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Re: Digest Number 2312

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Does anybody know any agencies providing AVB (applied verbal behavior)

services

I am currently getting 25 hours of ABA but am terribly unhappy with the

current providers. What's the most hours I can get with a full day of school

for next year. Ilive in brooklyn NY my son is will be five next january. Edie

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  • 1 year later...

In a message dated 1/15/2004 7:24:12 PM Central Standard Time,

writes:

> : Wed, 14 Jan 2004 03:51:15 -0000

> From: " jana5522 " <jana5522@...>

> Subject: Re: New Pic..

>

> Wow Gloria those are awesome! I hate to use that

> word...um..fantastic, amazing, stupendous!

>

> Well I don't think they are all *that*, but I appreciate the kindness...Go

> BFL'ers!!!!

okay I don't know what happened there and why it was copied so much...I am

not real computer literate...lol sorry......derrrr gloria....

Gloria

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  • 1 month later...
Guest guest

To Maureen

Good luck. Docs are really expensive if you buy retail,but if you are adept

at the internet you can probably find some reasonable. Also, since their

popularity is among a certain type of young person, the " in " styles are

usually priced higher, but I have found that the " out " styles are often

quite reasonable, and I am more into making my feet feel better than being

in style, D

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  • 1 year later...

8. Re: Stage 4 Colorectal Cancer - Know of Anyone Who has Survived?

My fiance has been a survivor for 2 years and 9 months now and whilst we are

panicked about the future (because it is hard to be certain) sometimes you reach

the 4 year mark and then you could get a recurrence, but fingers crossed I will

be on this group saying my fiance is a 4 year survivor in another 1 year and 3

months. Her main test nowadays is a CA-125 test every three months or so and a

blood sample analysis using a frequency machine, there have been a few CT scans

here and there but she avoids conventional doctors as much as possible other

than a couple of general practitioners who are more open to alternatives

I am always looking out for more things and innovations in existing products,

so whilst she will continue taking things like pau d'arco, renee, hoxsey and

various other things if I come across something new like " tumor shrinker " I will

give it a go, in addition to things like the frequency machine, cesium chloride,

alkaline water, vascustatin, vitamin C injections, graviola, immune boosting

tablets and so on. She tends to eat sushi but this is probably more a liking

than a health thing, but then again japanese people do live a long time.

In terms of her attitude, it is generally one of defiance, almost an angry

" I'll show you " attitude towards the doctors that diagnosed her in March 2003

(15cm tumor in bowel, 2 lymph nodes involved and a bit on the stomach lining)

Nick

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

Win a Vespa NEW - Cars has 3 Vespa LX125s to be won Enter Now!

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Thank you Nick for the information about your fiancé. You are correct in

that the scourge can come back, however, you are already ahead of the

conventional game and hopefully your efforts will continue to be positive.

I will be delighted to pass this on to a cousin that is 'toying' with

alternative efforts for a stage 4 colon cancer. I say 'toying' because he

is beginning to listen and try what many of us believe helpful. What he

has done constructive is tell the Oncologist, after his surgery and after

one harrowing chemo treatment, " I am going to beat this without this

horrible treatment " . Joe C.

Re: [ ] Digest Number 2312

> 8. Re: Stage 4 Colorectal Cancer - Know of Anyone Who has Survived?

>

> My fiance has been a survivor for 2 years and 9 months

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  • 4 weeks later...

Yes, I have had colon hydrotherapy on two separate occasions. Both times while

on a green juice & protein powder fast, also using psyllium/bentonite. It went

fine, took about an hour each time, on a Monday/Wednesday/ Friday routine.

OjaiRene

RRAERoth@...

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  • 4 years later...
Guest guest

Like the other I'm sorry to hear about your pain and your struggles. I have vivid memories of the time before I stumbled onto the combination of MTX, weekly (not bi-weekly) Humira, and ibuprofen that has worked for me for the last few years. When I first started Humira, I got the standard dosage, which didn't work adequately. I forced the issue and eventually made the MD and the insurance co. up the dosage, which has worked.You may be in a similar situation where you need to force the system to give you the relief you need. Have you tried various combinations of the drugs? Have you tried them at higher than the advertised dosages? I discovered after I called Abbott Pharmaceuticals that many people now take Humira weekly, even though the suggested dose is half that. Busy doctors and cost-conscious insurance companies are not going to suggest such

strategies, but they are effective in cases like mine. I am not an MD, but swelling around your waist sounds to me like something other than RA is going on since there are no joints near there. And painful ribs also doesn't sound like any kind of RA I've ever heard of. Have you pushed to get help with these?HTH,Stan

>

>

> Hi Everyone! I had to stop taking Simponi. Each time I took it, it made me

> swell more, then I would have to take two rounds of prednisone dosepacks and

> a cortizone shot to get the swelling and inflammation under control.

>

> Anyone else have this problem with Simponi? It's been added to all the

> other failures for me: vioxx, celebrex, methotrexate, humira, enbrel, and

> now simponi.

>

> I'm still swelling and hurting and I'm beginning to lose range of motion.

> The bone scan showed damage in my hands, shoulders, hips, and knees. But now

> I don't just swell in my lower extremities, I also swell around my waist as

> the day wears on. And my ribs hurt when I breathe.

>

> My rheumy is leaning towards orencia.

>

> Thanks,

>

> Kathy

>

>

>

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1c.

Re: Simponi is history for me

Posted by: "Harold Van Tuyl"

hvantuyl@...

grandpavan1927

Sat Jun 12, 2010 4:26 pm (PDT)

I'm sorry you haven't had success in spite of many treatments that are

usually effective for RA. I do well on Methotrexate plus Remicade, and

haven't tried anything else. You might make sure you have been checked by

the most sensitive test for Lyme disease because that is often mistaken for

RA. Also you might get a second opinion from a different rheumatologist.

Even if there are no new suggestions I think it will help emotionally to

feel you are getting the best possible treatment. I hope something works

for you. God bless.

From: rheumatoid_arthriti sgroups (DOT) com

[mailto:rheumatoid_arthriti sgroups (DOT) com] On Behalf Of kathy_d87

Sent: Saturday, June 12, 2010 2:13 PM

rheumatoid_arthriti sgroups (DOT) com

Subject: [rheumatoid_ arthritis] Simponi is history for me

Hi Everyone! I had to stop taking Simponi. Each time I took it, it made me

swell more, then I would have to take two rounds of prednisone dosepacks and

a cortizone shot to get the swelling and inflammation under control.

Anyone else have this problem with Simponi? It's been added to all the other

failures for me: vioxx, celebrex, methotrexate, humira, enbrel, and now

simponi.

I'm still swelling and hurting and I'm beginning to lose range of motion.

The bone scan showed damage in my hands, shoulders, hips, and knees. But now

I don't just swell in my lower extremities, I also swell around my waist as

the day wears on. And my ribs hurt when I breathe.

My rheumy is leaning towards orencia.

Thanks,

Kathy

No virus found in this incoming message.

Checked by AVG - www.avg.com

Version: 9.0.829 / Virus Database: 271.1.1/2932 - Release Date: 06/11/10

11:35:00

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Messages in this topic (4)

1d.

Re: Simponi is history for me

Posted by: " Beyke"

karenbeyke@...

needsbeach

Sun Jun 13, 2010 7:09 am (PDT)

So sorry to hear about your difficulties. I've never tried Simponi, but

I've had much better results with Orencia/MTX combo. Enbrel and Rituxan

didn't work for me as well.

I know it's disheartening and takes awhile to figure out (then re-figure

out), but just hang in there. Everyone reacts differently. Talk to your

rheumy, though, in case there's something else going on that s/he'd like to

rule out. I found that just knowing it wasn't something even worse made me

feel better.

<http://www.lifeisgo od.com/>

_____

From: rheumatoid_arthriti sgroups (DOT) com

[mailto:rheumatoid_arthriti sgroups (DOT) com] On Behalf Of kathy_d87

Sent: Saturday, June 12, 2010 4:13 PM

rheumatoid_arthriti sgroups (DOT) com

Subject: [rheumatoid_ arthritis] Simponi is history for me

Hi Everyone! I had to stop taking Simponi. Each time I took it, it made me

swell more, then I would have to take two rounds of prednisone dosepacks and

a cortizone shot to get the swelling and inflammation under control.

Anyone else have this problem with Simponi? It's been added to all the other

failures for me: vioxx, celebrex, methotrexate, humira, enbrel, and now

simponi.

I'm still swelling and hurting and I'm beginning to lose range of motion.

The bone scan showed damage in my hands, shoulders, hips, and knees. But now

I don't just swell in my lower extremities, I also swell around my waist as

the day wears on. And my ribs hurt when I breathe.

My rheumy is leaning towards orencia.

Thanks,

Kathy

No virus found in this incoming message.

Checked by AVG - www.avg.com

Version: 9.0.829 / Virus Database: 271.1.1/2932 - Release Date: 06/11/10

13:35:00

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Messages in this topic (4)

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