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,

The Minocin may be a good choice for you. Often when one has a

reaction like you did, it's because it is effective. You probably

were having a herxheimer reaction -- die-off from mycoplasma.

Have you read " The New Arthritis Breakthrough " ? If not, that would

be the first suggestion I might have for you. It is a wonderful

book, and a facinating and interesting " easy read. " It will also

support you in your decision not to take the other drugs you

mentioned. Everyone interested in this therapy should definitely

read the book.

bg

> Hi ,

>

> They want to start me on two chemo drugs and prednisone (sp?).

> My dad was on one and prednisone when he died so I am not jumping

on

> that wagon. I have been on doxy for about 4 months. I did mino

for

> about a week and then tapered down and started back up but it made

me

> so ill. I am ill enough without it. Doxy does not give me

headaches

> or anything. I will post to this group about it too. : )

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  • 3 years later...

All those drug names sound familiar - she has suppositories, pills and also some sort of cream to rub on her wrist that is supposed to stop nausea instantly. It all used to work for her - but she's not keeping any of her medicine down right now. Her system has just shut down totally and we'll get it going slowly if I can get her to just relax about it for a couple days at least. :)) It really excited her that she was able to drink that potassium broth tonight!

Becky

Many people have eaten my cooking and gone on to lead normal lives.

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  • 1 year later...
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Hi All,

I am doing chemo now. Any reiki and/or prayer is welcome.

I would like to feel stronger, my tummy more comfortable, my joints

less achy. Comfort in my joints and throughout my body. I would like

my healthy cells to stay that way and for anything innappropriate to

leave my body forever.

and so, it is. Thank you God!

Thanks and Love,

Kanta

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  • 1 year later...

Bless you, Lynda. Thank you for keeping us posted. You are one

amazing woman.

Sis

>

> Will get back to everyone after Friday when I see the doc.

Hopefully

> he is communicating with MD (Dr. Vicente Volare) in

Houston,

> and I have told him my expectations for next Friday are to have a

> plan in place that is aggressive enough to kill off the cancer. I

> have brought up trials of new drugs, with my expectations for what

I

> would need to have as minimal requirements (you don't know if you

are

> getting the trial drug, but they have to give you something that

is

> pretty effective against cancer). I have researched many options

> online. I will be taking them to him. I will know more by

Friday,

> but as of now, everything is up in the air and the chemo kept me

> stable but did not kill off any more of the tumors since April.

>

> So, you may not hear much from me for a few days. I am working on

> things. My therapist thinks I have it more together than my

> doctor. Don't know about that, but I did send him an email with

my

> expectations and my disappointment that he seems to have given up

on

> me. He denies this, but I am not ready for Palliative treatment

(the

> anti-hormone) and I made that VERY clear to him.

>

> Thanks for all the thoughts and prayers, when I have info. to

share I

> will share it, but for now I just need to take care of me.

>

> Love,

> Lynda

>

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