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Re: Digest Number 926

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Does anyone recommend a particular water filtration system for their home?

I am just starting to research them and was wondering what you all thought

of different brands...

Thanks,

Timary

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We have a reverse osmosis system for our drinking water. Very expensive, but I was told that is the best. Nothing filtering our other water though, which is a bit of a concern to me.

(Cary, NC)persistentC@...http://www.rtphome.org/mariposa

Re: [ ] Digest Number 926

Does anyone recommend a particular water filtration system for their home?I am just starting to research them and was wondering what you all thoughtof different brands...Thanks,Timary

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  • 4 weeks later...
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I will be back in my office on 3/30/01 (bright and early).

Thank you

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  • 1 month later...
Guest guest

Hi Everyone...this is a catch up email....

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

lmao...thanks!

Subject: MATURITY IS UNDER ATTACK!

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

...I agree ,,,,that's how i feel as well...we all have things happen

to us...how we choose to feel about them in time is our choice...attitude

is so important! Positive is best!

< I think that with any major bit of bad

news, there's a bit of time where I just want to be depressed and feel

sorry for myself. >

< There's so much that I wanted to do that I've

always thought there would be

plenty of time later for or that it would happen in due time and now

there may not be enough time for any of it at all. > what do you dream

of doing ?

i read this quote a couple days ago...plan your life like you'll life forever

and live each day like it's your last... live for the moment....the present...i

find worrying about tommorrow takes away stuff that i could have enjoyed

today and thinking about the past is useless because theres no way to change...the

only thing that i can change is my view of it....tell us about what you

dream of????? maybe theres a way to fulfill it??????? Always have hope!!!

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Welcome......I'm sure you'll love this group!

<Can you tell me what the focus of this egroup

is? Is it to offer support to others and to swap info on what works?> all

of the above and more....venting , joking, having fun!

What do you do for your fibro? My friend has some super exciting stuff

going on with her fibro problems- advanced medicine. That must be awful

to have a headache that long? Do you have children? family? hubby? Others

to help you cope?

~~~~~~~~~~~~~~~~~~~~~~~~

rotflmao...that's good!

Subject: Some health tips we can really use(joke)

Straight Dope On Food, Health, & Exercise:

~~~~~~~~~~~~~~~~~~~~~~`

Helen...(((hugs))))) hope you are feeling better!what's wrong?

~~~~~~~~~~~~~~~~~~~~

Chelle, Sorry to hear about brother....that's depressing!

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Jessi....this is not good...do they know what is

causing it? Do you get low blood sugar? do you eart frequent meals? Or

is it like a seizure?

< The bad news is i passed out again today! This is the third

time since August this has happened. I don't remember falling but i

woke up when

i hit the floor>.

~~~~~~~~~~~~~~~~~~~~~~~

Happy Birthday Marilyn...!!!!How did you celebrate it?

~~~~~~~~~~~~~~~~~~~~

Well...i've got house cleaning to do..hopefully people

who look at my house this week will buy it..please -say your prayers, good

wishes etc for me.....living here really wears me down....it's an ongoing

struggle to be postive....i hate having a life that is beyond my control....ahhhh...thats

my negative side coming out...*trout slap* .....on the positive side i

know....all things happen for a reason ....and the shine always shines

after it rains...i wish you all a great life and renewed health and spirits.....love

sheena:)

Sounds like we all need a group hug.....

((((((HUGS TO ALL OF YOU)))))))))

..

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  • 2 months later...
Guest guest

My daughter, (achon), had an MRI at nine months over at ish

Rite in Atlanta. She had met previously with Dr. Hudgins a month prior

and he didn't see anything wrong with her during the examination. He

requested that she have an MRI so that he could foresee anything

decompression, etc. that's common for all achons.

With her age, it was advise that she be sedated (no anesthesia was

given). I don't know the name the liquid, but she was given a small

amount. It started with a " C " (someone on the list will probably know

the name). It took her about ten minutes to go to sleep. We were allowed

to set in the room while the scanning was taken place. It was

understandable why she had to be sedated. The noise was loud, that we

had to wear headsets. They even placed a small set over her ears. The

process took about 20-30 minutes. She was awake in no time and after she

took a bottle of juice, we were allowed to leave. While she was in

recovery, she was hooked up to a pulse machine.

There may not be anything wrong with your son at this time; however,

it's good to have the tests for follow-up up visits.

I hope this helps you.

Cheryl

> 7. Doubts about having an MRI or CT.

> From: sussy_amezcua@...

>

> ________________________________________________________________________

> ________________________________________________________________________

> Message: 7

> Date: Sat, 21 Jul 2001 23:56:32 -0000

> From: sussy_amezcua@...

> Subject: Doubts about having an MRI or CT.

>

> Hello to every body.

> I am worried because I asked before if my 17 month old baby boy

> should have an MRI or CT, and a lot of people told be he must, but

> now I am really worried because of the things some people advise me

> of anesthesia.

> I want to know if every Lp needs that test or if is to dangerous to

> have it because of the anesthesia.

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  • 9 months later...
Guest guest

Thank you for the option of a newsletter. The daily digest was too

much, especially after this weekend. I agree with the other mother who said

" I have kids to tend to, not to mention a neglected husband, house, job

etc.... This is a valuable resource but I was about to unsubscribe when I

read this post. Thank You Again, Kara

[ ] Digest Number 926

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  • 1 month later...
Guest guest

I believe when someone has been or sais cured of autism its simply no

different than being cured of cancer or in remisson. If there is no reason or

signs of autism showing why yes they can say their cured at least at that

point in their life. There is nothing wrong with those words if your child is

cured in your eyes or the doctor's eye's good for you ,your child ,and your

family do not feel bad about using those word's we just wish we all could say

that. Just my opinion!!!!!!!!!!!!!!!

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  • 1 month later...
Guest guest

If you put a few drops of regular grocery store hydrogen peroxide in each ear and leave it in for 15 min. or 'till it stops bubbling, you may get help. If an infection in the area is part of the problem this will definitely help and maybe cure. Best wishes, pj

Dr wrote:

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Guest guest

Hi Shirley,

I do not have an infection in my ear. Thanks for the

good advice, I do use H2O2 for infections also. LuLu

--- Shirley <pj20844@...> wrote:

>

> If you put a few drops of regular grocery store

> hydrogen peroxide in each ear and leave it in for 15

> min. or 'till it stops bubbling, you may get help.

> If an infection in the area is part of the problem

> this will definitely help and maybe cure. Best

> wishes, pj

>

>

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Guest guest

Hi Shirley,

I do not have an infection in my ear. Thanks for the

good advice, I do use H2O2 for infections also. LuLu

--- Shirley <pj20844@...> wrote:

>

> If you put a few drops of regular grocery store

> hydrogen peroxide in each ear and leave it in for 15

> min. or 'till it stops bubbling, you may get help.

> If an infection in the area is part of the problem

> this will definitely help and maybe cure. Best

> wishes, pj

>

>

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  • 9 months later...
  • 8 months later...

Hi, Dougie,

You have raised some complex questions here!

I wonder if you are sure you have " Harrington " rods? I am surprised to

hear that someone was still using this type of nonsegmental

instrumentation as late as 1992. I am having my own original,

nonfunctional Harrington rod (from 1986, which was already kind of late)

removed next week, along with several newer rods (Isola, I believe) plus

other assorted hardware. In my case, the removal of implants is part of

a more complex spinal revision procedure. This will be my fifth spinal

surgery to date.

Rod removal is NOT something I would rush off to do. I would want to

get several opinions from spinal deformity specialists who have done

plenty of complex revision surgery. I trust you are seeing more than

one revision surgeon -- ideally, also, a specialist in pain medicine or

physical medicine and rehabilitation, as appropriate -- for the best

possible diagnosis and advice. I think our intuition about our problems

and needs is often very good. Still, I would not rely completely on my

own sense of what ails me, or on opinions at a Web forum -- much as I

value and appreciate groups like this one.

Although I trust the recommendation to get my own hardware taken out, I

still need several more tests. These should give my surgeon the best

possible idea of what is going on with me and help him to map out his

strategy for my surgery.

Occasionally I hear about people who benefited from hardware removal

only, but often this is done as part of a much more complex procedure --

involving new grafts, new osteotomies, etc. I have run into a number

of people who mistakenly believe that getting rid of a rod or two will

make everything all right. Usually the solution is more complicated,

and may or may not involve having more surgery.

You might be interested in our group for veterans of previous scoliosis

surgery, particularly those with problems relating to Harrington rod

instrumentation: www.. This group

would be most helpful to you if you have the specific problem called

" flatback syndrome " or " fixed sagittal imbalance. " Otherwise, there may

be people posting to the group who can refer you to a better and more

informative place on the Web. At least two or three members -- maybe

more -- have had surgery for both scoliosis and spina bifida.

Best,

| HI THERE

|

| MY NAME IS DOUGIE

|

| I HAVE SCOLISIS AND SPINEBIFDA.. I HAVE 2 HARRINGTON RODS IN.. MY BACK

I HAVE HAD THEM IN SINCE 1992 AND WOULD LIKE TO HAVE THEM REMOVED...

THEY BEEN CAUSING ME MENTAL EMTIONAL STRESS ALONG WITH THE PSYCHICAL

PAIN THAT GOSE ALONG WITH... IS THERE ANY WAY I CAN HAVE REMOVED?

| WHAT DOSE EVERYONE THINK OF THAT? IS AN ALT OR AM I JUST CRAZY ?

| THANKS DOUGIE

|

|

---

Outgoing mail is certified Virus Free.

Checked by AVG anti-virus system (http://www.grisoft.com).

Version: 6.0.577 / Virus Database: 366 - Release Date: 2/3/04

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Dougie...

So, are you sure that you have Harrington implants? As indicated,

they haven't been in general use for many years. I know that there are

certain situations where Harrington rods are still the best choice, but I

think those incidences are rare.

Who was your surgeon? And, do you have scoliosis, kyphosis, or

kyphoscoliosis?

Regards,

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  • 8 months later...

, I would like to have you use by photos for the slide show... You did a

faboulous job on the one at Bash.... is there any way we can purchase a copy of

it. I'd love to have one and be able to play it when I need a good boost.

Esther in Bremerton

Dr. Kuri 9/25/01

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Many people have chosen not to put their pictures on the

group " Photos " file, possibly because they don't want their picture

(s) " out there " . If the photos will be used for anything other than

the presentation at Bash, you should let people know.

a

//, I would like to have you use by photos for the slide

show... You did a faboulous job on the one at Bash.... is there any

way we can purchase a copy of it. I'd love to have one and be able

to play it when I need a good boost.//

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  • 1 year later...
Guest guest

In a message dated 3/26/06 5:20:42 PM, mrnuts@... writes:

Dr.Grim,

Am I missing something? I looked for your Digest Number 926 - "read my

review paper in the files" and could not find any reference. Is the

reference perchance to the BP group files? (I'm no longer a member)

In passing may I say how valuable I find the information in this Group -

Hyperaldosteronism. I realise how fortunate I am to have a treatable and

controllable medical condition.

You may also be interested to learn that Pfizer have recently released

Inspra in Australia - it is available relatively cheaply under the PBS

(Pharmaceutical Benefit Scheme) but only for LVH patients. I am

investigating via my specialist becoming a 'special case' trial under the

PBS to replace the amiloride that I'm currently taking. The main reason for

this trial is the hope that Inspra will help reduce the gynecomastia

side-effect.

Many thanks for your continued contribution to our special Group.

From Mark Nuttall (Australia)

PS In my case, I was treated for 25 years for hypertension before a

perceptive local physician noted my low potassium, did the tests and reached

the correct diagnosis.

If it is OKed for LVH then ask to have an echo done and review your EKG (before sprio) as you most likely had and may still have LVH.

Depends on how well your BP has been controlled.

I wil look it is called the evolution of primary aldsoteronism.

I spent a year in Melbourne at the Florey and at the Royal Mebloure Hosp. Know many HTN experts in Aussie land and it is interesting that over the last 30 years more chairs of medicine have been HTN experts in Aust than any other place in the world.

I may know one in your area but sounds like you have found one.

May your pressure be low!

CE Grim, BS(Chem/Math), MS(Biochem), MD.

Board Certified in Internal Medicine, Geriatrics and Hypertension

Former Epidemiologic Intelligence Services Officer (Lt. Comdr.), CDC

Specializing in Difficult to Manage High Blood Pressure

Clinical Professor of Medicine, Medical College of Wisconsin

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Guest guest

Dr.Grim,

Am I missing something? I looked for your Digest Number 926 - " read my

review paper in the files " and could not find any reference. Is the

reference perchance to the BP group files? (I'm no longer a member)

In passing may I say how valuable I find the information in this Group -

Hyperaldosteronism. I realise how fortunate I am to have a treatable and

controllable medical condition.

You may also be interested to learn that Pfizer have recently released

Inspra in Australia - it is available relatively cheaply under the PBS

(Pharmaceutical Benefit Scheme) but only for LVH patients. I am

investigating via my specialist becoming a 'special case' trial under the

PBS to replace the amiloride that I'm currently taking. The main reason for

this trial is the hope that Inspra will help reduce the gynecomastia

side-effect.

Many thanks for your continued contribution to our special Group.

From Mark Nuttall (Australia)

PS In my case, I was treated for 25 years for hypertension before a

perceptive local physician noted my low potassium, did the tests and reached

the correct diagnosis.

Re: Did most of you have high B/P or low potassium???

Read my reivew paper in the files.

May your pressure be low!

CE Grim, BS(Chem/Math), MS(Biochem), MD.

Board Certified in Internal Medicine, Geriatrics and Hypertension

Former Epidemiologic Intelligence Services Officer (Lt. Comdr.), CDC

Specializing in Difficult to Manage High Blood Pressure

Clinical Professor of Medicine, Medical College of Wisconsin

[This message contained attachments]

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