UnderGround Forum >> F*&%K Cancer! TAP CANCER OUT!

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Bukkake -

TTT for KRS. 

Good luck and God bless to all you that are fighting.

wreckker -

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Hang in there ace!

I have empathy for you, knowing your side effects are much worse And for alot longer than what i felt.

Steroids they are giving you are not enough to make u eat? Have you tried cannabis? I am eating constantly, your treatment is so much harsher chemically so i know it affects appetite alot


Im curious What are your Dr.s giving you to help you cope with side effects?

Hope they are doing right therapies for you ace.

Im doing alot of my own dietary plans, Tbe dieticians from hospital mostly SUCKED.

One of my Dr.s was also so bad i want to smash him.

Message me anytime ace if u want to chat in private. If i can help even just by listening hit me up:)

UGCTT_NKTKDace - 

wreckker -

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Hang in there ace!

I have empathy for you, knowing your side effects are much worse And for alot longer than what i felt.

Steroids they are giving you are not enough to make u eat? Have you tried cannabis? I am eating constantly, your treatment is so much harsher chemically so i know it affects appetite alot


Im curious What are your Dr.s giving you to help you cope with side effects?

Hope they are doing right therapies for you ace.

Im doing alot of my own dietary plans, Tbe dieticians from hospital mostly SUCKED.

One of my Dr.s was also so bad i want to smash him.

Message me anytime ace if u want to chat in private. If i can help even just by listening hit me up:)

My only side effects right now are having no taste buds and just how weak I am. The weakness will get better over time and when my taste buds come back. I have marinol pills and the ability to smoke but its not a appetite problem. Trust me I'm starving lol ...the problem is everything tastes like medal or cardboard and that's just nasty. I'm not on any type of steroids just multi vitamins, folic acid, potassium, magnesium and stuff for nauseous and my liver. Ramen noodles are all I can force myself to eat at the moment but I'm thinking about some stuffed shells tonight. I have till the end of April to recover is the way I see it lol

I was given some strong nausea meds and steroid called decatron.

im suprised they are nbot giving you setroid or nausea med?

very powerful antinflammatory, gives me tons of energy , and it increased mny appetite

smoked pot i found helps your taste buds alot more than marinol or edibles

i only had that metallic tatse with my first treatment after that i could eat like a horse

As harsh as your chemo is I wonder why they are nbot giving you steroid for energy, antinflammaotry and appetite?

Maybe it doesnt react well with your chermo?  Gives me alot of energy in addition to other efffects

Frank im just skeptical that western drs do all they can do.

 I know mine didnt

I went from feeling like hell to feeling good very fast, i hope you get the right therapies so you can have a fast improvement too

Have you tried smoked pot to improve tatse of your food?

wreckker -

UGCTT_NKTKDace - 

wreckker -

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Hang in there ace!

I have empathy for you, knowing your side effects are much worse And for alot longer than what i felt.

Steroids they are giving you are not enough to make u eat? Have you tried cannabis? I am eating constantly, your treatment is so much harsher chemically so i know it affects appetite alot


Im curious What are your Dr.s giving you to help you cope with side effects?

Hope they are doing right therapies for you ace.

Im doing alot of my own dietary plans, Tbe dieticians from hospital mostly SUCKED.

One of my Dr.s was also so bad i want to smash him.

Message me anytime ace if u want to chat in private. If i can help even just by listening hit me up:)

My only side effects right now are having no taste buds and just how weak I am. The weakness will get better over time and when my taste buds come back. I have marinol pills and the ability to smoke but its not a appetite problem. Trust me I'm starving lol ...the problem is everything tastes like medal or cardboard and that's just nasty. I'm not on any type of steroids just multi vitamins, folic acid, potassium, magnesium and stuff for nauseous and my liver. Ramen noodles are all I can force myself to eat at the moment but I'm thinking about some stuffed shells tonight. I have till the end of April to recover is the way I see it lol

I was given some strong nausea meds and steroid called decatron.

im suprised they are nbot giving you setroid or nausea med?

 

very powerful antinflammatory, gives me tons of energy , and it increased mny appetite

smoked pot i found helps your taste buds alot more than marinol or edibles

 

i only had that metallic tatse with my first treatment after that i could eat like a horse

As harsh as your chemo is I wonder why they are nbot giving you steroid for energy, antinflammaotry and appetite?

Maybe it doesnt react well with your chermo?  Gives me alot of energy in addition to other efffects

Frank im just skeptical that western drs do all they can do.

 

 I know mine didnt

I went from feeling like hell to feeling good very fast, i hope you get the right therapies so you can have a fast improvement too

 

Have you tried smoked pot to improve tatse of your food?

 

UGCTT_NKTKDace -

wreckker -

UGCTT_NKTKDace - 

wreckker -

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Hang in there ace!

I have empathy for you, knowing your side effects are much worse And for alot longer than what i felt.

Steroids they are giving you are not enough to make u eat? Have you tried cannabis? I am eating constantly, your treatment is so much harsher chemically so i know it affects appetite alot


Im curious What are your Dr.s giving you to help you cope with side effects?

Hope they are doing right therapies for you ace.

Im doing alot of my own dietary plans, Tbe dieticians from hospital mostly SUCKED.

One of my Dr.s was also so bad i want to smash him.

Message me anytime ace if u want to chat in private. If i can help even just by listening hit me up:)

My only side effects right now are having no taste buds and just how weak I am. The weakness will get better over time and when my taste buds come back. I have marinol pills and the ability to smoke but its not a appetite problem. Trust me I'm starving lol ...the problem is everything tastes like medal or cardboard and that's just nasty. I'm not on any type of steroids just multi vitamins, folic acid, potassium, magnesium and stuff for nauseous and my liver. Ramen noodles are all I can force myself to eat at the moment but I'm thinking about some stuffed shells tonight. I have till the end of April to recover is the way I see it lol

I was given some strong nausea meds and steroid called decatron.

im suprised they are nbot giving you setroid or nausea med?

 

very powerful antinflammatory, gives me tons of energy , and it increased mny appetite

smoked pot i found helps your taste buds alot more than marinol or edibles

 

i only had that metallic tatse with my first treatment after that i could eat like a horse

As harsh as your chemo is I wonder why they are nbot giving you steroid for energy, antinflammaotry and appetite?

Maybe it doesnt react well with your chermo?  Gives me alot of energy in addition to other efffects

Frank im just skeptical that western drs do all they can do.

 

 I know mine didnt

I went from feeling like hell to feeling good very fast, i hope you get the right therapies so you can have a fast improvement too

 

Have you tried smoked pot to improve tatse of your food?

 

Does not change my taste at all lol .... I have been on decatron many times but only for 5 days after chemo. After that becomes bad for the system and liver. That's what I was told and have done a crazy amount of research. For nauseous meds I have compazine, zofran, marinol and reglan. Reglan is all I use because the others are the suck. Some days it doesn't matter what I have.

FUCK CANCER!

I wish I could do more for you guys, but currently in the midst of helping my cousin rebuild after Sandy. In a few months after I replenish my funds I will check in and see whats what. Best of luck to you guys, you're all in my heart. 

WAR FRANK! WAR WENDY!!!

Krs10KO.com -

UGCTT_NKTKDace -

wreckker -

UGCTT_NKTKDace - 

wreckker -

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Hang in there ace!

I have empathy for you, knowing your side effects are much worse And for alot longer than what i felt.

Steroids they are giving you are not enough to make u eat? Have you tried cannabis? I am eating constantly, your treatment is so much harsher chemically so i know it affects appetite alot


Im curious What are your Dr.s giving you to help you cope with side effects?

Hope they are doing right therapies for you ace.

Im doing alot of my own dietary plans, Tbe dieticians from hospital mostly SUCKED.

One of my Dr.s was also so bad i want to smash him.

Message me anytime ace if u want to chat in private. If i can help even just by listening hit me up:)

My only side effects right now are having no taste buds and just how weak I am. The weakness will get better over time and when my taste buds come back. I have marinol pills and the ability to smoke but its not a appetite problem. Trust me I'm starving lol ...the problem is everything tastes like medal or cardboard and that's just nasty. I'm not on any type of steroids just multi vitamins, folic acid, potassium, magnesium and stuff for nauseous and my liver. Ramen noodles are all I can force myself to eat at the moment but I'm thinking about some stuffed shells tonight. I have till the end of April to recover is the way I see it lol

I was given some strong nausea meds and steroid called decatron.

im suprised they are nbot giving you setroid or nausea med?

 

very powerful antinflammatory, gives me tons of energy , and it increased mny appetite

smoked pot i found helps your taste buds alot more than marinol or edibles

 

i only had that metallic tatse with my first treatment after that i could eat like a horse

As harsh as your chemo is I wonder why they are nbot giving you steroid for energy, antinflammaotry and appetite?

Maybe it doesnt react well with your chermo?  Gives me alot of energy in addition to other efffects

Frank im just skeptical that western drs do all they can do.

 

 I know mine didnt

I went from feeling like hell to feeling good very fast, i hope you get the right therapies so you can have a fast improvement too

 

Have you tried smoked pot to improve tatse of your food?

 

Does not change my taste at all lol .... I have been on decatron many times but only for 5 days after chemo. After that becomes bad for the system and liver. That's what I was told and have done a crazy amount of research. For nauseous meds I have compazine, zofran, marinol and reglan. Reglan is all I use because the others are the suck. Some days it doesn't matter what I have.

Was just about to ask about anti-emetics u guys have used.
Can't take reglan. Makes me feel like I'm going to jump out of my skin. Tried Zophran, compazine, phenagrin. All crap.
What's the Marinol?
Thanks :)

Allen Hood -  GOOGLE RICK SIMPSON..

UGCTT_NKTKDace -

wreckker -

UGCTT_NKTKDace - 

wreckker -

UGCTT_NKTKDace - Slow slow recovery. The stem cell transplant with high dose chemo is no joke. I've done 7 rounds of chemo in the past but nothing prepares you for the high dose chemo. It has been a month since having it done and I'm still having trouble just moving room to room. My skin is all burned up and peeling and eating is still almost impossible. I have declined a second transplant so now we wait to see what is next. Till then just relax and try to get better.

Hang in there ace!

I have empathy for you, knowing your side effects are much worse And for alot longer than what i felt.

Steroids they are giving you are not enough to make u eat? Have you tried cannabis? I am eating constantly, your treatment is so much harsher chemically so i know it affects appetite alot


Im curious What are your Dr.s giving you to help you cope with side effects?

Hope they are doing right therapies for you ace.

Im doing alot of my own dietary plans, Tbe dieticians from hospital mostly SUCKED.

One of my Dr.s was also so bad i want to smash him.

Message me anytime ace if u want to chat in private. If i can help even just by listening hit me up:)

My only side effects right now are having no taste buds and just how weak I am. The weakness will get better over time and when my taste buds come back. I have marinol pills and the ability to smoke but its not a appetite problem. Trust me I'm starving lol ...the problem is everything tastes like medal or cardboard and that's just nasty. I'm not on any type of steroids just multi vitamins, folic acid, potassium, magnesium and stuff for nauseous and my liver. Ramen noodles are all I can force myself to eat at the moment but I'm thinking about some stuffed shells tonight. I have till the end of April to recover is the way I see it lol

I was given some strong nausea meds and steroid called decatron.

im suprised they are nbot giving you setroid or nausea med?

 

very powerful antinflammatory, gives me tons of energy , and it increased mny appetite

smoked pot i found helps your taste buds alot more than marinol or edibles

 

i only had that metallic tatse with my first treatment after that i could eat like a horse

As harsh as your chemo is I wonder why they are nbot giving you steroid for energy, antinflammaotry and appetite?

Maybe it doesnt react well with your chermo?  Gives me alot of energy in addition to other efffects

Frank im just skeptical that western drs do all they can do.

 

 I know mine didnt

I went from feeling like hell to feeling good very fast, i hope you get the right therapies so you can have a fast improvement too

 

Have you tried smoked pot to improve tatse of your food?

 

Does not change my taste at all lol .... I have been on decatron many times but only for 5 days after chemo. After that becomes bad for the system and liver. That's what I was told and have done a crazy amount of research. For nauseous meds I have compazine, zofran, marinol and reglan. Reglan is all I use because the others are the suck. Some days it doesn't matter what I have.

ttt for a great cause

ttt for a great cause and Krs10 because she's awesome.

DamnSevern -

ttt for a great cause and Krs10 because she's awesome.

Bump

Krs10KO.com - 

DamnSevern -

ttt for a great cause and Krs10 because she's awesome.

Oh man, thanks DS!! Youre just saying that bc I said I had a secret UG crush on you on another thread, aren't you?? I Kid I kid :) You and Pro Ice have like the best threads EVAR!!!

hhahaha, nope I didn't see that, but thank you.

you're awesome

ttt