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--- Hi lonnie-

I'm new too. Surprised your GP diagnosed you--- I've been to several

doctors, had several x-rays, MRI's and work before a

Rhuemitologist (sp?) told me I had FM.

He ha sput me on Neurontin, a anti-seizure medication that is

supposed to have a side effect that helps reduce pain. The way he

explained it to me was that it's like you're hardwired wrond. There

is often a chemical imbalance which is why many people with FM also

usually have been on anti-anxiety meds, serontin lifters like

Lexepro, and anti-depressants. He says the difference is that these

signals come from the spine instead of the brain. But they register

pain that should be 0-1-2 as a 10,20 (100 if you were to ask me)

I am new to the Neurontin so I can't say if it works or not. My aunt

has been diagnosed with it for several years now and has a pretty

well working set of she takes. I just have that list in front

of me. Email me if you are interested. Also, go to a specialist

(arthritis usually I think) if you don't get the desired results from

your GP..........

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Dear Lorrie,

You said you were thinking about trying to go back to work... are you on

SSD right now? They have a back to work program that lets you try it

for 9 months, and if during that time, you find you can't work, your

benefits will be reinstated with no questions asked. My problem is that

I can never predict when I am going to have a good pain day and when it

is going to be a bad one. Weather plays a huge part, and who is going

to hire someone who says that she cannot come in if the weather is cold,

damp or rainy?? If I knew ahead that I could only work every other day

or something, part time work might be an option for me. But there is no

rhyme or reason to my pain. I am feeling pretty good today, at least

painwise, even though I am under tremendous stress with my surgery on

the 12th fast approaching. But for several days before today, I was

having a major flare. So I am not willing to risk my disability by

trying to work when I know in my heart of hearts that I really am not

able to. I believe that SSD also has a program where you can work part

time and draw partial SSD benefits, but I could be wrong on that. Best

bet would be to call SS.

hugs and prayers,

Sharon - Memphis, TN

Faith...with it, miracles *CAN* and *DO* happen!

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Be very careful about this. I had no flack from SS until I told them I wanted

to try to go back to work. All of a sudden, I was under investigation to make

sure I was still disabled. Even though their doctors said that my condition

hadn't changed, they still kicked me off of SSDI & told me I owed them $13,000+

in overpayments.

in Jax

<><><><><>

Re: new here

Dear Lorrie,

You said you were thinking about trying to go back to work... are you on

SSD right now? They have a back to work program that lets you try it

for 9 months, and if during that time, you find you can't work, your

benefits will be reinstated with no questions asked. ...

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Guest guest

Be very careful about this. I had no flack from SS until I told them I wanted

to try to go back to work. All of a sudden, I was under investigation to make

sure I was still disabled. Even though their doctors said that my condition

hadn't changed, they still kicked me off of SSDI & told me I owed them $13,000+

in overpayments.

in Jax

<><><><><>

Re: new here

Dear Lorrie,

You said you were thinking about trying to go back to work... are you on

SSD right now? They have a back to work program that lets you try it

for 9 months, and if during that time, you find you can't work, your

benefits will be reinstated with no questions asked. ...

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  • 1 month later...
Guest guest

Hi Keri,

Welcome to the group! I am sort of behind in reading posts. Like two days

behind. Every since I wrecked my truck last Sat. I am running a couple days

behind. Oh well Ill catch up eventually. Maybe. Nice to meet ya! Write

anytime. G.

new here

Hi my name is Keri age 32 and not only am I the mother of 4 children

ages 15, 13, 12 and 10....two of whom are autistic...I was jsut

diagnosed with fibromyalgia less than 3 months ago. The doctor put me

on Relefen and tramadol...after a month I decided that they really do

not help me; so i am currently " eating " 600-800mg of Ibroprofen! (An

over the counter med that I cannot live without! :)! At the same time

I was diagnosed with Fibro. I was also diagnosed with the Epstein

Barr Virus and Chronic Fatigue....Was wondering if anyone on here

shares any of the same diagnosis?? I look forward to getting to know

everyone and hopfully learning everything that I can from evveryone!

I also look forward to hopefully being able to contribute to this

list and being here for others! Take care everyone and hope to chat

soon!

Love

Keri

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