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With what lumbar spondylosis is does this mean I'm going to get worse?

Does this mean I'll just keep degenerating and being in more pain? How

fast will all this occur? Because, I don't know if I can handle more

pain which will only bring more depression. I know that I have four

discs so far that are affected and I also have a lot of weakness on my

right side mainly. How do I respond, react, or handle any of this.

Except to accept my lot in life and bawl my eyes out.

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Oh Sweetie, No it doesn't necessarily mean any of those things. A

Rhuematologist can give you a script for medication that helps rebuild

cartiledge and exercizes that strengthen the muscles on either side of your

spine. It doesn't sound like the pain could get any worse. Just try to deal

with the pain you're already in and try not to worry about the future right now.

Taking it day by day is the only way any of us can go right now.

Keep writing into this site and we will support you in anything you are going

through. A good crying jag can do you a lot of good and get everything out, but

then it will start to make you worse. All that tension and stress will start to

make you hurt more - and mess up your sinuses.

I've definitely been depressed over the pain and brain fog of fibromyalgia,

and other things that I have, so I can empathize with you. 12 years ago I had

two discs fused in my neck, c1 and c2 and have done fine with it. They had

deteriorated and were pressing against nerves and were very painful.

I hope you have someone or someones who can give you the gentle hugs you need.

You will get through this and it will get better. And you have friends here

who will listen.

Take care,

Marti

lyriczada wrote:

With what lumbar spondylosis is does this mean I'm going to get worse?

Does this mean I'll just keep degenerating and being in more pain? How

fast will all this occur? Because, I don't know if I can handle more

pain which will only bring more depression. I know that I have four

discs so far that are affected and I also have a lot of weakness on my

right side mainly. How do I respond, react, or handle any of this.

Except to accept my lot in life and bawl my eyes out.

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

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In a message dated 12/9/2007 6:01:45 P.M. Pacific Standard Time,

lisaannbogue@... writes:

lumbar spondylosis

This is what I found on it...go to this website...

_http://www.myelectronicmd.com/get_reference.php?Id=1263_

(http://www.myelectronicmd.com/get_reference.php?Id=1263)

Love and gentle hugs,

Debi/So. Cal.-54

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I certainly hope there is something that can be done. A surgery? My heart is

with you. I read a little about spondylosis.... what I basically understand is

that it is deterioration of the areas between the bones of the spine which can

cause the nerves and possibly the spinal chord to become compressed between the

bones. This obviously causes great amounts of pain in some instances. It was

also described as " spinal arthritis " in one article I looked at.

love,

Debra V.

lyriczada wrote:

With what lumbar spondylosis is does this mean I'm going to get worse?

Does this mean I'll just keep degenerating and being in more pain? How

fast will all this occur? Because, I don't know if I can handle more

pain which will only bring more depression. I know that I have four

discs so far that are affected and I also have a lot of weakness on my

right side mainly. How do I respond, react, or handle any of this.

Except to accept my lot in life and bawl my eyes out.

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

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In a message dated 12/10/2007 3:37:46 A.M. Pacific Standard Time,

raburtongdyr@... writes:

Anyone ever feel like giving up!

I do every day, but my 4 grandkids (the ones that I live with) give me

reason not to give up and to keep fighting.

Love and gentle hugs,

Debi/So. Cal.-54

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Be a good e-mail buddy, and ALWAYS

protect your friends from email address harvesters which can lead to more

Spam, unwanted mail, and even viruses.

Copy and paste into a new email and place parenthesis around the addresses.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

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Anyone ever feel like giving up!

Sent from my Verizon Wireless BlackBerry

Re: When do I stop crying

In a message dated 12/9/2007 6:01:45 P.M. Pacific Standard Time,

lisaannbogue@ <mailto:lisaannbogue%40verizon.net> verizon.net writes:

lumbar spondylosis

This is what I found on it...go to this website...

_http://www.myelectr <http://www.myelectronicmd.com/get_reference.php?Id=1263_>

onicmd.com/get_reference.php?Id=1263_

(http://www.myelectr <http://www.myelectronicmd.com/get_reference.php?Id=1263>

onicmd.com/get_reference.php?Id=1263)

Love and gentle hugs,

Debi/So. Cal.-54

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

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protect your friends from email address harvesters which can lead to more

Spam, unwanted mail, and even viruses.

Copy and paste into a new email and place parenthesis around the addresses.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

**************************************Check out AOL's list of 2007's hottest

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<http://money.aol.com/special/hot-products-2007?NCID=aoltop00030000000001>

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Hi DebiA, Yes, I go through spells all the time, particularly during a flare,

when I feel like giving up. It's so hard when I'm in terrible pain and no one

seems to care. I can work myself into a downward spiral fast.

But then I start remembering the things that are good in my life, even though

I am being bombarded with money problems and other things along with being sick.

I have my grandchildren who are a delight. They would miss me.

When I was in a bad Sarcoidosis flare and in the hospital, my daughter and son

gave me a list of reasons I couldn't die. Mostly they needed me to do things

for them (they are grown), but then it was supposed to be funny but true. My

daughter included that she didn't want her in-laws to be the only grandparent

influence on the kids while they were growing up. Anyway it brought a smile to

my face.

I try to hang on to the word " hope " because as long as there's hope then the

possibility of change is still there. I told my kids, among other things, when

they were growing up that the only thing they could depend on was change - and

it's true, things will change.

I also told them that they could do anything they wanted to in life. Now both

their lives are so crowded with things they are doing, that my son said " when

you told us we could do anything, I wish you had added, not all a one time! "

Just a funny for your day.

Take care of yourself, I know it's hard,

Marti

raburtongdyr@... wrote:

Anyone ever feel like giving up!

Sent from my Verizon Wireless BlackBerry

Re: When do I stop crying

In a message dated 12/9/2007 6:01:45 P.M. Pacific Standard Time,

lisaannbogue@ verizon.net writes:

lumbar spondylosis

This is what I found on it...go to this website...

_http://www.myelectr onicmd.com/get_reference.php?Id=1263_

(http://www.myelectr onicmd.com/get_reference.php?Id=1263)

Love and gentle hugs,

Debi/So. Cal.-54

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Be a good e-mail buddy, and ALWAYS

protect your friends from email address harvesters which can lead to more

Spam, unwanted mail, and even viruses.

Copy and paste into a new email and place parenthesis around the addresses.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

**************************************Check out AOL's list of 2007's hottest

products.

(http://money. aol.com/special/hot-products-2007?NCID=aoltop00030000000001)

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Ann, you definitely are not in this fight alone and you can always say

exactly what you are feeling here...we will understand better than anyone who

doesn't have it and this is the best place to look for empathy. Email me

anytime you want to or IM me...DebiAC012553.

Love and gentle hugs,

Debi/So. Cal.-54

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Be a good e-mail buddy, and ALWAYS

protect your friends from email address harvesters which can lead to more

Spam, unwanted mail, and even viruses.

Copy and paste into a new email and place parenthesis around the addresses.

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I'm sorry you are in so much pain. It is a difficult adjustment to make

getting the FM diagnosis and then having the back problems along with it.

I've been diagnosed with FM for almost 10 years now. Back problems have

gotten very bad over the past year. I spent almost a year and a half in bed

being very depressed and reading books to distract myself from how miserable

I was. So when I finally started to come out of the depression, my back

wasn't able to handle certain things anymore. I have 3 disc that are

effected.(lol! did I use the right word?)

Sorry, we were having a discussion on effect and affect.

Anyhow, an orthopedic surgeon said a spinal fusion would probably not work

for me because I will just transfer the weak muscles to another area and

still have pain. I had some PT on the back which helped some. I'm supposed

to do exercises to build up the core strength so my muscles aren't so weak

and causing the back to spasm so easily. My quality of life has definitely

decreased. I cannot sit and relax in a chair. I have to sit forward and

keep my back straight or the spasms will be awful when I try to get up.

It's tiring to have to sit straight up all the time. So I still have to get

into the bed during the day to rest.

You sound like you're about at the end of your rope. Wish I had a name to

address you, even if it's not your " real " name. Are you getting any

counseling, being treated for depression? These are very crucial parts of

surviving FM as well as the other diseases and such that we deal with. I

hope at least you realize you're not alone here. We know what you're going

through. Take care.

Jeanne in WI

> With what lumbar spondylosis is does this mean I'm going to get worse?

> Does this mean I'll just keep degenerating and being in more pain? How

> fast will all this occur? Because, I don't know if I can handle more pain

> which will only bring more depression. I know that I have four discs so

> far that are affected and I also have a lot of weakness on my right side

> mainly. How do I respond, react, or handle any of this.

> Except to accept my lot in life and bawl my eyes out.

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Share on other sites

I am at the end of my rope. It's like always walking on egg shells. My email

address is lisaannbogue@... and my real name is Ann. Thank you for

responding it's always a comfort to know that I'm not in this fight alone. I'm

married and have a wonderful husband but when it comes to this illness he's

clueless.

Sincerely

Ann

Date: 2007/12/11 Tue AM 09:48:55 CST

To: Fibromyalgia_Support_Group

Subject: Re: When do I stop crying

I'm sorry you are in so much pain. It is a difficult adjustment to make

getting the FM diagnosis and then having the back problems along with it.

I've been diagnosed with FM for almost 10 years now. Back problems have

gotten very bad over the past year. I spent almost a year and a half in bed

being very depressed and reading books to distract myself from how miserable

I was. So when I finally started to come out of the depression, my back

wasn't able to handle certain things anymore. I have 3 disc that are

effected.(lol! did I use the right word?)

Sorry, we were having a discussion on effect and affect.

Anyhow, an orthopedic surgeon said a spinal fusion would probably not work

for me because I will just transfer the weak muscles to another area and

still have pain. I had some PT on the back which helped some. I'm supposed

to do exercises to build up the core strength so my muscles aren't so weak

and causing the back to spasm so easily. My quality of life has definitely

decreased. I cannot sit and relax in a chair. I have to sit forward and

keep my back straight or the spasms will be awful when I try to get up.

It's tiring to have to sit straight up all the time. So I still have to get

into the bed during the day to rest.

You sound like you're about at the end of your rope. Wish I had a name to

address you, even if it's not your " real " name. Are you getting any

counseling, being treated for depression? These are very crucial parts of

surviving FM as well as the other diseases and such that we deal with. I

hope at least you realize you're not alone here. We know what you're going

through. Take care.

Jeanne in WI

> With what lumbar spondylosis is does this mean I'm going to get worse?

> Does this mean I'll just keep degenerating and being in more pain? How

> fast will all this occur? Because, I don't know if I can handle more pain

> which will only bring more depression. I know that I have four discs so

> far that are affected and I also have a lot of weakness on my right side

> mainly. How do I respond, react, or handle any of this.

> Except to accept my lot in life and bawl my eyes out.

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Share on other sites

Thank you for sharing your name, Ann. That's the main purpose for this

group, to help you realize that you aren't the only one dealing with this

monster. When you have time, look through the files and link on the website

for information to share with your husband. Educating him and yourself will

help you both adjust. Just remember that you will have good days ahead.

The future is not all " black clouds. " You may email me privately anytime.

Jeanne in WI

djgraves9497@...

>I am at the end of my rope. It's like always walking on egg shells. My

>email address is lisaannbogue@... and my real name is Ann.

>Thank you for responding it's always a comfort to know that I'm not in this

>fight alone. I'm married and have a wonderful husband but when it comes to

>this illness he's clueless.

> Sincerely

> Ann

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