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Hello,

I'm 37 and living in Louisville, KY US and was diagnosed late last

year after suffering begining just over a year ago. My rhumetoligist

sent me to another DR that specilizes in Fibro (Healing Options is

the name of the office) and we're still finding a balance.

Still have to have hydrocodone for the spikes in pain during the

day. Also taking Lyrica (300mg day) Cymbalta (60mg/d) and Ambien

(20mg/n) to sleep along with supplements for Adrenals, DHEA, vitamin

D, and testosterone. Also doing hydro therapy.

Started in my left hand, diagnosed as carpal tunnel til a nerve

induction test showed no narrowing of the bridge. Soon it was in my

right hand too, then feet, hips and back. Had several rounds of

cortizone pills til the diagnosis... horrible side effects and

eventually little effect/duration of pain management.

Dr says it's the stress/trauma that started it all along with some

other triggers. 'Severly' sensitive in 17 of the 18 points. Though

the nice (young) assistant/RN feels I'll be 100% back to normal...

I'm not so sure, but it's no where near as bad now as it was (could

barely walk for a couple of months).

Side effects I'm dealing with is coated tounge (everything just

doesn't taste right) and some loss of smell. Strange body odor/sweat

and that's about it.

Off to the Dr here in a few hours. Now have TMJ with it (clenching

teeth because of the pain) so have to figure out how to get that

helped. Also to ask about disability.

Have aunt diagnosed with it (and supposedly every other person in her

office as well) who calls it 'normal aches and pains of living' and

that I should 'get over it'. Only sister felt the same way about it

til she saw how bad it could be. Mum diagnosed with rhumetoid

arthritis (caught it early in the process so prevented a lot of

damage to her system) a year before so she totally understands.

Looking forward to other perspectives about how to deal with it.

This actually took me about 50 mins to write and post. Can't stick

at the keyboard long on even medium days before things start feeling

like I'm being stabbed into the keyboard or desk.

*Wave*

Tom

P.S. Can't get away without mentioning I love kilts, and my 2 boys

and wifey. :) So this was more of the medical intro and not the

craziness I live with.

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>

> Hello,

>

> I'm 37 and living in Louisville, KY

Hi Tom, Welcome to our group of sickies!!! I think you will like it

here, lots of info and support.

/Mi

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> >

> > Hello,

> >

> > I'm 37 and living in Louisville, KY

>

>

> Hi Tom, Welcome to our group of sickies!!! I think you will like it

> here, lots of info and support.

> /Mi

>Hello I am from Buffalo just wanted to say hello and welcome

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Hello Missy,

I am just getting started answering to the messages, they were right though, the

number of mail is outstanding ! Hope to talk to you soon.

Pam

missy8632 wrote: Hello,

I am new to the board as well.

---------------------------------

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Hi Missy - welcome :) Jump right in - the water's fine! LOL

missy8632 wrote: Hello,

I am new to the board as well.

------------------------------------

1. While it is wonderful to share our experiences with everyone on the list as

to what treatments do and don't work for us, pls always check with your dr. Some

treatments are dangerous when given along with other meds as well as to certain

health conditions or just dangerous in general.

2. If you are in a difficult situation (doesn't matter what it is) pls don't be

afraid to ask for help. It is the first step to trying to make that situation

better.

3. To unsubscribe the e-mail is:

Fibromyalgia_Support_Group-unsubscribe

4. Also, it is not uncommon for more than one member to be feeling bad at the

same time when it comes to flares and b/c of that potentially take something

another member says the wrong way. And that includes the things that one member

may find funny (even if it's laughing at fibro itself) even though we who deal

with illness whether one such as fibro or multiple illnesses try to keep a sense

of humor.

5. Pls let's be gentle with each other, and if you are having a bad day pls let

us know so that we can do our best to offer our support.

Have a nice day everyone.

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Re: Re: Saluations

Hi Missy - welcome :) Jump right in - the water's fine! LOL

missy8632 wrote: Hello,

I am new to the board as well.

Hi Missy, Welcome 2 group. Hope it helps. Jodi M.

------------------------------------

1. While it is wonderful to share our experiences with everyone on the list as

to what treatments do and don't work for us, pls always check with your dr. Some

treatments are dangerous when given along with other meds as well as to certain

health conditions or just dangerous in general.

2. If you are in a difficult situation (doesn't matter what it is) pls don't be

afraid to ask for help. It is the first step to trying to make that situation

better.

3. To unsubscribe the e-mail is:

Fibromyalgia_Support_Group-unsubscribe

4. Also, it is not uncommon for more than one member to be feeling bad at the

same time when it comes to flares and b/c of that potentially take something

another member says the wrong way. And that includes the things that one member

may find funny (even if it's laughing at fibro itself) even though we who deal

with illness whether one such as fibro or multiple illnesses try to keep a sense

of humor.

5. Pls let's be gentle with each other, and if you are having a bad day pls let

us know so that we can do our best to offer our support.

Have a nice day everyone.

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