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Re: WHAT WOULD YOU DO?

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Hi Rach! I saw this on another list and wanted to respond. I don't

understand why you'd wait till March; is it that your insurance is

different form what we have in teh states? Not that it matters much.

LOL One thing that occurred to me: What if you had the lap band now

and the DS in MArch. Could you do this? Then your weight would be

lower and you'd be part way to goal and have a jump on things. I say

this assuming that the band does not alter stomach anatomy.

Of course you wouldn't want to lose so much that you were

disqualified!

Chris

> I have been offered gastric banding instead of bpd/ds I don't think

it would

> be nearly as good . what would you do? the 2 are options I have now

is have

> gastric banding or wait till March and have open bpd/ds I was going

to have

> it lap but I think I will have to change surgeons now. any advise

would be

> very helpful

> Love auzzie mate Rach

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  • 10 months later...

Lori, So glad to see you posting. Yes, we have all heard of Dr. T. He has

great info, but you must remember that even his writings are somewhat out of

date, so don't believe all that you read on the outlook of RP. WE all were

scared when we were first diagnosed and read all the terrible things. Just

remember that RP is treatable and you aren't going to die in 5-8 years.

I also had to wait a LONG time to get into a rheumy. I think this country is

really short on rheumy's. My syptoms were like yours when I was first dx.

So I was able to wait for an appt. One dr had a 6-8 month waiting list. I

would do what Dawn suggests and try some over the counter anti inflammatory

meds for now but PLEASE do not hesitate to get to a dr or ER if your symptoms

become worse. Red, swollen, thobbing ear, nose, ribs, or trouble breathing.

With every flare, damage can be done.

Don't be afraid to post any questions or problems to the group. There are a

lot of us here and always someone to listen.

Hang in there and be sure to keep us updated. Some people in the group tend

to worry a lot. LOL

hugs

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--- lori3kidsmom wrote:

> I would like to ask you guys your opinion on

> something. My ENT

> mentioned the possibility of RP to me. I went back

> to see my

> regular Dr. (Internal Medicine) and he suggested we

> set up an

> appointment with a Rheumatologist. He set up my

> appointment but the

> Rheumatologist can't see me until NOVEMBER!!! So

> here I am left

> wondering and worrying and reading all these nasty

> things about RP.

> My Dr. knows very little and just looks at me and

> says, 'I don't

> know!' Would you INSIST on seeing someone prior to

> November? The

> only symptom I have is occasional right ear pain, no

> swelling, no

> redness. It only lasts a day or two and then goes

> away. I have

> questions and I need to talk to someone with some

> medical experience

> in RP or I'm going to make myself nuts with worry!

> What would you do?

> Thanks!

>

> Lori, that is a very difficult one. Obviously for

your peace of mind it would be much better to see a

rheumy sooner, rather than later. On the other hand

if you make a fuss and get to see him earlier he might

well say something like 'well the symptoms are not

severe, so we cannot really tell' and you are no

better off!!! As relapsing polychondritis is

diagnosed by symptom rather than tests, they can't

always say. I think I might wait and see, and diary

ANY symptoms to take to your appointment. If anything

should happen between now and your appointment that

causes worry, get on the phone straight away!!!

Although untreated RP can cause damage, I believe it

is usually only when one is flaring that this happens.

If I am not being clear it is better to see the

doctor when you are actually having the problem, so he

can see it for himself.

Of course this is only my opinion!!!! . Most of us

had a long hard road before we got a diagnosis so we

do sympathise!! I know this is impossible, but try not

to worry. Even if it should be rp it is not a death

sentence. (Although I am sure most of us have gone

through a phase of thinking it is!!) Keep us in touch

with your progress.

Take care, love Liz

__________________________________________________

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Lori,

my name is chuck, i was diagnosed with RP a few years ago and the

diagnoses is scary, but as you get information about it, it tends to

lead off the craziness i was thinking about. mine started with the

red ears, and very very painful. i was finally diagnosed by a great

rhumy, and now i see a specialist in Boston who is in my opinion

awesome, DR.T. he understands what your going through and it is

treatable. i was on different meds for a while until i found the best

one to cotrol the sever flareups and i still work every day, as a

matter of a fact i work two jobs. i find that if i can keep my stress

level down it help me immensly. hope your doing better and keep your

chin up although you may feel like it, it is not the end of the world

and you WILL get through it...chuck...(cistn@...) if you have any

more questions as far as the long awated appointment, it is not

unusuall i think i waiting 4 months

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