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Hello everyone...not sure if I'm doing this right...but wanted to jump right

on in. I'm Anita (known online as ButterflyKisses) I'm a 45, married mother

of two, grandmother of one, and am owned by my two mini dach's...lol

After 8 years of pain, going from one doctor to the next...5 years ago I was

diagnosed with MS...but that didn't account for the daily pain...now I'm

sure I'm not the only one out there that has went through the following...

Q. Where do you hurt. A. Depends on the day, and what I'm doing. Q. How

bad is the pain A. Depends on the day, and what I'm doing. Q. Is it a

stabbing pain? A. Depends on the day and what I'm doing (see a pattern

forming??? LOL What other symptoms do you have...well let's see... Fatigue,

numbness, tingling, pin pricks, ... Okay where... UUHHH depends on the day

and what I'm doing! Now I've been playing this little cat and mouse game

for years! My family doctor cared, but had NO clue what was happening. I

ended up being on a Duragesic Patch (75 MG)... Which when taken with my

Neurontin and Elavil really did wonders! Was I pain free? Nope... But at

least I could function.

My world came crashing down last November. You see my family doctor got

sick and ended up having of all things...open heart surgery. She's been my

doctor for over 8 years, and knew all about my struggle. When she got ill,

I had to see another doctor in the same building, since you can't get refill

s on the Patch. This doctor told me it was all in my head, that I just like

getting high, and that it was over. I put on my last patch on the 2nd of

January... Now I'm not sure if you all know this...but...you are NEVER

suppose to go off that patch cold turkey, you're suppose to be weaned...not

me...oohhh nooo... And to be honest....for over a week...I went through the

worst withdraws... I went through hell!

The only GOOD thing about it... I finally was sent to the Cleveland Clinic

(no one within 200 miles wanted to touch me)... But I digress.... Finally .

..I have an answer...it's Fibro....which by the way was the FIRST thing my

family doctor thought it was....will the Cleveland Clinic treat me and help

me??? Not unless I go to Cleveland, stay for a month (in a motel room....)

and go to Physical Therapy, Group Therapy (long story..lol), Individual

Therapy, and various other therapies! Welllll.... Number one my husbands

insurance would have a cow! And we would go bankrupt between the motel cost

and food costs. So where does that leave me??? Struggling! All those

symptoms that had become bearable are now back with fury! Right now it's

impossible to do anything for any length of time. I never wanted to get

high.....I wanted to be able to function!!!

Okay, I'm sorry...I've screamed long enough...I don't want to push you all

away with my first post.... Someone, anyone...tell me there's hope out

there!!!

Thanks for listening...uuhh reading

Anita

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Hi Anita,

I want to welcome you to the group (and all the newbies I have missed).

You probably haven't seen my name a lot as I am having sight issues and having

trouble reading and replying to posts. I was able to magnify your letter (some

I can't or I lose the right side of the letter - go figure).

You're right about a lot of people going through several of things you have

mentioned, so don't feel bad at all " screaming " about them, as you say. We are

use to doctors and others who say we are drug seekers and don't have any reason

for wanting pain meds except to get high. It makes me want to growl just typing

it. GRRRRRR

I'm so sorry you lost the doctor who was so helpful. I haven't used the

patch, but can imagine the withdrawal was terrible. I read about this " cold

turkey " business a lot on here and don't know why the doctors don't wean people

when they have to know they should.

I hope you find a solution soon and I'm sorry you are in such pain. We are

here to support and comfort you so you have come to the right place.

Welcome,

Marti

" tubelover2u@... " wrote:

Hello everyone...not sure if I'm doing this right...but wanted to jump

right

on in. I'm Anita (known online as ButterflyKisses) I'm a 45, married mother

of two, grandmother of one, and am owned by my two mini dach's...lol

After 8 years of pain, going from one doctor to the next...5 years ago I was

diagnosed with MS...but that didn't account for the daily pain...now I'm

sure I'm not the only one out there that has went through the following...

Q. Where do you hurt. A. Depends on the day, and what I'm doing. Q. How

bad is the pain A. Depends on the day, and what I'm doing. Q. Is it a

stabbing pain? A. Depends on the day and what I'm doing (see a pattern

forming??? LOL What other symptoms do you have...well let's see... Fatigue,

numbness, tingling, pin pricks, ... Okay where... UUHHH depends on the day

and what I'm doing! Now I've been playing this little cat and mouse game

for years! My family doctor cared, but had NO clue what was happening. I

ended up being on a Duragesic Patch (75 MG)... Which when taken with my

Neurontin and Elavil really did wonders! Was I pain free? Nope... But at

least I could function.

My world came crashing down last November. You see my family doctor got

sick and ended up having of all things...open heart surgery. She's been my

doctor for over 8 years, and knew all about my struggle. When she got ill,

I had to see another doctor in the same building, since you can't get refill

s on the Patch. This doctor told me it was all in my head, that I just like

getting high, and that it was over. I put on my last patch on the 2nd of

January... Now I'm not sure if you all know this...but...you are NEVER

suppose to go off that patch cold turkey, you're suppose to be weaned...not

me...oohhh nooo... And to be honest....for over a week...I went through the

worst withdraws... I went through hell!

The only GOOD thing about it... I finally was sent to the Cleveland Clinic

(no one within 200 miles wanted to touch me)... But I digress.... Finally .

...I have an answer...it's Fibro....which by the way was the FIRST thing my

family doctor thought it was....will the Cleveland Clinic treat me and help

me??? Not unless I go to Cleveland, stay for a month (in a motel room....)

and go to Physical Therapy, Group Therapy (long story..lol), Individual

Therapy, and various other therapies! Welllll.... Number one my husbands

insurance would have a cow! And we would go bankrupt between the motel cost

and food costs. So where does that leave me??? Struggling! All those

symptoms that had become bearable are now back with fury! Right now it's

impossible to do anything for any length of time. I never wanted to get

high.....I wanted to be able to function!!!

Okay, I'm sorry...I've screamed long enough...I don't want to push you all

away with my first post.... Someone, anyone...tell me there's hope out

there!!!

Thanks for listening...uuhh reading

Anita

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Hi Anita - Is your wonderful doctor going to be able to continue with her

practice after recovering from the surgery? Keep searching for another good

doc. They are out there. Take care.

Jeanne in WI

> Hello everyone...not sure if I'm doing this right...but wanted to jump

> right on in. I'm Anita (known online as ButterflyKisses) I'm a 45,

> married mother of two, grandmother of one, and am owned by my two mini

> dach's...lol

>

> After 8 years of pain, going from one doctor to the next...5 years ago I

> was diagnosed with MS...but that didn't account for the daily pain...now

> I'm sure I'm not the only one out there that has went through the

> following...

> Q. Where do you hurt. A. Depends on the day, and what I'm doing. Q. How

> bad is the pain A. Depends on the day, and what I'm doing. Q. Is it a

> stabbing pain? A. Depends on the day and what I'm doing (see a pattern

> forming??? LOL What other symptoms do you have...well let's see...

> Fatigue, numbness, tingling, pin pricks, ... Okay where... UUHHH depends

> on the day

> and what I'm doing! Now I've been playing this little cat and mouse game

> for years! My family doctor cared, but had NO clue what was happening. I

> ended up being on a Duragesic Patch (75 MG)... Which when taken with my

> Neurontin and Elavil really did wonders! Was I pain free? Nope... But at

> least I could function.

>

> My world came crashing down last November. You see my family doctor got

> sick and ended up having of all things...open heart surgery. She's been

> my doctor for over 8 years, and knew all about my struggle. When she got

> ill, I had to see another doctor in the same building, since you can't get

> refills on the Patch. This doctor told me it was all in my head, that I

> just like getting high, and that it was over. I put on my last patch on

> the 2nd of

January... Now I'm not sure if you all know this...but...you are NEVER

suppose to go off that patch cold turkey, you're suppose to be weaned...not

me...oohhh nooo... And to be honest....for over a week...I went through the

worst withdraws... I went through hell!

>

> The only GOOD thing about it... I finally was sent to the Cleveland Clinic

> (no one within 200 miles wanted to touch me)... But I digress.... Finally

> .I have an answer...it's Fibro....which by the way was the FIRST thing my

> family doctor thought it was....will the Cleveland Clinic treat me and

> help me??? Not unless I go to Cleveland, stay for a month (in a motel

> room....)

and go to Physical Therapy, Group Therapy (long story..lol), Individual

Therapy, and various other therapies! Welllll.... Number one my husbands

> insurance would have a cow! And we would go bankrupt between the motel

> cost and food costs. So where does that leave me??? Struggling! All

> those

symptoms that had become bearable are now back with fury! Right now it's

impossible to do anything for any length of time. I never wanted to get

high.....I wanted to be able to function!!!

>

> Okay, I'm sorry...I've screamed long enough...I don't want to push you all

> away with my first post.... Someone, anyone...tell me there's hope out

> there!!!

>

> Thanks for listening...uuhh reading

>

> Anita

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Welcome, Anita!!

You're right on -- it's simultaneously " terrifying " and frustrating

that the dx, tx, good doctors, etc., are so hard to find, then when

you do find one and all is beginning to improve, even stabilize, one

tiny little pebble or grain of sand in the system fan blow it all

away. I think that is part of what makes this group so great -- no

matter where we are or how often we do or do not get out, we are able

to hear others' experiences and realize that we are not alone!!!! Now,

even the soap box NYT stirred up has to be enlarged!

For example, I know that for me, it's given me another reference point

to be able to tell my dr that I've started participating in this

group, and for example, I am not the only one (although the only one

he/d ever heard of) that had the reaction that I did to Lyrica.

Anyway, I am pretty new here too and I have already found it to have

very supportive benefits. Welcome!!

Cheryl M.

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