Skin Cancer

[Guest guest]

Hey Marshal,

Got some information for you. I have had cancer three times, healed

naturally twice. I've read alot & studied alot. In particular I am really

attracted to a certain system of care it's called medical dowsing and is

very helpful in determining what you got and how to get rid of it. I don't

mean to sound glib about this. I do find this technique so extremely useful

at helping us pin point causes and effects of disease. You can also send

your saliva away to be analyzed for an inexpensive price. Peaceful Meadow

Retreat, 7075 Valmont Dr., Boulder, CO and Hanna's Herbs also in Boulder,

Co. Hanna was a Master Herbalist who died last year at the age of 80

something. The Retreat is a teaching institute where one can take week long

classes in medical dowsing inorder to be able to help themselves and of

course others. There is also a naturopath in Socorro, NM her name is Dr.

Marcy Foley. I don't have my phone book with me or I'd give you the

numbers. But directory asssitance should be able to help you. Also

anything you read by Hanna Kroeger, her herb shop carries all her books and

can tell you what books will help you understand more. And Dr. Hazel

Parcell's who died a few yrs. ago at abe 106. Her Institute is in Santa Fe,

NM I think.

This is a great website and full of information. It's what we need. Thank

you one and all.

Ria

>From: Dusan Stojkovic <dusan@...>

>Reply- onelist

>ZACKSAM@... (MARSHALL PALMER)

>CC: onelist

>Subject: [ ] Re: Skin cancer

>Date: Tue, 04 May 1999 11:20:34 +0200

>

>From: Dusan Stojkovic <dusan@...>

>

>At 06:49 02.05.99 -0400, you wrote:

> >Dusan, can you give me advice? I have skin cancers, and after treating

> >them with Efudex creme they get better but won`t go away! Can

> >you advise me what to try? Diet, or anything? I`ll try your advice.

> >Thanks

> >Marshall

> >

> >

>

>

>

>

>

>Hello Marshall.

>

>Skin cancer is one of the most simple cancers to cure.

>

>To cure skin cancer, just folow this program:

>

>http://home.sol.no/~dusan/cancer.html

>It will take 3 - 6 months to be cured.

>

>

>

>

>Take care about what you eat, after the program, so that you do not get

>cancer again.

>

>

>Read also testimonials of the people who have used only a small fraction of

>this program:

>

>http://www.geocities.com/HotSprings/1158/MAILBAG.HTM

>

>

>Join also Cancer cured discussion group.

>People from that group will help you and will have more time to answer your

>questions.

>

>Cancercured - Discussion and Support Group:

>People who have cured cancer, and people who are doing it!

>

>Subscribe to the list: /subscribe.cgi/

>List Archives: /archives.cgi/

>

>

>----------------------------------------------------------------------------

>----

>

>

>Take care

>

>Dusan Stojkovic

>Norway

>http://home.sol.no/~dusan/

>_________________________________________

>

>

>

>

>

>

>

>

>

>

>

>Here is one story from this page:

> http://www.geocities.com/HotSprings/1158/MAILBAG.HTM

>

>

>Subject: The Miracle of Flax

>Date: Sun, 8 Feb 1998 23:50:25 EST

>From: Parentbd@...

>av984@...

>Dear Shirley:

>

>A few months ago, my mother was diagnosed with an agressively growing,

>squamous cell carcinoma on her left arm. Her doctor wanted to operated

>immediately, but she was opposed to the idea of invasive surgery; so she

>asked her doctor for two weeks to find an alternative. She discovered

>Fischer's " How to Fight Cancer and Win " , used the 1 Tbs Flax and 1/4 cup

>cottage cheese, plus she rubbed a little of the oil on the cancerous

>tissue. After two weeks she returned to her doctor with a completely healed

>arm. Her doctor was floored! He insisted that he take another biopsy, even

>though the cancerous tissue was gone. When the results came back negative,

>he dubbed her recovery as " spontaneous remission, " failing to believe that

>flax oil had cured my mom of cancer.

>

>I have since found your website, and I have copied much of the info.

>(including Beckworth's testimonial) and have given the info. to people with

>cancer who have found the testimonial pursuasive enough to at least give

>the oil a shot. One man, a friend of my husband's, has already reported

>back that his doctor found that his blood appears to have changed from the

>greenish color of cancer patients, back to a healthy reddish color--just as

>described in Fischer's book!!

>

>Thank you so much for sharing this information, I'm sure you have saved

>lives!

>

>Incidentally, my mom and dad have been taking flax oil everyday since the

>diagnosis. Each morning, their mostly empty bowls have been given to

>Scooter (their 15 year old Bichen Frise dog), who has been licking them

>clean! Scooter, amazingly, has become a puppy again. All of the effects of

>age that she had displayed are now gone--her cataracks are even going away!

>

>All the best,

>

> Parent Parentbd@...

>

>PS. I would be delighted if you shared my mom's story-and so would she. In

>fact, here is her address in case anyone would like to contact her:

>Ede P.O. Box 434 Pine Valley, CA 91962

>

>Thanks Again for your wonderful website!

>

>

>

>

>------------------------------------------------------------------------

>The possibilities are endless!

>

>ONElist has something for everyone!

>------------------------------------------------------------------------

>-List Archives:

>/archives.cgi/

>Web Sites:

>http://home.sol.no/~dusan/cancerpage.html

>

>http://www.geocities.com/~dusan_s/

>http://www.geocities.com/~mycleanse/

>http://www.geocities.com/HotSprings/1158

>

>By joining the list you agree to hold yourself FULLY responsible FOR

>yourself. The things you will find here are for information and research

>purposes only!!!

>

_______________________________________________________________

Get Free Email and Do More On The Web. Visit http://www.msn.com

[Guest guest]

Ria,

Can you give us the address of the web site that you refer to as great.

Thank you

> The Miracle of Flax

> >Date: Sun, 8 Feb 1998 23:50:25 EST

> >From: Parentbd@...

> >av984@...

> >Dear Shirley:

> >

> >A few months ago, my mother was diagnosed with an agressively growing,

> >squamous cell carcinoma on her left arm. Her doctor wanted to operated

> >immediately, but she was opposed to the idea of invasive surgery; so she

> >asked her doctor for two weeks to find an alternative. She discovered

> >Fischer's " How to Fight Cancer and Win " , used the 1 Tbs Flax and 1/4 cup

> >cottage cheese, plus she rubbed a little of the oil on the cancerous

> >tissue. After two weeks she returned to her doctor with a

> completely healed

> >arm. Her doctor was floored! He insisted that he take another

> biopsy, even

> >though the cancerous tissue was gone. When the results came back

> negative,

> >he dubbed her recovery as " spontaneous remission, " failing to

> believe that

> >flax oil had cured my mom of cancer.

> >

> >I have since found your website, and I have copied much of the info.

> >(including Beckworth's testimonial) and have given the info. to

> people with

> >cancer who have found the testimonial pursuasive enough to at least give

> >the oil a shot. One man, a friend of my husband's, has already reported

> >back that his doctor found that his blood appears to have

> changed from the

> >greenish color of cancer patients, back to a healthy reddish

> color--just as

> >described in Fischer's book!!

> >

> >Thank you so much for sharing this information, I'm sure you have saved

> >lives!

> >

> >Incidentally, my mom and dad have been taking flax oil everyday since the

> >diagnosis. Each morning, their mostly empty bowls have been given to

> >Scooter (their 15 year old Bichen Frise dog), who has been licking them

> >clean! Scooter, amazingly, has become a puppy again. All of the

> effects of

> >age that she had displayed are now gone--her cataracks are even

> going away!

> >

> >All the best,

> >

> > Parent Parentbd@...

> >

> >PS. I would be delighted if you shared my mom's story-and so

> would she. In

> >fact, here is her address in case anyone would like to contact her:

> >Ede P.O. Box 434 Pine Valley, CA 91962

> >

> >Thanks Again for your wonderful website!

> >

> >

> >

> >

> >------------------------------------------------------------------------

> >The possibilities are endless!

> >

> >ONElist has something for everyone!

> >------------------------------------------------------------------------

> >-List Archives:

> >/archives.cgi/

> >Web Sites:

> >http://home.sol.no/~dusan/cancerpage.html

> >

> >http://www.geocities.com/~dusan_s/

> >http://www.geocities.com/~mycleanse/

> >http://www.geocities.com/HotSprings/1158

> >

> >By joining the list you agree to hold yourself FULLY responsible FOR

> >yourself. The things you will find here are for information and research

> >purposes only!!!

> >

>

>

> _______________________________________________________________

> Get Free Email and Do More On The Web. Visit http://www.msn.com

>

> ------------------------------------------------------------------------

> Attention Star Wars fans!

>

> ONElist is the best place for your Star Wars list!

> ------------------------------------------------------------------------

> -List Archives:

> /archives.cgi/

> Web Sites:

> http://home.sol.no/~dusan/cancerpage.html

>

http://www.geocities.com/~dusan_s/

http://www.geocities.com/~mycleanse/

http://www.geocities.com/HotSprings/1158

By joining the list you agree to hold yourself FULLY responsible FOR

yourself. The things you will find here are for information and research

purposes only!!!

[Guest guest]

What a positive approach you have taken to your affliction, Patty! I applaud you for your brave heart, and your kindness in warning others of the dangers that may lie ahead for sun "worshippers". Many thanks--------------and prayers and best wishes to you.

-------------Rosie, St. Louis, MO

(We may be related. My mother's maiden name------O'Brien!! )

[Guest guest]

Thank you for sharing your story and caring enough to warn others. I have

been a " sun worshipper " all of my life, and was quite bummed when I had heard

about skin cancer and imuran (I have been taking 50mg daily since January of

this year), but after reading your story I will definitely start using sun

screens, and even staying out of the sun when possible.

You sound like you have a very positive outlook, that can make all the

difference in the world. Once again THANK YOU!! Keep us updated on your

surgeries, and remember that you are in our prayers.

AIH (01/01)

Illinois

[Guest guest]

> To All,

>

Patty,

Thanks for the words of wisdom. I'm sorry that you had to come upon

them in this manner. I would like to add to your warning that

prednisone use and sun do not mix either. I grew up pale and

freckled. Every summer I would spend many countless hours trying to

get a sun tan and not a burn. I now live in Florida and I'm teased

by my northern friends and relatives and even my students (yes, I'm a

teacher) about being so " white " . My father has skin cancer but has

been spared, so far, the carcinoma. I went to a dermatologist when I

first moved down here. He took one look at me and said, you've got

to stay out of the sun. You already have a lot of skin damage.

I wish I could say that I keep sun screen on all of the time but I

don't. I'm listening to you and I'm going to start using it when I'm

just out and about. I hope that I haven't waited too long.

My prayers and my thoughts are with you. I love the rainbow striped

band-aids. What a great addition to any ensemble. :?)

Debbie/FL

> Some time back I read several postings about avoiding the sun

> while taking Imuran due to it's potential to increase skin

cancers.

> In Palmer's book (pg. 192) she states " Skin cancers,

> lymphoma, and leukemia are the cancers most attributable to

> azathioprine (Imuran) use, although these cancers occur as a side

> effect in rare circumstances. " Although I do NOT attribute my

recent

> bout with skin cancer to Imuran use as the first visible signs

began

> 5 months before I began Imuran, I want to share my experience so

that

> others do not minimize the need for skin blocks and protection.

>

> My AIH symptoms began in June 2000 and at the same time a

small

> sore developed on my nose. The sore finally healed in November,

but

> broke open again in January. I saw a local dermatologist last

month

> who diagnosed it as basal cell carcinoma (BCC) and my friends

laughed

> at how concerned I was as many had family members with up to 15 BCC

> removals frozen off at their dermatologist. But my dermatologist

> warned me that the location and size would complicate removal and

he

> urged me to hook up with the best plastic surgeon and

dermatologistat

> Scripps. I did.

>

> Monday two surgeries were performed to remove what turned out

> to be squamous carcinoma, a more aggressive type than BCC. Tuesday

> the plastic surgeon cut skin from the top of my cheek down to my

chin

> to pull over & reconstruct my nose. Another 3 or 4 surgeries will

be

> performed at three week intervals in hopes of restoring my face.

At

> best I will have scars on my nose and cheeks for life.

>

> I'm over my pity-party and recovering well. Today as I dress

> my scars and bandage my skin I'll put rainbow colored " Peace "

> bandages over the most repulsive areas so people won't gasp in

> horror. I'm laughing at myself again and feeling optimistic about

the

> future. But I urge everyone, especially those on Imuran to use a

> sunblock and avoid undergoing the pain and cuttings of skin cancer.

> Summer approaches and tans look good for a short time but there may

> be a future price to pay. I thank God I have great doctors or I'd

be

> signing off as " Elephant Man Wanna-Be " .

>

> Patty O

[Guest guest]

Hi Debbie,

I read your Pred. warning about the sun. I live in

Florida and love the sun. I have been trying to use a

sunscreen for several yrs. now because of skin getting

older and trying to prevent wrinkles. at this point

I'll take the wrinkles but want to leave the cancer

behind. We all have enough things going on without

adding something that we can try to prevent.There

seems to be a lot of teachers in this group. I am an

L.P.N. but have worked for a periodontist for the last

17 yrs. AIH was new to me and also to other medical

professionals I've asked. This seem to be a great

group of people. Where in Florida do you live?

Judy/Pensacola

-- dfisher4140@... wrote:

>

> > To All,

> >

> Patty,

> Thanks for the words of wisdom. I'm sorry that you

> had to come upon

> them in this manner. I would like to add to your

> warning that

> prednisone use and sun do not mix either. I grew up

> pale and

> freckled. Every summer I would spend many countless

> hours trying to

> get a sun tan and not a burn. I now live in Florida

> and I'm teased

> by my northern friends and relatives and even my

> students (yes, I'm a

> teacher) about being so " white " . My father has skin

> cancer but has

> been spared, so far, the carcinoma. I went to a

> dermatologist when I

> first moved down here. He took one look at me and

> said, you've got

> to stay out of the sun. You already have a lot of

> skin damage.

> I wish I could say that I keep sun screen on all of

> the time but I

> don't. I'm listening to you and I'm going to start

> using it when I'm

> just out and about. I hope that I haven't waited

> too long.

> My prayers and my thoughts are with you. I love the

> rainbow striped

> band-aids. What a great addition to any ensemble.

> :?)

>

> Debbie/FL

>

> > Some time back I read several postings about

> avoiding the sun

> > while taking Imuran due to it's potential to

> increase skin

> cancers.

> > In Palmer's book (pg. 192) she states

> " Skin cancers,

> > lymphoma, and leukemia are the cancers most

> attributable to

> > azathioprine (Imuran) use, although these cancers

> occur as a side

> > effect in rare circumstances. " Although I do NOT

> attribute my

> recent

> > bout with skin cancer to Imuran use as the first

> visible signs

> began

> > 5 months before I began Imuran, I want to share my

> experience so

> that

> > others do not minimize the need for skin blocks

> and protection.

> >

> > My AIH symptoms began in June 2000 and at

> the same time a

> small

> > sore developed on my nose. The sore finally

> healed in November,

> but

> > broke open again in January. I saw a local

> dermatologist last

> month

> > who diagnosed it as basal cell carcinoma (BCC) and

> my friends

> laughed

> > at how concerned I was as many had family members

> with up to 15 BCC

> > removals frozen off at their dermatologist. But

> my dermatologist

> > warned me that the location and size would

> complicate removal and

> he

> > urged me to hook up with the best plastic surgeon

> and

> dermatologistat

> > Scripps. I did.

> >

> > Monday two surgeries were performed to

> remove what turned out

> > to be squamous carcinoma, a more aggressive type

> than BCC. Tuesday

> > the plastic surgeon cut skin from the top of my

> cheek down to my

> chin

> > to pull over & reconstruct my nose. Another 3 or

> 4 surgeries will

> be

> > performed at three week intervals in hopes of

> restoring my face.

> At

> > best I will have scars on my nose and cheeks for

> life.

> >

> > I'm over my pity-party and recovering well.

> Today as I dress

> > my scars and bandage my skin I'll put rainbow

> colored " Peace "

> > bandages over the most repulsive areas so people

> won't gasp in

> > horror. I'm laughing at myself again and feeling

> optimistic about

> the

> > future. But I urge everyone, especially those on

> Imuran to use a

> > sunblock and avoid undergoing the pain and

> cuttings of skin cancer.

> > Summer approaches and tans look good for a short

> time but there may

> > be a future price to pay. I thank God I have

> great doctors or I'd

> be

> > signing off as " Elephant Man Wanna-Be " .

> >

> > Patty O

>

>

__________________________________________________

[Guest guest]

Judy,

I live in West Palm Beach. I'm umbilically connected to the

temperate zone. LOL I've lived here for 12yrs. I love it. I grew

up in West Virginia. No hillbilly jokes!!!

Debbie/FL

[Guest guest]

Patty,

I am so sorry to hear about all you have gone through. Thank you for the advise. I have very fair skin, and burn very easily. I never thought about how the meds would even affect me...I guess it's another thing to worry about.

Keep up your positive attitude and humor. You have a lot of people praying for you. Don' t worry about the pity parties either. We all need to throw them every once in awhile. You can come to one of mine anytime!!!

Sincerely,

Pam in CT

[Guest guest]

Hi Patty,

Extra prayers sent to you...2 yrs ago my mom had a squamous cell CA removed from her nose too. She was always so careful with her fair freckled skin and was devastated with the initial looks of her face after the first surgery. The second reconstruction made it look better after a while, but she still thinks her face is no longer pretty. She is wrong. Yes, we do see the scar but when she smiles, it goes away. She massaged Vitamin E oil in it for the last 6 months and honestly, I can't see the scar anymore. And we are just thankful that this skin CA didn't take her life.......I still need her so much, just as your family needs you. It sounds like you have a lot of loving people around you and that helps. God bless you, Patty. My recent surgery for cervical cancer only shows on my belly, but I'm thankful too for my life.

One of the first things I noticed when I started Imuran Jan 2000 was the appearance of small nodules (like moles or warts) on my skin -- legs, neck, face. I have them removed by freezing (nitrogen) about every 6 months, but they keep popping up. Doc says these lesions should not be worrisome.

My prayers to you for quick healing.

God bless,

[Guest guest]

Patti....your story really gave me a pause to reflect and be thankful for

all that I have. You wear that rainbow band-aid with pride and be thankful

too. Living in Ohio I never see much sun and have never gone " tanning " at

any of those shops. Now that my son is on the Pred and will be on the Imuran

soon, I will be lathering on the SPF 30 each and every day! Thanks so much

for your message and good luck to you on your future sx. I'm certain

everything will turn out great and you are a beautiful person, rainbow

band-aids and all! :-)

Hang in there!

Kathy (Mom of Ronnie AIH 4/01)

[ ] Re: Skin Cancer

>

> > To All,

> >

> Patty,

> Thanks for the words of wisdom. I'm sorry that you had to come upon

> them in this manner. I would like to add to your warning that

> prednisone use and sun do not mix either. I grew up pale and

> freckled. Every summer I would spend many countless hours trying to

> get a sun tan and not a burn. I now live in Florida and I'm teased

> by my northern friends and relatives and even my students (yes, I'm a

> teacher) about being so " white " . My father has skin cancer but has

> been spared, so far, the carcinoma. I went to a dermatologist when I

> first moved down here. He took one look at me and said, you've got

> to stay out of the sun. You already have a lot of skin damage.

> I wish I could say that I keep sun screen on all of the time but I

> don't. I'm listening to you and I'm going to start using it when I'm

> just out and about. I hope that I haven't waited too long.

> My prayers and my thoughts are with you. I love the rainbow striped

> band-aids. What a great addition to any ensemble. :?)

>

> Debbie/FL

>

> > Some time back I read several postings about avoiding the sun

> > while taking Imuran due to it's potential to increase skin

> cancers.

> > In Palmer's book (pg. 192) she states " Skin cancers,

> > lymphoma, and leukemia are the cancers most attributable to

> > azathioprine (Imuran) use, although these cancers occur as a side

> > effect in rare circumstances. " Although I do NOT attribute my

> recent

> > bout with skin cancer to Imuran use as the first visible signs

> began

> > 5 months before I began Imuran, I want to share my experience so

> that

> > others do not minimize the need for skin blocks and protection.

> >

> > My AIH symptoms began in June 2000 and at the same time a

> small

> > sore developed on my nose. The sore finally healed in November,

> but

> > broke open again in January. I saw a local dermatologist last

> month

> > who diagnosed it as basal cell carcinoma (BCC) and my friends

> laughed

> > at how concerned I was as many had family members with up to 15 BCC

> > removals frozen off at their dermatologist. But my dermatologist

> > warned me that the location and size would complicate removal and

> he

> > urged me to hook up with the best plastic surgeon and

> dermatologistat

> > Scripps. I did.

> >

> > Monday two surgeries were performed to remove what turned out

> > to be squamous carcinoma, a more aggressive type than BCC. Tuesday

> > the plastic surgeon cut skin from the top of my cheek down to my

> chin

> > to pull over & reconstruct my nose. Another 3 or 4 surgeries will

> be

> > performed at three week intervals in hopes of restoring my face.

> At

> > best I will have scars on my nose and cheeks for life.

> >

> > I'm over my pity-party and recovering well. Today as I dress

> > my scars and bandage my skin I'll put rainbow colored " Peace "

> > bandages over the most repulsive areas so people won't gasp in

> > horror. I'm laughing at myself again and feeling optimistic about

> the

> > future. But I urge everyone, especially those on Imuran to use a

> > sunblock and avoid undergoing the pain and cuttings of skin cancer.

> > Summer approaches and tans look good for a short time but there may

> > be a future price to pay. I thank God I have great doctors or I'd

> be

> > signing off as " Elephant Man Wanna-Be " .

> >

> > Patty O

>

>

>

>

[Guest guest]

Debby,

Yes my hepatologist has warned me against sun exposure. Hat's, sunscreen,

cover up as much as possible. If you read the inserts on the Cellcept and

Imuran they mention an increase risk of melanoma's. But what do you do. We

have to take the immunosupression drugs due to the AIH. So it is just

something we have to be aware of.

[Guest guest]

In a message dated 1/6/02 9:08:59 PM Pacific Standard Time, MKANTZLE@... writes:

Yes my hepatologist has warned me against sun exposure. Hat's, sunscreen, cover up as much as possible. If you read the inserts on the Cellcept and Imuran they mention an increase risk of melanoma's. But what do you do. We have to take the immunosupression drugs due to the AIH. So it is just something we have to be aware of.

My gastro-enterologist told me he had never heard of a connection between Imuran and skin cancer. I'm quite sure he was wrong. (Years ago my dermatologist told me there was no connection between tetracycline and sunburn. He was wrong.)

Harper

[Guest guest]

Harper,

I read the inserts religiously. It is mentioned in both Imuran and Cellcept.

I think if I remember correctly there is a higher risk on Cellcept but it is

mentioned in both.

.

[Guest guest]

In a message dated 1/6/02 10:32:11 PM Pacific Standard Time, MKANTZLE@... writes:

Harper,

I read the inserts religiously. It is mentioned in both Imuran and Cellcept. I think if I remember correctly there is a higher risk on Cellcept but it is mentioned in both.

.

Yes, I know. That's why I was dismayed to find my highly respected doctor didn't know about it. At the time (early Prednisone), I was so uncertain of my thinking processes that I thought I might be mistaken, might have mis-read.

Harper

[Guest guest]

In a message dated 1/7/02 4:07:43 PM Pacific Standard Time, nneW5@... writes:

.....last summer even with all the

precautions (super sunblock, umbrella, tshirts) I still had a reaction

to the sun (itchy, red raised rash) and had to practically dress like

an eskimo to go out on the beach!

nne

I'm lucky -- the place where we're building a vacation house is noted for frequent fog! And I'm very pale.

Harper

[Guest guest]

Thanks nne,

I have always been a sun lover and this has been hard for me because one of

the only things I did to relax was to go the the pool and VEG OUT. So this

is gone too. Just have to find a new way to VEG OUT.

I too now look like a FAT ESKIMO when I go out but I am very careful.

Thanks for your concern.

[Guest guest]

In a message dated 1/7/02 6:24:57 PM Pacific Standard Time, tdcc2000@... writes:

Thanks for the info. I have to admit that I have not read any of the literature on cellcept yet. I guess it is time!

debby

Read about any medication you use, prescribed or not. Don't depend entirely on anyone else.

Harper

[Guest guest]

,

Also one thing to keep in mind re sun exposure...prednisone (if I

recall correctly) is photo sensitive as is 6mp (which I take instead

of imuran) Many drugs are, (e.g., HCTZ),so even if the risk of skin

cancer is minimal, be careful to cover up to avoid other more

immediate and uncomfortable reactions....last summer even with all the

precautions (super sunblock, umbrella, tshirts) I still had a reaction

to the sun (itchy, red raised rash) and had to practically dress like

an eskimo to go out on the beach!

nne

> Debby,

>

> Yes my hepatologist has warned me against sun exposure. Hat's,

sunscreen,

> cover up as much as possible. If you read the inserts on the

Cellcept and

> Imuran they mention an increase risk of melanoma's. But what do you

do. We

> have to take the immunosupression drugs due to the AIH. So it is just

> something we have to be aware of.

>

>

[Guest guest]

Thanks for the info. I have to admit that I have not read any of the literature on cellcept yet. I guess it is time!

debby

Re: [ ] Skin cancer

Debby,Yes my hepatologist has warned me against sun exposure. Hat's, sunscreen, cover up as much as possible. If you read the inserts on the Cellcept and Imuran they mention an increase risk of melanoma's. But what do you do. We have to take the immunosupression drugs due to the AIH. So it is just something we have to be aware of.

[Guest guest]

Has she tried Cansema? It is a topical that eats away the cancer. I've heard

many testimonials.

Kathy

lren@... wrote:

My mother in-law has skin cancer (basal cell mostly) and is constantly

getting zapped by the dermatologist. Can anyone tell me if there is something

specifically for that cancer that will help her from the inside out?

Thank you,

R

[Guest guest]

>My mother in-law has skin cancer (basal cell mostly) and is constantly

>getting zapped by the dermatologist. Can anyone tell me if there is

>something

>specifically for that cancer that will help her from the inside out?

I made the comment in the post on ulcerated

BC earlier today that, and as K Ott mentioned,

" cansema appears incredibly effective for any type

of skin cancer. I have heard of only one case where

additional measures were necessary. " This is used

after the fact, though.

As far as preventing it from the inside, the three

main supplements that come to mind are a good

multivitamin that contains at least 70mcg selenium

with other antioxidants, PABA (1000mg per day), and

omega 3 fish oil (molecularly distilled type like Enzymatic

Therapy Eskimo-3 or Carlson's).

turf

[Guest guest]

High gauss north pole stationary magnets. The north pole attracts oxygen

(cancer's arch enemy) and repels hydrogen. Read H. Philpott's book

Magnetic Therapy' for details. DON'T let them cut on it! It will spread of

they do. No biopsies either, you can tell be looking at it what it is.

http://www.amazon

com/gp/product/1887299211/sr=8-6/qid=1149091310/ref=pd_bbs_6/002-7344692-9299

49?%5Fencoding=UTF8

-- [ ] Skin cancer

[WDDTY e-News Broadcast - 30 May 2006]

Skin cancer: This reader requests help for a friend?s mother with basal

cell carcinoma (a form of skin cancer) of the head. She?s been

prescribed Imiquimod cream (Aldara) but has become very ill since taking

it. She experienced nausea, lethargy, depression and very painful

headaches. She?s now been advised by the hospital to stop using it

(after three weeks of daily use). Does anyone know if there are any

long-term side effects? Are there any natural approaches that can

Help

<SNIP>

[Guest guest]

Try Miracle II products. Sold on e-bay if you do not know where to

find it. Very cheap. Works well on almost all cancers. Non toxic.

Write me off line after you have the products if you need specific

directions on how to use it.

Start with soap and neutralizer. Also get gel or cream for topical

use.

robert-blau@... wrote:

> [WDDTY e-News Broadcast - 30 May 2006]

> Skin cancer: This reader requests help for a friend?s mother with basal cell

carcinoma (a form of skin cancer) of the head. She?s been

> prescribed Imiquimod cream (Aldara) but has become very ill since taking it.

She experienced nausea, lethargy, depression and very painful headaches. She?s

now been advised by the hospital to stop using it (after three weeks of daily

use). Does anyone know if there are any long-term side effects? Are there any

natural approaches that can help?

>

> GIVE YOUR FELLOW READERS A HELPING HAND: If you have tips or suggestions that

you think may be useful for any of the readers' health queries, send to us at:

e-news@...

>

[Guest guest]

Hi Thanks for that. Went to the website. It seems that it costs $115 and only

treats a small amount of spots. Is that right? Is there any pain with the

treatment? Does anyone know of any other skin cancer treatments. I know I was

impressed about reading about rasberry cream a long while ago but cant find the

site again.

Thanks

Toni

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

PDQ Herbal Skin Cream works on all kinds of skin cancers, usually in

about ten days. I have used it with great success on my face and

neck. It is available from: http://behealed.biz/

Bonnie

[Guest guest]

Hi Toni--

The cost is $89.97 plus $5 shipping. They say one bottle will treat

20 lesions. In my experience, one treatment (2 drops) can cover a

size about as large as a silver dollar so you can stretch it out a

bit. I used it for a lesion on my lip and after it finished healing,

there was no scarring whatsoever. There can be quite a bit of pain

for the first day and a half depending on the size of the lesion and

where it is on your body. Some areas have less nerve endings than

others. But after all is said and done, a little pain is well worth

the results, especially where one's face is concerned.

Here is a recent posting from WDDTY that might interest you regarding

skin cancer:

As for alternatives, several creams have been suggested, including

SunSpot (a blend of glycoalkaloids, aloe vera, salicylic acid, tea

tree oil and menthol), Curaderm (see www.curaderm.net) and Raspex

(containing ellagitannins from raspberry extract). These have worked

for individual readers, but obviously they may not work for everyone.

Always carry out your own research before embarking on any treatment.