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Well, not knowing all the goings on and not having the medical education, it

SOUNDS as though you COULD just fix the stenosis, as long as it's outside the

fusion area.  That's my guess.

 

Lj

From: beckybugkins <beckybugkins@...>

Subject: Help!

Scoliosis Treatment

Date: Tuesday, January 6, 2009, 10:36 PM

Here's my problem. I have had the fusion for Scoliosis. I now need a

laminenctomy for spinal stenosis. I am scared and confused. One doctor

said that I need a lot of things done with opening me up front and back

and fusing the rest of my spine, trimming my rods and more. Another

well respected Brain and Spine surgeon says that she can go in and just

fix the stenosis without all of the trimming and fusing. I am wonder

which one is correct. I am wondering if putting off the surgery will

cause damage to my spine. The stenosis is severe. I am really

scared. What would you do?

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  • 3 months later...
Guest guest

Hi Meredith,

Your password expired on June 24th of last year.

You can re-register at http://www.CureDrive.org

I see what you mean. You are onto something there. You have to keep

curing; that's the essence of healing and being a healer. You have

slipped and allowed yourself to be compromised.

Love,

Greg

At 10:00 PM 4/18/2009, you wrote:

>I'm having a senior moment and can't remember my id and password to

>get on the web college. As far as I know, my donation is in order.

>If there is a problem with that, please let me know.

>

>Thanks for your help. I have had a suspicion that some of my

>conditions have to do with being an empath and need to figure out

>how to keep the gift without keeping the conditions, so I really

>need to go digging. Since Carl's accident I have gotten out of my

>usual immunic routine and have neglected working on myself and

>learning new things.

>

>Thanks again,

>Meredith

>

>--

> " We don't see things as they are. We see things as we are. " Anais Nin

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Guest guest

Hey girl,

I was nervous in the beginning too, but now I know that there was really no need

to be. The needle is really thin and only 1/2 " long. My doctor told me to inject

into the stomach fat, there are no blood vessels there so you barely feel it,

really. The needle goes all the way in. After the first time it is no big deal.

Be brave. You can do this and boy is it worth it.

>

> I'm waiting for my hcg to arrive, I'm starting to have second thoughts about

this. How deep do you have to stick the needles? What does aspirate mean? What

if I hit a vein? I know it's alot of questions but I'm not so sure I can do

this. Please help!

>

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Guest guest

I don't know how this board works. I thought I signed up to use a different name

than my own name.

I am having trouble following this board.

In , SuzanneSH <SuzanneSH@...> wrote:

>

> ,

>

> All that you have is your name and this 1st E-mail you send to the board,so

that is why no responded to it I am sure.

>

> Suzanne

>

>

>

> In a message dated 08/03/09 08:44:10 Pacific Daylight Time, denisef822@...

writes:

>

>

>

>

>

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First, relax. Stressing releases cortisol, which causes fat storage.

The calories on P3/P4 depend on your current weight. Go to one of the online calorie calculators and see what you should be eating. The most frequent mistake on P3 is to eat too few calories, too little food, which will bring about a gain. While eating no starch/sugar, you can eat more fat. P3 should be about adding good fats back in. Eat as many grams of fat as you do of protein, and half that much or less of carb grams.

CC

A moderator of the hCGDieters group

Guide to Implementing the Weight Loss Cure http://www.weightlosscureonline.com

DO NOT ORDER FROM THE LINK ABOVE. As a member of this group, you can get my over 100-page eBook for $19.95 by sending it to me at apracticalidealist at dot com using PayPal.

ALERT: Please use an email that is NOT comcast.net since the files cannot be sent there successfully. For faster access to the eBook, use a credit card if you can.

From: easybreezycoversgirl <easybreezycoversgirl@...> Sent: Sunday, August 16, 2009 2:02:49 AMSubject: HELP!

OK, this is what's happened.I ended the 23 days last sunday and then did the 500 calories till the following wednesday. I then went on a boat trip to Arizona. 1) It's extremely hot down there, 2) I retain water easily when I go on vacation trips, 3) I never over ate while I was down there. But, I have gained back 4.6 pounds since wednesday. I know I was supposed to do a steak day immedialtely once I hit over two pounds but I was worried I'd pass out from being on a boat all day so I just took it easy and ate some eggs in the morning, chicken for lunch, and a small steak for dinner with fruit and vegetables throughout the day. I also ran 2 miles every night down there which I haven't done in a LONG time. But, getting on the scale scares me now. Have I completely ruined what I've been doing the last month? And how can I get it back down to my lowest point?One more question I've been wondering is when he says going back to eating normal

after your 26 days, what does that REALLY mean? Like how many grams of fat should I be eating a day? I know there's no sugar or starch and that's fine. But calorie intake? I don't know if it's like 2000 calories a day, or like 1200 calories a day. Can someone help me clear this mess up? I'd appreciate it SO MUCH! I'm so worried I've ruined it.

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Guest guest

Hi, I don't know if I have posted incorrectly but I joined recently and haven't

seen anything come up. I have a new knee replacement and would love to get some

feedback from members. Thanks Judith

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Guest guest

Dear Phoebe,

Sorry to be the bearer of bad news but this disease will teach you patience

whether it's a lesson you want to learn or not.  Steroids should give immediate

relief but long-term use can have bad consequences and you need long-term help

since it looks like you're not one of the few lucky ones where the disease goes

away and stays away.  Methotrexate and all the long-term treatments take awhile

to kick in so that's why your rheumy isn't concerned about three weeks and no

effect.  Methotrexate didn't help me either but a biologic gave me my life back

after many years of the pain you're experiencing.  I was a single parent with

two kids and a rotten boss at the time so I hid the pain as best I could and

kept up the job.  People at work thought I was short-tempered and asocial

because I was in that relentless pain but refused to tell a soul.  When the

Enbrel kicked in my doc in a nice way and my boss in a mocking way both

commented how I turned into

Sunshine with a smile on my face for the whole human race.    Have

patience.  Hang in there.  Someday, I hope soon, your doc will find the right

med for you and you can get your life back and experience the joy of being

pain-free.  It is a joy only experienced after going through the hellacious

pain we have. 

Take care,

Janette in Indiana

From: Phoebe <phoebe214@...>

Subject: HELP!

Date: Monday, August 8, 2011, 1:11 AM

 

I am newly re-diagnosed with Reactive Arthritis. I guess I've had it since

adolescence but had been under the impression that it went away. I realize now

that is a bunch of phooey and that indeed I have been suffering the symptoms all

along only attributing them to other issues.

Here is my problem. I am in horrible pain. My hips, and feet are currently

effected. I'm on steriods, methotrexate, and folic acid. To no avail. It's not

getting any better. I'm so frustrated. Can anyone give me any ideas. My

rheumatologist is supposed to be one of the leading specialists of the field but

it has been 3 weeks since I saw him without much improvement. In fact, It might

be worse. This is interrupting my sleep. I've been prescribed every kind of pain

killer and frankly- it doesn't work.

I have been missing lots of work too. This is a problem for me, but I find

myself absolutely exhausted by 3pm, and Thursday & Friday are nearly impossible

for me to navigate.

Can anyone help me figure out how to get to feeling better quickly?

Thank you,

-p

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Guest guest

Hi Phoebe,

I have been suffering from ReA for 33 years [i am 56], I have tried every drug

out there, until I started getting Remicade infusions a year now.

It has worked great, I call it my Wonder Drug. It costs a lot my Rheumy gets

mine free from the manufacturer. Hope this helps! Harv in MI

HELP!

I am newly re-diagnosed with Reactive Arthritis. I guess I've had it since

adolescence but had been under the impression that it went away. I realize now

that is a bunch of phooey and that indeed I have been suffering the symptoms all

along only attributing them to other issues.

Here is my problem. I am in horrible pain. My hips, and feet are currently

effected. I'm on steriods, methotrexate, and folic acid. To no avail. It's not

getting any better. I'm so frustrated. Can anyone give me any ideas. My

rheumatologist is supposed to be one of the leading specialists of the field but

it has been 3 weeks since I saw him without much improvement. In fact, It might

be worse. This is interrupting my sleep. I've been prescribed every kind of pain

killer and frankly- it doesn't work.

I have been missing lots of work too. This is a problem for me, but I find

myself absolutely exhausted by 3pm, and Thursday & Friday are nearly impossible

for me to navigate.

Can anyone help me figure out how to get to feeling better quickly?

Thank you,

-p

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