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Re: Digest Number 6313

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My 5 year old Abby is pauci extended, not systemic, but has been on MXT for

about 9 months at a dose of 20mg to start and now at 20.5 now. I guess jaws

don't respond as well as the other joints. She has also gained weight so the

rheumy increased it. She has responded well to the med. We inject her once a

week in her sleep and she doesn't even wake up anymore. She is on folic acid as

well and has had no side effects.

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On May 2, 2010, at 6:11 AM, wrote:

The Juvenile Arthritis Forum

Messages In This Digest (14 Messages)

1a.

OT - BPPV From: veristroud@...

1b.

Re: OT - BPPV From: and Schulz

1c.

Re: OT - BPPV From: Beth Yohnk

1d.

Re: OT - BPPV From: veristroud@...

1e.

Re: OT - BPPV From: veristroud@...

2a.

Re: introduction; any advice on living with systemic day to day?? From: nn

2b.

Re: introduction; any advice on living with systemic day to day?? From: nn

2c.

Re: introduction; any advice on living with systemic day to day?? From: nn

2d.

Re: introduction; any advice on living with systemic day to day?? From: nn

2e.

Re: introduction; any advice on living with systemic day to day?? From:

Price

2f.

Re: introduction; any advice on living with systemic day to day?? From: Amy

Hendrickson

2g.

Re: introduction; any advice on living with systemic day to day?? From:

redfeather03@...

2h.

Re: introduction; any advice on living with systemic day to day?? From:

Price

3a.

@ Ford From: Joann Bullock

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1a.

OT - BPPV

Posted by: " veristroud@... " veristroud@... veri_stroud

Sat May 1, 2010 4:32 am (PDT)

I am in need of information and know there must be at least one person on this

list with some help for me. Does anyone know much about BPPV - Benign Paroxysmal

Positional Vertigo? I have recently been diagnosed with this and am struggling.

The only people I have found with any knowledge about this are my doctors. Which

I am thankful they have the knowledge but itis difficult to talk to them every

day. they have all the book knowledge but not the personal experience. I have

several other things going on within my body at this time as well and am

convinced that they are connected although the doctor seems to think they are

not. HMmmm. I am just not sure where to turn. Jaye is quite concerned and

has become Dr. Mom and given direct insturctions on getting an MRI done and

other things. She told me that now I have to listen to her and do what needs to

be done. She is more impatient with my testing then I think I may have been with

her stuff. She told

me that I made her this way, she learned all she knows from me. She also told

me that she thinks she could probably become a doctor with less schooling then

most. She is quite funny. Any input is appreciated. Thanks

Veri

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