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Virginia...

I'm glad you are working on your books! Since I've returned to work full

time, I've not gotten any writing done. I have 3 fantasy/romance books in

work. One I need to finish and polish up this year if I can. I don't push

myself cause I know how I am. I could write all nite and then be too

exhausted to go to work and I need the money and the insurance right now to

work on this hep. Eventually our plan, hubby's and mine, is for me to quit

work, prolly on disability, and write full time (as full time as a hepper

can). No use in trying to do that now. Besides the money and insurance

issues, my daughter, her husband and their two babies live with us and being

home is NOT restful. Keep us informed!

alley/

ICQ 12631861

alleypat@...

http://www.flash.net/~alleypat

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Virginia...

I'm glad you are working on your books! Since I've returned to work full

time, I've not gotten any writing done. I have 3 fantasy/romance books in

work. One I need to finish and polish up this year if I can. I don't push

myself cause I know how I am. I could write all nite and then be too

exhausted to go to work and I need the money and the insurance right now to

work on this hep. Eventually our plan, hubby's and mine, is for me to quit

work, prolly on disability, and write full time (as full time as a hepper

can). No use in trying to do that now. Besides the money and insurance

issues, my daughter, her husband and their two babies live with us and being

home is NOT restful. Keep us informed!

alley/

ICQ 12631861

alleypat@...

http://www.flash.net/~alleypat

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  • 2 months later...
Guest guest

Hi Alley! it's called 'Duragesic' patch. I believe it is timed release

Fentanyl. My doc didn't want to try that on me. He wrote for Oxycontin

instead. that is also a narcotic pain reliever (oral) that I will only take

at night. it lasts (or is suppose to last..) 12 hours. It DID help me sleep

better, altho' I took it much too late. I too, have tried my shots at

different times...it always turns out to have the same effect at night. I

hae yet to try any in the early afternoon. The earliest I've done a shot is

3:00. I'm done for this week (thank GOD!) and I know I can look forward to

feeling better on Sunday and Monday. YAY!!!!!!!!!! :o)

I seem to be able to deal with the fatigue (so what else is new?) and I

have just really started feeling nauseous (moreso than b/4 Tx) the past

couple of days...but I can also deal with that. I hope you are still feeling

well.........please let me know. God Bless, gee

" We can do no great things; only small things with great Love. " Mother

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Hi Alley! it's called 'Duragesic' patch. I believe it is timed release

Fentanyl. My doc didn't want to try that on me. He wrote for Oxycontin

instead. that is also a narcotic pain reliever (oral) that I will only take

at night. it lasts (or is suppose to last..) 12 hours. It DID help me sleep

better, altho' I took it much too late. I too, have tried my shots at

different times...it always turns out to have the same effect at night. I

hae yet to try any in the early afternoon. The earliest I've done a shot is

3:00. I'm done for this week (thank GOD!) and I know I can look forward to

feeling better on Sunday and Monday. YAY!!!!!!!!!! :o)

I seem to be able to deal with the fatigue (so what else is new?) and I

have just really started feeling nauseous (moreso than b/4 Tx) the past

couple of days...but I can also deal with that. I hope you are still feeling

well.........please let me know. God Bless, gee

" We can do no great things; only small things with great Love. " Mother

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  • 10 months later...
Guest guest

I've never actually checked this place out myself, but

maybe you could and let us know how it works. I bet

by the time 'paperwork' is done though your husband's

insurance will be in effect!

Accessing Free Medication - The Patient's Advocate

< TARGET= " _blank " >http://www.themedicineprogram.com/>

" This organization was established by volunteers

dedicated to

alleviating

the plight of an ever increasing number of patients

who cannot afford

their

prescription medication. "

__________________________________________________

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Guest guest

I've never actually checked this place out myself, but

maybe you could and let us know how it works. I bet

by the time 'paperwork' is done though your husband's

insurance will be in effect!

Accessing Free Medication - The Patient's Advocate

< TARGET= " _blank " >http://www.themedicineprogram.com/>

" This organization was established by volunteers

dedicated to

alleviating

the plight of an ever increasing number of patients

who cannot afford

their

prescription medication. "

__________________________________________________

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  • 4 months later...

He gril (as we used to say)!!!!!!!!!!

Thoughts and prayers are with you. Get a good nights sleep. Daivd says it's

great fun.........until the pain meds wear off. I'd just as soon take his

word for it.

LOL,

Anne

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He gril (as we used to say)!!!!!!!!!!

Thoughts and prayers are with you. Get a good nights sleep. Daivd says it's

great fun.........until the pain meds wear off. I'd just as soon take his

word for it.

LOL,

Anne

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Yep me too, Good Luck Alley and I hope it doesn't hurt

much. You have been through so much

Take Care, Connie

Daivd says it's

> great fun.........until the pain meds wear off. I'd

> just as soon take his

> word for it.

> LOL,

> Anne

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________

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Yep me too, Good Luck Alley and I hope it doesn't hurt

much. You have been through so much

Take Care, Connie

Daivd says it's

> great fun.........until the pain meds wear off. I'd

> just as soon take his

> word for it.

> LOL,

> Anne

>

>

> [Non-text portions of this message have been

> removed]

>

>

__________________________________________________

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  • 5 months later...
Guest guest

Hi Alley,

Thanks for the big hug.

It is really different being the patient. I am so used to be the care

giver that it is hard to let others do for me. :-)) I am slowly

healing...the ortho doc is happy with my progress and all 3 doctors are

working together !! The big mystery is why my leg broke. No one can

find the cause. One of the great mysteries of life...LOL

I will be turning 55 next month and I plan on using every little SENIOR

discount that I can get ...hahaha

hugs,

Judy

http://community.webtv.net/jcmmo/Affirmation

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  • 3 weeks later...
Guest guest

Exactamundo Alley. You stated that properly. Went to GI Doc, Canada

has approved the peg....BUT, not the funding....the government won't pay

for it, at least not yet. Dr. said if I had $50,000 to pay for it, he

could write me a prescription right now. So the government decides who

lives and dies? Not right. Not at all.

Oh yeah, we don't do viral loads in Canada anymore either....guess it

was too costly. Now my only option is getting on a serious sedative

from my pcDoc, then try the standard combo again and see if it helps the

speedy sides. Dr. did say that feeling like I was on speed is

definitely not a normal side effect. I'm not a happy camper today :-(

Hugggggs

Carol

wrote:

> , true, but then we aren't turned down for specialists and if

> we ask

> for treatment we get it, etc (if we have insurance that is). If I

> lived in

> Canada, my normal liver enzymes wouldn't have even warranted a biopsy

> or

> genotype, maybe not even a viral load, much less treatment. From what

> I

> hear, a lot of Canadian doctors give no options for treatment, because

> the

> gov controls the restrictions. And the last thing I want in my life

> is the

> gov controlling what meds I can or can't have. That'd be worse than

> HMO.

>

> I don't mean to pick on Canada. It's just the people I know are from

> there.

>

> alley

>

>

>

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Exactamundo Alley. You stated that properly. Went to GI Doc, Canada

has approved the peg....BUT, not the funding....the government won't pay

for it, at least not yet. Dr. said if I had $50,000 to pay for it, he

could write me a prescription right now. So the government decides who

lives and dies? Not right. Not at all.

Oh yeah, we don't do viral loads in Canada anymore either....guess it

was too costly. Now my only option is getting on a serious sedative

from my pcDoc, then try the standard combo again and see if it helps the

speedy sides. Dr. did say that feeling like I was on speed is

definitely not a normal side effect. I'm not a happy camper today :-(

Hugggggs

Carol

wrote:

> , true, but then we aren't turned down for specialists and if

> we ask

> for treatment we get it, etc (if we have insurance that is). If I

> lived in

> Canada, my normal liver enzymes wouldn't have even warranted a biopsy

> or

> genotype, maybe not even a viral load, much less treatment. From what

> I

> hear, a lot of Canadian doctors give no options for treatment, because

> the

> gov controls the restrictions. And the last thing I want in my life

> is the

> gov controlling what meds I can or can't have. That'd be worse than

> HMO.

>

> I don't mean to pick on Canada. It's just the people I know are from

> there.

>

> alley

>

>

>

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Guest guest

I have a friend in Canada who has a rough time with their medical care

also. She's not a hepper but has serious candida.

I'm pro socialized medicine but I think that it needs a lot of

improvement. But at the same time, I believe that every person should

have the right to some form of medical care...it should not be a

privilege that only those with money or insurance can have.

I think, and Willem will need to confirm this, that Holland has worked

out the kinks in socialized medicine. My friend from Holland who lives

here now, has never had a bad word to say about their medical program.

But Canada has a lot of problems with their socialized medicine and I

don't know why they can't get it worked out.

blessings

Tatezi

Carol wrote:

> Exactamundo Alley. You stated that properly. Went to GI Doc, Canada

>

> has approved the peg....BUT, not the funding....the government won't

> pay

> for it, at least not yet. Dr. said if I had $50,000 to pay for it, he

>

> could write me a prescription right now. So the government decides

> who

> lives and dies? Not right. Not at all.

>

> Oh yeah, we don't do viral loads in Canada anymore either....guess it

> was too costly. Now my only option is getting on a serious sedative

> from my pcDoc, then try the standard combo again and see if it helps

> the

> speedy sides. Dr. did say that feeling like I was on speed is

> definitely not a normal side effect. I'm not a happy camper today :-(

>

> Hugggggs

> Carol

>

> wrote:

>

> > , true, but then we aren't turned down for specialists and

> if

> > we ask

> > for treatment we get it, etc (if we have insurance that is). If I

> > lived in

> > Canada, my normal liver enzymes wouldn't have even warranted a

> biopsy

> > or

> > genotype, maybe not even a viral load, much less treatment. From

> what

> > I

> > hear, a lot of Canadian doctors give no options for treatment,

> because

> > the

> > gov controls the restrictions. And the last thing I want in my life

>

> > is the

> > gov controlling what meds I can or can't have. That'd be worse than

>

> > HMO.

> >

> > I don't mean to pick on Canada. It's just the people I know are from

>

> > there.

> >

> > alley

> >

> >

> >

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  • 1 year later...

Hi Alley....your first paragraph is exactly what I'd like to know too. I even

mentioned it to the GI doc about my level going down could mean this, and he

agreed that a person could have normal enzymes and still be end stage. So

damned if I know what's going on....I'm just a grain of sand on the beach (a

larger grain, but a grain).

I understand what you're saying about Overeaters Anon. I attended one meeting

years ago with a friend and had to stifle my laughter....it was just so petty.

When compared to AA where people battle a disease, where you can hear gut

wrenching stories about someone who ran over their child while drinking and

driving, to wondering if she ate too much at lunch, I just couldn't take it

anymore and went outside and lmao. First and last meeting.

Huggggs

Carol

Re: RE: I'm giving up too / Carol

Ah well Carol, that explains it. Sorry I didnt remember. However, I have

read that people with cirrhosis and even end stage liver disease will have

normal liver enzymes because there are no more liver cells to kill

(oversimplification but at 2am it'll do, you know what I mean :). So, if that

is your case, what do they base no treatment on then? How do they know?

(curious)

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Carol,

If you can possibly afford it, why not get a liver biopsy and find out, if

just for your own knowledge, what is going on. At least that way you know what

you are up against, and if it's time to take drastic measures, like moving to

another country, or whatever it takes. Don't ever give up the fight against

this dragon!

Re: Alley

Hi Alley....your first paragraph is exactly what I'd like to know too. I even

mentioned it to the GI doc about my level going down could mean this, and he

agreed that a person could have normal enzymes and still be end stage. So

damned if I know what's going on....I'm just a grain of sand on the beach (a

larger grain, but a grain).

Carol

Ah well Carol, that explains it. Sorry I didnt remember. However, I have

read that people with cirrhosis and even end stage liver disease will have

normal liver enzymes because there are no more liver cells to kill

(oversimplification but at 2am it'll do, you know what I mean :). So, if that

is your case, what do they base no treatment on then? How do they know?

(curious)

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Carol,

If you can possibly afford it, why not get a liver biopsy and find out, if

just for your own knowledge, what is going on. At least that way you know what

you are up against, and if it's time to take drastic measures, like moving to

another country, or whatever it takes. Don't ever give up the fight against

this dragon!

Re: Alley

Hi Alley....your first paragraph is exactly what I'd like to know too. I even

mentioned it to the GI doc about my level going down could mean this, and he

agreed that a person could have normal enzymes and still be end stage. So

damned if I know what's going on....I'm just a grain of sand on the beach (a

larger grain, but a grain).

Carol

Ah well Carol, that explains it. Sorry I didnt remember. However, I have

read that people with cirrhosis and even end stage liver disease will have

normal liver enzymes because there are no more liver cells to kill

(oversimplification but at 2am it'll do, you know what I mean :). So, if that

is your case, what do they base no treatment on then? How do they know?

(curious)

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  • 3 years later...
Guest guest

Happy Easter Alley and everyone....glad you saw the hockey game...Dallas plays

our team, the Vancouver Canucks...I guess we'll be cheering for different teams

lol.

Carol in Vancouver, Canada

Hubby and I attended the Dallas Stars hockey game today and we won! (we've

already lost our division title, but are in the playoffs, yipppeeee)

Have a great Sunday yall!

Alley

www.geocities.com/dfwhcv

www.alleypat.com

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Guest guest

<<Dallas plays our team, the Vancouver Canucks>>

Cool Carol!!! :) I wish I could attend the Vancouver games! But we have our

playoff tickets for the home games. I'm crossing my fingers!!!

Good luck to us both!

Hockey Alley :)

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