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Yes, I met Dr. Steenblock at the Hyperbaric Oxygen for Stroke conference

of mainly physicians at the Washington-Marriott Hotel in May 1998. He felt

confident he could help my wife, but she was in no condition to make a long

trip. At that time she was totally paralyzed both in speech and mobility as

well as cognitive powers. Now she is much improved, but his clinic is in

Calif. and the patient needs to be ambulatory. Also, he has other therapies

such as chelation which help to reinforce his program. I hear he is getting

some excellent results. I am now trying to get her some local HBO therapy,

but thus far, have not been able to get those who have an HBO capability to

use it for stroke. They limit their patients to the 13 or 14 indications

approved by Hyperbaric Undersea Medical Society, FDA, Medicare and many of the

insurance companies. I do believe the rules and attitudes for stroke are in

transition, and that soon stroke, Cerebral Palsy and other oxygen responsive

diseases will be included in the approved list. Thanks for the suggestion.

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,

I was wondering if you already know Dr. Steenblock, out here in

California. He is trying to do what you are, getting the medical

establishment to understand the implications of HBOT in treating

stroke. If you don't know him, maybe you guys should talk.

" My objective at the moment is to spread the word about hyperbaric

oxygen

therapy for stroke victims as well as cerebral palsy, MS and other

difficult

to treat diseases. HBOT is approved by Medicare for 14 indications but

excludes stroke, CP and MS all of which are proving responsive to HBOT.

I

personally know of an estimated 100 stroke patients, from Baltimore to

California, including Florida, Louisiana, Texas currently receiving HBOT

and

each and all improving both in speech and mobility. Yet HBOT therapy is

not

approved for stroke and the others. "

And thanks for your support,

Tangerine

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  • 4 weeks later...

Message here is in response to Merry's recent email and her upcoming shot

refusal. When your flight surgeon says he wouldn't recommend getting the shot

if you were a civilian, but you should as a " vulnerable " member of the

military, that argument is totally bogus with a capital B. Chances are your

flight surgeon knows little about the OPERATIONAL threat of anthrax. Who were

the targets/victims in OK City, the World Trade Center and the recent embassy

bombings? Primarily civilian. OK, we had Khobar towers--one terrible

terrorist incident. But the anthrax threats last year that I know of--Federal

Building in Los Angeles, 2 guys in the North West who threatened local

officials, and a letter bomb, were all targeted hoaxes at CIVILIANS.

Why don't terrorists target the military? Because they'd be beyond stupid.

Our response to such a bio or chem attack in the Gulf War was, " You slime us,

we'll nuke you! " This modern day threat of " massive retaliation " seemed to

suffice against Iraq as a proven bio/chem aggressor. No potential enemy of

the U. S. should be convinced that the U. S. military is abandoning such

massive retaliation if it is known who perpetrates such an act. So it's the

Civilians who are really vulnerable and are not getting this so-called

" protection " . Why? Who in the civilian community would be gullible or

cooperative enough to subject themselves to such a program? It's the military

culture which cannot effectively protect itself against such requirements that

allows them to be abused in this manner.

The administration would like to do more to protect civilians, but has no plan

to stockpile this vaccine for their protection. Why? Administration

officials say they expect better non-toxic vaccines to be available in 2-3

years and don't want to invest in using the current questionably-safe

inventory. But it's surely good enough for our second-class citizens in

uniform, apparently. (This info from a NY Times article).

Your flight surgeon, along with many others, has bought the threat hook, line

and sinker. Even with radar, counter air, gas masks, antibiotics, ship air

filtration systems, emergency vent closing procedures, etc., etc., there

seems to be nearly universal conviction that all current defensive measures

will fail simultaneously, exposing thousands of troops to lethally-inhalable

anthrax. Statistics from the Iran/Iraq War should indicate how effective the

biowarfare attempts were. Has anyone researched this angle? Statements from

a few articles here and some other thoughts may give one pause in this rush to

vaccinate environment:

1. If a 5 lb bag of anthrax drops from the air and falls on the ground, it

affects the 2 ft diameter area in lands on.

2. If the bag breaks open, it disperses over a larger area depending on the

release height and assuming the aircraft dropping it is not detected or shot

down.

3. No one seems to know how many anthrax spores it takes to lethally be

inhaled. One estimate indicates maybe 10,000 spores. Another 100,000,000.

4. Anthrax doesn't penetrate solid materials like concrete buildings.

Individuals inside wouldn't be affected.

5. If the 5 lb bag falls on Washington, D. C. and would kill half the

population as has been claimed, how does that actually occur? Would the 5 lb

bag be dispersed over the whole city? Would 1/2 the people be outside to

inhale it? Would it be concentrated enough to get in the lungs of 300,000

people over the entire city? Or would a single plane with a single bag have

to make numerous passes over the mall area on a concentrated crowd during an

event such as the Million Man March and all of them remain stationary while

the " people-dusting " takes place?

6. Anthrax in liquid form is dangerous if swallowed or injected, but is not

an inhaled threat even though Iraq may have 20,000 gallons (which we

apparently sold to them along with the vaccine).

The somewhat ludicrous conjectures on this subject have become accepted as

almost unavoidable threats.

Some other anecdotal indication of the real level of concern over this threat:

After hearing an overseas briefing about the anthrax threat and vaccination

program, a pregnant servicemember asked if she would be reassigned safely out

of the theater and back to the states since the vaccine is considered risky

for pregnant women. She was told no. Apparently, the government wants to

protect males and non-pregnant women against this " threat " , but is perfectly

willing to EXPOSE PREGNANT WOMEN since they will not be removed from the area

for their own protection. That's how much the government really thinks the

military is exposed to anthrax. Where the hell is the logic here? Seems to

me, the government doesn't really believe there is a threat or someone is

trying to punish all the women who dared enter the realm of the formerly male-

dominated military.

How about both the men and women who don't want to risk the health of yet

unconceived children they might have in future families, or who have to delay

conception until the 18 month shot-series is over? The government policy

apparently condones this health risk even though plenty of veterans with Gulf

War Syndrome are living proof this policy constitutes inexcusable abuse on the

part of the military leadership and medical community. But then again, since

when have these groups been held accountable for their actions? Not often.

Merry, there are consequences for not obeying a " lawful " order to vaccinate

against this " threat " . Apparently, you see the consequences of obeying such

an order even more of a threat. I understand.

Redmond Handy

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  • 7 months later...
  • 5 months later...

Hi, Everyone......Nothing like a special needs kid getting the stomach

flu!!!! Poor Gareth.......doesn't quite seem to know what end to put on the

toilet. Anyways........I was going through the Medscape review for

the week and there is an article in there about the coexistence of Tourettes'

Syndrome and Autism. Seems one study has the rate at 8% of kids with Autism

having both, along with the good ole ADD and OCD. For 6 yrs. we went back

and forth between the two dx., depending on which psych. saw him. Perhaps

he's got both!!! Oh well, what's one more label ?!?!?! Thanks

for the advice on the Buspar. Gareth has an appt. with a new psych. tomorrow

night. His 'NO' is getting pretty loud and the ODD is making a comeback.

He's on 3 mg. of Risperdal now and I really don't want to raise that if I

don't have to. It's been a miracle drug for him, so I am really hesitant

about taking him off it too. I do know (like a lot of you have said) that

they tend to become immune to the affects after a while. We will wait and

see what the Dr. says. Take care everyone.

Margaret

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Hi, Everyone......Nothing like a special needs kid getting the stomach

flu!!!! Poor Gareth.......doesn't quite seem to know what end to put on the

toilet. Anyways........I was going through the Medscape review for

the week and there is an article in there about the coexistence of Tourettes'

Syndrome and Autism. Seems one study has the rate at 8% of kids with Autism

having both, along with the good ole ADD and OCD. For 6 yrs. we went back

and forth between the two dx., depending on which psych. saw him. Perhaps

he's got both!!! Oh well, what's one more label ?!?!?! Thanks

for the advice on the Buspar. Gareth has an appt. with a new psych. tomorrow

night. His 'NO' is getting pretty loud and the ODD is making a comeback.

He's on 3 mg. of Risperdal now and I really don't want to raise that if I

don't have to. It's been a miracle drug for him, so I am really hesitant

about taking him off it too. I do know (like a lot of you have said) that

they tend to become immune to the affects after a while. We will wait and

see what the Dr. says. Take care everyone.

Margaret

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:

I feel your frustration when you said your child is up at 6 and down at

midnight... seems to go in " cycles " ....he'll go for weeks sleeping

regularly (with or without med. help) and all of a sudden, he'll want to stay

up all night....you would think after going to bed so late they would be

exhausted and sleep in later in the a.m. right?? This is the most

frustrating part.....they'll get up at the crack of dawn and START ALL OVER

AGAIN.....

Don't know the answer to this one.....only that I've been there, and am doing

that..notice I've said " doing " and not " done " because we're STILL DOING IT...

Off the soapbox,

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did an all-nighter last night. He had the ceiling fan going, all

the lights on and was trying to call someone on the phone. I had crashed and

the sound of the telephone woke me up.

His cheeks are red, eyes are glassy and he had only about 20 min of nap today

(I hope it is a good sign)

Ann with , and

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was awake until 1am last night and about 7.3o am got into bed with

us,its school half term here and its now 9.15 and both boys are asleep in our

bed,I know I should wake them or we will get a re run tonight but it is so

peaceful,I find as I get older I cant take the lack of sleep,makes me very

bad tempered Pat

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In a message dated 02/22/2000 11:22:32 PM Central Standard Time,

mfroof@... writes:

<< Nothing like a special needs kid getting the stomach

flu!!!! Poor Gareth.......doesn't quite seem to know what end to put on the

toilet. >>

Oh, Margaret, can I relate! Stomach flu is truly a trial for all. I hope

Gareth is feeling better now.

Maureen

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  • 1 month later...
Guest guest

Hi Phyllis,

Thanks for the note - it does help to have someone else who understands. How

long have you been dealing with the fibro? And the lupus? I am slowly feeling

better about myself and where I am at with my pain (except on my PMSing days :)

!! I used to be alot worse, and had to stay doped up on muscle relaxants and

pain meds most of the time. Nowadays I just take 1 pain pill at night and

sometimes during the day after working out or doing something strenuous around

the house, lots of vitamins, and an antidepressant, both for help sleeping and

with depression/stress (too many things going on in my life - not even counting

the fibro!) Luckily I have one of the most supportive, understanding dh's in

the world!

I really want to increase my strength and endurance, but it's just so hard to

measure how far you can go. I feel ok during a workout, and then 15 min after

stopping I can feel my neck tensing up. Or sometimes, unexpectedly, I will have

to hold my ds for more than a couple of minutes, and I am down for the count.

(He's 2.5 years old and weighs 41 pounds! Very big, just like my dd was and

is!) I know that Taebo is helping, and I am going to continue, because it does

make me feel better. I wish I saw a little quicker results with size and losing

weight but I figure just seeing my muscles actually getting tight is pretty

good. Haven't seen them for awhile! :)

I do have a question...How do you modify the SA floorwork? Do you have any

issues with your neck? I tried to do alot of those crunches, leaving my neck on

the floor, doing reverse crunches lifting my hips, but I could still feel the

strain on the top of my shoulders into the neck. My dh and I are going to watch

it and see what I can do to modify it ahead of time and be prepared, instead of

trying to modify as I go. Any suggestions from anyone would be welcome!

Talk to you later!

in Texas

Message: 17

Date: Tue, 11 Apr 2000 16:32:02 -040

From: Phyl <paw@...>

Subject: Re: Re: feeling guilty

>

> Hi , just wanted to say I know exactly how you feel. With lupus and

fibro, I really have to be careful about what I do, just wanted you to know you

are not alone. Tae Bo has really helped me feel better about myself, I feel

strong and healthy while doing tae bo, even on days when I can only do it for a

short time and I always modify, it really makes me feel good about

myself....which isn't easy considering what fibro takes away from our lives.

> I also want to do many things I cannot do and I want to exercise for longer

periods of time but I know I can't....or like you, I am in bed for days. I am

slowly learning to be happy with what I can do and not feel so guilty, tae bo

helps me get through the rough times, and I know even doing 10 mins of exercise

helps me become a stronger and healthier person....I did 20 mins today and feel

good.

> I am so thankful to Blanks, I can't say that enough.

> Phyllis

>

> K wrote:

>

> > Oh, Angie, do I know about feeling guilty! Guilty about not being able to

pick up my dd anymore, and now my ds. Guilty about not being able to push a

vacuum cleaner or mop, I have to double check the shopping carts at the grocery

store to make sure they don't lean to the left. You HAVE to listen to your

body, if it is tired, you have to let it rest. Pushing it when it's tired or

sick will only hurt it. I have learned this a very hard way. I want to

exercise and play and roughhouse, but my body tells me different. When I have

pushed it, I end up in bed or on pain meds for the next 3 days. My muscles are

weaker, but it's still the same thing. The myofascial pain syndrome, trigger

points and fibro all have taught me to measure and watch my body and its

strength carefully.

> >

>

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In a message dated 04/11/2000 11:35:20 PM Eastern Daylight Time,

susan@... writes:

<< I do have a question...How do you modify the SA floorwork? Do you have

any issues with your neck? I tried to do alot of those crunches, leaving my

neck on the floor, doing reverse crunches lifting my hips, but I could still

feel the strain on the top of my shoulders into the neck. My dh and I are

going to watch it and see what I can do to modify it ahead of time and be

prepared, instead of trying to modify as I go. Any suggestions from anyone

would be welcome! >>

you have to really concentrate not to involve your shoulders, neck and head

when doing crunches by focusing on the upper abs, Go for less movement,

keeping chin pointed to the ceiling and arms crossed on chest. Try to stay in

the contraction going up and down with minimum movement.

You can also try extending one arm at a time with the upwards movement

alittle diagonally to involve other muscles

Barb

who is always trying to protect my neck

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  • 4 months later...

Hi Kathy,

This sounds to me like it might be one of those cases when it would

be advisable to invite the teacher to your home.

Be supportive of Sara and let the teacher see for herself that Sara

is competent in whatever areas you think best.

Talk to the teacher - try to draw her out - as to just what her

instructions are, and how they are given.

If Sara is doing so well in her regular 2nd grade class, and had no

problems with the resource room last year, _and_ she is complaining

about the noise in the resource room...well altogether it sounds like

it may require some adjustment on the teacher's part, as well as on

Sara's part.

Good luck,

Israela

At 11:54 25/08/00 +0000, you wrote:

>Message: 7

> Date: Thu, 24 Aug 2000 21:52:52 EDT

> From: M4858@...

>Subject: A Letter from the teacher :(

>

>Hi :)

>

>Well, Sara's been in school almost 2 weeks now!!!!!!!!!!!! AND I received

>this letter today from her Resource teacher/Sped teacher. Letter is below:

>

> " Sara would not do her Reading this morning. She would not follow directions

>in Math. Please help her with the work she REFUSED to do. If you have any

>suggestions to help correct her behavior I would be happy to try them in

>class. I have already tried rewards, stickers, candy, stars. I have also

>tried the time out. She is happy to sit and not work.

>

>Thanks for your help

>

>Mrs. teacher

> PS. Sara did do one math sheet after about 30 min. (a happy face next to

>this) "

>

>Now I'm really wondering what's going on, Sara did not have these problems

>before and not in summer school. This is a new teacher, and Sara is missing

>some sleep lately (we've been making her stay in her OWN bed at night now) or

>maybe the classroom has changed. For years she's been educated with kids in

>Resource with LD labels, I think this classroom has now become a " Sped room "

>for lack of a better description :) Sara has told me all week, she hates

>going to the Resource room......AKA Learning Lab. Sara told me it's loud and

>she even copied some of the behaviors that she said that does bothered her

>(screaming, yelling etc........)

>

>I did reem her out and all night when she asked me for things like having a

>friend spend the night this weekend, or going to Britney Spears again in Oct.

>I told her " NO " not until she starts to work in the Learning Lab. Does anyone

>have any suggestions I can pass on to the teacher? or any little tricks I can

>use :) She is having no problems in the Reg 2nd grade class, the teacher has

>even called me at home and said Sara's been awsome!!!!!!!!!!! I know it's

>just the beginning of the year but I don't want this to become a habit with

>her :)

>

>Next Ill address to the teachers that they are to be sending a communication

>notebook home with her DAILY Heehee positive and negative stuff :) as says

>her IEP :)

>

>Kathy mom to Sara 8................who was stripped of all privileges today :(

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  • 5 months later...
  • 3 years later...
Guest guest

In a message dated 5/13/2004 9:36:07 PM Eastern Daylight Time, health writes:

From: "Anne" <pokergirl212000@...>Subject: Re: Nerve Formula side effectsI am currently taking the Nerve Formula in extract form which contains: Black Cohosh Root, Cayenne Pepper, Hops flower, Lobelia herb, Scullcap herb, Valerian Root, Wood Betony herb, & Mistletoe Leaves. The bottle says serving size is 15 drops between meals, but I only take 7 drops in the evenings. I have not taken any Valium for over a month. I made sure I was off Valium before I started the Nerve Formula. I am only on 3 other prescriptions Propranolol 40mg & Diltiazem 120mg (these are for tremors and blood pressure), and Oral Contraceptives (this is for primary dysmenorrhea not to prevent pregnancy). In addition to the numbness and tingling in my arms and hands, I have also had little headache the past 3 days. Just want to make sure it is not side effects of the Nerve Formula causing this. If this is something that requires more looking into I want to know, before I have a stroke.

..

..

>>> It can take a whole lot of time with many side effects before valium is out of your system. You may be experiencing withdrawal still.

Fish oil and Magnesium are great from tremors and blood pressure, by the way.

mjhhttp://foxhillfarm.us/FireBasil/

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>

> >>> It can take a whole lot of time with many side effects before

> valium is out of your system.  You may be experiencing withdrawal

> still.

>

I forget the half life of Valium exactly but remember that it's OFF THE

CHARTS....take care this drug stores in the tissues a long long time

and when it periodically releases it can be quite a ride. Take your

time and be careful detoxing.

Whole Life Essentials.

Outstanding Organic Essential Oils & Products

http://www.WholeLifeEssentials.com

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