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Barb

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Jenn, I have a couple of ideas for you. Go into several pizza shops,

wawas or places like that. Make up containers with a picture on it and

a slit on the top. Tell your story and what you want the money to go to.

ALso I have a epilepsy support group

EpilepsyApproach/

You can sign up and place the info there and address you want to send

the money too.

I place that info in my links area till you collect your money needed

and then take it off after you let me know.

Hope this helps.

> I wish no one ever had to even think about $. Anyway, one day I'm

sure it

> will some how be covered, until then trust God to provide the funds,

He has

> for us. Also The Centre (Claudie) has helped our daughter so much

that I do

> not feel overcharged. I realize there is no way at knowing that

before you

> try a treatment. They realize that too, so I believe there is some

kind of

> money back guarantee. I'm not sure though, because I've had no need to

> inquire about it.

>

> Barb

>

>

>

>

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  • 8 months later...

-a,

Thanks for your reply. Besides my elbows I am having problems with my

hands, wrists and ankles. They are really baffled as to what is wrong

with me. Up until today the rheumatologist what certian I have RA but

my Rheumatoid factor was only 24, which they said is only a slight

elevation and that my liver panel and other blood tests were ok. Now

she thinks that maybe it might be nerve compression. I was on 20 mgs

of Prednisone and now for the last 2 days I am on 10mgs. I Was

supposed to taper off in 3 days but my R tologist told me not to. In

addition to scanning my elbows she has now ordered my wrists to be

scanned too. I was not scheduled to see her offically until the 14th

but had to have an emergency appointment today because my wrists and

elbows hurt so badly last night that I was up crying all night with

no relief despite the prednisone. So it boils down to this, went in

today dr. said not really sure now, still have MRI but add wrists

into scan, here is tylenol 3 and call on the 14th to discuss results

and decide what to do from there. I hate not knowing what the heck is

going on!! They don't know, I don't know! ARRRGHH!

Barb

-- In , a <a54@s...> wrote:

> Barb,

>

> In time, talking to us as a group may feel more comfortable. I

> understand how you feel. It is great to get the collective

> experience from so many knowledgeable members. Between us all,

we've

> taken ever med and had every treatment.

> The MRI doesn't sound like fun, but hopefully it will be tolerable

> for you.

> Mood swings is one of the major side effects of prednisone.

> Prednisone has a lot of side effects, so hopefully you won't be on

it

> for long.

> Does your doctor intend on starting you on RA meds soon? Do you

have

> any other joints that are affected besides your elbows?

>

> a

>

>

> On Sep 5, 2005, at 8:10 PM, sassyone3173 wrote:

>

> > Hi guys. I am not really good at the group thing, i never know

what

> > to

> > say. One on one I am okay, but in a group I am a " chicken " . This

> > Thursday I go for an MRI on both elbows, an hour each side! Ouch!

My

> > Rheumatologist asked if i could handle it, I just responded with

> > " hope

> > so. " They are using the new extremity MRI where only the joint

being

> > examined is placed in the machine, but holding my elbows that

long is

> > what concerns me. The prednisone they started me on last Tuesday

is

> > making me really moody. Has anyone else experienced that? If so

how

> > did you deal with it? Was there anything you did that helped it?

I am

> > usually a patient person and now I am crabbing at my kids and

hubby a

> > lot. Any imput would help greatly, I am new to this.

> >

> > Sincerely,

> >

> > Barb ( Sassyone3173)

>

>

>

>

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Barb,

Your rheumatoid factor doesn't have to be positive in order to have

RA. I've never had a positive RF in 30 years.

20% of rheumatoid patients have a negative rheumatoid factor. That

is what is so frustrating about diagnosing this disease.

It CANNOT be diagnosed with blood tests alone. Nerve compression to

me sounds unlikely since so many joints are involved,

but I'm not a doctor. When you get your MRI results it may show

erosion. If it shows bone erosion it may help with the

diagnosis. I hope you get answers soon so that you can get on

medication and get some relief.

a

On Sep 6, 2005, at 6:32 PM, sassyone3173 wrote:

> -a,

>

> Thanks for your reply. Besides my elbows I am having problems with my

> hands, wrists and ankles. They are really baffled as to what is wrong

> with me. Up until today the rheumatologist what certian I have RA but

> my Rheumatoid factor was only 24, which they said is only a slight

> elevation and that my liver panel and other blood tests were ok. Now

> she thinks that maybe it might be nerve compression. I was on 20 mgs

> of Prednisone and now for the last 2 days I am on 10mgs. I Was

> supposed to taper off in 3 days but my R tologist told me not to. In

> addition to scanning my elbows she has now ordered my wrists to be

> scanned too. I was not scheduled to see her offically until the 14th

> but had to have an emergency appointment today because my wrists and

> elbows hurt so badly last night that I was up crying all night with

> no relief despite the prednisone. So it boils down to this, went in

> today dr. said not really sure now, still have MRI but add wrists

> into scan, here is tylenol 3 and call on the 14th to discuss results

> and decide what to do from there. I hate not knowing what the heck is

> going on!! They don't know, I don't know! ARRRGHH!

>

> Barb

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  • 5 months later...
Guest guest

Barb,

Did you decide to give him 100mg based on his weight? I don't know how to

decide the dosage for my daughter who is about 20 lbs.

Thanks,

[ ] Digest Number 7699

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Guest guest

> I don't know how to decide the dosage for my daughter who is about 20 lbs.

1/8 to 1/2 mg per pound of body weight, per dose.

That means 2.5 to 10 mg.

What chelator are we talking about? DMSA, ALA?

Valentina

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

I love you a, and thanks!   Hugs,  Barb

From: rascalsniche@... <rascalsniche@...>

Subject: [ ] Barb

Date: Saturday, May 22, 2010, 5:46 PM

 

I agree with all the others...you're the best Barb!!

Hugs...a

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  • 3 months later...

my insurance company does not authorize pre-therapy so I am just riding my

stationery bike and some simple

leg exercises and trying to lose some weight to help with therapy

afterwards.......

my pain in the hip gets worse daily......some days I wonder if I can last

until 11/11.....

Gayle, I have not noticed. Are you having a hip or knee done?

BARB in Florida

Re: day two

Barb, I may be a rarity here, but day two was fine for me. I was up walking

around my hospital room unaided on day two. And it just got easier with

each passing day. The worse day was the day before the op! But I guess I am

one of the lucky ones.

>

> I have been talking about hip replacement with another group of

> people and they seem to agree that day two after the surgery is

> the worst day of the first week. Do you guys agree? BARB

>

>

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I'll be having my right knee replaced.  Is yours a hip or knee?

 

Gayle

From: BARB <barbmch@...>

Subject: Re: Re: day two

Joint Replacement

Date: Monday, September 6, 2010, 8:29 AM

Maybe I will be one of the lucky ones too.......11/11 gets closer and

closer........

BARB

Re: day two

Barb, I may be a rarity here, but day two was fine for me. I was up walking

around my hospital room unaided on day two. And it just got easier with

each passing day. The worse day was the day before the op! But I guess I am

one of the lucky ones.

>

> I have been talking about hip replacement with another group of

> people and they seem to agree that day two after the surgery is

> the worst day of the first week. Do you guys agree? BARB

>

>

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right hip

Re: day two

Barb, I may be a rarity here, but day two was fine for me. I was up walking

around my hospital room unaided on day two. And it just got easier with

each passing day. The worse day was the day before the op! But I guess I am

one of the lucky ones.

>

> I have been talking about hip replacement with another group of

> people and they seem to agree that day two after the surgery is

> the worst day of the first week. Do you guys agree? BARB

>

>

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Brickey, I have a recumbent bike.......a Schwinn 230.......we paid $377 on

Amazon.

I didn't know what to get or in what price range. So I picked a mid-range

one.

I am very satisfied. Not hard to assemble. Works so smoothly. I ride it

twice a

day for 30 minutes each. After my new hip, I should be able to ride it a

lot more

than that. BARB

Re: Barb

In a message dated 9/7/2010 5:02:14 P.M. Pacific Daylight Time,

barbmch@... writes:

I am just riding my

stationery bike and some simple

I am thinking of buying a recumbent stationary bike as I know I will be

kicked out of PT pretty soon. My PT has me riding the bike for at least 10

minutes. Just started to turn the pedals 360 last week. I was looking at the

Walmart Weslo Pursuit at $167 and the Sears Nordic Trac C3 at $349.88. Sears

also has a Pro Form 10.8 at $249.99.

I placed an add on Craig's list and had only two responses. Both canceled

when their mates heard what they were up to and both said they plan on using

it.

Any advice from users?

Brickey

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