body aches, and depressed. I've had none of those so far. My lab

results from yesterday aren't looking as good as they were, though.

My coordinator called me today and told me my numbers have been going

up. I didn't ask her because I didn't feel like knowing the answer

right now, but I'm assuming she's talking about my liver numbers.

I'll know when I get my lab results in the mail Thursday. It can do

that when first starting treatment. Hopefully, they will be going

back down again soon. Also, my white and red blood cell counts are

dropping, but I knew that would probably happen. They're still in

range right now, but soon I will have to get shots to keep those up

in the normal range. My glucose was up to 119 yesterday, but today

it's back down to 98. That's another thing I have to check twice a

day because the treatment can cause the blood sugar to rise, and then

I would need insulin. I've been getting more and more tired, and no

wonder since my white and red blood cell counts are dropping. My

coordinator told me from here on out I need to just rest, and if

things need to be done, to let my husband do them. She's really

stressing that. She thought I might be out shopping for Christmas,

and she doesn't want me doing that. I haven't been since I hate

shopping anyway. I usually do all my shopping online, and had that

all done before Thanksgiving. Anything else that we need to get my

husband goes out to get. doesn't let me run around and wear

myself out anyway, so she doesn't have to worry about that...lol.

I hope you all are doing well.

Penny

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Continuing to pray for you Penny.

________________________________

To: livercirrhosissupport

Sent: Tuesday, December 16, 2008 4:53:22 PM

Subject: Third Shot Tonight

I will be doing my third shot tonight for the Hep C treatment. So

far, so good, as you all know. I went to my family doctor yesterday

for a check up. She is watching me locally, while my transplant

coordinator watches me from there. My family doctor was amazed at

how well treatment has been going for me so far. She was dreading

seeing me because she thought I would be sick with fever, chills,

body aches, and depressed. I've had none of those so far. My lab

results from yesterday aren't looking as good as they were, though.

My coordinator called me today and told me my numbers have been going

up. I didn't ask her because I didn't feel like knowing the answer

right now, but I'm assuming she's talking about my liver numbers.

I'll know when I get my lab results in the mail Thursday. It can do

that when first starting treatment. Hopefully, they will be going

back down again soon. Also, my white and red blood cell counts are

dropping, but I knew that would probably happen. They're still in

range right now, but soon I will have to get shots to keep those up

in the normal range. My glucose was up to 119 yesterday, but today

it's back down to 98. That's another thing I have to check twice a

day because the treatment can cause the blood sugar to rise, and then

I would need insulin. I've been getting more and more tired, and no

wonder since my white and red blood cell counts are dropping. My

coordinator told me from here on out I need to just rest, and if

things need to be done, to let my husband do them. She's really

stressing that. She thought I might be out shopping for Christmas,

and she doesn't want me doing that. I haven't been since I hate

shopping anyway. I usually do all my shopping online, and had that

all done before Thanksgiving. Anything else that we need to get my

husband goes out to get. doesn't let me run around and wear

myself out anyway, so she doesn't have to worry about that...lol.

I hope you all are doing well.

Penny

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rest rest rest penny, you take it easy and just rest, let us know

your results when you get them. know i am thinking of you and praying

too,much love barby

>

> I will be doing my third shot tonight for the Hep C treatment. So

> far, so good, as you all know. I went to my family doctor

yesterday

> for a check up. She is watching me locally, while my transplant

> coordinator watches me from there. My family doctor was amazed at

> how well treatment has been going for me so far. She was dreading

> seeing me because she thought I would be sick with fever, chills,

> body aches, and depressed. I've had none of those so far. My lab

> results from yesterday aren't looking as good as they were,

though.

> My coordinator called me today and told me my numbers have been

going

> up. I didn't ask her because I didn't feel like knowing the answer

> right now, but I'm assuming she's talking about my liver numbers.

> I'll know when I get my lab results in the mail Thursday. It can

do

> that when first starting treatment. Hopefully, they will be going

> back down again soon. Also, my white and red blood cell counts are

> dropping, but I knew that would probably happen. They're still in

> range right now, but soon I will have to get shots to keep those up

> in the normal range. My glucose was up to 119 yesterday, but today

> it's back down to 98. That's another thing I have to check twice a

> day because the treatment can cause the blood sugar to rise, and

then

> I would need insulin. I've been getting more and more tired, and

no

> wonder since my white and red blood cell counts are dropping. My

> coordinator told me from here on out I need to just rest, and if

> things need to be done, to let my husband do them. She's really

> stressing that. She thought I might be out shopping for Christmas,

> and she doesn't want me doing that. I haven't been since I hate

> shopping anyway. I usually do all my shopping online, and had that

> all done before Thanksgiving. Anything else that we need to get my

> husband goes out to get. doesn't let me run around and wear

> myself out anyway, so she doesn't have to worry about that...lol.

>

> I hope you all are doing well.

>

> Penny

>

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Thanks, Barby & Diane.

I just did my third shot. I actually did it myself this time. My

friend, Lori, came over and just supported me and guided me through

it. I had the needle next to my leg, and I thought, " I can't poke

myself with this " . Then I just did it and it slid right in and

didn't hurt. It was a piece of cake! That's the part I was most

nervous about was putting the needle into my skin, but it's such a

thin, tiny little needle, it just slid in like a hot knife through

butter and didn't hurt a bit.

Penny

> >

> > I will be doing my third shot tonight for the Hep C treatment.

So

> > far, so good, as you all know. I went to my family doctor

> yesterday

> > for a check up. She is watching me locally, while my transplant

> > coordinator watches me from there. My family doctor was amazed

at

> > how well treatment has been going for me so far. She was

dreading

> > seeing me because she thought I would be sick with fever, chills,

> > body aches, and depressed. I've had none of those so far. My

lab

> > results from yesterday aren't looking as good as they were,

> though.

> > My coordinator called me today and told me my numbers have been

> going

> > up. I didn't ask her because I didn't feel like knowing the

answer

> > right now, but I'm assuming she's talking about my liver

numbers.

> > I'll know when I get my lab results in the mail Thursday. It can

> do

> > that when first starting treatment. Hopefully, they will be

going

> > back down again soon. Also, my white and red blood cell counts

are

> > dropping, but I knew that would probably happen. They're still

in

> > range right now, but soon I will have to get shots to keep those

up

> > in the normal range. My glucose was up to 119 yesterday, but

today

> > it's back down to 98. That's another thing I have to check twice

a

> > day because the treatment can cause the blood sugar to rise, and

> then

> > I would need insulin. I've been getting more and more tired, and

> no

> > wonder since my white and red blood cell counts are dropping. My

> > coordinator told me from here on out I need to just rest, and if

> > things need to be done, to let my husband do them. She's really

> > stressing that. She thought I might be out shopping for

Christmas,

> > and she doesn't want me doing that. I haven't been since I hate

> > shopping anyway. I usually do all my shopping online, and had

that

> > all done before Thanksgiving. Anything else that we need to get

my

> > husband goes out to get. doesn't let me run around and

wear

> > myself out anyway, so she doesn't have to worry about that...lol.

> >

> > I hope you all are doing well.

> >

> > Penny

> >

>

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Good for you Penny!  Isn't it wonderful how brave you can be when you're

tested?!  Continuing to pray for you as you move forward.

________________________________

To: livercirrhosissupport

Sent: Tuesday, December 16, 2008 9:01:54 PM

Subject: Re: Third Shot Tonight

Thanks, Barby & Diane.

I just did my third shot. I actually did it myself this time. My

friend, Lori, came over and just supported me and guided me through

it. I had the needle next to my leg, and I thought, " I can't poke

myself with this " . Then I just did it and it slid right in and

didn't hurt. It was a piece of cake! That's the part I was most

nervous about was putting the needle into my skin, but it's such a

thin, tiny little needle, it just slid in like a hot knife through

butter and didn't hurt a bit.

Penny

> >

> > I will be doing my third shot tonight for the Hep C treatment.

So

> > far, so good, as you all know. I went to my family doctor

> yesterday

> > for a check up. She is watching me locally, while my transplant

> > coordinator watches me from there. My family doctor was amazed

at

> > how well treatment has been going for me so far. She was

dreading

> > seeing me because she thought I would be sick with fever, chills,

> > body aches, and depressed. I've had none of those so far. My

lab

> > results from yesterday aren't looking as good as they were,

> though.

> > My coordinator called me today and told me my numbers have been

> going

> > up. I didn't ask her because I didn't feel like knowing the

answer

> > right now, but I'm assuming she's talking about my liver

numbers.

> > I'll know when I get my lab results in the mail Thursday. It can

> do

> > that when first starting treatment. Hopefully, they will be

going

> > back down again soon. Also, my white and red blood cell counts

are

> > dropping, but I knew that would probably happen. They're still

in

> > range right now, but soon I will have to get shots to keep those

up

> > in the normal range. My glucose was up to 119 yesterday, but

today

> > it's back down to 98. That's another thing I have to check twice

a

> > day because the treatment can cause the blood sugar to rise, and

> then

> > I would need insulin. I've been getting more and more tired, and

> no

> > wonder since my white and red blood cell counts are dropping. My

> > coordinator told me from here on out I need to just rest, and if

> > things need to be done, to let my husband do them. She's really

> > stressing that. She thought I might be out shopping for

Christmas,

> > and she doesn't want me doing that. I haven't been since I hate

> > shopping anyway. I usually do all my shopping online, and had

that

> > all done before Thanksgiving. Anything else that we need to get

my

> > husband goes out to get. doesn't let me run around and

wear

> > myself out anyway, so she doesn't have to worry about that...lol.

> >

> > I hope you all are doing well.

> >

> > Penny

> >

>

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Thanks, Diane. Yeah, you can do anything when you have to.

Again, on this third shot, I've had no side effects at all. Whoo

hoo! It seems my only side effects are going to be tiredness, and

what's going on with my lab tests. I like having no side effects! I

just hope it continues.

Penny

> > >

> > > I will be doing my third shot tonight for the Hep C treatment.

> So

> > > far, so good, as you all know. I went to my family doctor

> > yesterday

> > > for a check up. She is watching me locally, while my transplant

> > > coordinator watches me from there. My family doctor was amazed

> at

> > > how well treatment has been going for me so far. She was

> dreading

> > > seeing me because she thought I would be sick with fever,

chills,

> > > body aches, and depressed. I've had none of those so far. My

> lab

> > > results from yesterday aren't looking as good as they were,

> > though.

> > > My coordinator called me today and told me my numbers have been

> > going

> > > up. I didn't ask her because I didn't feel like knowing the

> answer

> > > right now, but I'm assuming she's talking about my liver

> numbers.

> > > I'll know when I get my lab results in the mail Thursday. It

can

> > do

> > > that when first starting treatment. Hopefully, they will be

> going

> > > back down again soon. Also, my white and red blood cell counts

> are

> > > dropping, but I knew that would probably happen. They're still

> in

> > > range right now, but soon I will have to get shots to keep

those

> up

> > > in the normal range. My glucose was up to 119 yesterday, but

> today

> > > it's back down to 98. That's another thing I have to check

twice

> a

> > > day because the treatment can cause the blood sugar to rise,

and

> > then

> > > I would need insulin. I've been getting more and more tired,

and

> > no

> > > wonder since my white and red blood cell counts are dropping.

My

> > > coordinator told me from here on out I need to just rest, and

if

> > > things need to be done, to let my husband do them. She's really

> > > stressing that. She thought I might be out shopping for

> Christmas,

> > > and she doesn't want me doing that. I haven't been since I hate

> > > shopping anyway. I usually do all my shopping online, and had

> that

> > > all done before Thanksgiving. Anything else that we need to get

> my

> > > husband goes out to get. doesn't let me run around and

> wear

> > > myself out anyway, so she doesn't have to worry about

that...lol.

> > >

> > > I hope you all are doing well.

> > >

> > > Penny

> > >

> >

>

>

>

>

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I am so excited for you!  I'm sorry you're being tired and that the labs are

being wonky, but maybe all of that will sort itself out.  Continuing to pray for

you Penny.

________________________________

To: livercirrhosissupport

Sent: Wednesday, December 17, 2008 1:49:51 PM

Subject: Re: Third Shot Tonight

Thanks, Diane. Yeah, you can do anything when you have to.

Again, on this third shot, I've had no side effects at all. Whoo

hoo! It seems my only side effects are going to be tiredness, and

what's going on with my lab tests. I like having no side effects! I

just hope it continues.

Penny

> > >

> > > I will be doing my third shot tonight for the Hep C treatment.

> So

> > > far, so good, as you all know. I went to my family doctor

> > yesterday

> > > for a check up. She is watching me locally, while my transplant

> > > coordinator watches me from there. My family doctor was amazed

> at

> > > how well treatment has been going for me so far. She was

> dreading

> > > seeing me because she thought I would be sick with fever,

chills,

> > > body aches, and depressed. I've had none of those so far. My

> lab

> > > results from yesterday aren't looking as good as they were,

> > though.

> > > My coordinator called me today and told me my numbers have been

> > going

> > > up. I didn't ask her because I didn't feel like knowing the

> answer

> > > right now, but I'm assuming she's talking about my liver

> numbers.

> > > I'll know when I get my lab results in the mail Thursday. It

can

> > do

> > > that when first starting treatment. Hopefully, they will be

> going

> > > back down again soon. Also, my white and red blood cell counts

> are

> > > dropping, but I knew that would probably happen. They're still

> in

> > > range right now, but soon I will have to get shots to keep

those

> up

> > > in the normal range. My glucose was up to 119 yesterday, but

> today

> > > it's back down to 98. That's another thing I have to check

twice

> a

> > > day because the treatment can cause the blood sugar to rise,

and

> > then

> > > I would need insulin. I've been getting more and more tired,

and

> > no

> > > wonder since my white and red blood cell counts are dropping.

My

> > > coordinator told me from here on out I need to just rest, and

if

> > > things need to be done, to let my husband do them. She's really

> > > stressing that. She thought I might be out shopping for

> Christmas,

> > > and she doesn't want me doing that. I haven't been since I hate

> > > shopping anyway. I usually do all my shopping online, and had

> that

> > > all done before Thanksgiving. Anything else that we need to get

> my

> > > husband goes out to get. doesn't let me run around and

> wear

> > > myself out anyway, so she doesn't have to worry about

that...lol.

> > >

> > > I hope you all are doing well.

> > >

> > > Penny

> > >

> >

>

>

>

>

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Thanks, Diane.

Penny

> > > >

> > > > I will be doing my third shot tonight for the Hep C

treatment.

> > So

> > > > far, so good, as you all know. I went to my family doctor

> > > yesterday

> > > > for a check up. She is watching me locally, while my

transplant

> > > > coordinator watches me from there. My family doctor was

amazed

> > at

> > > > how well treatment has been going for me so far. She was

> > dreading

> > > > seeing me because she thought I would be sick with fever,

> chills,

> > > > body aches, and depressed. I've had none of those so far. My

> > lab

> > > > results from yesterday aren't looking as good as they were,

> > > though.

> > > > My coordinator called me today and told me my numbers have

been

> > > going

> > > > up. I didn't ask her because I didn't feel like knowing the

> > answer

> > > > right now, but I'm assuming she's talking about my liver

> > numbers.

> > > > I'll know when I get my lab results in the mail Thursday. It

> can

> > > do

> > > > that when first starting treatment. Hopefully, they will be

> > going

> > > > back down again soon. Also, my white and red blood cell

counts

> > are

> > > > dropping, but I knew that would probably happen. They're

still

> > in

> > > > range right now, but soon I will have to get shots to keep

> those

> > up

> > > > in the normal range. My glucose was up to 119 yesterday, but

> > today

> > > > it's back down to 98. That's another thing I have to check

> twice

> > a

> > > > day because the treatment can cause the blood sugar to rise,

> and

> > > then

> > > > I would need insulin. I've been getting more and more tired,

> and

> > > no

> > > > wonder since my white and red blood cell counts are dropping.

> My

> > > > coordinator told me from here on out I need to just rest, and

> if

> > > > things need to be done, to let my husband do them. She's

really

> > > > stressing that. She thought I might be out shopping for

> > Christmas,

> > > > and she doesn't want me doing that. I haven't been since I

hate

> > > > shopping anyway. I usually do all my shopping online, and had

> > that

> > > > all done before Thanksgiving. Anything else that we need to

get

> > my

> > > > husband goes out to get. doesn't let me run around and

> > wear

> > > > myself out anyway, so she doesn't have to worry about

> that...lol.

> > > >

> > > > I hope you all are doing well.

> > > >

> > > > Penny

> > > >

> > >

> >

> >

> >

> >

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I am glad you aren't suffering any severe side effects Penny! You and

I are in the same boat....I can't go anywhere either except Dr appt's,

the lab and dialysis......I am not doing much Christmas shopping

either but like you I prefer online.

Although since my transplant was before Thanksgiving I miss seeing a

lot of the decorations and music in the stores, etc.....

We can rest together! Enjoy the holidays....

Hugs,

>

> I will be doing my third shot tonight for the Hep C treatment. So

> far, so good, as you all know. I went to my family doctor yesterday

> for a check up. She is watching me locally, while my transplant

> coordinator watches me from there. My family doctor was amazed at

> how well treatment has been going for me so far. She was dreading

> seeing me because she thought I would be sick with fever, chills,

> body aches, and depressed. I've had none of those so far. My lab

> results from yesterday aren't looking as good as they were, though.

> My coordinator called me today and told me my numbers have been going

> up. I didn't ask her because I didn't feel like knowing the answer

> right now, but I'm assuming she's talking about my liver numbers.

> I'll know when I get my lab results in the mail Thursday. It can do

> that when first starting treatment. Hopefully, they will be going

> back down again soon. Also, my white and red blood cell counts are

> dropping, but I knew that would probably happen. They're still in

> range right now, but soon I will have to get shots to keep those up

> in the normal range. My glucose was up to 119 yesterday, but today

> it's back down to 98. That's another thing I have to check twice a

> day because the treatment can cause the blood sugar to rise, and then

> I would need insulin. I've been getting more and more tired, and no

> wonder since my white and red blood cell counts are dropping. My

> coordinator told me from here on out I need to just rest, and if

> things need to be done, to let my husband do them. She's really

> stressing that. She thought I might be out shopping for Christmas,

> and she doesn't want me doing that. I haven't been since I hate

> shopping anyway. I usually do all my shopping online, and had that

> all done before Thanksgiving. Anything else that we need to get my

> husband goes out to get. doesn't let me run around and wear

> myself out anyway, so she doesn't have to worry about that...lol.

>

> I hope you all are doing well.

>

> Penny

>

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hi there nancy. glad to see ya back, we have all been praying for

you,you definatlety deserve to rest with penny:)i hope you have a

wonderful christmas!!!!! stay well and take care of yourself,much

love barby

> >

> > I will be doing my third shot tonight for the Hep C treatment.

So

> > far, so good, as you all know. I went to my family doctor

yesterday

> > for a check up. She is watching me locally, while my transplant

> > coordinator watches me from there. My family doctor was amazed

at

> > how well treatment has been going for me so far. She was

dreading

> > seeing me because she thought I would be sick with fever, chills,

> > body aches, and depressed. I've had none of those so far. My

lab

> > results from yesterday aren't looking as good as they were,

though.

> > My coordinator called me today and told me my numbers have been

going

> > up. I didn't ask her because I didn't feel like knowing the

answer

> > right now, but I'm assuming she's talking about my liver

numbers.

> > I'll know when I get my lab results in the mail Thursday. It can

do

> > that when first starting treatment. Hopefully, they will be

going

> > back down again soon. Also, my white and red blood cell counts

are

> > dropping, but I knew that would probably happen. They're still

in

> > range right now, but soon I will have to get shots to keep those

up

> > in the normal range. My glucose was up to 119 yesterday, but

today

> > it's back down to 98. That's another thing I have to check twice

a

> > day because the treatment can cause the blood sugar to rise, and

then

> > I would need insulin. I've been getting more and more tired, and

no

> > wonder since my white and red blood cell counts are dropping. My

> > coordinator told me from here on out I need to just rest, and if

> > things need to be done, to let my husband do them. She's really

> > stressing that. She thought I might be out shopping for

Christmas,

> > and she doesn't want me doing that. I haven't been since I hate

> > shopping anyway. I usually do all my shopping online, and had

that

> > all done before Thanksgiving. Anything else that we need to get

my

> > husband goes out to get. doesn't let me run around and

wear

> > myself out anyway, so she doesn't have to worry about that...lol.

> >

> > I hope you all are doing well.

> >

> > Penny

> >

>

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it isso good to hear from you!  I am so thankful you are able to be home

and that things are going as well as they are.  You are an inspiration to all of

us!  Just take care of yourself.  Those you love have received the best

Christmas gift ever, someone gave you another chance at life.  What else could

they possibly want?!  Continuing to pray for you.

Hugs.............

Diane

________________________________

To: livercirrhosissupport

Sent: Wednesday, December 17, 2008 7:51:16 PM

Subject: Re: Third Shot Tonight

I am glad you aren't suffering any severe side effects Penny! You and

I are in the same boat....I can't go anywhere either except Dr appt's,

the lab and dialysis.... ..I am not doing much Christmas shopping

either but like you I prefer online.

Although since my transplant was before Thanksgiving I miss seeing a

lot of the decorations and music in the stores, etc.....

We can rest together! Enjoy the holidays....

Hugs,

>

> I will be doing my third shot tonight for the Hep C treatment. So

> far, so good, as you all know. I went to my family doctor yesterday

> for a check up. She is watching me locally, while my transplant

> coordinator watches me from there. My family doctor was amazed at

> how well treatment has been going for me so far. She was dreading

> seeing me because she thought I would be sick with fever, chills,

> body aches, and depressed. I've had none of those so far. My lab

> results from yesterday aren't looking as good as they were, though.

> My coordinator called me today and told me my numbers have been going

> up. I didn't ask her because I didn't feel like knowing the answer

> right now, but I'm assuming she's talking about my liver numbers.

> I'll know when I get my lab results in the mail Thursday. It can do

> that when first starting treatment. Hopefully, they will be going

> back down again soon. Also, my white and red blood cell counts are

> dropping, but I knew that would probably happen. They're still in

> range right now, but soon I will have to get shots to keep those up

> in the normal range. My glucose was up to 119 yesterday, but today

> it's back down to 98. That's another thing I have to check twice a

> day because the treatment can cause the blood sugar to rise, and then

> I would need insulin. I've been getting more and more tired, and no

> wonder since my white and red blood cell counts are dropping. My

> coordinator told me from here on out I need to just rest, and if

> things need to be done, to let my husband do them. She's really

> stressing that. She thought I might be out shopping for Christmas,

> and she doesn't want me doing that. I haven't been since I hate

> shopping anyway. I usually do all my shopping online, and had that

> all done before Thanksgiving. Anything else that we need to get my

> husband goes out to get. doesn't let me run around and wear

> myself out anyway, so she doesn't have to worry about that...lol.

>

> I hope you all are doing well.

>

> Penny

>

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Thanks Barby...I don't want to *highjack* Penny's post just wanted to

tell her I would be thinking about her from my couch..... :-)

> > >

> > > I will be doing my third shot tonight for the Hep C treatment.

> So

> > > far, so good, as you all know. I went to my family doctor

> yesterday

> > > for a check up. She is watching me locally, while my transplant

> > > coordinator watches me from there. My family doctor was amazed

> at

> > > how well treatment has been going for me so far. She was

> dreading

> > > seeing me because she thought I would be sick with fever, chills,

> > > body aches, and depressed. I've had none of those so far. My

> lab

> > > results from yesterday aren't looking as good as they were,

> though.

> > > My coordinator called me today and told me my numbers have been

> going

> > > up. I didn't ask her because I didn't feel like knowing the

> answer

> > > right now, but I'm assuming she's talking about my liver

> numbers.

> > > I'll know when I get my lab results in the mail Thursday. It can

> do

> > > that when first starting treatment. Hopefully, they will be

> going

> > > back down again soon. Also, my white and red blood cell counts

> are

> > > dropping, but I knew that would probably happen. They're still

> in

> > > range right now, but soon I will have to get shots to keep those

> up

> > > in the normal range. My glucose was up to 119 yesterday, but

> today

> > > it's back down to 98. That's another thing I have to check twice

> a

> > > day because the treatment can cause the blood sugar to rise, and

> then

> > > I would need insulin. I've been getting more and more tired, and

> no

> > > wonder since my white and red blood cell counts are dropping. My

> > > coordinator told me from here on out I need to just rest, and if

> > > things need to be done, to let my husband do them. She's really

> > > stressing that. She thought I might be out shopping for

> Christmas,

> > > and she doesn't want me doing that. I haven't been since I hate

> > > shopping anyway. I usually do all my shopping online, and had

> that

> > > all done before Thanksgiving. Anything else that we need to get

> my

> > > husband goes out to get. doesn't let me run around and

> wear

> > > myself out anyway, so she doesn't have to worry about that...lol.

> > >

> > > I hope you all are doing well.

> > >

> > > Penny

> > >

> >

>

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Hi ,

I'm glad to see you posting. I hope you are feeling ok. I know what

you are going through. I was sick last Thanksgiving, and in the

hospital last Christmas, New Year's, my birthday, and our wedding

anniversary, but it was ok because I got a new liver which was the

best present for all those special days. Even though we can't go

anywhere, at least we are home. It's good to be home!

I really needed the rest today because I got a terrible headache and

nausea. After I threw up, I was fine again. The headache

disappeared immediately. I think I am reacting to the increase in my

pills. I started the treatment with one pill twice a day, then

yesterday I had to increase it to two pills twice a day.

Keep up with your healing. I wish your healing to be as smooth as

mine was after transplant.

Penny

> >

> > I will be doing my third shot tonight for the Hep C treatment.

So

> > far, so good, as you all know. I went to my family doctor

yesterday

> > for a check up. She is watching me locally, while my transplant

> > coordinator watches me from there. My family doctor was amazed

at

> > how well treatment has been going for me so far. She was

dreading

> > seeing me because she thought I would be sick with fever, chills,

> > body aches, and depressed. I've had none of those so far. My

lab

> > results from yesterday aren't looking as good as they were,

though.

> > My coordinator called me today and told me my numbers have been

going

> > up. I didn't ask her because I didn't feel like knowing the

answer

> > right now, but I'm assuming she's talking about my liver

numbers.

> > I'll know when I get my lab results in the mail Thursday. It can

do

> > that when first starting treatment. Hopefully, they will be

going

> > back down again soon. Also, my white and red blood cell counts

are

> > dropping, but I knew that would probably happen. They're still

in

> > range right now, but soon I will have to get shots to keep those

up

> > in the normal range. My glucose was up to 119 yesterday, but

today

> > it's back down to 98. That's another thing I have to check twice

a

> > day because the treatment can cause the blood sugar to rise, and

then

> > I would need insulin. I've been getting more and more tired, and

no

> > wonder since my white and red blood cell counts are dropping. My

> > coordinator told me from here on out I need to just rest, and if

> > things need to be done, to let my husband do them. She's really

> > stressing that. She thought I might be out shopping for

Christmas,

> > and she doesn't want me doing that. I haven't been since I hate

> > shopping anyway. I usually do all my shopping online, and had

that

> > all done before Thanksgiving. Anything else that we need to get

my

> > husband goes out to get. doesn't let me run around and

wear

> > myself out anyway, so she doesn't have to worry about that...lol.

> >

> > I hope you all are doing well.

> >

> > Penny

> >

>

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That's great! You didn't " highjack " my post. We're just all glad to

hear from you that you are doing alright.

Penny

> > > >

> > > > I will be doing my third shot tonight for the Hep C

treatment.

> > So

> > > > far, so good, as you all know. I went to my family doctor

> > yesterday

> > > > for a check up. She is watching me locally, while my

transplant

> > > > coordinator watches me from there. My family doctor was

amazed

> > at

> > > > how well treatment has been going for me so far. She was

> > dreading

> > > > seeing me because she thought I would be sick with fever,

chills,

> > > > body aches, and depressed. I've had none of those so far.

My

> > lab

> > > > results from yesterday aren't looking as good as they were,

> > though.

> > > > My coordinator called me today and told me my numbers have

been

> > going

> > > > up. I didn't ask her because I didn't feel like knowing the

> > answer

> > > > right now, but I'm assuming she's talking about my liver

> > numbers.

> > > > I'll know when I get my lab results in the mail Thursday. It

can

> > do

> > > > that when first starting treatment. Hopefully, they will be

> > going

> > > > back down again soon. Also, my white and red blood cell

counts

> > are

> > > > dropping, but I knew that would probably happen. They're

still

> > in

> > > > range right now, but soon I will have to get shots to keep

those

> > up

> > > > in the normal range. My glucose was up to 119 yesterday, but

> > today

> > > > it's back down to 98. That's another thing I have to check

twice

> > a

> > > > day because the treatment can cause the blood sugar to rise,

and

> > then

> > > > I would need insulin. I've been getting more and more tired,

and

> > no

> > > > wonder since my white and red blood cell counts are

dropping. My

> > > > coordinator told me from here on out I need to just rest, and

if

> > > > things need to be done, to let my husband do them. She's

really

> > > > stressing that. She thought I might be out shopping for

> > Christmas,

> > > > and she doesn't want me doing that. I haven't been since I

hate

> > > > shopping anyway. I usually do all my shopping online, and

had

> > that

> > > > all done before Thanksgiving. Anything else that we need to

get

> > my

> > > > husband goes out to get. doesn't let me run around and

> > wear

> > > > myself out anyway, so she doesn't have to worry about

that...lol.

> > > >

> > > > I hope you all are doing well.

> > > >

> > > > Penny

> > > >

> > >

> >

>

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