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Joe goes monday for his first post op chemo appt. , we are praying that all

stays good news!!

He has to go Sept 7th for the nerve study , but I am pretty sure the neuropathy

is just caused by the chemo and not the syrinx ( we can hope cant we?)

He is feeling pretty good , other than the neuropathy and some twinges in

stomach but we are saying HECK its just normal twinges, and not even thinking

about anything else ( umm yeah right )

Dani went to the neurosurgeon for her first post op visit today , they have set

her up to have another MRI on Sept 10th to see if they can figure out why she is

having the headaches,

Also gave her a note for school that says she cant carry backpack or gym for at

least 3 months ( no not carry gym lol you know what I mean)

As for mom she went to the oncologist today first time since her diagnoses (

this time)

And we found out that she has squamous cell(Lung) cancer tumor in her

mediastinium area, inoperable.

They are going to start chemo on Tuesday, the oncologist said that the chemo

will not cure it , but will arrest it , hmmm does this mean then mom will have

to be on chemo the rest of her life??

The chemo she will be on is Taxol and Carboplatin, she begins Tuesday and then

goes every 3 weeks, for she thinks they said 10 treatments??

I have questions , like she was recently diagnosed with Congestive heart failure

, how is she to combat becoming dehyrdrated during chemo, since if she drinks to

much the CHF kicks in??

Will she definately loose her hair ? And how much do wigs run?? She isnt a vain

woman by any means , but she is very upset over the thought of this, mom and dad

are on a fixed income and cant afford much extra's , also they have no

prescription coverage , I told mom to let the doctor know so maybe they will

give her anti nausea samples????????

One of the drugs she is going to be on is platinum based so she will have the

cold issues ( not eating /touching cold things ) like oxaplatin .

Mom is VERY independent and not one to listen to others lol.

I told her she MUST do what the docs say, like drink etc

I also told her that ultimately the decision to continue chemo will be HERS and

no one , not my father , not my siblings, not myself , can or will force her to

do it .

My mom and dad have been married for 57yrs , and she is more worried about dad

being at the chemo place for 6hours with her than she is for herself :(

I realize that this is the Colon cancer list but I feel more like family here so

I hope yall dont mind me ranting here.

Me?? I still need to dye my hair , my driving is coming along slowly but surely

havent hit anything so thats a GOOD THING!!!!!!!!!! lol still havent left my

neighborhood yet , I want to get totally comfortable first lol

Thanks for listening

Deb

33yrold husband Joe, was diagnosed with CC in Sept,

resection on Sept 27th 2004

found mets to the abdominal wall lining 3 lymph nodes involved

open wound from infection until Jan 2005

Ileostomy reversal Dec 7th 2004

Chemo regiment begun Jan 2005

5fu/levorican/Oxaplatin/ Avastin added Feb 14 2005 (Happy Valentines :(

Calcium Magnesium added for the Tingles Feb 28 2005

Ct Scan done March 23rd 2005 , 16 millimeter cyst like object on liver found

April 1 2005 PET scan done awaiting results

April 11 PET SCAN SHOWS

NED!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

May 9 Plateletts are low 75,000

---------------------------------

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Deb, Hamilton has a cancer site that lists all the different chemos and

what they do to you, its http://www.chemocare.com/ And my sister had chemo that

caused her to lose all her hair after the 2nd treatment, the American Cancer

Society gave her completely free a really nice quality wig, they had lots for

her to choose from, it's very nice, brand new and they do this all over the

country she was told, just call them. They also give away large packages of

makeup to make cancer victims feel a bit better, all kinds of brand name

cosmetics, regular size, it is worth giving them a call. ~Dianna

deb vamdembos debbied31@...> wrote:Joe goes monday for his first post op

chemo appt. , we are praying that all stays good news!!

He has to go Sept 7th for the nerve study , but I am pretty sure the neuropathy

is just caused by the chemo and not the syrinx ( we can hope cant we?)

He is feeling pretty good , other than the neuropathy and some twinges in

stomach but we are saying HECK its just normal twinges, and not even thinking

about anything else ( umm yeah right )

Dani went to the neurosurgeon for her first post op visit today , they have set

her up to have another MRI on Sept 10th to see if they can figure out why she is

having the headaches,

Also gave her a note for school that says she cant carry backpack or gym for at

least 3 months ( no not carry gym lol you know what I mean)

As for mom she went to the oncologist today first time since her diagnoses (

this time)

And we found out that she has squamous cell(Lung) cancer tumor in her

mediastinium area, inoperable.

They are going to start chemo on Tuesday, the oncologist said that the chemo

will not cure it , but will arrest it , hmmm does this mean then mom will have

to be on chemo the rest of her life??

The chemo she will be on is Taxol and Carboplatin, she begins Tuesday and then

goes every 3 weeks, for she thinks they said 10 treatments??

I have questions , like she was recently diagnosed with Congestive heart failure

, how is she to combat becoming dehyrdrated during chemo, since if she drinks to

much the CHF kicks in??

Will she definately loose her hair ? And how much do wigs run?? She isnt a vain

woman by any means , but she is very upset over the thought of this, mom and dad

are on a fixed income and cant afford much extra's , also they have no

prescription coverage , I told mom to let the doctor know so maybe they will

give her anti nausea samples????????

One of the drugs she is going to be on is platinum based so she will have the

cold issues ( not eating /touching cold things ) like oxaplatin .

Mom is VERY independent and not one to listen to others lol.

I told her she MUST do what the docs say, like drink etc

I also told her that ultimately the decision to continue chemo will be HERS and

no one , not my father , not my siblings, not myself , can or will force her to

do it .

My mom and dad have been married for 57yrs , and she is more worried about dad

being at the chemo place for 6hours with her than she is for herself :(

I realize that this is the Colon cancer list but I feel more like family here so

I hope yall dont mind me ranting here.

Me?? I still need to dye my hair , my driving is coming along slowly but surely

havent hit anything so thats a GOOD THING!!!!!!!!!! lol still havent left my

neighborhood yet , I want to get totally comfortable first lol

Thanks for listening

Deb

33yrold husband Joe, was diagnosed with CC in Sept,

resection on Sept 27th 2004

found mets to the abdominal wall lining 3 lymph nodes involved

open wound from infection until Jan 2005

Ileostomy reversal Dec 7th 2004

Chemo regiment begun Jan 2005

5fu/levorican/Oxaplatin/ Avastin added Feb 14 2005 (Happy Valentines :(

Calcium Magnesium added for the Tingles Feb 28 2005

Ct Scan done March 23rd 2005 , 16 millimeter cyst like object on liver found

April 1 2005 PET scan done awaiting results

April 11 PET SCAN SHOWS

NED!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

May 9 Plateletts are low 75,000

---------------------------------

Start your day with Yahoo! - make it your home page

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Share on other sites

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