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Sherri,

Welcome to the group. So sorry to hear your depression is so bad. The

only advice I can give is to keep trying different doctors(I know,

hard when you don't have insurance), and eventually you will find one

who is sympathetic and helpful. Also, keep trying different

medications and supplements and therapies. What works for one person

doesn't necessarily work for another. I'm sure everyone here will be

willing to offer advice on alternative meds to try. I'm currently

trying drug therapy pretty much for the first time. I tried for years

to treat my fibro with vitamins and supplements and herbs, and it

just didn't help nearly enough. So a lot of these drugs are new to

me. I'm learning. :-)

Take care,

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Sherri,

Welcome to the group. So sorry to hear your depression is so bad. The

only advice I can give is to keep trying different doctors(I know,

hard when you don't have insurance), and eventually you will find one

who is sympathetic and helpful. Also, keep trying different

medications and supplements and therapies. What works for one person

doesn't necessarily work for another. I'm sure everyone here will be

willing to offer advice on alternative meds to try. I'm currently

trying drug therapy pretty much for the first time. I tried for years

to treat my fibro with vitamins and supplements and herbs, and it

just didn't help nearly enough. So a lot of these drugs are new to

me. I'm learning. :-)

Take care,

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Hello all! I have been reading all your messages the past few days and

decided it was time to jump right in. (oh,oh bad choice of words, LOL!)

My name is Sherri and I am 40 yrs old. I was diagnosed with CFS in 2000 but

think I've been suffering since 1993. Back then, I just thought it was

depression. I had lost my sister who was 9 months pregnant in a car

accident. We were in the military at the time (and I was healthy) We were

2000 miles away when it happened. Had to get on a plane and come back home

to Indiana. It was the worst time in my life then. Anyway, we got out of

the service in March of 93 and moved home to try and take care of the 5 kids

she left behind.

In 1996 I got pregnant and that is when alot of my physical problems

started. Thought I was gonna die! Had so many problems so when I had my

son I thought I was going to get better and never did. Even after having my

baby (which is another story in itself) I was suffering from deep

depression, tired all the time (extremely). I cried almost all day and

night. Couldn't figure out why I felt this way because I had this beautiful

baby boy. In the years before I had him, I was crying and thought about

dying all the time. I would actually pray to God everynight before I went

to bed asking him to take me. I couldn't stand the thought of facing one

more day. Thought my kids would be better off without me.

In 1997 I finally went to another doctor and she diagnosed me with sever

clinical depression and put me on prozac. I also was hypothyroid at the

time and helped me with that. So far, my thyroid is working okay. Just had

it tested a couple weeks ago. The prozac worked some, at least I wasn't

crying all the time. I was still in pain (meaning sadness) but could at

least cope with the daily things in life. Decided to try and get a job in

2000. Was a cashier at Wal-mart. Started out just a few hours a week

because of being tired. Really thought working would help with that. The

last day that I worked there was on a Saturday and I had worked a couple of

hours and suddenly got very tired and sick. Went home at 2 p.m. and slept

the rest of the day and night, got up Sun morning for about 15 min and went

back to bed until Monday. Got up and made appt to see doctor. She

diagnosed me with CFS but didn't do anything except up my prozac. I had to

quit work because I couldn't cope, which was only a couple months after I

started.

This past January I woke up with a really sore and stiff neck. Thought it

would go away so waited a few days. It got worse so went to a chiropractor.

He said that my neck was curved the wrong way and my back went at an angle.

I had 3 treatments a week for 6 weeks and was still getting worse. Went to

my reg doc and she thought it was a pinched nerve so gave me Skelaxin and

saw me the next week. Then she decided to put me on prednisone for 15 days.

I was sicker than a dog and it seems to me that is when my whole entire body

went bad. Now, I have all of the 18 tender points, can hardly walk. Can't

do my regular household chores. Getting severe fibro fog. The whole

shebang. I didn't realize that FMS could come on so fast????

I do not have insurance so we decided to do two tests last week. One was my

thyroid and the other was an ANA test which both came back okay. Thyroid

was normal and the ANA was negative. She also changed me to Effexor XR (In

2001) and gave me Zanaflex and Celebrex. Celebrex isn't doing any good.

Neither are the relaxers. I called her back yesterday to see what tests we

could do next and she said that we could do all the blood tests in the world

and I would still have to see a Rheumy so she is done with me now. Just

wants to forget about me and send me to the RH.

I am soooo confused and aggrivated. Dr also told me a month ago to try for

disability. I called the SSS office and they told me since I haven't worked

(oh, they haven't raised kids?) in the past ten years I was out of luck. I

have tried and tried to get insurance but everyone turns me down. So now I

am kinda stuck.

Thanks for listening and sorry this was soooo long. Hope to get to know you

all better. I may not post that much because of the depression but will at

least try.

Cyberhugs,

Sherri

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Sherri,

welcome - I think you have reached a site in which many can relate to you.

Don't give up !!!!

And for disability - I am fighting Wal-Mart & Hartford for simple short term.

( I say fight - but truely I don't have much of that in me anymore)

As for SS - there is such a thing as SSI. This is for those who have not paid in

enough SS from a public job. They don't consider housewife and mother as a job -

but personally I think it is the most important one in the world !!!!! Check out

the site for posts on SS disability - there are several good ones with useful

information that might help you.

gentle hugs,

Cinda

New here also/long

Hello all! I have been reading all your messages the past few days and

decided it was time to jump right in. (oh,oh bad choice of words, LOL!)

My name is Sherri and I am 40 yrs old. I was diagnosed with CFS in 2000 but

think I've been suffering since 1993. Back then, I just thought it was

depression. I had lost my sister who was 9 months pregnant in a car

accident. We were in the military at the time (and I was healthy) We were

2000 miles away when it happened. Had to get on a plane and come back home

to Indiana. It was the worst time in my life then. Anyway, we got out of

the service in March of 93 and moved home to try and take care of the 5 kids

she left behind.

In 1996 I got pregnant and that is when alot of my physical problems

started. Thought I was gonna die! Had so many problems so when I had my

son I thought I was going to get better and never did. Even after having my

baby (which is another story in itself) I was suffering from deep

depression, tired all the time (extremely). I cried almost all day and

night. Couldn't figure out why I felt this way because I had this beautiful

baby boy. In the years before I had him, I was crying and thought about

dying all the time. I would actually pray to God everynight before I went

to bed asking him to take me. I couldn't stand the thought of facing one

more day. Thought my kids would be better off without me.

In 1997 I finally went to another doctor and she diagnosed me with sever

clinical depression and put me on prozac. I also was hypothyroid at the

time and helped me with that. So far, my thyroid is working okay. Just had

it tested a couple weeks ago. The prozac worked some, at least I wasn't

crying all the time. I was still in pain (meaning sadness) but could at

least cope with the daily things in life. Decided to try and get a job in

2000. Was a cashier at Wal-mart. Started out just a few hours a week

because of being tired. Really thought working would help with that. The

last day that I worked there was on a Saturday and I had worked a couple of

hours and suddenly got very tired and sick. Went home at 2 p.m. and slept

the rest of the day and night, got up Sun morning for about 15 min and went

back to bed until Monday. Got up and made appt to see doctor. She

diagnosed me with CFS but didn't do anything except up my prozac. I had to

quit work because I couldn't cope, which was only a couple months after I

started.

This past January I woke up with a really sore and stiff neck. Thought it

would go away so waited a few days. It got worse so went to a chiropractor.

He said that my neck was curved the wrong way and my back went at an angle.

I had 3 treatments a week for 6 weeks and was still getting worse. Went to

my reg doc and she thought it was a pinched nerve so gave me Skelaxin and

saw me the next week. Then she decided to put me on prednisone for 15 days.

I was sicker than a dog and it seems to me that is when my whole entire body

went bad. Now, I have all of the 18 tender points, can hardly walk. Can't

do my regular household chores. Getting severe fibro fog. The whole

shebang. I didn't realize that FMS could come on so fast????

I do not have insurance so we decided to do two tests last week. One was my

thyroid and the other was an ANA test which both came back okay. Thyroid

was normal and the ANA was negative. She also changed me to Effexor XR (In

2001) and gave me Zanaflex and Celebrex. Celebrex isn't doing any good.

Neither are the relaxers. I called her back yesterday to see what tests we

could do next and she said that we could do all the blood tests in the world

and I would still have to see a Rheumy so she is done with me now. Just

wants to forget about me and send me to the RH.

I am soooo confused and aggrivated. Dr also told me a month ago to try for

disability. I called the SSS office and they told me since I haven't worked

(oh, they haven't raised kids?) in the past ten years I was out of luck. I

have tried and tried to get insurance but everyone turns me down. So now I

am kinda stuck.

Thanks for listening and sorry this was soooo long. Hope to get to know you

all better. I may not post that much because of the depression but will at

least try.

Cyberhugs,

Sherri

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Guest guest

Sherri,

welcome - I think you have reached a site in which many can relate to you.

Don't give up !!!!

And for disability - I am fighting Wal-Mart & Hartford for simple short term.

( I say fight - but truely I don't have much of that in me anymore)

As for SS - there is such a thing as SSI. This is for those who have not paid in

enough SS from a public job. They don't consider housewife and mother as a job -

but personally I think it is the most important one in the world !!!!! Check out

the site for posts on SS disability - there are several good ones with useful

information that might help you.

gentle hugs,

Cinda

New here also/long

Hello all! I have been reading all your messages the past few days and

decided it was time to jump right in. (oh,oh bad choice of words, LOL!)

My name is Sherri and I am 40 yrs old. I was diagnosed with CFS in 2000 but

think I've been suffering since 1993. Back then, I just thought it was

depression. I had lost my sister who was 9 months pregnant in a car

accident. We were in the military at the time (and I was healthy) We were

2000 miles away when it happened. Had to get on a plane and come back home

to Indiana. It was the worst time in my life then. Anyway, we got out of

the service in March of 93 and moved home to try and take care of the 5 kids

she left behind.

In 1996 I got pregnant and that is when alot of my physical problems

started. Thought I was gonna die! Had so many problems so when I had my

son I thought I was going to get better and never did. Even after having my

baby (which is another story in itself) I was suffering from deep

depression, tired all the time (extremely). I cried almost all day and

night. Couldn't figure out why I felt this way because I had this beautiful

baby boy. In the years before I had him, I was crying and thought about

dying all the time. I would actually pray to God everynight before I went

to bed asking him to take me. I couldn't stand the thought of facing one

more day. Thought my kids would be better off without me.

In 1997 I finally went to another doctor and she diagnosed me with sever

clinical depression and put me on prozac. I also was hypothyroid at the

time and helped me with that. So far, my thyroid is working okay. Just had

it tested a couple weeks ago. The prozac worked some, at least I wasn't

crying all the time. I was still in pain (meaning sadness) but could at

least cope with the daily things in life. Decided to try and get a job in

2000. Was a cashier at Wal-mart. Started out just a few hours a week

because of being tired. Really thought working would help with that. The

last day that I worked there was on a Saturday and I had worked a couple of

hours and suddenly got very tired and sick. Went home at 2 p.m. and slept

the rest of the day and night, got up Sun morning for about 15 min and went

back to bed until Monday. Got up and made appt to see doctor. She

diagnosed me with CFS but didn't do anything except up my prozac. I had to

quit work because I couldn't cope, which was only a couple months after I

started.

This past January I woke up with a really sore and stiff neck. Thought it

would go away so waited a few days. It got worse so went to a chiropractor.

He said that my neck was curved the wrong way and my back went at an angle.

I had 3 treatments a week for 6 weeks and was still getting worse. Went to

my reg doc and she thought it was a pinched nerve so gave me Skelaxin and

saw me the next week. Then she decided to put me on prednisone for 15 days.

I was sicker than a dog and it seems to me that is when my whole entire body

went bad. Now, I have all of the 18 tender points, can hardly walk. Can't

do my regular household chores. Getting severe fibro fog. The whole

shebang. I didn't realize that FMS could come on so fast????

I do not have insurance so we decided to do two tests last week. One was my

thyroid and the other was an ANA test which both came back okay. Thyroid

was normal and the ANA was negative. She also changed me to Effexor XR (In

2001) and gave me Zanaflex and Celebrex. Celebrex isn't doing any good.

Neither are the relaxers. I called her back yesterday to see what tests we

could do next and she said that we could do all the blood tests in the world

and I would still have to see a Rheumy so she is done with me now. Just

wants to forget about me and send me to the RH.

I am soooo confused and aggrivated. Dr also told me a month ago to try for

disability. I called the SSS office and they told me since I haven't worked

(oh, they haven't raised kids?) in the past ten years I was out of luck. I

have tried and tried to get insurance but everyone turns me down. So now I

am kinda stuck.

Thanks for listening and sorry this was soooo long. Hope to get to know you

all better. I may not post that much because of the depression but will at

least try.

Cyberhugs,

Sherri

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Guest guest

Big cyber hug to you, Sherri. SSI/Disability is one of my sore spots (pun

intended). I have been trying to avoid filing, but I don't think I really have

a choice at this point. Sounds to me as if the stress you were under really

kicked things off. If you are in Indiana, there are several state programs that

might assist you with medical help. I've recently lost my job and am scrambling

amongst my family for my COBRA premiums each month, but I know I could not

survive without insurance. Even if I qualify for Disability immediately, it's

still a two year wait for Medicare and, after working in health insurance for

nearly 15 years, I can honestly say Medicare stinks.

I really hope things work out for you. Please take care!

~ :-D

New here also/long

Hello all! I have been reading all your messages the past few days and

decided it was time to jump right in. (oh,oh bad choice of words, LOL!)

My name is Sherri and I am 40 yrs old. I was diagnosed with CFS in 2000 but

think I've been suffering since 1993. Back then, I just thought it was

depression. I had lost my sister who was 9 months pregnant in a car

accident. We were in the military at the time (and I was healthy) We were

2000 miles away when it happened. Had to get on a plane and come back home

to Indiana. It was the worst time in my life then. Anyway, we got out of

the service in March of 93 and moved home to try and take care of the 5 kids

she left behind.

In 1996 I got pregnant and that is when alot of my physical problems

started. Thought I was gonna die! Had so many problems so when I had my

son I thought I was going to get better and never did. Even after having my

baby (which is another story in itself) I was suffering from deep

depression, tired all the time (extremely). I cried almost all day and

night. Couldn't figure out why I felt this way because I had this beautiful

baby boy. In the years before I had him, I was crying and thought about

dying all the time. I would actually pray to God everynight before I went

to bed asking him to take me. I couldn't stand the thought of facing one

more day. Thought my kids would be better off without me.

In 1997 I finally went to another doctor and she diagnosed me with sever

clinical depression and put me on prozac. I also was hypothyroid at the

time and helped me with that. So far, my thyroid is working okay. Just had

it tested a couple weeks ago. The prozac worked some, at least I wasn't

crying all the time. I was still in pain (meaning sadness) but could at

least cope with the daily things in life. Decided to try and get a job in

2000. Was a cashier at Wal-mart. Started out just a few hours a week

because of being tired. Really thought working would help with that. The

last day that I worked there was on a Saturday and I had worked a couple of

hours and suddenly got very tired and sick. Went home at 2 p.m. and slept

the rest of the day and night, got up Sun morning for about 15 min and went

back to bed until Monday. Got up and made appt to see doctor. She

diagnosed me with CFS but didn't do anything except up my prozac. I had to

quit work because I couldn't cope, which was only a couple months after I

started.

This past January I woke up with a really sore and stiff neck. Thought it

would go away so waited a few days. It got worse so went to a chiropractor.

He said that my neck was curved the wrong way and my back went at an angle.

I had 3 treatments a week for 6 weeks and was still getting worse. Went to

my reg doc and she thought it was a pinched nerve so gave me Skelaxin and

saw me the next week. Then she decided to put me on prednisone for 15 days.

I was sicker than a dog and it seems to me that is when my whole entire body

went bad. Now, I have all of the 18 tender points, can hardly walk. Can't

do my regular household chores. Getting severe fibro fog. The whole

shebang. I didn't realize that FMS could come on so fast????

I do not have insurance so we decided to do two tests last week. One was my

thyroid and the other was an ANA test which both came back okay. Thyroid

was normal and the ANA was negative. She also changed me to Effexor XR (In

2001) and gave me Zanaflex and Celebrex. Celebrex isn't doing any good.

Neither are the relaxers. I called her back yesterday to see what tests we

could do next and she said that we could do all the blood tests in the world

and I would still have to see a Rheumy so she is done with me now. Just

wants to forget about me and send me to the RH.

I am soooo confused and aggrivated. Dr also told me a month ago to try for

disability. I called the SSS office and they told me since I haven't worked

(oh, they haven't raised kids?) in the past ten years I was out of luck. I

have tried and tried to get insurance but everyone turns me down. So now I

am kinda stuck.

Thanks for listening and sorry this was soooo long. Hope to get to know you

all better. I may not post that much because of the depression but will at

least try.

Cyberhugs,

Sherri

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Guest guest

Big cyber hug to you, Sherri. SSI/Disability is one of my sore spots (pun

intended). I have been trying to avoid filing, but I don't think I really have

a choice at this point. Sounds to me as if the stress you were under really

kicked things off. If you are in Indiana, there are several state programs that

might assist you with medical help. I've recently lost my job and am scrambling

amongst my family for my COBRA premiums each month, but I know I could not

survive without insurance. Even if I qualify for Disability immediately, it's

still a two year wait for Medicare and, after working in health insurance for

nearly 15 years, I can honestly say Medicare stinks.

I really hope things work out for you. Please take care!

~ :-D

New here also/long

Hello all! I have been reading all your messages the past few days and

decided it was time to jump right in. (oh,oh bad choice of words, LOL!)

My name is Sherri and I am 40 yrs old. I was diagnosed with CFS in 2000 but

think I've been suffering since 1993. Back then, I just thought it was

depression. I had lost my sister who was 9 months pregnant in a car

accident. We were in the military at the time (and I was healthy) We were

2000 miles away when it happened. Had to get on a plane and come back home

to Indiana. It was the worst time in my life then. Anyway, we got out of

the service in March of 93 and moved home to try and take care of the 5 kids

she left behind.

In 1996 I got pregnant and that is when alot of my physical problems

started. Thought I was gonna die! Had so many problems so when I had my

son I thought I was going to get better and never did. Even after having my

baby (which is another story in itself) I was suffering from deep

depression, tired all the time (extremely). I cried almost all day and

night. Couldn't figure out why I felt this way because I had this beautiful

baby boy. In the years before I had him, I was crying and thought about

dying all the time. I would actually pray to God everynight before I went

to bed asking him to take me. I couldn't stand the thought of facing one

more day. Thought my kids would be better off without me.

In 1997 I finally went to another doctor and she diagnosed me with sever

clinical depression and put me on prozac. I also was hypothyroid at the

time and helped me with that. So far, my thyroid is working okay. Just had

it tested a couple weeks ago. The prozac worked some, at least I wasn't

crying all the time. I was still in pain (meaning sadness) but could at

least cope with the daily things in life. Decided to try and get a job in

2000. Was a cashier at Wal-mart. Started out just a few hours a week

because of being tired. Really thought working would help with that. The

last day that I worked there was on a Saturday and I had worked a couple of

hours and suddenly got very tired and sick. Went home at 2 p.m. and slept

the rest of the day and night, got up Sun morning for about 15 min and went

back to bed until Monday. Got up and made appt to see doctor. She

diagnosed me with CFS but didn't do anything except up my prozac. I had to

quit work because I couldn't cope, which was only a couple months after I

started.

This past January I woke up with a really sore and stiff neck. Thought it

would go away so waited a few days. It got worse so went to a chiropractor.

He said that my neck was curved the wrong way and my back went at an angle.

I had 3 treatments a week for 6 weeks and was still getting worse. Went to

my reg doc and she thought it was a pinched nerve so gave me Skelaxin and

saw me the next week. Then she decided to put me on prednisone for 15 days.

I was sicker than a dog and it seems to me that is when my whole entire body

went bad. Now, I have all of the 18 tender points, can hardly walk. Can't

do my regular household chores. Getting severe fibro fog. The whole

shebang. I didn't realize that FMS could come on so fast????

I do not have insurance so we decided to do two tests last week. One was my

thyroid and the other was an ANA test which both came back okay. Thyroid

was normal and the ANA was negative. She also changed me to Effexor XR (In

2001) and gave me Zanaflex and Celebrex. Celebrex isn't doing any good.

Neither are the relaxers. I called her back yesterday to see what tests we

could do next and she said that we could do all the blood tests in the world

and I would still have to see a Rheumy so she is done with me now. Just

wants to forget about me and send me to the RH.

I am soooo confused and aggrivated. Dr also told me a month ago to try for

disability. I called the SSS office and they told me since I haven't worked

(oh, they haven't raised kids?) in the past ten years I was out of luck. I

have tried and tried to get insurance but everyone turns me down. So now I

am kinda stuck.

Thanks for listening and sorry this was soooo long. Hope to get to know you

all better. I may not post that much because of the depression but will at

least try.

Cyberhugs,

Sherri

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Guest guest

Welcome, Sherri to our group. I think that when you find out that you are

not alone and that many of us have gone through a lot of the things that you

are going through will help you to cope. In my mind, one of the hardest

thing about fibro.

Our fibromyalgia family are very caring, loving and very supportive. If you

feel that you need to vent or you are going to start screaming, vent here.

We will listen and you will know that we do care about you.

Take care,

Irene

Books may well be the only true magic

Alice Hoffman

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Guest guest

>disability. I called the SSS office and they told me since I haven't

>worked

>(oh, they haven't raised kids?) in the past ten years I was out of luck. I

>have tried and tried to get insurance but everyone turns me down. So now I

>am kinda stuck.

WOAH!!! Stop right there and go BACK to the SS office... Tell them you want

to apply for SSI.. There are *two* programs... SS Disability for those who

have enough quarters of work and SSI for those who don't... one is

income-based, one is not!!

What state are you in? They cannot deny you the right to apply!!!

Go to ssa.gov and check it out...

Kit

_________________________________________________________________

MSN Photos is the easiest way to share and print your photos:

http://photos.msn.com/support/worldwide.aspx

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Guest guest

>disability. I called the SSS office and they told me since I haven't

>worked

>(oh, they haven't raised kids?) in the past ten years I was out of luck. I

>have tried and tried to get insurance but everyone turns me down. So now I

>am kinda stuck.

WOAH!!! Stop right there and go BACK to the SS office... Tell them you want

to apply for SSI.. There are *two* programs... SS Disability for those who

have enough quarters of work and SSI for those who don't... one is

income-based, one is not!!

What state are you in? They cannot deny you the right to apply!!!

Go to ssa.gov and check it out...

Kit

_________________________________________________________________

MSN Photos is the easiest way to share and print your photos:

http://photos.msn.com/support/worldwide.aspx

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Share on other sites

Guest guest

>disability. I called the SSS office and they told me since I haven't

>worked

>(oh, they haven't raised kids?) in the past ten years I was out of luck. I

>have tried and tried to get insurance but everyone turns me down. So now I

>am kinda stuck.

WOAH!!! Stop right there and go BACK to the SS office... Tell them you want

to apply for SSI.. There are *two* programs... SS Disability for those who

have enough quarters of work and SSI for those who don't... one is

income-based, one is not!!

What state are you in? They cannot deny you the right to apply!!!

Go to ssa.gov and check it out...

Kit

_________________________________________________________________

MSN Photos is the easiest way to share and print your photos:

http://photos.msn.com/support/worldwide.aspx

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