THERE IS HOPE FOR GETTING BETTER

[Guest guest]

How did you recover from cfs?

--- Cheryl Spaulding <cspau2@...> wrote:

> I know this is out of the norm for this web site -

> but for whatever it's

> worth I wanted to share a few comments with you all.

>

> I have just recovered from 6 months of EBV. It has

> been very difficult

> at times but I am just about back to 100%. Last

> night as I walked my

> dogs around a beautiful lake near my house I took a

> moment to remind

> myself - how lucky I was. I will never forget for a

> minute how

> wonderful it is to feel good and I will never take

> my health for granted

> again. I haved learned so much over these past 6

> months about sickness

> and about the immune system and CFS. About dealing

> with tolerance, faith

> and hope. I realize there is always a chance for a

> relapse, and I pray

> that I can do everything in my power to avoid this

> from happening. I

> continue to read all of your posts and attend my

> local support group

> meetings. If any of you are interested in my

> recovery story I will be

> happy to respond to you individually.

>

> God Bless!

>

>

> [Non-text portions of this message have been

> removed]

>

>

> -------------------------- eGroups Sponsor

>

> This list is intended for patients to share personal

> experiences with each other, not to give medical

> advice. If you are interested in any treatment

> discussed here, please consult your doctor.

>

__________________________________________________

[Guest guest]

Now now, don't be stingy! Lol! Just kidding. Really though, my

opinion is that ANYONE'S RECOVERY STORY IS MOST WELCOME HERE. I'm

sure that Ken and all our Experimental list members would agree.

Amid all the technical posts, the questions, the " how much do I

take? " , the " This symptom got worse, this got better? " , the " am I

herxing? " and the " where's that website? " , we NEED to hear about it

when someone turns a corner towards that magical and sometimes

seemingly unreachable place of good health.

Ok maybe " we " don't need it, but " I " sure do!!!!!!!!

If any of you are interested in my recovery story I will be

> happy to respond to you individually.

>

> God Bless!

[Guest guest]

Now now, don't be stingy! Lol! Just kidding. Really though, my

opinion is that ANYONE'S RECOVERY STORY IS MOST WELCOME HERE. I'm

sure that Ken and all our Experimental list members would agree.

Amid all the technical posts, the questions, the " how much do I

take? " , the " This symptom got worse, this got better? " , the " am I

herxing? " and the " where's that website? " , we NEED to hear about it

when someone turns a corner towards that magical and sometimes

seemingly unreachable place of good health.

Ok maybe " we " don't need it, but " I " sure do!!!!!!!!

If any of you are interested in my recovery story I will be

> happy to respond to you individually.

>

> God Bless!

[Guest guest]

Cheryl, I think you could

guess that people trying to get well would want to know how someone else got

well. So please post here to the group.

I'm glad you are doing so well. However, a bout with EBV is not CFIDS. It is a

bout with EBV. When I was in high school,I got Mono (caused by EBV). I was in

the hospital for 10 days, in bed for 6 weeks. I then fully recovered. It was 20

years later that I got CFIDS, which has lasted 15 years.

Katrina

[Guest guest]

I would like to hear your story.

Lucey001@...

>How did you recover from cfs?

>--- Cheryl Spaulding <cspau2@...> wrote:

>> I know this is out of the norm for this web site -

>> but for whatever it's

>> worth I wanted to share a few comments with you all.

>>

>> I have just recovered from 6 months of EBV. It has

>> been very difficult

>> at times but I am just about back to 100%. Last

>> night as I walked my

>> dogs around a beautiful lake near my house I took a

>> moment to remind

>> myself - how lucky I was. I will never forget for a

>> minute how

>> wonderful it is to feel good and I will never take

>> my health for granted

>> again. I haved learned so much over these past 6

>> months about sickness

>> and about the immune system and CFS. About dealing

>> with tolerance, faith

>> and hope. I realize there is always a chance for a

>> relapse, and I pray

>> that I can do everything in my power to avoid this

>> from happening. I

>> continue to read all of your posts and attend my

>> local support group

>> meetings. If any of you are interested in my

>> recovery story I will be

>> happy to respond to you individually.

>>

>> God Bless!

>>

>>

>> [Non-text portions of this message have been

>> removed]

>>

>>

>> -------------------------- eGroups Sponsor

>>

>> This list is intended for patients to share personal

>> experiences with each other, not to give medical

>> advice. If you are interested in any treatment

>> discussed here, please consult your doctor.

>>

>

>

>__________________________________________________

>

[Guest guest]

lucey001@... writes:

> >> meetings. If any of you are interested in my recovery story I will be

> >> happy to respond to you individually.God Bless!

Hello , It would be even better for your health to just post what has

helped you Recover instead of all these individual e-mails. Believe me their

will be more requests from your posting. of getting better & or recovery.

Be very careful! You mentioned 6 months, most of us aren't even dxd by 6mnths

of illness. Relapses, Reprieves, Please be careful of your good health take

caution and keep Drs. informed esp. on titer levels.

This is an advance Thank You ........Thank You ........ God Bless

Still Riding The Wave ......

[Guest guest]

Hello Cheryl,

I just remembered, Aren't you the kind lady in line with me waiting

to

purchase Humfry ? That must have been 6 months ago in the drugstore. Well,

wouldn't you know Humfry's stuffing fell out and I can't get anyone to go to

the store. cspau2@... (Cheryl

Spaulding) cspau2@...

Been e-mailing them. Maybe you could help ? <A HREF= " service@... " >

service@...</A>

[Guest guest]

Hello Cheryl,

I'm sorry I don't backchannel, I was able to copy & paste your

question. Your slip is showing that's how I knew lol,. See > @eckerd.com &

Missy's shows @hcs.harvard.edu. Laurie's is @Folkarts.com . I remembered

Humfry was an exclusive teddy from eckerd & or jcp.

I do like peanut butter,grape juice & ezkeil bread. Just copy & paste your

info like I did, it might be easier for you to answer on help items. Thanks

>>>>In a message dated 10/17/2000 1:43:55 PM cspau2@... writes: I just

read your post, I could have been the lady in line when you were buying

Humphrey, how did you know this was me?Received: from i005.jcpenney.com

(jcpint2a.jcpenney.com <<<<