Don't know what to do

[Guest guest]

In a message dated 8/7/2009 1:33:01 P.M. Central Daylight Time, dipghater writes:

Please all continue to think and pray for my little man, and my strength to fight this battle forhim and with him!

_____________

Rhonda, I'm not a big poster to this list and am not dealing with cancer right now myself or my family, so take what I am going to say at your own discretion.

 

In my personal opinion, I think Reid should be told exactly what's going on with him. You'd be amazed how children can deal with things. Talking about the truth with him empowers him. Kids have a way of knowing when we're hiding something from them. Disease can be changed to health. It happens all the time. The way the person thinks is a critical part of healing. You are, in essence, enlisting his help in the fight. In the Catholic faith, 7 is the age of reason. Maybe telling him his protocol is for a purpose will be a turning point in his journey to health.

 

Please, follow your own heart.

 

Terri

 

[Guest guest]

Tony, Marc, ,

Reid has become resistant to taking all of his pills, as I said

before he is foinf enzymes, NAC, curcumin and ipf inostitol. He takes

5 pills three times a day, or he was until he decided he didn't want

too. I struggle everyday with keeping things " normal " for us so he

doesn't get any incling that he has cancer . When we started all of

his treatment he knew he was having headaches so he knew he needed to

take his pills and do his " therapy " to make the headaches go away, but

now he doesn't get it because he isn't having headaches so to him that

means he doesn't have to take any pills. I'm at such a loss right

now, his MRI is on the 12th of August, and I'm very nervous to get the

results altho I try not to be because I know that no matter what it

shows, that's what it will show, I can't change that.

So what I'm writing to ask is, I know that all the pills are

important, but if there was just one or two that I could get him to

take which ones are the most important? Would it be the NAC and ip6?

I'm much more likely to get him to take 6 or 9 pills per day vs the 15

he was getting, also I'm still unsure of what a theraputic dose would

be for the ip6 and NAC? As it stands now Reid takes his OPC in

organic oj because he just won't drink anything else besides water and

I made him try it straight one time and he gagged. Think he is gettin

tire of the oj 3 times a day, I'm really just lost and confused and

want to do whatever I can for the boy that I can do for him. Its hard

to convince a 7 yo that he needs to take pills when he feels fine

without telling him what could happen if he doesn't.

On a side note, Reid is still doing outstanding. I registered

him for 2nd grade this week and it was an emotional day for me. Back

in Feb we weren't sure if he was going to feel well enough to finish

the 1st grade and we sure as heck weren't sure he was going to go to

2nd grade!!!!!! School starts on the 24th and we couldn't be more

excited or feel more blessed than we do! Please all continue to think

and pray for my little man, and my strength to fight this battle for

him and with him!

All my love

Rhonda

www.caringbridge.org/visit/reidebrom

 

--

Sent from my mobile device

[Guest guest]

Hi Rhonda -

 

I know this wasn't addressed to me, but maybe getting creative and putting

everything into one or 2 doses a day if possible may help - like smoothies -

make it fun for him since he's 7.

 

I fully understand that all the supplements can be overwhelming sometimes. I've

had to get creative myself and I mix as many as possible into a couple of doses

a day.

 

The IP-6 is more citrus flavored so maybe that can go in his juice and water it

down a bit. Even freeze the juice and make it frozen/creamy.

 

I would suggest whey or rice protein with lots of blueberries or strawberries

and put the enzymes, curcumin and NAC into it. NAC would have to be crushed a

bit though.

 

Please try and focus on the positive only - for him and for yourself. Visualize

positive MRI results and hold on to the positive things are are happening with

him.

 

Thank you for sharing the date of the MRI - I will visualize this with you. I'm

sure others will as well.

 

Help him understand that continued therapy helps keep the headaches away.

 

Being responsible for a child is challenging - am praying for continued strength

for you.

 

cathy

 

oleander soup , rhonda ebrom <dipghater wrote:

>

> Tony, Marc, ,

> Reid has become resistant to taking all of his pills, as I said

> before he is foinf enzymes, NAC, curcumin and ipf inostitol. He takes

> 5 pills three times a day, or he was until he decided he didn't want

> too. I struggle everyday with keeping things " normal " for us so he

> doesn't get any incling that he has cancer . When we started all of

> his treatment he knew he was having headaches so he knew he needed to

> take his pills and do his " therapy " to make the headaches go away, but

> now he doesn't get it because he isn't having headaches so to him that

> means he doesn't have to take any pills. I'm at such a loss right

> now, his MRI is on the 12th of August, and I'm very nervous to get the

> results altho I try not to be because I know that no matter what it

> shows, that's what it will show, I can't change that.

> So what I'm writing to ask is, I know that all the pills are

> important, but if there was just one or two that I could get him to

> take which ones are the most important? Would it be the NAC and ip6?

> I'm much more likely to get him to take 6 or 9 pills per day vs the 15

> he was getting, also I'm still unsure of what a theraputic dose would

> be for the ip6 and NAC? As it stands now Reid takes his OPC in

> organic oj because he just won't drink anything else besides water and

> I made him try it straight one time and he gagged. Think he is gettin

> tire of the oj 3 times a day, I'm really just lost and confused and

> want to do whatever I can for the boy that I can do for him. Its hard

> to convince a 7 yo that he needs to take pills when he feels fine

> without telling him what could happen if he doesn't.

> On a side note, Reid is still doing outstanding. I registered

> him for 2nd grade this week and it was an emotional day for me. Back

> in Feb we weren't sure if he was going to feel well enough to finish

> the 1st grade and we sure as heck weren't sure he was going to go to

> 2nd grade!!!!!! School starts on the 24th and we couldn't be more

> excited or feel more blessed than we do! Please all continue to think

> and pray for my little man, and my strength to fight this battle for

> him and with him!

> All my love

> Rhonda

> www.caringbridge.org/visit/reidebrom

>

> --

> Sent from my mobile device

>

[Guest guest]

Thank your for the suggestions, sadly my child is VERY particular with

what he eats or drinks. He will eat fruit like its going out of style

but not smoothies, he will eat apples but not applesauce (I thought

about pills in applesauce) he won't eat yogurt or cottage cheese. Its

very hard to get him to drink the oj with the OPC in it as it has a

taste that he is not fond of. Its so very frustrating!

Rhonda

 

On 8/7/09, plantenergy1 <plantenergy1 wrote:

> Hi Rhonda -

>

> I know this wasn't addressed to me, but maybe getting creative and putting

> everything into one or 2 doses a day if possible may help - like smoothies -

> make it fun for him since he's 7.

>

> I fully understand that all the supplements can be overwhelming sometimes.

> I've had to get creative myself and I mix as many as possible into a couple

> of doses a day.

>

> The IP-6 is more citrus flavored so maybe that can go in his juice and water

> it down a bit. Even freeze the juice and make it frozen/creamy.

>

> I would suggest whey or rice protein with lots of blueberries or

> strawberries and put the enzymes, curcumin and NAC into it. NAC would have

> to be crushed a bit though.

>

> Please try and focus on the positive only - for him and for yourself.

> Visualize positive MRI results and hold on to the positive things are are

> happening with him.

>

> Thank you for sharing the date of the MRI - I will visualize this with you.

> I'm sure others will as well.

>

> Help him understand that continued therapy helps keep the headaches away.

>

> Being responsible for a child is challenging - am praying for continued

> strength for you.

>

> cathy

>

> oleander soup , rhonda ebrom <dipghater wrote:

>>

>> Tony, Marc, ,

>> Reid has become resistant to taking all of his pills, as I said

>> before he is foinf enzymes, NAC, curcumin and ipf inostitol. He takes

>> 5 pills three times a day, or he was until he decided he didn't want

>> too. I struggle everyday with keeping things " normal " for us so he

>> doesn't get any incling that he has cancer . When we started all of

>> his treatment he knew he was having headaches so he knew he needed to

>> take his pills and do his " therapy " to make the headaches go away, but

>> now he doesn't get it because he isn't having headaches so to him that

>> means he doesn't have to take any pills. I'm at such a loss right

>> now, his MRI is on the 12th of August, and I'm very nervous to get the

>> results altho I try not to be because I know that no matter what it

>> shows, that's what it will show, I can't change that.

>> So what I'm writing to ask is, I know that all the pills are

>> important, but if there was just one or two that I could get him to

>> take which ones are the most important? Would it be the NAC and ip6?

>> I'm much more likely to get him to take 6 or 9 pills per day vs the 15

>> he was getting, also I'm still unsure of what a theraputic dose would

>> be for the ip6 and NAC? As it stands now Reid takes his OPC in

>> organic oj because he just won't drink anything else besides water and

>> I made him try it straight one time and he gagged. Think he is gettin

>> tire of the oj 3 times a day, I'm really just lost and confused and

>> want to do whatever I can for the boy that I can do for him. Its hard

>> to convince a 7 yo that he needs to take pills when he feels fine

>> without telling him what could happen if he doesn't.

>> On a side note, Reid is still doing outstanding. I registered

>> him for 2nd grade this week and it was an emotional day for me. Back

>> in Feb we weren't sure if he was going to feel well enough to finish

>> the 1st grade and we sure as heck weren't sure he was going to go to

>> 2nd grade!!!!!! School starts on the 24th and we couldn't be more

>> excited or feel more blessed than we do! Please all continue to think

>> and pray for my little man, and my strength to fight this battle for

>> him and with him!

>> All my love

>> Rhonda

>> www.caringbridge.org/visit/reidebrom

>>

>> --

>> Sent from my mobile device

>>

>

>

>

 

--

Sent from my mobile device

[Guest guest]

Rhonda,

 

I'm glad to hear Reid is still doing well. Right now we have Luke on every

one of these same supplements. He takes these all in his yogurt, due to the

fact that he was having swallowing issues. The curcumin has a taste, but the

rest are rather flavorless. You'll need to invest in a pill crusher for the

IP6/Inositol tablets. The capsules you can just pull apart and dump into the

yogurt or pudding.

Perhaps you could let Reid know that this is to keep the headaches away.

We'll be praying for a good scan for Reid.

 

Darren (Luke's dad)

http://www.caringbridge.org/visit/lukepollok

 

 

oleander soup , rhonda ebrom <dipghater wrote:

>

> Tony, Marc, ,

> Reid has become resistant to taking all of his pills, as I said

> before he is foinf enzymes, NAC, curcumin and ipf inostitol. He takes

> 5 pills three times a day, or he was until he decided he didn't want

> too. I struggle everyday with keeping things " normal " for us so he

> doesn't get any incling that he has cancer . When we started all of

> his treatment he knew he was having headaches so he knew he needed to

> take his pills and do his " therapy " to make the headaches go away, but

> now he doesn't get it because he isn't having headaches so to him that

> means he doesn't have to take any pills. I'm at such a loss right

> now, his MRI is on the 12th of August, and I'm very nervous to get the

> results altho I try not to be because I know that no matter what it

> shows, that's what it will show, I can't change that.

> So what I'm writing to ask is, I know that all the pills are

> important, but if there was just one or two that I could get him to

> take which ones are the most important? Would it be the NAC and ip6?

> I'm much more likely to get him to take 6 or 9 pills per day vs the 15

> he was getting, also I'm still unsure of what a theraputic dose would

> be for the ip6 and NAC? As it stands now Reid takes his OPC in

> organic oj because he just won't drink anything else besides water and

> I made him try it straight one time and he gagged. Think he is gettin

> tire of the oj 3 times a day, I'm really just lost and confused and

> want to do whatever I can for the boy that I can do for him. Its hard

> to convince a 7 yo that he needs to take pills when he feels fine

> without telling him what could happen if he doesn't.

> On a side note, Reid is still doing outstanding. I registered

> him for 2nd grade this week and it was an emotional day for me. Back

> in Feb we weren't sure if he was going to feel well enough to finish

> the 1st grade and we sure as heck weren't sure he was going to go to

> 2nd grade!!!!!! School starts on the 24th and we couldn't be more

> excited or feel more blessed than we do! Please all continue to think

> and pray for my little man, and my strength to fight this battle for

> him and with him!

> All my love

> Rhonda

> www.caringbridge.org/visit/reidebrom

>

> --

> Sent from my mobile device

>

[Guest guest]

Maybe Ice Cream? Does he like Ice Cream? Put it in whatever he likes! Get one of those electric ice cream makers, he likes fruit, put fruit in it! You can keep some handy in the freezer, and give him a bit a few times a day with his meds in it! Whatever it takes to make him well! Love and Prayers, Elizabeth

 

 

 

rhonda ebrom <dipghateroleander soup Sent: Friday, August 7, 2009 2:42:32 PM Re: Don't know what to do

Thank your for the suggestions, sadly my child is VERY particular withwhat he eats or drinks. He will eat fruit like its going out of stylebut not smoothies, he will eat apples but not applesauce (I thoughtabout pills in applesauce) he won't eat yogurt or cottage cheese. Itsvery hard to get him to drink the oj with the OPC in it as it has ataste that he is not fond of. Its so very frustrating!RhondaOn 8/7/09, plantenergy1 <plantenergy1@ > wrote:> Hi Rhonda ->> I know this wasn't addressed to me, but maybe getting creative and putting> everything into one or 2 doses a day if possible may help - like smoothies -> make it fun for him since he's 7.>> I fully understand that all the supplements can be overwhelming sometimes.> I've had to get

creative myself and I mix as many as possible into a couple> of doses a day.>> The IP-6 is more citrus flavored so maybe that can go in his juice and water> it down a bit. Even freeze the juice and make it frozen/creamy.>> I would suggest whey or rice protein with lots of blueberries or> strawberries and put the enzymes, curcumin and NAC into it. NAC would have> to be crushed a bit though.>> Please try and focus on the positive only - for him and for yourself.> Visualize positive MRI results and hold on to the positive things are are> happening with him.>> Thank you for sharing the date of the MRI - I will visualize this with you.> I'm sure others will as well.>> Help him understand that continued therapy helps keep the headaches away.>> Being responsible for a child is challenging - am praying for continued>

strength for you.>> cathy>> oleander soup, rhonda ebrom <dipghater@. ..> wrote:>>>> Tony, Marc, ,>> Reid has become resistant to taking all of his pills, as I said>> before he is foinf enzymes, NAC, curcumin and ipf inostitol. He takes>> 5 pills three times a day, or he was until he decided he didn't want>> too. I struggle everyday with keeping things "normal" for us so he>> doesn't get any incling that he has cancer . When we started all of>> his treatment he knew he was having headaches so he knew he needed to>> take his pills and do his "therapy" to make the headaches go away, but>> now he doesn't get it because he isn't having headaches so to him that>>

means he doesn't have to take any pills. I'm at such a loss right>> now, his MRI is on the 12th of August, and I'm very nervous to get the>> results altho I try not to be because I know that no matter what it>> shows, that's what it will show, I can't change that.>> So what I'm writing to ask is, I know that all the pills are>> important, but if there was just one or two that I could get him to>> take which ones are the most important? Would it be the NAC and ip6?>> I'm much more likely to get him to take 6 or 9 pills per day vs the 15>> he was getting, also I'm still unsure of what a theraputic dose would>> be for the ip6 and NAC? As it stands now Reid takes his OPC in>> organic oj because he just won't drink anything else besides water and>> I made him try it straight one time and he gagged. Think he is gettin>> tire of the oj 3

times a day, I'm really just lost and confused and>> want to do whatever I can for the boy that I can do for him. Its hard>> to convince a 7 yo that he needs to take pills when he feels fine>> without telling him what could happen if he doesn't.>> On a side note, Reid is still doing outstanding. I registered>> him for 2nd grade this week and it was an emotional day for me. Back>> in Feb we weren't sure if he was going to feel well enough to finish>> the 1st grade and we sure as heck weren't sure he was going to go to>> 2nd grade!!!!!! School starts on the 24th and we couldn't be more>> excited or feel more blessed than we do! Please all continue to think>> and pray for my little man, and my strength to fight this battle for>> him and with him!>> All my love>> Rhonda>> www.caringbridge. org/visit/

reidebrom>>>> -->> Sent from my mobile device>>>>>-- Sent from my mobile device

[Guest guest]

Rhonda,

 

Hugs to you and your little man there.

 

It seems to me that you have two options:

 

1)While keeping the truth about cancer from him is very understandable at his

tender age, it may be time to begin to open the truth up to him. Especially in

light of your comment about him being willing to take things 'for the headache'

while he had it and now he sees no need, it seems that perhaps the serious truth

is needed to gain his cooperation.

 

2)Otherwise, what would seem to be called for is a serious stance of you being

the parent in charge, determining what priviledge or activity in his life is

important enough to him to be compliant for and then disallowing it unless he

takes whatever you determine needs to go in him for his own good. Lovingly

explain to him first that you are the one in charge for good reason, that you

love him sooooooo very much, that even though he cannot understand why he needs

to do what you say that he must and this is how it must be. As hard as it is to

do with any child (and certainly more one who is ill), it is needful and gives

the child security.

 

In care and prayer,

Judy

 

oleander soup , rhonda ebrom <dipghater wrote:

>

> Thank your for the suggestions, sadly my child is VERY particular with

> what he eats or drinks. He will eat fruit like its going out of style

> but not smoothies, he will eat apples but not applesauce (I thought

> about pills in applesauce) he won't eat yogurt or cottage cheese. Its

> very hard to get him to drink the oj with the OPC in it as it has a

> taste that he is not fond of. Its so very frustrating!

> Rhonda

>

> On 8/7/09, plantenergy1 <plantenergy1 wrote:

> > Hi Rhonda -

> >

> > I know this wasn't addressed to me, but maybe getting creative and putting

> > everything into one or 2 doses a day if possible may help - like smoothies -

> > make it fun for him since he's 7.

> >

> > I fully understand that all the supplements can be overwhelming sometimes.

> > I've had to get creative myself and I mix as many as possible into a couple

> > of doses a day.

> >

> > The IP-6 is more citrus flavored so maybe that can go in his juice and water

> > it down a bit. Even freeze the juice and make it frozen/creamy.

> >

> > I would suggest whey or rice protein with lots of blueberries or

> > strawberries and put the enzymes, curcumin and NAC into it. NAC would have

> > to be crushed a bit though.

> >

> > Please try and focus on the positive only - for him and for yourself.

> > Visualize positive MRI results and hold on to the positive things are are

> > happening with him.

> >

> > Thank you for sharing the date of the MRI - I will visualize this with you.

> > I'm sure others will as well.

> >

> > Help him understand that continued therapy helps keep the headaches away.

> >

> > Being responsible for a child is challenging - am praying for continued

> > strength for you.

> >

> > cathy

> >

> > oleander soup , rhonda ebrom <dipghater@> wrote:

> >>

> >> Tony, Marc, ,

> >> Reid has become resistant to taking all of his pills, as I said

> >> before he is foinf enzymes, NAC, curcumin and ipf inostitol. He takes

> >> 5 pills three times a day, or he was until he decided he didn't want

> >> too. I struggle everyday with keeping things " normal " for us so he

> >> doesn't get any incling that he has cancer . When we started all of

> >> his treatment he knew he was having headaches so he knew he needed to

> >> take his pills and do his " therapy " to make the headaches go away, but

> >> now he doesn't get it because he isn't having headaches so to him that

> >> means he doesn't have to take any pills. I'm at such a loss right

> >> now, his MRI is on the 12th of August, and I'm very nervous to get the

> >> results altho I try not to be because I know that no matter what it

> >> shows, that's what it will show, I can't change that.

> >> So what I'm writing to ask is, I know that all the pills are

> >> important, but if there was just one or two that I could get him to

> >> take which ones are the most important? Would it be the NAC and ip6?

> >> I'm much more likely to get him to take 6 or 9 pills per day vs the 15

> >> he was getting, also I'm still unsure of what a theraputic dose would

> >> be for the ip6 and NAC? As it stands now Reid takes his OPC in

> >> organic oj because he just won't drink anything else besides water and

> >> I made him try it straight one time and he gagged. Think he is gettin

> >> tire of the oj 3 times a day, I'm really just lost and confused and

> >> want to do whatever I can for the boy that I can do for him. Its hard

> >> to convince a 7 yo that he needs to take pills when he feels fine

> >> without telling him what could happen if he doesn't.

> >> On a side note, Reid is still doing outstanding. I registered

> >> him for 2nd grade this week and it was an emotional day for me. Back

> >> in Feb we weren't sure if he was going to feel well enough to finish

> >> the 1st grade and we sure as heck weren't sure he was going to go to

> >> 2nd grade!!!!!! School starts on the 24th and we couldn't be more

> >> excited or feel more blessed than we do! Please all continue to think

> >> and pray for my little man, and my strength to fight this battle for

> >> him and with him!

> >> All my love

> >> Rhonda

> >> www.caringbridge.org/visit/reidebrom

> >>

> >> --

> >> Sent from my mobile device

> >>

> >

> >

> >

>

> --

> Sent from my mobile device

>

[Guest guest]

I have to agree with Terri; I raised 4 boys, and I believe based on that

experience, that an upbeat explanation of the treatment for, if you don't want

to use the word cancer, then a bad sickness, will encourage him to get on board

with the treatment. He needs to understand that you are giving him medicine

that will make him better, and if he doesn't take it, he won't get better.

Ted

oleander soup , sstenycat wrote:

>

> In a message dated 8/7/2009 1:33:01 P.M. Central Daylight Time,

> dipghater writes:

>

> Please all continue to think and pray for my little man, and my strength

> to fight this battle for

> him and with him!

> _____________

> Rhonda, I'm not a big poster to this list and am not dealing with cancer

> right now myself or my family, so take what I am going to say at your own

> discretion.

>

> In my personal opinion, I think Reid should be told exactly what's going on

> with him. You'd be amazed how children can deal with things. Talking

> about the truth with him empowers him. Kids have a way of knowing when we're

> hiding something from them. Disease can be changed to health. It happens

> all the time. The way the person thinks is a critical part of healing.

> You are, in essence, enlisting his help in the fight. In the Catholic faith,

> 7 is the age of reason. Maybe telling him his protocol is for a purpose

> will be a turning point in his journey to health.

>

> Please, follow your own heart.

>

> Terri

>

[Guest guest]

My son is currently battling a brain tumor dx one year ago he is 34. He is a 32 year survivor of ALL leukemia whic was diagnosed at age 2. We told him that he had to fight to be healthy at about the age of 5. In additon to enlisting him in the battle we killed bad cells (pacman was big then)! Kids do not need to know all the details but can fight better if they know that you are a team working on it! It worked for us! If there is a social worker accessable use the service! You can even tell him that the pills keep the headaches away that they destroy the headaches that might be hiding.......good time to work on some visualiztion...take the pills and imagine they are looking for..destroying the headaches tha might be hiding.....you can even make it a

game! Good luck ......you all are in my prayers! You are not walking alone!

 

Sandy Barber

 

 

 

"sstenycat" <sstenycatoleander soup Sent: Friday, August 7, 2009 2:35:22 PMRe: Don't know what to do

 

In a message dated 8/7/2009 1:33:01 P.M. Central Daylight Time, dipghater (AT) gmail (DOT) com writes:

Please all continue to think and pray for my little man, and my strength to fight this battle forhim and with him!

____________ _

Rhonda, I'm not a big poster to this list and am not dealing with cancer right now myself or my family, so take what I am going to say at your own discretion.

 

In my personal opinion, I think Reid should be told exactly what's going on with him. You'd be amazed how children can deal with things. Talking about the truth with him empowers him. Kids have a way of knowing when we're hiding something from them. Disease can be changed to health. It happens all the time. The way the person thinks is a critical part of healing. You are, in essence, enlisting his help in the fight. In the Catholic faith, 7 is the age of reason. Maybe telling him his protocol is for a purpose will be a turning point in his journey to health.

 

Please, follow your own heart.

 

Terri

 

[Guest guest]

I know this is going to sound strange, considering what response the word radiation evokes in people today. But--many years ago low dose radiation was considered a powerful healer. All that information was basically "lost" once Hiroshima happened and people became terrified of radiation. Man made radiation is just that--terrifying. But natural radiation can truly help people heal.

 

I have been researching it because I'm on a list where a scientist, that I respect and trust his information, has been talking about using natural low dose radiation in the form of stones that you place on your body.

 

You can buy these stones from various places on the web, but the one I trust (and that the scientist also trusts) actually rates the strength of his stones so you know for sure what you are getting.

 

Here is an interview link where the seller of these stones talks about how he got started in using these stones for healing (he's a native American shaman) after making jewelry with the stones and being told his jewelry seemed to help people get well.

 

He started on his journey to learn all about using natural low dose radiation and then began cutting the stones to get certain amounts of energy per stone. He started lecturing about this "new" method and now hundreds of doctors from all over the world have approached him and are using his stones in healing.

 

I know this sounds crazy, but please do listen to the recording and check out his web site. I have seen people talking here about brain cancer in their children and just felt like I had to let you know--as one of the first major success stories Jay (the stone owner) has is from curing brain cancer in a young girl.

 

There are many testimonials on his web site, it's a small, friendly business. You can email or call and they are very helpful. I have just purchased a kit and extra healing stone for us, even though we don't have cancer. But I believe in prevention--and I think these stones are another powerful tool to have in our alternative healing kit. It is certainly worth investigating, and not just denying because of the word "radiation". I think using the stones along with all our other powerful healing tools, such as oleander, MMS, herbs, CS, DMSO, etc can overcome anything.

 

Remember--many people think oleander is poison until they research and learn better. :-)

 

Interview with Jay Gutierrez: www.radiationhormesis.com

 

 

His site is www.nighthawkminerals.com

There is a link on this site that says "research it" and from there you can read many reports from independent labs and groups about low dose radiation.

 

Samala,

Renee

 

 

----

 

My son is currently battling a brain tumor dx one year ago he is 34. He is a 32 year survivor of ALL leukemia whic was diagnosed at age 2. We told him that he had to fight to be healthy at about the age of 5. In additon to enlisting him in the battle we killed bad cells (pacman was big then)! Kids do not need to know all the details but can fight better if they know that you are a team working on it! It worked for us! If there is a social worker accessable use the service! You can even tell him that the pills keep the headaches away that they destroy the headaches that might be hiding.......good time to work on some visualiztion...take the pills and imagine they are looking for..destroying the headaches tha might be hiding.....you can even make it a game! Good luck ......you all are in my prayers! You are not walking alone!

 

[Guest guest]

Noooooo...... Not ice cream. Cancer feeds on sugar.

Hugs,

 

oleander soup , Elizabeth Deedrick <elizabethdeedrick wrote:>> Maybe Ice Cream? Does he like Ice Cream? Put it in whatever he likes! Get one of those electric ice cream makers, he likes fruit, put fruit in it! You can keep some handy in the freezer, and give him a bit a few times a day with his meds in it! Whatever it takes to make him well! Love and Prayers, Elizabeth>

[Guest guest]

Oooops!

 

 

 

May <luellamay129oleander soup Sent: Sunday, August 9, 2009 4:57:12 PM Re: Don't know what to do

 

Noooooo..... . Not ice cream. Cancer feeds on sugar.

Hugs,

 

oleander soup, Elizabeth Deedrick <elizabethdeedrick@ ...> wrote:>> Maybe Ice Cream? Does he like Ice Cream? Put it in whatever he likes! Get one of those electric ice cream makers, he likes fruit, put fruit in it! You can keep some handy in the freezer, and give him a bit a few times a day with his meds in it! Whatever it takes to make him well! Love and Prayers, Elizabeth>

[Guest guest]

Sorry about the ice cream thing, trying to think of something a little child would like, to get his meds in him. I didn't know that cancer feeds on suger. Thank You for that information! Sincerely, Elizabeth

 

 

 

Elizabeth Deedrick <elizabethdeedrickoleander soup Sent: Sunday, August 9, 2009 5:10:15 PMRe: Re: Don't know what to do

 

 

Oooops!

 

 

 

May <luellamay129@ >oleander soupSunday, August 9, 2009 4:57:12 PM Re: Don't know what to do

 

Noooooo..... . Not ice cream. Cancer feeds on sugar.

Hugs,

 

oleander soup, Elizabeth Deedrick <elizabethdeedrick@ ...> wrote:>> Maybe Ice Cream? Does he like Ice Cream? Put it in whatever he likes! Get one of those electric ice cream makers, he likes fruit, put fruit in it! You can keep some handy in the freezer, and give him a bit a few times a day with his meds in it! Whatever it takes to make him well! Love and Prayers, Elizabeth>

[Guest guest]

Not to worry Elizabeth. I understand your reasoning. Yeah..... Normally ice cream would work.

Hugs,

 

[Guest guest]

Oh bless your heart Rhonda! Please forgive this tardy response. My computer is down and I'm sharing Tony's computer (again) so until I get it back from the shop my time online is limited.

What to do.........

It is extremely important that Reid take his supplements and the fact that he is feeling so well may very well be attributable to these very supplements and the care that you give him.

I don't know your particular situation, so I cannot advise you whether or not to tell Reid about the brain cancer. I do not know him or how he would react. But at this point, somehow, maybe using psychology, I would stress to him the importance of these supplements and why he needs to take them. Maybe telling him that the headaches were the result of a very serious condition and the reason he is feeling so well is because of these very supplements. Maybe explain to him that he cannot drop the ball now and risk going back to those horrible headaches. Maybe tell him just what he needs to know, but no more. Yet, stressing how very important it is that these supplements be taken. Kind of being honest without being too honest?

It is wonderful news that you will be enrolling Reid in the second grade! I can imagine the joy you feel.

We are praying for the MRI on August 12th. Please be sure and let us know.

Lots of love,