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Please respond to vaikakul@...

need help

To whom it may concern :

I am in the stage of settlement with the school district for re-imbursement

and requested of teaching one-to- one with ABA/DTT to my daughter. I would

like to

know parent who has settlement agreemnet already which I can use as a

guideline. My daughter is 16 yrs.old (high school level) and in Southern

California. The initial settlement already came out and agreed only pay,

re-imbursement, but not talk about the trainning 1:1 with ABA/DTT

which I already try with my daughter for 6 months and knew that it is the

teaching that work effective with my daughter.

Please spread my e-mail to anyone who can give me the suggestion.

Thank you very much in advance, also please excused me for my limited

English (from Thailand).

Pat Vaikakul

vaikakul@...

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At 05:22 AM 09/03/2000 +0000, wrote:

>

>Does anyone know if anyone in Australia follows Dr Goldberg's

>protocol or work? Does anyone know if and how my sister can contact

>Dr Goldberg? We have taken the list of necessary blood tests from

>the web, and think we can have them done here (in

>Australia).........but then what?

delurking :). I was given the names of 2 doctors in Australia but know

nothing about them

*** Australia ***

Dodds M.D.

6 Roslyn Ave.

Roseville

Sydney NSW 2069

Australia

ph: 612-416-1935

fax: 612 415 6870

Kahler, M.D.

10th Floor, Royal Children's Hospital

Flemington Road

Parkville 3052

Melbourne

Australia

ph: 3-8341-6201

http://www.autism.com/ari/danlist.html

I am trying to find a doctor a bit closer to Brisbane if anyone can help

anna v

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I'm pretty sure that Dr. Goldberg goes to Australia and/or New Zealand to see

patients; meanwhile, have your sister call Dr. G's office @(818) 343-1010

and talk to his staff. In the early days I had better success contacting

Dr.G's office with a fax:

(818)343-6585

Good luck!

Kate

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,

I am an Australian living in Singapore. Our son has been a patient of Dr

Goldberg for 10 months now. We just completed our 2nd trip to CA to see him.

In between visits, we have a phone consult every 6 weeks, plus regular

updates by phone and fax and e'mail. He visits Australia for conferences

(how we came to know of him) and has a number of patients from Australia and

now Asia.

E'mail us direct if you want any more help.

need help

Hello group members

I joined this group recently in the hope of being able to find some

help for my nephew, aged almost 4, who is a real worry. My sister is

so tired and flat out just managing him (he's also up at all hours of

the night),that she doesn't have a minute to do much else, so I have

been doing some searching for solutins or help for my nephew.

Does anyone know if anyone in Australia follows Dr Goldberg's

protocol or work? Does anyone know if and how my sister can contact

Dr Goldberg? We have taken the list of necessary blood tests from

the web, and think we can have them done here (in

Australia).........but then what?

My nephew has been diagnosed as autistic (although some of his

behaviours are typical, and some are not)and ADHD; has no speech

(makes some sounds);has allergies;sleeps terribly; and his bahaviour

is basically out of control. My sister has a little girl, aged 7,

and a husband who (we are sure!)has ADD (and is not much help or

support).

I so desperately want to be able to help my sister find some

solutions and / or help. I just hate seeing what this is all doing

to her.

I believe that finding this list has been the first step, and THANK

YOU ALL for the information and leads (through your posts) that you

have already given us.

Looking forward to any more help or suggestions you might be able to

give.

THANKS HEAPS!

(in Canberra, Australia)

Responsibility for the content of this message lies strictly with

the original author, and is not necessarily endorsed by or the

opinion of the Research Institute.

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On Sun, 03 Sep 2000 16:40:18 +1000 V & Ged M <annaged@...> wrote:

>-------------------------- eGroups Sponsor -------------------------~-~>

>GET A NEXTCARD VISA, in 30 seconds! Get rates

>of 2.9% Intro or 9.9% Ongoing APR* and no annual fee!

>Apply NOW!

>1/7872/12/_/472608/_/968005529/

>---------------------------------------------------------------------_->

>

>At 05:22 AM 09/03/2000 +0000, wrote:

>>

>>Does anyone know if anyone in Australia follows Dr Goldberg's

>>protocol or work? Does anyone know if and how my sister can contact

>>Dr Goldberg? We have taken the list of necessary blood tests from

>>the web, and think we can have them done here (in

>>Australia).........but then what?

>

>delurking :). I was given the names of 2 doctors in Australia but know

>nothing about them

>

>*** Australia ***

> Dodds M.D.

>6 Roslyn Ave.

>Roseville

>Sydney NSW 2069

>Australia

>ph: 612-416-1935

>fax: 612 415 6870

> Kahler, M.D.

>10th Floor, Royal Children's Hospital

>Flemington Road

>Parkville 3052

>Melbourne

>Australia

>ph: 3-8341-6201

>

>http://www.autism.com/ari/danlist.html

>

>I am trying to find a doctor a bit closer to Brisbane if anyone can help

>

>anna v

>Hi ,

You need to copy all of the child's records and write the parent's account of

the child's development, get the necessary bloodwork done and actually firstly,

I would just call the office or e-mail them at the office. The phone, which you

probably already know is 1-818-343-1010. There is also a Dr. in Australia who I

read is working on the gut/brain issue. It sounds like he is having some

progress. His name is Borody, first initial T. If you have any luck with him,

let me know. Thanks.. Kathy

>

>Responsibility for the content of this message lies strictly with

>the original author, and is not necessarily endorsed by or the

>opinion of the Research Institute.

>

>

>

_______________________________________________

Get your free e-mail at http://www.ourhouse.net

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All you have to do is contact Dr. G's office at 818-343-1010. Your sister

will get an appointment from the office staff. I would wait until I get the

instruction from the office before I would get blood work done because there

are more than one list of necessary tests. Kathy R

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Hello everyone

i have three nids kids and am currently working towards my masters in

environmental studies----I have to evaluate the latest primary scientific

literature regarding the evidence for immunomodulatory effects of lead, uvb,

ozone, or MY CHOICE (with professor's approval). i'd like to research

something useful for our kids, because my end goal for this degree is to

help EFFECT some change for our kids (this degree incorporates government

policy). If anyone has suggestions (specific journal citings would be MOST

helpful), please email me them privately and write in the subject heading

" for nids research " so i won't inadvertently delete them. So far I've

considered Peptide T, organophosphates, and of COURSE mercury and combined

immunizations.

THANKS!!

Kate

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specific food additives/dyes???

Re: need help

>

> Hello everyone

> i have three nids kids and am currently working towards my masters in

> environmental studies----I have to evaluate the latest primary scientific

> literature regarding the evidence for immunomodulatory effects of lead,

uvb,

> ozone, or MY CHOICE (with professor's approval). i'd like to research

> something useful for our kids, because my end goal for this degree is to

> help EFFECT some change for our kids (this degree incorporates

government

> policy). If anyone has suggestions (specific journal citings would be

MOST

> helpful), please email me them privately and write in the subject heading

> " for nids research " so i won't inadvertently delete them. So far I've

> considered Peptide T, organophosphates, and of COURSE mercury and combined

> immunizations.

> THANKS!!

> Kate

>

> Responsibility for the content of this message lies strictly with

> the original author, and is not necessarily endorsed by or the

> opinion of the Research Institute.

>

>

>

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Kathy,

Dr. G mentioned Peptide T a while ago; I have another phone consult coming

up this month so I'll ask again.

kate

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The majority of Health Care Practitioners are well meaning people who have

chosen their fields of endeavor because they want to help people. The

majority of Health Care Practitioners have never been exposed to the theory

of . They are practicing responsible medicine based upon the information

that is available to them. We have to get the information out. Once it is

accepted theory you will see a change in the schedule of immunizations for

susceptible children. Kathy R

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The area of Government policy on ensuring safety in vaccinations:

eg compulsory testing for possible immune dysfunction or autoimmune

antibodies before administering.

Today we just took our 2yo daughter for her MMR after waiting 9 more months,

after discussion with Dr G and our local pediactrician. (our 5yo son Chris

is ) She didn't even squeak bless her. I did keep the box and

instructions for the vaccine inside, and it says " xxx should not be given to

subjects with impaired immune responses. These include patients with primary

or secondary immunodeficiencies. " Hmmmmmmm!!

Here I was, sitting with the doctor using a magnifying glass to read this

thing it was so small! How many medical professionals actually read all of

these. And if they don't check for the presence of contra-indications, then

what is the recourse of the patient?

Good luck Kate,

Re: need help

Hello everyone

i have three nids kids and am currently working towards my masters in

environmental studies----I have to evaluate the latest primary scientific

literature regarding the evidence for immunomodulatory effects of lead, uvb,

ozone, or MY CHOICE (with professor's approval). i'd like to research

something useful for our kids, because my end goal for this degree is to

help EFFECT some change for our kids (this degree incorporates government

policy). If anyone has suggestions (specific journal citings would be

MOST

helpful), please email me them privately and write in the subject heading

" for nids research " so i won't inadvertently delete them. So far I've

considered Peptide T, organophosphates, and of COURSE mercury and combined

immunizations.

THANKS!!

Kate

Responsibility for the content of this message lies strictly with

the original author, and is not necessarily endorsed by or the

opinion of the Research Institute.

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need help

>

>

>

> Hello group members

>

> THANKS HEAPS!

>

>

> (in Canberra, Australia)

>

>

>

>

>

, ring me oo 62966734 in Canberra , I may be able to give you some

leads.

Windsor, ADD Support Group.

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Kathy,

Dr. Galpin, an infectious disease specialist who frequently consults

with Dr. Goldberg, spoke about peptide T at the conference in Bethesda

in June 1999. I have a tape of his portion of the conference....

mary nunan

rhemary@...

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Hallo können, vielleicht Sie die folgende Website versuchen zu helfen, Ihre

Fragen in Englisch zu übersetzen, und den wir können versuchen, Ihnen zu

helfen. Ich spreche sehr kleines Deutsch aber werde helfen während viel

während ich zu können. http: //ets.freetranslation.com/

Kari

need help

> hallo ich hoffe hier ist jemand in der gruppe der deutsch spricht.ich

> habe so viele fragen die ich einfach nicht ins englische uebersetzen

> kann.

>

>

> For more plagio info

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Hallo, wenn das Kettenglied, das ich habe gegeben nicht arbeitet, versucht

www. freetranslation. com Und wenn das noch arbeitet fühlt nicht befreit,

auf deutsch aufzustellen, ist es sehr möglich, daß jemand auf diesem

Ausschuß Deutsch spricht, und, wenn nicht ich Ihre Fragen in Englisch und

irgendeine Antworten Sie revieve Rückseite in Deutsch für Sie übersetzen

kann. Haben Sie ein Kind mit plagiocephaly? Gutes Glück!

Kari

need help

> hallo ich hoffe hier ist jemand in der gruppe der deutsch spricht.ich

> habe so viele fragen die ich einfach nicht ins englische uebersetzen

> kann.

>

>

> For more plagio info

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Hey Kari,

You're awesome. I can try and help you translate as well. I'm very rusty, but so far have understood everything. I've got a good dictionary around her someplace. Good for you for stepping up on this.

Gail

need help> hallo ich hoffe hier ist jemand in der gruppe der deutsch spricht.ich> habe so viele fragen die ich einfach nicht ins englische uebersetzen> kann.>>> For more plagio info

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Marie, that neuro has no idea what he is talking about! LDN stops progression, why would it matter if you had MS for one year or 20! I was diagnosed 3 yrs ago, been on ldn 10 months and have not progressed since.

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Marie

I was diagnosed in April 7 2003 on LDN already had great results in only 10 days -gone off copaxone for a while-its very individual I feel this drug (as to its effects quickly or over longer term of use for some)from what I research but 85% get great results on the 3 mg dose- love from kell in australia

----- Original Message -----

From: Marie Deady

low dose naltrexone

Sent: Saturday, April 24, 2004 3:31 AM

Subject: [low dose naltrexone] Need help

I wrote a post a while ago about my neice's husband that was just diagnosed with MS. He saw a neurologist and that neuro knows of LDN but said that it only worked on people that have had MS for a long time. So he suggested that he go on one of the crab's. Fran is starting to get interested in LDN. He wants to know if there is anyone out there that has recently been diagnosed with MS and have been helped by LDN. I guess that I am of no help with this because I have had MS for 27 years. Can any of you that have only had MS for a short time and have been helped by it respond to this. And please say how long that you have been on LDN. Thanks for help with this matter. I appreciate it.

Marie

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thissal@... wrote:

> See Message 5208 > >Thanks for the link Suzi. Now I feel like I should break my fast and dose up on MSM. ;)Don't you dare quit your cleanse.. you can take MSM afterwards... what are you going to take it for?

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roni_slye wrote:

>

> Hi everyone,

> I've got a tough one, and I would appreciate any help you guys can

> give me. Much to my amazement my mother, who has been very resistant

> to anything other than what her doctors give her, asked me what kind

> of herbs etc would be helpful for her osteo arthritis and pain. I am

> thrilled at the prospect that she may be opening a little to natural

> remedies, but I'm hesitant to suggest anything because she is on so

> many medications. I told her this and she said that she was really

> only on a few medications now because they had stopped some of them.

> So, I asked her what she was currently taking. Here is the list:

> celebrex, prednisone, oxycotin, hydrocodone, valium, prevacid,

> methyltrixate,lopressor, lipitor, and just a few days ago they also

> put her on insulin pills as she is now diabetic as well. If this is

> just a few I can't even imagine what she used to be taking. Now I

> know that diet is a huge issue in all of this, but she will not

> change her lifestyle or eating habits. Even now that she is

> diabetic, she is still eating candy bars and cookies. I realize that

> nothing is really going to help as long as she continues eating

> poorly (to put it mildly), and taking all of these medications, but

> since she did ask I'd like to make at least a small baby step with

> her by suggesting some supplements. I am thinking MSM for starters

> since it is a pill I think she will be more open to it. I'd also

> like to suggest Super tonic and complete nutrition though I doubt

> she will take them. I thought about organic iron, but am not sure

> about the sugar in the molasses with her being diabetic. I was also

> thinking about making her some herbal teas, but am unsure what would

> be safe given all the medication she is on. So, my question is will

> any of these things cause a problem with her medications? Does

> anyone have any other ideas on things that might be helpful? I

> really appreciate any help and advice anyone can give me.

>

> Love,

> Roni

========================

Hi Roni,

Your mom sounds like my dad. He is a walking drug store for sure. Your

mother must be in some pain to be taking all those pain meds. It is

saddening to hear this. She is taking so much that there is a

possibility of drug-drug or drug-herb or drug-supplement or drug-food

interaction. She probably wouldn't need the prevacid if she weren't

eating all those other drugs, wouldn't need the valium if she weren't

taking all the narcotics, probably wouldn't need the insulin if she got

off the prednisone and wouldn't need the lipitor if her liver wasn't so

polluted and toxic from all these drugs.

Shoot!!! The Super tonic and complete nutrition should be safe enough

and at least might help her get off the lopressor or at least reduce it

to bare minimum. The prednisone just raises the blood sugar levels. This

is probably one of the reasons she is now on insulin. Yes, you should

leave out the sugar. Not something she needs right now.

There is very little research into drug-herb interactions to date. There

are some herbs that do react quite strongly with various drugs.

Chamomile, valerian, ginger and goldenseal can increase the effects of

valium. Licorice, black cohosh and goldenseal would not be useful where

she is taking lopressor (a beta blocker). Ginseng wouldn't be too good

to take while taking insulin.

I am sure there is more out there, I just haven't found it yet. However,

you are right, unless she is willing to change her lifestyle and

diet.....well she will just continue to help fill the pharmaceutical

coffers like my father I guess. :-(

Just about everything she is taking is toxic, toxic, toxic and is only

slowly shutting down her liver, pancreas, and probably a few more organs

until it completely shuts down the body.

I guess I haven't helped you much here Roni. Do go with the complete

nutrition and super tonic but do research whatever other herbs you plan

on for any kind of drug interactions.

Peace be with you Roni.

--

Peace, love and light,

Don " Quai " Eitner

" Spirit sleeps in the mineral, breathes in the vegetable, dreams in the animal

and wakes in man. "

--

In compliance with the highest standards of Universal Law, this email has been

thoroughly disinfected and purified in the solar flares of the sun.

Outgoing mail is certified Virus Free.

Checked by AVG Anti-Virus.

Version: 7.0.302 / Virus Database: 265.6.11 - Release Date: 1/12/05

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Thank you Suzi,

The problem with getting my mom off the medications is, one the

drs tell her she will not get out of bed without the meds and she

believes them, two I think she likes them and is probably addicted

to them. My mom believes that medications are the answer to

everything and has taken a lot of medications for as long as I

remember. If you have a headache at her house and happen to mention

it, she will offer you some tylenol with codeine.

Her problems are numerous (I believe largley due to the meds,

diet, and inactivity). She has a form of arthritis called ankylosing

Spondylitis, osteo arthritis in her knees (she has had a knee

replacement), bursitis, IBS, high cholestrol, high blood pressure,

osteoporosis, restless leg syndrome, acid reflux, and just a few

days ago was diagnosed with diabetis. I think this is it, but I may

be forgetting a few things.

My only hope is that if she has even a small success with

alternative treatments, she may be more open to getting off the meds

and changing her lifestyle. I know these are high hopes, but since

she has given me the opportunity I have to try. I have Deep tissue

repair oil and BF & C, but I am concerned about reactions with the

meds, and liver damage due to the fact that the meds are already so

hard on the liver. Are these concerns valid or is it redundant due

to the fact that the meds are already so damaging? I think the MSM

should be pretty safe. If anyone knows of any concerns with MSM and

meds please let me know. So, given the fact that she is probably not

going to quit taking the meds what alternative remedies would be

pretty safe. They also must be easy and pleasant or she will not do

it (she may not anyway). I know this is a lot to ask, but again I

have to try.

Thank you so much for your input Suzi, and I will show Mom your

response. I just hope I don't completely alienate her. I am walking

a very fine line as she gets very defensive about her meds and drs,

but it is worth the risk if I can get through to her in even a small

way.

Love,

Roni

-- In health , Suzanne

<suziesgoats@y...> wrote:

> Hi Roni.

> I know Don will have alot in the a.m. however, tell your mother

from me... one mother to another well, actually a grandmother to ...

(I'm 51, if that helps)

> that Celebrex is the worst she can take... they prescribed that

for me... after surgery and I took it in the hosp... didn't do

anything for the pain and arthritis... (oh yes, forgot to mention

that they also told me that the arthritis was a combo osteo and

rhumatoid) now let me tell you what did work. We're talking

level 4 on the knee cap... and that I would always have some

swelling and pain..... (Some swelling?? It was twice the size of the

other one even months after and they drained it 3 times)...and pain.

> Now if you can get the powder MSM and capsule it yourself the

better... take 3-4 capsules 3 times a day for the first week then

cut back to 6 -9 - as the pain lessens cut back the following week

to 4-6.... and this can vary some... Also, get some deep tissue oil,

BF & C ... use these as a rub or salve on the afflicted area 2-3 times

a day or as needed...

> Get your mother off these drugs.(the combo of all of them is

really screwing with her body) .. what are her problems? Please

tell her for me (let her read this) that these meds are only making

matters worse...

> My knee only aches slightly when there are weather changes and I

am going up steps (at the same time)... only time I notice it.. They

told me I would not run again... HAAAA! What do they know... I also

did alot of juicing and raw veggies, salads, etc during this time...

No it wasn't easy, but I did not want to live with pain and an ugly

knee.. Your mom is going to have to make some tough decisions...

Detox baths are also very good... and hot/cold therapy.. (did them

too).....

> Wait for Don's reply in the a.m. and add these together...

>

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Thank you Don,

Actually, you have helped me. I completely agree that the meds are

causing many of her problems, unfortunately she doesn't see this.

When I have talked to her about side effects of meds, she swears she

has never had any problems from her meds. I have seen a slight

glimmer of hope lately though, as I explained to her that perhaps

she did have side effects from her medications but just didn't

realize that it was the medications causing the " new " problem she

was having, she seemed to actually give this some thought.

Unfortunately she doesn't want to " give up " anything she likes, and

wants a pill to take care of everything so that she will not have to

change. I think, perhaps, she might be starting to realize that the

pills are not taking care of everything. I hope this is the case,

because it is very sad to see her growing sicker by the day. Do you

know of any problems with MSM and the meds, Don? Take care and thank

you for your help.

Love,

Roni

> ========================

> Hi Roni,

>

> Your mom sounds like my dad. He is a walking drug store for sure.

Your

> mother must be in some pain to be taking all those pain meds. It

is

> saddening to hear this. She is taking so much that there is a

> possibility of drug-drug or drug-herb or drug-supplement or drug-

food

> interaction. She probably wouldn't need the prevacid if she

weren't

> eating all those other drugs, wouldn't need the valium if she

weren't

> taking all the narcotics, probably wouldn't need the insulin if

she got

> off the prednisone and wouldn't need the lipitor if her liver

wasn't so

> polluted and toxic from all these drugs.

>

> Shoot!!! The Super tonic and complete nutrition should be safe

enough

> and at least might help her get off the lopressor or at least

reduce it

> to bare minimum. The prednisone just raises the blood sugar

levels. This

> is probably one of the reasons she is now on insulin. Yes, you

should

> leave out the sugar. Not something she needs right now.

>

> There is very little research into drug-herb interactions to date.

There

> are some herbs that do react quite strongly with various drugs.

> Chamomile, valerian, ginger and goldenseal can increase the

effects of

> valium. Licorice, black cohosh and goldenseal would not be useful

where

> she is taking lopressor (a beta blocker). Ginseng wouldn't be too

good

> to take while taking insulin.

>

> I am sure there is more out there, I just haven't found it yet.

However,

> you are right, unless she is willing to change her lifestyle and

> diet.....well she will just continue to help fill the

pharmaceutical

> coffers like my father I guess. :-(

>

> Just about everything she is taking is toxic, toxic, toxic and is

only

> slowly shutting down her liver, pancreas, and probably a few more

organs

> until it completely shuts down the body.

>

> I guess I haven't helped you much here Roni. Do go with the

complete

> nutrition and super tonic but do research whatever other herbs you

plan

> on for any kind of drug interactions.

>

> Peace be with you Roni.

>

> --

> Peace, love and light,

>

> Don " Quai " Eitner

>

> " Spirit sleeps in the mineral, breathes in the vegetable, dreams

in the animal and wakes in man. "

>

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Thank you

Yes, I tried to talk to her about her diet and the diabetis, and she

said she just didn't take the diabetis very seriously since she

felt " fine " . I tried to explain to her that by the time she didn't

feel fine the damage would already be done, but she just said she

wasn't going to give up all the things she liked. And, I do realize

that until she decides to make the changes, change will not happen.

I will keep the blue green algae in mind for when the day,

hopefully, comes that she decides it's time to try a new approach.

Love,

Roni

> Hi Roni,

>

> When a diabetic knows they are eating sugar and it will hurt them,

it shows

> they haven't changed their mindset yet. They really need to

change this

> before more harm is done to their organs.

>

> If I were a diabetic, I would be taking blue-green algae and

gymnema

> sylvestre to balance my blood sugar. I REALLY HATE to tell 'them'

of a

> natural anything to do this because it will be zeroed in on and

removed if

> at all possible! Guess I'd better stock up on it by the lb. I'm

quite

> serious about this and not joking in the least. I cured a case of

the worst

> ketosis I'd ever seen in an animal, diagnosed by a vet, which

merely means

> blood sugar imbalance. All but dead, refused to eat or drink,

body weight

> loss over half, too weak to get up and then, a miraculous

turnaround. I

> wouldn't want to risk going this far ever again but it worked.

>

> Once a top vet (on a panel no less), wrote me to ask if I knew of

any cures

> using natural means? I nearly fell into the trap and told him of

all the

> wonderful cures but stopped short just in time and told him I

would tell him

> nothing because the information would be used to harm us, not to

help us. A

> top vet who would write a letter like I received, only meant harm

(sold out

> his soul).

>

> If your mother is anything like my sister, she will start falling

without

> warning. Just one of the side effects (nice, calm name for

something

> serious and possibly deadly side effect of prescription meds).

The muscle

> weakness and falling was increasing and a matter of time until

bones were

> broken. Wonder how many broken bones leading to death, is

reported by

> 'them', as a side effect? Then my uncle called to talk with my

sister and

> he told her his wife was having falling spells. My sister asked

if she was

> taking Lipitor. Amazingly, she was! There was nothing like that

moment to

> make my sister realize what deadly drugs were being dispensed as

casually as

> candy.

>

> Jean

>

>

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