Re: Mantle Cell Lymphoma and LDN

[Guest guest]

>

> This is a call for help on behalf of my dad.

> Earlier this week my dad (he's 65 years old) was diagnosed with

> Mantle Cell Lymphoma. The Mantle Cell lymphoma most likely

> originated from a nasal adenoid snd is now residing in the sinus

> cavities high up in the nose. We do not yet know what stage my dad

> is in - bone marrow puncture and CT scan scheduled for next week.

> Blood work doesn't yet show too many abnormalities.

>

> The little bit of research I've been able to do (we only got the

> word yesterday) re: Mantle Cell Lymphoma is not good. Chemo doesn't

> seem to do much, not that we were that interested in pursuing chemo

> anyway (we've had other family members get diagnosed with blood

> cancers at a relatively young age, and the chemo did nothing except

> for enormously magnifying the person's suffering and completely

> robbing them from their dignity).

>

> I have been using LDN for myself and my two boys (one with autism,

> the other one with extensive allergies) with absolutely wonderful

> results. Dr. Jacquelyn McCandless (she's been keeping an eye on how

> my boys are doing on LDN) strongly recommended LDN for my dad as

> well, and I totally agree that this would be a very wise course of

> action.

>

> One issue here - my dad is in the Netherlands. So I am desperately

> questing for 1) a doc in the Netherlands, or maybe even here in the

> US that will prescribe LDN to a Mantle Cell Lymphoma patient, 2) a

> pharmacy either in the Netherlands or in the UK (I've browsed MS UK

> boards, apparently there is a pharmacy in the UK that dispenses LDN)

> that could fill the prescription.

>

> Any thoughts, ideas, suggestions on how to get my dad on LDN as soon

> as possible will be greatly appreciated. Needless to say that LDN

> will only be one part of our 'arsenal', so any other suggestions you

> may have (on or off board) will be greatly appreciated to0,

>

> Thanks in advance from the bottom of my heart.

>

> Petra

>

> Feel free to contact me, if you have any information, either on or

> off board, what ever works best for you.

>

=====

This was buried in the spam so decided to push it to the current page.

[Guest guest]

Dear Petra,

Perhaps Dr. Bruce Guillmette can help you with some leads for your father.

If anyone has his email address it would be a great help.

Sent via BlackBerry from Cingular Wireless

[low dose naltrexone] Mantle Cell Lymphoma and LDN

This is a call for help on behalf of my dad.

Earlier this week my dad (he's 65 years old) was diagnosed with

Mantle Cell Lymphoma. The Mantle Cell lymphoma most likely

originated from a nasal adenoid snd is now residing in the sinus

cavities high up in the nose. We do not yet know what stage my dad

is in - bone marrow puncture and CT scan scheduled for next week.

Blood work doesn't yet show too many abnormalities.

The little bit of research I've been able to do (we only got the

word yesterday) re: Mantle Cell Lymphoma is not good. Chemo doesn't

seem to do much, not that we were that interested in pursuing chemo

anyway (we've had other family members get diagnosed with blood

cancers at a relatively young age, and the chemo did nothing except

for enormously magnifying the person's suffering and completely

robbing them from their dignity).

I have been using LDN for myself and my two boys (one with autism,

the other one with extensive allergies) with absolutely wonderful

results. Dr. Jacquelyn McCandless (she's been keeping an eye on how

my boys are doing on LDN) strongly recommended LDN for my dad as

well, and I totally agree that this would be a very wise course of

action.

One issue here - my dad is in the Netherlands. So I am desperately

questing for 1) a doc in the Netherlands, or maybe even here in the

US that will prescribe LDN to a Mantle Cell Lymphoma patient, 2) a

pharmacy either in the Netherlands or in the UK (I've browsed MS UK

boards, apparently there is a pharmacy in the UK that dispenses LDN)

that could fill the prescription.

Any thoughts, ideas, suggestions on how to get my dad on LDN as soon

as possible will be greatly appreciated. Needless to say that LDN

will only be one part of our 'arsenal', so any other suggestions you

may have (on or off board) will be greatly appreciated to0,

Thanks in advance from the bottom of my heart.

Petra

Feel free to contact me, if you have any information, either on or

off board, what ever works best for you.

[Guest guest]

bruce@...

Good luck

Arlene

--------- [low dose naltrexone] Mantle Cell Lymphoma and LDN > > This is a call for help on behalf of my dad. > Earlier this week my dad (he's 65 years old) was diagnosed with > Mantle Cell Lymphoma. The Mantle Cell lymphoma most likely > originated from a nasal adenoid snd is now residing in the sinus > cavities high up

in the nose. We do not yet know what stage my dad > is in - bone marrow puncture and CT scan scheduled for next week. > Blood work doesn't yet show too many abnormalities. > > The little bit of research I've been able to do (we only got the > word yesterday) re: Mantle Cell Lymphoma is not good. Chemo doesn't > seem to do much, not that we were that interested in pursuing chemo > anyway (we've had other family members get diagnosed with blood > cancers at a relatively young age, and the chemo did nothing except > for enormously magnifying the person's suffering and completely > robbing them from their dignity). > > I have been using LDN for myself and my two boys (one with autism, > the other one with extensive allergies) with absolutely wonderful > results. Dr. Jacquelyn McCandless (she's been keeping an eye on how > my boys are doing on LDN) strongly recommended LDN for my da

d as > well, and I totally agree that this would be a very wise course of > action. > > One issue here - my dad is in the Netherlands. So I am desperately > questing for 1) a doc in the Netherlands, or maybe even here in the > US that will prescribe LDN to a Mantle Cell Lymphoma patient, 2) a > pharmacy either in the Netherlands or in the UK (I've browsed MS UK > boards, apparently there is a pharmacy in the UK that dispenses LDN) > that could fill the prescription. > > Any thoughts, ideas, suggestions on how to get my dad on LDN as soon > as possible will be greatly appreciated. Needless to say that LDN > will only be one part of our 'arsenal', so any other suggestions you > may have (on or off board) will be greatly appreciated to0, > > Thanks in advance from the bottom of my heart. > > Petra > > Feel free to contact me, if you have any infor

mation, either on or > off board, what ever works best for you. > > > > > >

[Guest guest]

I have heard from a reliable source ( White from the Brewer Library) that LDN is good for this type of cancer. Perhaps you could call them and research Hans Neiper's cancer protocol. Also, has two large newsletters dedicated solely to cancer. There is a multitude of info in these articles. God Bless you and your family. Oh the phone number to the library is 608-647-6513. Kathy

[low dose naltrexone] Re: Mantle Cell Lymphoma and LDN

>> This is a call for help on behalf of my dad. > Earlier this week my dad (he's 65 years old) was diagnosed with > Mantle Cell Lymphoma. The Mantle Cell lymphoma most likely > originated from a nasal adenoid snd is now residing in the sinus > cavities high up in the nose. We do not yet know what stage my dad > is in - bone marrow puncture and CT scan scheduled for next week. > Blood work doesn't yet show too many abnormalities.> > The little bit of research I've been able to do (we only got the > word yesterday) re: Mantle Cell Lymphoma is not good. Chemo doesn't > seem to do much, not that we were that interested in pursuing chemo > anyway (we've had other family members get diagnosed with blood > cancers at a relatively young age, and the chemo did nothing except > for enormously magnifying the person's suffering and completely > robbing them from their dignity).> > I have been using LDN for myself and my two boys (one with autism, > the other one with extensive allergies) with absolutely wonderful > results. Dr. Jacquelyn McCandless (she's been keeping an eye on how > my boys are doing on LDN) strongly recommended LDN for my dad as > well, and I totally agree that this would be a very wise course of > action.> > One issue here - my dad is in the Netherlands. So I am desperately > questing for 1) a doc in the Netherlands, or maybe even here in the > US that will prescribe LDN to a Mantle Cell Lymphoma patient, 2) a > pharmacy either in the Netherlands or in the UK (I've browsed MS UK > boards, apparently there is a pharmacy in the UK that dispenses LDN) > that could fill the prescription.> > Any thoughts, ideas, suggestions on how to get my dad on LDN as soon > as possible will be greatly appreciated. Needless to say that LDN > will only be one part of our 'arsenal', so any other suggestions you > may have (on or off board) will be greatly appreciated to0,> > Thanks in advance from the bottom of my heart.> > Petra> > Feel free to contact me, if you have any information, either on or > off board, what ever works best for you.>=====This was buried in the spam so decided to push it to the current page.

[Guest guest]

Hi, I live in Richland Center WI, home of the Brewer Science Library. There is a website. If you google Brewer Science Library, you will find it. This is how I came across LDN. White runs this part of the library and writes a newsletter you may subscribe to or read archived copies. Eve

http://www.mwt.net

[low dose naltrexone] Re: Mantle Cell Lymphoma and LDN

>> This is a call for help on behalf of my dad. > Earlier this week my dad (he's 65 years old) was diagnosed with > Mantle Cell Lymphoma. The Mantle Cell lymphoma most likely > originated from a nasal adenoid snd is now residing in the sinus > cavities high up in the nose. We do not yet know what stage my dad > is in - bone marrow puncture and CT scan scheduled for next week. > Blood work doesn't yet show too many abnormalities.> > The little bit of research I've been able to do (we only got the > word yesterday) re: Mantle Cell Lymphoma is not good. Chemo doesn't > seem to do much, not that we were that interested in pursuing chemo > anyway (we've had other family members get diagnosed with blood > cancers at a relatively young age, and the chemo did nothing except > for enormously magnifying the person's suffering and completely > robbing them from their dignity).> > I have been using LDN for myself and my two boys (one with autism, > the other one with extensive allergies) with absolutely wonderful > results. Dr. Jacquelyn McCandless (she's been keeping an eye on how > my boys are doing on LDN) strongly recommended LDN for my dad as > well, and I totally agree that this would be a very wise course of > action.> > One issue here - my dad is in the Netherlands. So I am desperately > questing for 1) a doc in the Netherlands, or maybe even here in the > US that will prescribe LDN to a Mantle Cell Lymphoma patient, 2) a > pharmacy either in the Netherlands or in the UK (I've browsed MS UK > boards, apparently there is a pharmacy in the UK that dispenses LDN) > that could fill the prescription.> > Any thoughts, ideas, suggestions on how to get my dad on LDN as soon > as possible will be greatly appreciated. Needless to say that LDN > will only be one part of our 'arsenal', so any other suggestions you > may have (on or off board) will be greatly appreciated to0,> > Thanks in advance from the bottom of my heart.> > Petra> > Feel free to contact me, if you have any information, either on or > off board, what ever works best for you.>=====This was buried in the spam so decided to push it to the current page.

[Guest guest]

Yes, it is brewersciencelibrary@....

[low dose naltrexone] Re: Mantle Cell Lymphoma and LDN

>> This is a call for help on behalf of my dad. > Earlier this week my dad (he's 65 years old) was diagnosed with > Mantle Cell Lymphoma. The Mantle Cell lymphoma most likely > originated from a nasal adenoid snd is now residing in the sinus > cavities high up in the nose. We do not yet know what stage my dad > is in - bone marrow puncture and CT scan scheduled for next week. > Blood work doesn't yet show too many abnormalities.> > The little bit of research I've been able to do (we only got the > word yesterday) re: Mantle Cell Lymphoma is not good. Chemo doesn't > seem to do much, not that we were that interested in pursuing chemo > anyway (we've had other family members get diagnosed with blood > cancers at a relatively young age, and the chemo did nothing except > for enormously magnifying the person's suffering and completely > robbing them from their dignity).> > I have been using LDN for myself and my two boys (one with autism, > the other one with extensive allergies) with absolutely wonderful > results. Dr. Jacquelyn McCandless (she's been keeping an eye on how > my boys are doing on LDN) strongly recommended LDN for my dad as > well, and I totally agree that this would be a very wise course of > action.> > One issue here - my dad is in the Netherlands. So I am desperately > questing for 1) a doc in the Netherlands, or maybe even here in the > US that will prescribe LDN to a Mantle Cell Lymphoma patient, 2) a > pharmacy either in the Netherlands or in the UK (I've browsed MS UK > boards, apparently there is a pharmacy in the UK that dispenses LDN) > that could fill the prescription.> > Any thoughts, ideas, suggestions on how to get my dad on LDN as soon > as possible will be greatly appreciated. Needless to say that LDN > will only be one part of our 'arsenal', so any other suggestions you > may have (on or off board) will be greatly appreciated to0,> > Thanks in advance from the bottom of my heart.> > Petra> > Feel free to contact me, if you have any information, either on or > off board, what ever works best for you.>=====This was buried in the spam so decided to push it to the current page.