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Hello all,

At the symposium a medical school student, Peggy Wang, who attended was

interested in seeing if anyone would like to participate in a research

project. They worked on a questionnaire on alternative therapies to collect

some preliminary data for a possible grant request in the future.

I'm enclosing the questionnaire as attachment

The purpose of this questionnaire is to gauge interest levels in chronic pain

sufferers for alternative therapies and is at this stage, a gathering of

preliminary data. They can't tell at this point whether or not (or when) a

formal study might be undertaken. They are interested in finding out what

treatments, both conventional and alternative, help chronic pain sufferers

and this survey might help shape a future study.

I hope you will be willing to help them. Please feel free to call the her at

or email at nharrierpw@... if you have any questions or if

the files don't transfer.

Her mailing address is:

Peggy Wang

5465 Barlby Dr.

Indianapolis, IN 46237

Karyn , RN

Founder / Executive Director

http://www.pancassociation.org

1- / KarynWms@...

PAI Home Office: Indianapolis, Indiana, USA

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In a message dated 10/30/2002 22:06:21 US Eastern Standard Time,

hominid2@... writes:

>>>> afraid the questionaire didn't make it. Remember, all attachments are

> stripped from the postings. Maybe you can add it to the files database and

> people can download it from there. Kimber <<<

I knew that. Gheeze. (Hand across the forehead). I'll put it on a text file

in the files section.---tomorrow.

Karyn , RN

Founder / Executive Director

http://www.pancassociation.org

1- / KarynWms@...

PAI Home Office: Indianapolis, Indiana, USA

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In a message dated 10/30/2002 22:06:21 US Eastern Standard Time,

hominid2@... writes:

>>>> afraid the questionaire didn't make it. Remember, all attachments are

> stripped from the postings. Maybe you can add it to the files database and

> people can download it from there. Kimber <<<

I knew that. Gheeze. (Hand across the forehead). I'll put it on a text file

in the files section.---tomorrow.

Karyn , RN

Founder / Executive Director

http://www.pancassociation.org

1- / KarynWms@...

PAI Home Office: Indianapolis, Indiana, USA

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Karyn,

afraid the questionaire didn't make it. Remember, all

attachments are stripped from the postings. Maybe you can

add it to the files database and people can download it from

there.

Kimber

--

Kimber

Vallejo, CA

hominid2@...

Southwest and California Representative

Pancreatitis Association, International

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Karyn,

afraid the questionaire didn't make it. Remember, all

attachments are stripped from the postings. Maybe you can

add it to the files database and people can download it from

there.

Kimber

--

Kimber

Vallejo, CA

hominid2@...

Southwest and California Representative

Pancreatitis Association, International

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Karyn,

afraid the questionaire didn't make it. Remember, all

attachments are stripped from the postings. Maybe you can

add it to the files database and people can download it from

there.

Kimber

--

Kimber

Vallejo, CA

hominid2@...

Southwest and California Representative

Pancreatitis Association, International

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  • 1 year later...
Guest guest

had it

since a teen, dxed in my 40’s. Dr. asked lots of questions on a questionnaire

and took bloodtests.

2

Aralen, Celebrex

Sarna

From: nursealso

Sent: Sunday, June 20, 2004 8:44

AM

To: lupies

Subject: Re: ?'s and Mojo

Here are the questions:

1. How where you tested for lupus and how long between your first symptoms to

diagnosis?

The first sign I had was in 1997 and the Doctor I worked for(an OB/GYN) looked

at a rash I had on my back that wouldn't go away, and told me that it looked

like a lupus rash and tested my ANA. It was 1/121 ? I can't remember but I

had a bx that came back inconclusive. So, I blew it off until I had another

rash or two. Then after a few years or so I started having alot of other sx's.

More test, then in May of 2002 I went to Vanderbilt in Nashville, and had another bx that was

positive. I was already seeing a Rhumy so he just continued my Plaqunil.

2. What medication are you taking strictly for lupus. I know most of these are

not actually " for " lupus, but I need the names of the ones that are

given to treat lupus, not the secondary illnesses associated with lupus. Also,

please mention what symptoms this medication is for and whether it is helping

you or

not.

The only Lupus medication is Plaqunil 200mg three times a day. So far the only

side effect has been increased acne. Not sure if it's from plaqunil or the DHEA

that I use for fatigue.

3. Skin lupus: please give me your input on medication

used.

I use a steriod cream called Clobetasol Propionate 0.05% It helps alot

with the rashes.

4. What alternative medicine are you using, for how long and with what result.

Not using

Mojo, I hope this helps some. I would like to see other responces as

well. This could be helpful for all of

us.

Helen

" The

LUPIES Store " Come check out our store...

http://www.cafepress.com/thelupies

" The LUPIES Web Page "

http://www.itzarion.com/lupusgroup.html

" The LUPIES online photo albums! "

Check out what your fellow Lupies look like...

http://www.picturetrail.com/lupies

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