Re: New MRI

[Guest guest]

Gosh Carol, sounds like you really opened your neuro's eyes. Seems like you ought to give her another visit to see if she will have indeed read the LDN info and become a believer. Sometimes it seems like it has to be done one doctor at a time--but at least that is progress. And think of how many other of her patients you can help if you have led her to believe in the efficacy of LDN.

And best wishes with your breast cancer. May all go positively for you on that account.

Kathie Arnold

On Fri, 3 Mar 2006 17:29:39 EST sunynbrite56@... writes:

I have news that I feel the need to share with you all.

To start, I've just been dx. with Breast Cancer. (it gets better, I promise!) Now, this was my first mamogram, I'm 49. The size is just about a centimeter, and very faint. Which, thank God is removable being it was detected early. But, it made me wonder how long I could have had this, and did the LDN keep it from getting any worse? So, I called Dr. Bihari's office, and was told "Absolutley". I could have had this for years and the LDN kept it from progressing. I, Fully and Honestly believe that in my heart. How lucky am I? Next step, surgery. Keep me in your prayers. I'd really appreciate that.

LDN has done so much for my MS, and just proved that to the new Neuro who told me she couldn't take me on as a patient because I don't follow the "conventional protocol for MS". We had quite a debate last week in her office. She told me, "Go for an MRI, I'm SURE you have ACTIVE lesions, and when we see that on the report, you must agree to start an IV treatment, then we'll talk about going back to the injectables".....Needless to say, I looked at her like she had 8 eyeballs, but agreed to the MRI for my own curiosity, and told her I'd be crazy to change anything I was doing for myself. Well, the report is in. It remains exactly the same as when first starting LDN in Sept. of 2002. Keeping in mind, my First MRI, in 1999 when dx. with RRMS, showed 4 prominent lesions, the MRI's since LDN show only 2, and one is difficult to see. She swallowed hard and said, "Your MS is doing wonderful, nothing active, its not progressed, it's stayed the same" I said, "Well, maybe now you'll read all the information I gave you about LDN, and Oh, next time I come in, we'll discuss whether or not I want to keep You on as My Neuro!" She told me to please come back. I told her I'd think about it. She hugged me and I left. I'll give her some time to read up on LDN and think about things, and decide if I really want to go back.

Anyway, I just wanted to share this with you. I have been a believer in LDN since the day I started it in 2002, and now with the thought of it keeping this cancer at bay just reinforces it all.

Until There's A Cure.............There's LDN

God Bless You All

Carol

[Guest guest]

Way to go Carol!! I'll keep you in my prayers for you surgery.

On Mar 3, 2006, at 5:29 PM, sunynbrite56@... wrote:

> I have news that I feel the need to share with you all. 

> To start, I've just been dx. with Breast Cancer. (it gets better, I

> promise!) Now, this was my first mamogram, I'm 49.  The size is just

> about a centimeter, and very faint. Which, thank God is removable

> being it was detected early.  But, it made me wonder how long I could

> have had this, and did the LDN keep it from getting any worse? So, I

> called Dr. Bihari's office, and was told " Absolutley " .  I could have

> had this for years and the LDN  kept it from progressing.  I, Fully

> and Honestly believe that in my heart. How lucky am I? Next step,

> surgery.  Keep me in your prayers.  I'd really appreciate that. 

>      LDN has done so much for my MS, and just proved that to the new

> Neuro who told me she couldn't take me on as a patient because I don't

> follow the " conventional protocol for MS " .  We had quite a debate last

> week in her office.  She told me, " Go for an MRI, I'm SURE you have

> ACTIVE lesions, and when we see that on the report, you must agree to

> start an IV treatment, then we'll talk about going back to the

> injectables " .....Needless to say, I looked at her like she had 8

> eyeballs, but agreed to the MRI for my own curiosity, and told her I'd

> be crazy to change anything I was doing for myself.  Well, the report

> is in.  It remains exactly the same as when first starting LDN in

> Sept. of 2002.  Keeping in mind, my First MRI, in 1999 when dx. with

> RRMS, showed 4 prominent lesions, the MRI's since LDN show only 2, and

> one is difficult to see. She swallowed hard and said, " Your MS is

> doing wonderful, nothing active, its not progressed, it's stayed the

> same "   I said, " Well, maybe now you'll read all the information I gave

> you about LDN, and Oh, next time I come in, we'll discuss whether or

> not I want to keep You on as My Neuro! "   She told me to please come

> back.  I told her I'd think about it.  She hugged me and I left.  I'll

> give her some time to read up on LDN and think about things, and

> decide if I really want to go back.

>    Anyway, I just wanted to share this with you.  I have been a

> believer in LDN since the day I started it in 2002, and now with the

> thought of it keeping this cancer at bay just reinforces it all. 

> Until There's A Cure.............There's LDN

>                God Bless You All

>            Carol

>

>

>

[Guest guest]

I am alw, doctor found cancer in my bladder and found

cancer with a spider web thing covering the cancer.

It did not spred it was arrested.

--- sunynbrite56@... wrote:

>

>

> I have news that I feel the need to share with you

> all.

> To start, I've just been dx. with Breast Cancer.

> (it gets better, I

> promise!) Now, this was my first mamogram, I'm 49.

> The size is just about a

> centimeter, and very faint. Which, thank God is

> removable being it was detected

> early. But, it made me wonder how long I could

> have had this, and did the LDN

> keep it from getting any worse? So, I called Dr.

> Bihari's office, and was told

> " Absolutley " . I could have had this for years and

> the LDN kept it from

> progressing. I, Fully and Honestly believe that in

> my heart. How lucky am I?

> Next step, surgery. Keep me in your prayers. I'd

> really appreciate that.

> LDN has done so much for my MS, and just

> proved that to the new Neuro

> who told me she couldn't take me on as a patient

> because I don't follow the

> " conventional protocol for MS " . We had quite a

> debate last week in her

> office. She told me, " Go for an MRI, I'm SURE you

> have ACTIVE lesions, and when we

> see that on the report, you must agree to start an

> IV treatment, then we'll

> talk about going back to the

> injectables " .....Needless to say, I looked at

> her like she had 8 eyeballs, but agreed to the MRI

> for my own curiosity, and

> told her I'd be crazy to change anything I was

> doing for myself. Well, the

> report is in. It remains exactly the same as when

> first starting LDN in Sept.

> of 2002. Keeping in mind, my First MRI, in 1999

> when dx. with RRMS, showed 4

> prominent lesions, the MRI's since LDN show only 2,

> and one is difficult to

> see. She swallowed hard and said, " Your MS is doing

> wonderful, nothing

> active, its not progressed, it's stayed the same "

> I said, " Well, maybe now you'll

> read all the information I gave you about LDN, and

> Oh, next time I come in,

> we'll discuss whether or not I want to keep You on

> as My Neuro! " She told me

> to please come back. I told her I'd think about

> it. She hugged me and I

> left. I'll give her some time to read up on LDN

> and think about things, and

> decide if I really want to go back.

> Anyway, I just wanted to share this with you. I

> have been a believer in

> LDN since the day I started it in 2002, and now

> with the thought of it

> keeping this cancer at bay just reinforces it all.

>

> Until There's A Cure.............There's LDN

> God Bless You All

> Carol

>

>

>

__________________________________________________

[Guest guest]

Hi Carole,

I would log onto http://www.survivecancer.net/. Or e-mail Bruce directly. He has a fasting diet that he can tell you about that you do for 2 weeks once a year to kill any cancer that might be in your body.

I had a friend that got rid of all of his cancer that had spread in many areas of his body. He did mostly juicing to get more alkaline and then he had gone into a clinic to have some other things done. But he attributes a lot of his success to balancing his PH by juicing. That is basically what Bruce's two week diet does too.

Below is a link to a list of foods that are more alkaline and foods that are more acid.

http://www.thewolfeclinic.com/acidalkfoods.html

I hope it is helpful.

My very best

Aletha

[low dose naltrexone] New MRI

I have news that I feel the need to share with you all.

To start, I've just been dx. with Breast Cancer. (it gets better, I promise!) Now, this was my first mamogram, I'm 49. The size is just about a centimeter, and very faint. Which, thank God is removable being it was detected early. But, it made me wonder how long I could have had this, and did the LDN keep it from getting any worse? So, I called Dr. Bihari's office, and was told "Absolutley". I could have had this for years and the LDN kept it from progressing. I, Fully and Honestly believe that in my heart. How lucky am I? Next step, surgery. Keep me in your prayers. I'd really appreciate that.

LDN has done so much for my MS, and just proved that to the new Neuro who told me she couldn't take me on as a patient because I don't follow the "conventional protocol for MS". We had quite a debate last week in her office. She told me, "Go for an MRI, I'm SURE you have ACTIVE lesions, and when we see that on the report, you must agree to start an IV treatment, then we'll talk about going back to the injectables".....Needless to say, I looked at her like she had 8 eyeballs, but agreed to the MRI for my own curiosity, and told her I'd be crazy to change anything I was doing for myself. Well, the report is in. It remains exactly the same as when first starting LDN in Sept. of 2002. Keeping in mind, my First MRI, in 1999 when dx. with RRMS, showed 4 prominent lesions, the MRI's since LDN show only 2, and one is difficult to see. She swallowed hard and said, "Your MS is doing wonderful, nothing active, its not progressed, it's stayed the same" I said, "Well, maybe now you'll read all the information I gave you about LDN, and Oh, next time I come in, we'll discuss whether or not I want to keep You on as My Neuro!" She told me to please come back. I told her I'd think about it. She hugged me and I left. I'll give her some time to read up on LDN and think about things, and decide if I really want to go back.

Anyway, I just wanted to share this with you. I have been a believer in LDN since the day I started it in 2002, and now with the thought of it keeping this cancer at bay just reinforces it all.

Until There's A Cure.............There's LDN

God Bless You All

Carol

[Guest guest]

Good luck Carol! I'll be praying for you! Way to go with the neuro!

Take care

>

> I have news that I feel the need to share with you all.

> To start, I've just been dx. with Breast Cancer. (it gets better,

I

> promise!) Now, this was my first mamogram, I'm 49. The size is

just about a

> centimeter, and very faint. Which, thank God is removable being

it was detected

> early. But, it made me wonder how long I could have had this,

and did the LDN

> keep it from getting any worse? So, I called Dr. Bihari's office,

and was told

> " Absolutley " . I could have had this for years and the LDN kept

it from

> progressing. I, Fully and Honestly believe that in my heart. How

lucky am I?

> Next step, surgery. Keep me in your prayers. I'd really

appreciate that.

> LDN has done so much for my MS, and just proved that to the

new Neuro

> who told me she couldn't take me on as a patient because I don't

follow the

> " conventional protocol for MS " . We had quite a debate last week

in her

> office. She told me, " Go for an MRI, I'm SURE you have ACTIVE

lesions, and when we

> see that on the report, you must agree to start an IV treatment,

then we'll

> talk about going back to the injectables " .....Needless to say, I

looked at

> her like she had 8 eyeballs, but agreed to the MRI for my own

curiosity, and

> told her I'd be crazy to change anything I was doing for myself.

Well, the

> report is in. It remains exactly the same as when first starting

LDN in Sept.

> of 2002. Keeping in mind, my First MRI, in 1999 when dx. with

RRMS, showed 4

> prominent lesions, the MRI's since LDN show only 2, and one is

difficult to

> see. She swallowed hard and said, " Your MS is doing wonderful,

nothing

> active, its not progressed, it's stayed the same " I said, " Well,

maybe now you'll

> read all the information I gave you about LDN, and Oh, next time

I come in,

> we'll discuss whether or not I want to keep You on as My Neuro! "

She told me

> to please come back. I told her I'd think about it. She hugged

me and I

> left. I'll give her some time to read up on LDN and think about

things, and

> decide if I really want to go back.

> Anyway, I just wanted to share this with you. I have been a

believer in

> LDN since the day I started it in 2002, and now with the thought

of it

> keeping this cancer at bay just reinforces it all.

> Until There's A Cure.............There's LDN

> God Bless You All

> Carol

>

[Guest guest]

That's a great testament to the power of LDN and the human spirit. I am so happy for your progress and I think this is possible for each and every one of us. Blessings, Kathy

[low dose naltrexone] New MRI

I have news that I feel the need to share with you all.

To start, I've just been dx. with Breast Cancer. (it gets better, I promise!) Now, this was my first mamogram, I'm 49. The size is just about a centimeter, and very faint. Which, thank God is removable being it was detected early. But, it made me wonder how long I could have had this, and did the LDN keep it from getting any worse? So, I called Dr. Bihari's office, and was told "Absolutley". I could have had this for years and the LDN kept it from progressing. I, Fully and Honestly believe that in my heart. How lucky am I? Next step, surgery. Keep me in your prayers. I'd really appreciate that.

LDN has done so much for my MS, and just proved that to the new Neuro who told me she couldn't take me on as a patient because I don't follow the "conventional protocol for MS". We had quite a debate last week in her office. She told me, "Go for an MRI, I'm SURE you have ACTIVE lesions, and when we see that on the report, you must agree to start an IV treatment, then we'll talk about going back to the injectables".....Needless to say, I looked at her like she had 8 eyeballs, but agreed to the MRI for my own curiosity, and told her I'd be crazy to change anything I was doing for myself. Well, the report is in. It remains exactly the same as when first starting LDN in Sept. of 2002. Keeping in mind, my First MRI, in 1999 when dx. with RRMS, showed 4 prominent lesions, the MRI's since LDN show only 2, and one is difficult to see. She swallowed hard and said, "Your MS is doing wonderful, nothing active, its not progressed, it's stayed the same" I said, "Well, maybe now you'll read all the information I gave you about LDN, and Oh, next time I come in, we'll discuss whether or not I want to keep You on as My Neuro!" She told me to please come back. I told her I'd think about it. She hugged me and I left. I'll give her some time to read up on LDN and think about things, and decide if I really want to go back.

Anyway, I just wanted to share this with you. I have been a believer in LDN since the day I started it in 2002, and now with the thought of it keeping this cancer at bay just reinforces it all.

Until There's A Cure.............There's LDN

God Bless You All

Carol

[Guest guest]

Prayers for you concerning your cancer as well.

[low dose naltrexone] New MRI

I have news that I feel the need to share with you all.

To start, I've just been dx. with Breast Cancer. (it gets better, I promise!) Now, this was my first mamogram, I'm 49. The size is just about a centimeter, and very faint. Which, thank God is removable being it was detected early. But, it made me wonder how long I could have had this, and did the LDN keep it from getting any worse? So, I called Dr. Bihari's office, and was told "Absolutley". I could have had this for years and the LDN kept it from progressing. I, Fully and Honestly believe that in my heart. How lucky am I? Next step, surgery. Keep me in your prayers. I'd really appreciate that.

LDN has done so much for my MS, and just proved that to the new Neuro who told me she couldn't take me on as a patient because I don't follow the "conventional protocol for MS". We had quite a debate last week in her office. She told me, "Go for an MRI, I'm SURE you have ACTIVE lesions, and when we see that on the report, you must agree to start an IV treatment, then we'll talk about going back to the injectables".....Needless to say, I looked at her like she had 8 eyeballs, but agreed to the MRI for my own curiosity, and told her I'd be crazy to change anything I was doing for myself. Well, the report is in. It remains exactly the same as when first starting LDN in Sept. of 2002. Keeping in mind, my First MRI, in 1999 when dx. with RRMS, showed 4 prominent lesions, the MRI's since LDN show only 2, and one is difficult to see. She swallowed hard and said, "Your MS is doing wonderful, nothing active, its not progressed, it's stayed the same" I said, "Well, maybe now you'll read all the information I gave you about LDN, and Oh, next time I come in, we'll discuss whether or not I want to keep You on as My Neuro!" She told me to please come back. I told her I'd think about it. She hugged me and I left. I'll give her some time to read up on LDN and think about things, and decide if I really want to go back.

Anyway, I just wanted to share this with you. I have been a believer in LDN since the day I started it in 2002, and now with the thought of it keeping this cancer at bay just reinforces it all.

Until There's A Cure.............There's LDN

God Bless You All

Carol

[Guest guest]

WO W this i s great!!!!! thank you for posting this wonderful and very encouraging news!

Nola

[low dose naltrexone] New MRI

I have news that I feel the need to share with you all.

To start, I've just been dx. with Breast Cancer. (it gets better, I promise!) Now, this was my first mamogram, I'm 49. The size is just about a centimeter, and very faint. Which, thank God is removable being it was detected early. But, it made me wonder how long I could have had this, and did the LDN keep it from getting any worse? So, I called Dr. Bihari's office, and was told "Absolutley". I could have had this for years and the LDN kept it from progressing. I, Fully and Honestly believe that in my heart. How lucky am I? Next step, surgery. Keep me in your prayers. I'd really appreciate that.

LDN has done so much for my MS, and just proved that to the new Neuro who told me she couldn't take me on as a patient because I don't follow the "conventional protocol for MS". We had quite a debate last week in her office. She told me, "Go for an MRI, I'm SURE you have ACTIVE lesions, and when we see that on the report, you must agree to start an IV treatment, then we'll talk about going back to the injectables".....Needless to say, I looked at her like she had 8 eyeballs, but agreed to the MRI for my own curiosity, and told her I'd be crazy to change anything I was doing for myself. Well, the report is in. It remains exactly the same as when first starting LDN in Sept. of 2002. Keeping in mind, my First MRI, in 1999 when dx. with RRMS, showed 4 prominent lesions, the MRI's since LDN show only 2, and one is difficult to see. She swallowed hard and said, "Your MS is doing wonderful, nothing active, its not progressed, it's stayed the same" I said, "Well, maybe now you'll read all the information I gave you about LDN, and Oh, next time I come in, we'll discuss whether or not I want to keep You on as My Neuro!" She told me to please come back. I told her I'd think about it. She hugged me and I left. I'll give her some time to read up on LDN and think about things, and decide if I really want to go back.

Anyway, I just wanted to share this with you. I have been a believer in LDN since the day I started it in 2002, and now with the thought of it keeping this cancer at bay just reinforces it all.

Until There's A Cure.............There's LDN

God Bless You All

Carol

[Guest guest]

>

>

>

> I have news that I feel the need to share with you all.

> To start, I've just been dx. with Breast Cancer. (it gets better,

I

> promise!) Now, this was my first mamogram, I'm 49. The size is

just about a

> centimeter, and very faint. Which, thank God is removable being

it was detected

> early. But, it made me wonder how long I could have had this,

and did the LDN

> keep it from getting any worse? So, I called Dr. Bihari's office,

and was told

> " Absolutley " . I could have had this for years and the LDN kept

it from

> progressing. I, Fully and Honestly believe that in my heart. How

lucky am I?

> Next step, surgery. Keep me in your prayers. I'd really

appreciate that.

> LDN has done so much for my MS, and just proved that to the

new Neuro

> who told me she couldn't take me on as a patient because I don't

follow the

> " conventional protocol for MS " . We had quite a debate last week

in her

> office. She told me, " Go for an MRI, I'm SURE you have ACTIVE

lesions, and when we

> see that on the report, you must agree to start an IV treatment,

then we'll

> talk about going back to the injectables " .....Needless to say, I

looked at

> her like she had 8 eyeballs, but agreed to the MRI for my own

curiosity, and

> told her I'd be crazy to change anything I was doing for myself.

Well, the

> report is in. It remains exactly the same as when first starting

LDN in Sept.

> of 2002. Keeping in mind, my First MRI, in 1999 when dx. with

RRMS, showed 4

> prominent lesions, the MRI's since LDN show only 2, and one is

difficult to

> see. She swallowed hard and said, " Your MS is doing wonderful,

nothing

> active, its not progressed, it's stayed the same " I said, " Well,

maybe now you'll

> read all the information I gave you about LDN, and Oh, next time

I come in,

> we'll discuss whether or not I want to keep You on as My Neuro! "

She told me

> to please come back. I told her I'd think about it. She hugged

me and I

> left. I'll give her some time to read up on LDN and think about

things, and

> decide if I really want to go back.

> Anyway, I just wanted to share this with you. I have been a

believer in

> LDN since the day I started it in 2002, and now with the thought

of it

> keeping this cancer at bay just reinforces it all.

> Until There's A Cure.............There's LDN

> God Bless You All

> Carol

>

Carol, thank you for your post and you will be in my prayers! I

also love your spirit!!