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Hi ,

I'm so glad you decided to contact the list. I really feel your sadness.

It is frustrating to think of the things you cannot do...but what if you tried

to focus on the things that you can do? You are here for a reason. We all

go through feeling bad, having good days and bad days. At the end of the day,

you have managed to survive yet another day. Please keep posting to us

.....take care.

Heidi

To those who believe, no explanation is necessary; to those who dont, no

explanation is possible

In a message dated 6/10/2008 10:31:21 A.M. Eastern Daylight Time,

emilyspivey@... writes:

Hi all. I've been a member for several years, since I was diagnosed,

but don't post alot. I need to vent/seek some support. I've become

disabled from a combination of diseases, RA, OA, FMS, DDD and

bursitis. I am so depressed that I don't know what to do. Not being

able to do things I've always done really makes me feel like my life,

as I knew it, is over. To make matters worse, my only 2 granddaughters

are moving 1400 miles away soon. I just don't know what to do. I'm on

an antidepressant already (the most I can take) but I feel so useless

and hopeless. I can't afford phsycotherapy, our insurance only pays

50%. So, I just sleep. I can't read much anymore because I have

dementia and forget what I've read if I put the book aside. I feel

like if I had someone to talk to I'd feel better. Does anyone know if

the State of Alabama has any service that I could utilize. I think

I'll research that. Thank you all for listening, I feel better

already , just having gotten this off my chest.

**************Vote for your city's best dining and nightlife. City's Best

2008. (http://citysbest.aol.com?ncid=aolacg00050000000102)

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I am so glad that you have posted for some support! As you know from reading the

posts, this group is full of amazing, courageous, supportive individuals WHO

CARE! I know how difficult it is being disabled and it leading to

depression. & nbsp; I'm 36 now and have been home for 6 years now. & nbsp; I only

got & nbsp; to work a couple of years out of college before it all ended. & nbsp; I

spend virtually all of my time alone, except for seeing my mom at the end of the

day, and my brother and nephew a couple of times a week. & nbsp; I have an anxiety

disorder with agoraphobia as well so getting out is a challenge in and of itself

but I am working on it. & nbsp; I'm not sure of your insurance, if you have

Medicare? There are some psychologists, most that I have worked with that have a

sliding fee scale. & nbsp; The psychiatrist I've been seeing for the past few

years to manage my anxiety/agoraphobia and treatment, only takes the money

Medicare pays him. & nbsp; & nbsp; He

doesn't charge me any copays. & nbsp; Some doctors do this and can use it as a

write off at the end of the year. & nbsp; Like pro bono. & nbsp; My Cognitive

Behavioral psychologist did the same. & nbsp; I'd pay $10 each visit and she would

take what Medicare paid and that would be it. & nbsp; There are also community

mental health agencies that might be less expensive. & nbsp; Support groups, which

are free can also be very helpful. & nbsp; I don't know if you have any pets, but

dogs have been proven to help lower blood pressure, help with depression,

anxiety. & nbsp; I actually have a prescribed therapy dog for my

agoraphobia. & nbsp; Antidepressants I have learned throughout the years, (as well

as my anxiety meds) simply do not work on their own. & nbsp; I know many

individuals think " oh the doctor will give me this pill and it will be

better " . & nbsp; Yet without some form of cognitive therapy behavior therapy they

don't seem to do much good on their own (except to keep

us from falling further). & nbsp; I hope that you can find someone to help soon!

From: eandsspivey & lt;emilyspivey@... & gt;

Subject: [ ] Disabled and Depressed

Date: Tuesday, June 10, 2008, 10:30 AM

Hi all. I've been a member for several years, since I was diagnosed,

but don't post alot. I need to vent/seek some support. I've become

disabled from a combination of diseases, RA, OA, FMS, DDD and

bursitis. I am so depressed that I don't know what to do. Not being

able to do things I've always done really makes me feel like my life,

as I knew it, is over. To make matters worse, my only 2 granddaughters

are moving 1400 miles away soon. I just don't know what to do. I'm on

an antidepressant already (the most I can take) but I feel so useless

and hopeless. I can't afford phsycotherapy, our insurance only pays

50%. So, I just sleep. I can't read much anymore because I have

dementia and forget what I've read if I put the book aside. I feel

like if I had someone to talk to I'd feel better. Does anyone know if

the State of Alabama has any service that I could utilize. I think

I'll research that. Thank you all for listening, I feel better

already , just having gotten this off my chest.

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,

I hate to hear you are having to go thru so much. I think its hard for

anyone to handle family moving out of the area but that in combination with

all the diseases you have is like adding insult to injury.I have the same Dx

as you and do to a really strange problem( that was no fault of ours) we had

to stop any contact my husbands grandchildren. ( His son is crazy and the

Daughter-in-law is pure evil) My Grandkids are in Texas and I am in NJ. I

wish there was some magic words or a magic pill that would make it all

better. Unfortunately I can't but know that there are people out there that

care and are here to listen. I will keep you in my prayers

Heidi M

On Tue, Jun 10, 2008 at 1:34 PM, stephanie <stephieann2@...> wrote:

>

> I am so glad that you have posted for some support! As you know from

> reading the posts, this group is full of amazing, courageous, supportive

> individuals WHO CARE! I know how difficult it is being disabled and it

> leading to depression. & nbsp; I'm 36 now and have been home for 6 years

> now. & nbsp; I only got & nbsp; to work a couple of years out of college before

> it all ended. & nbsp; I spend virtually all of my time alone, except for

> seeing my mom at the end of the day, and my brother and nephew a couple of

> times a week. & nbsp; I have an anxiety disorder with agoraphobia as well so

> getting out is a challenge in and of itself but I am working on it. & nbsp;

> I'm not sure of your insurance, if you have Medicare? There are some

> psychologists, most that I have worked with that have a sliding fee

> scale. & nbsp; The psychiatrist I've been seeing for the past few years to

> manage my anxiety/agoraphobia and treatment, only takes the money Medicare

> pays him. & nbsp; & nbsp; He

> doesn't charge me any copays. & nbsp; Some doctors do this and can use it as

> a write off at the end of the year. & nbsp; Like pro bono. & nbsp; My Cognitive

> Behavioral psychologist did the same. & nbsp; I'd pay $10 each visit and she

> would take what Medicare paid and that would be it. & nbsp; There are also

> community mental health agencies that might be less expensive. & nbsp; Support

> groups, which are free can also be very helpful. & nbsp; I don't know if you

> have any pets, but dogs have been proven to help lower blood pressure, help

> with depression, anxiety. & nbsp; I actually have a prescribed therapy dog for

> my agoraphobia. & nbsp; Antidepressants I have learned throughout the years,

> (as well as my anxiety meds) simply do not work on their own. & nbsp; I know

> many individuals think " oh the doctor will give me this pill and it will be

> better " . & nbsp; Yet without some form of cognitive therapy behavior therapy

> they don't seem to do much good on their own (except to keep

> us from falling further). & nbsp; I hope that you can find someone to help

> soon!

>

>

>

> From: eandsspivey & lt;emilyspivey@...<emilyspivey%40centurytel.net>

> & gt;

> Subject: [ ] Disabled and Depressed

> < %40>

> Date: Tuesday, June 10, 2008, 10:30 AM

>

> Hi all. I've been a member for several years, since I was diagnosed,

> but don't post alot. I need to vent/seek some support. I've become

> disabled from a combination of diseases, RA, OA, FMS, DDD and

> bursitis. I am so depressed that I don't know what to do. Not being

> able to do things I've always done really makes me feel like my life,

> as I knew it, is over. To make matters worse, my only 2 granddaughters

> are moving 1400 miles away soon. I just don't know what to do. I'm on

> an antidepressant already (the most I can take) but I feel so useless

> and hopeless. I can't afford phsycotherapy, our insurance only pays

> 50%. So, I just sleep. I can't read much anymore because I have

> dementia and forget what I've read if I put the book aside. I feel

> like if I had someone to talk to I'd feel better. Does anyone know if

> the State of Alabama has any service that I could utilize. I think

> I'll research that. Thank you all for listening, I feel better

> already , just having gotten this off my chest.

>

>

>

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-Dear , You are a part of a wonderful, caring group and I know

you will be helped alot by just being a part of the group as I am. I

do not post much myself. I read and I learn and I pray for all of us

and the meny others who live with such chalenges. Depression is a

hard one for me and just knowing that I am not alone helps. hang in

there and know that you are in the prayers of group members here. I

know nothing about Alabama. I must share that I came to Arizona for

a visit and I am having a 80% improvement pain-wise. I love it. I am

walking normally now without a cane or any device. So much less

pain. It's this dry heat. I am sooooooo happy. I had the claw hands

and so on. I haven't felt this good in along time. I know it has to

be this dry heat. I pray you feel better along with all our group

members. Peace and joy and much love, to you & yours, Marie

-- In , sposy@... wrote:

>

> Hi ,

>

> I'm so glad you decided to contact the list. I really feel your

sadness.

> It is frustrating to think of the things you cannot do...but what

if you tried

> to focus on the things that you can do? You are here for a

reason. We all

> go through feeling bad, having good days and bad days. At the

end of the day,

> you have managed to survive yet another day. Please keep posting

to us

> ....take care.

>

> Heidi

>

> To those who believe, no explanation is necessary; to those who

dont, no

> explanation is possible

>

>

> In a message dated 6/10/2008 10:31:21 A.M. Eastern Daylight Time,

> emilyspivey@... writes:

>

>

>

>

> Hi all. I've been a member for several years, since I was

diagnosed,

> but don't post alot. I need to vent/seek some support. I've

become

> disabled from a combination of diseases, RA, OA, FMS, DDD and

> bursitis. I am so depressed that I don't know what to do. Not

being

> able to do things I've always done really makes me feel like my

life,

> as I knew it, is over. To make matters worse, my only 2

granddaughters

> are moving 1400 miles away soon. I just don't know what to do. I'm

on

> an antidepressant already (the most I can take) but I feel so

useless

> and hopeless. I can't afford phsycotherapy, our insurance only

pays

> 50%. So, I just sleep. I can't read much anymore because I have

> dementia and forget what I've read if I put the book aside. I

feel

> like if I had someone to talk to I'd feel better. Does anyone know

if

> the State of Alabama has any service that I could utilize. I

think

> I'll research that. Thank you all for listening, I feel better

> already , just having gotten this off my chest.

>

>

>

>

>

>

> **************Vote for your city's best dining and nightlife.

City's Best

> 2008. (http://citysbest.aol.com?ncid=aolacg00050000000102)

>

>

>

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--- In , " eandsspivey " <emilyspivey@...>

wrote:

HI ,

I was sorry to hear about your situation. It is a shame for you

that your grandchildren are moving away. Have you got other friends

that could be there for you ? I really feel your frustration and I

too suffer from most of the conditions you have listed. Bursitis is

another one that I have got along with RA,FMS,Endometriosis, IBS,

and ME/CFS. I have a 15year old daughter who can only remember her

mother being unwell. She suffers from a rare autoimmune disorder

where her body rejects her blood cells and kills them off.

At times I feel useless as I need to care for her and I am stuggling

with pain and unable to get around properly.

I do hope that you get the support you need, as I live in Australia

I am unsure of your system over there. But I did sympathise with

you when I read your email.

Take care .

>

> Hi all. I've been a member for several years, since I was

diagnosed,

> but don't post alot. I need to vent/seek some support. I've

become

> disabled from a combination of diseases, RA, OA, FMS, DDD and

> bursitis. I am so depressed that I don't know what to do. Not

being

> able to do things I've always done really makes me feel like my

life,

> as I knew it, is over. To make matters worse, my only 2

granddaughters

> are moving 1400 miles away soon. I just don't know what to do.

I'm on

> an antidepressant already (the most I can take) but I feel so

useless

> and hopeless. I can't afford phsycotherapy, our insurance only

pays

> 50%. So, I just sleep. I can't read much anymore because I have

> dementia and forget what I've read if I put the book aside. I

feel

> like if I had someone to talk to I'd feel better. Does anyone

know if

> the State of Alabama has any service that I could utilize. I

think

> I'll research that. Thank you all for listening, I feel better

> already , just having gotten this off my chest.

>

>

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hi emily, my heart goes out to you. im SORRY about your situation & your

grandaughters leaving. i know what it's like when you can do something then it's

taken away, NOT A GOOD FEELING!!! may god be with you & bless you,melyndagamez

[ ] Re: Disabled and Depressed

--- In , " eandsspivey " <emilyspivey@...>

wrote:

HI ,

I was sorry to hear about your situation.  It is a shame for you

that your grandchildren are moving away.  Have you got other friends

that could be there for you ?  I really feel your frustration and I

too suffer from most of the conditions you have listed.  Bursitis is

another one that I have got along with RA,FMS,Endometriosis, IBS,

and ME/CFS.  I have a 15year old daughter who can only remember her

mother being unwell.  She suffers from a rare autoimmune disorder

where her body rejects her blood cells and kills them off.

At times I feel useless as I need to care for her and I am stuggling

with pain and unable to get around properly.

I do hope that you get the support you need, as I live in Australia

I am unsure of your system over there.  But I did sympathise with

you when I read your email.

Take care ..

>

> Hi all.  I've been a member for several years, since I was

diagnosed,

> but don't post alot.  I need to vent/seek some support.  I've

become

> disabled from a combination of diseases, RA, OA, FMS, DDD and

> bursitis.  I am so depressed that I don't know what to do.  Not

being

> able to do things I've always done really makes me feel like my

life,

> as I knew it, is over.  To make matters worse, my only 2

granddaughters

> are moving 1400 miles away soon.  I just don't know what to do. 

I'm on

> an antidepressant already (the most I can take) but I feel so

useless

> and hopeless.  I can't afford phsycotherapy, our insurance only

pays

> 50%.  So, I just sleep.  I can't read much anymore because I have

> dementia and forget what I've read if I put the book aside.  I

feel

> like if I had someone to talk to I'd feel better.  Does anyone

know if

> the State of Alabama has any service that I could utilize.  I

think

> I'll research that.  Thank you all for listening, I feel better

> already , just having gotten this off my chest. 

>

>

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

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hi marie, one question for you? you say the dry heat helps with your pain but

what about your BREATHING? i live here in TEXAS & sometimes it's very,very, hot.

i'm on several meds. & when i'm outside for maybe 30 to 45 minutes i can't

BREATH!! maybe it has to do with my meds., i don't know. any suggestions would

be GREAT!! thank-you & may god bless,melyndagamez

[ ] Re: Disabled and Depressed

-Dear , You are a part of a wonderful, caring group and I know

you will be helped alot by just being a part of the group as I am. I

do not post much myself. I read and I learn and I pray for all of us

and the meny others who live with such chalenges. Depression is a

hard one for me and just knowing that I am not alone helps. hang in

there and know that you are in the prayers of group members here. I

know nothing about Alabama. I must share that I came to Arizona for

a visit and I am having a 80% improvement pain-wise. I love it. I am

walking normally now without a cane or any device. So much less

pain. It's this dry heat. I am sooooooo happy. I had the claw hands

and so on. I haven't felt this good in along time. I know it has to

be this dry heat. I pray you feel better along with all our group

members. Peace and joy and much love, to you & yours, Marie

 

-- In , sposy@... wrote:

>

> Hi ,

> 

> I'm so glad you decided to contact the list.  I really  feel your

sadness. 

> It is frustrating to think of the things you cannot  do...but what

if you tried

> to focus on the things that you can do?  You are  here for a

reason. We all

> go through feeling bad, having good days and bad  days.  At the

end of the day,

> you have managed to survive yet another  day.  Please keep posting

to us

> ....take care.

> 

> Heidi

> 

> To those who believe, no explanation is necessary; to those who 

dont, no

> explanation is possible 

>

> 

> In a message dated 6/10/2008 10:31:21 A.M. Eastern Daylight Time, 

> emilyspivey@... writes:

>

> 

> 

> 

> Hi all. I've been a member for several years, since I was

diagnosed, 

> but don't post alot. I need to vent/seek some support. I've

become 

> disabled from a combination of diseases, RA, OA, FMS, DDD and 

> bursitis. I am so depressed that I don't know what to do. Not

being 

> able to do things I've always done really makes me feel like my

life, 

> as I knew it, is over. To make matters worse, my only 2

granddaughters 

> are moving 1400 miles away soon. I just don't know what to do. I'm

on 

> an antidepressant already (the most I can take) but I feel so

useless 

> and hopeless. I can't afford phsycotherapy, our insurance only

pays 

> 50%. So, I just sleep. I can't read much anymore because I have 

> dementia and forget what I've read if I put the book aside. I

feel 

> like if I had someone to talk to I'd feel better. Does anyone know

if 

> the State of Alabama has any service that I could utilize. I

think 

> I'll research that. Thank you all for listening, I feel better

> already  , just having gotten this off my chest.

>

>

>

> 

>

>

> **************Vote for your city's best dining and nightlife.

City's Best

> 2008.      (http://citysbest.aol.com?ncid=aolacg00050000000102)

>

>

>

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hi stephanie, it seems to me you're pretty much in the dumps!! what's up woman?

i use to be soo much like you until one day something SNAPPED IN MY HEAD &

said, " get up,get up & take CONTROL OF YOUR LIFE. " i even tried suicide know

that's some major problems i had to deal within myself & i did it, stephanie..

you know i have a hub & a 11yr.old daughter o.k. but he works alllll the time &

alyssa all she wants to do is play with her friends or go here or there with her

friends. so yes i know what it feels like to be alone cuz the majority of the

time i am!! so i have come up with all this CRAZY stuff to keep my mind off

being lonely & depressed! here it goes;

1.READ THE BIBLE

2.LISTEN TO SOME RELAXING SOUNDS(i prefer the waves at beach,windchimes,rain, &

last but least birds)

3.MEDITATE

4.LISTEN TO SOME TYPE OF MUSIC YOU LIKE(i prefer the classic oldies)

5.WATCH AN OLDIE BUT GOODIE MOVIE

6.READ MAYBE SOME OF YOUR SPECIAL BOOKS YOU LIKE(i like r.a.today,woman's

health, goodhousekeeping, & redbook)

7.SPEND TIME WITH " SPECIAL FRIENDS " ETC.

  I HOPE I could be of some help because everybody needs somebody!!!god

bless,melyndagamez 6/12/08 1:45a.m.central

[ ] Disabled and Depressed

Date: Tuesday, June 10, 2008, 10:30 AM

Hi all. I've been a member for several years, since I was diagnosed,

but don't post alot. I need to vent/seek some support. I've become

disabled from a combination of diseases, RA, OA, FMS, DDD and

bursitis. I am so depressed that I don't know what to do. Not being

able to do things I've always done really makes me feel like my life,

as I knew it, is over. To make matters worse, my only 2 granddaughters

are moving 1400 miles away soon. I just don't know what to do. I'm on

an antidepressant already (the most I can take) but I feel so useless

and hopeless. I can't afford phsycotherapy, our insurance only pays

50%. So, I just sleep. I can't read much anymore because I have

dementia and forget what I've read if I put the book aside. I feel

like if I had someone to talk to I'd feel better. Does anyone know if

the State of Alabama has any service that I could utilize. I think

I'll research that. Thank you all for listening, I feel better

already , just having gotten this off my chest.

     

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HEIDI,YOUR WORDS TO EMILY WERE A.W.E.S.O.M.E. if we had MORE people like YOU in

this RA SUPPORT GROUP to really speak from the HEART, they will get by by the

HELP of others & by the grace of god.

our god is an awesome god & an awesome god he is!!!!!!!!!!!!!!!!!! god

bless,melyndagamez 6/12/08 1:55a..m.central

Re: [ ] Disabled and Depressed

Hi ,

I'm so glad you decided to contact the list.  I really  feel your sadness. 

It is frustrating to think of the things you cannot  do...but what if you tried

to focus on the things that you can do?  You are  here for a reason. We all

go through feeling bad, having good days and bad  days.  At the end of the day,

you have managed to survive yet another  day.  Please keep posting to us

.....take care.

Heidi

To those who believe, no explanation is necessary; to those who  dont, no

explanation is possible 

In a message dated 6/10/2008 10:31:21 A.M. Eastern Daylight Time, 

emilyspivey@... writes:

Hi all. I've been a member for several years, since I was diagnosed, 

but don't post alot. I need to vent/seek some support. I've become 

disabled from a combination of diseases, RA, OA, FMS, DDD and 

bursitis. I am so depressed that I don't know what to do. Not being 

able to do things I've always done really makes me feel like my life, 

as I knew it, is over. To make matters worse, my only 2 granddaughters 

are moving 1400 miles away soon. I just don't know what to do. I'm on 

an antidepressant already (the most I can take) but I feel so useless 

and hopeless. I can't afford phsycotherapy, our insurance only pays 

50%. So, I just sleep. I can't read much anymore because I have 

dementia and forget what I've read if I put the book aside. I feel 

like if I had someone to talk to I'd feel better. Does anyone know if 

the State of Alabama has any service that I could utilize. I think 

I'll research that. Thank you all for listening, I feel better

already  , just having gotten this off my chest.

**************Vote for your city's best dining and nightlife. City's Best

2008.      (http://citysbest.aol.com?ncid=aolacg00050000000102)

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Hi : I just thought I would drop you a note to say I am praying for

you, and your family. I hope your troubles will lessen soon. I too, know

exactly what you are going through. I pray you will find the help you

need, so you won't feel so alone and depressed. We all care about you,

and you are never alone. We only have one life, and we all have to live

it the best we can. God will never abandon you, and He will help you

through this difficult time. It is good you decided to post so you can

see how much we all care about you. That is the first step in your

recovery. I really don't know anyone who has not gone through periods of

depresssion, and felt like their lives were over. But, life is for the

LIVING, and we owe it to ourselves to do the best we can everyday. I

went through a very terrible time years ago, and I just wanted to curl

up and die. That is what I thought at the time. But with help, I dusted

myself off, and slowly got my life back. I have always loved life, and

had such zest, I just couldn't believe what happened to me. Yes, I

sometimes have days that I just can't do anything with the RA pain,

etc., so I watch movies, love the old ones, read awhile, go on line,

etc. I love cards, so I play Solitare or the game 13, that my

Grandfather taught me. I too, am alone a lot, and those are long days. I

just try to focus my thoughts for the day, and what I would like to

accomplish. I only deal with one day at a time, otherwise, I get too

overwhelmed. I will try to do some house chores, and if I can't get it

all done, there is always tomorrow. I will continue praying for you,

. God Bless you in all ways. Hugs, Barbara

> >

> > Hi ,

> >

> > I'm so glad you decided to contact the list. I really feel your

> sadness.

> > It is frustrating to think of the things you cannot do...but what

> if you tried

> > to focus on the things that you can do? You are here for a

> reason. We all

> > go through feeling bad, having good days and bad days. At the

> end of the day,

> > you have managed to survive yet another day. Please keep posting

> to us

> > ....take care.

> >

> > Heidi

> >

> > To those who believe, no explanation is necessary; to those who

> dont, no

> > explanation is possible

> >

> >

> > In a message dated 6/10/2008 10:31:21 A.M. Eastern Daylight Time,

> > emilyspivey@ writes:

> >

> >

> >

> >

> > Hi all. I've been a member for several years, since I was

> diagnosed,

> > but don't post alot. I need to vent/seek some support. I've

> become

> > disabled from a combination of diseases, RA, OA, FMS, DDD and

> > bursitis. I am so depressed that I don't know what to do. Not

> being

> > able to do things I've always done really makes me feel like my

> life,

> > as I knew it, is over. To make matters worse, my only 2

> granddaughters

> > are moving 1400 miles away soon. I just don't know what to do. I'm

> on

> > an antidepressant already (the most I can take) but I feel so

> useless

> > and hopeless. I can't afford phsycotherapy, our insurance only

> pays

> > 50%. So, I just sleep. I can't read much anymore because I have

> > dementia and forget what I've read if I put the book aside. I

> feel

> > like if I had someone to talk to I'd feel better. Does anyone know

> if

> > the State of Alabama has any service that I could utilize. I

> think

> > I'll research that. Thank you all for listening, I feel better

> > already , just having gotten this off my chest.

> >

> >

> >

> >

> >

> >

> > **************Vote for your city's best dining and nightlife.

> City's Best

> > 2008. (http://citysbest.aol.com?ncid=aolacg00050000000102)

> >

> >

> >

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Guest guest

Heidis the best, she helped me alot.

Jolene

In a message dated 6/12/2008 2:53:54 A.M. Eastern Daylight Time,

melyndagamez@... writes:

HEIDI,YOUR WORDS TO EMILY WERE A.W.E.S.O.M.HEIDI,YOUR WORDS TO EMILY WERE

A.W.E.S.O.M.<WBR>E. if we had MORE people like YOU in this RA SUPPORT GROUP to

really speak from the HE & by the grace of god.

our god is an awesome god & an awesome god he is!!!!!!!!!! an awesome god he

is!!!!!!!!!!<WBR>!!!!!!!! god bless,m

Re: [ ] Disabled and Depressed

Hi ,

I'm so glad you decided to contact the list. I really feel your sadness.

It is frustrating to think of the things you cannot do...but what if you

tried

to focus on the things that you can do? You are here for a reason. We all

go through feeling bad, having good days and bad days. At the end of the

day,

you have managed to survive yet another day. Please keep posting to us

.....take care.

Heidi

To those who believe, no explanation is necessary; to those who dont, no

explanation is possible

In a message dated 6/10/2008 10:31:21 A.M. Eastern Daylight Time,

_emilyspivey@emilyspiveyemi_ (mailto:emilyspivey@...) writes:

Hi all. I've been a member for several years, since I was diagnosed,

but don't post alot. I need to vent/seek some support. I've become

disabled from a combination of diseases, RA, OA, FMS, DDD and

bursitis. I am so depressed that I don't know what to do. Not being

able to do things I've always done really makes me feel like my life,

as I knew it, is over. To make matters worse, my only 2 granddaughters

are moving 1400 miles away soon. I just don't know what to do. I'm on

an antidepressant already (the most I can take) but I feel so useless

and hopeless. I can't afford phsycotherapy, our insurance only pays

50%. So, I just sleep. I can't read much anymore because I have

dementia and forget what I've read if I put the book aside. I feel

like if I had someone to talk to I'd feel better. Does anyone know if

the State of Alabama has any service that I could utilize. I think

I'll research that. Thank you all for listening, I feel better

already , just having gotten this off my chest.

************************<WBR>**Vote for your city's best dining and nightl

2008. (_http://citysbest.http://citysbhttp://citysbesthttp_

(http://citysbest.aol.com/?ncid=aolacg00050000000102) )

[Non-text portions of this message have been removed]

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For archives or to change subscription options:

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( ) ! Groups Links

[Non-text portions of this message have been removed]

**************Vote for your city's best dining and nightlife. City's Best

2008. (http://citysbest.aol.com?ncid=aolacg00050000000102)

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