Lori

[Guest guest]

Lori,

thank you for the offer! I will definitely take you up on that.

Huggs

Sandy

[Guest guest]

wow i am empowered by your email you have been thru so much and i am so so

proud of you you have the right approuch to klife anf it seerms to be

working for you i am so happy you got out of this opioid rut but dfidnt you

suffer withdrawals? i am on a emoitonal rollalrcoaster but determined to make a

change with vhurcvh and postive people and not let my fmaily effect my

self esteeem. i wish i could drink 12 glassses of water a day with my chronicn

kidney stoneds but i can only get down 4 16.9 bottleds but it is working

for me i will read you email over and over again you really are a

inspriatation

netty

In a message dated 3/21/2012 9:02:27 A.M. Eastern Daylight Time,

lorijkarasek@... writes:

Hi,

I started this email to share about meds I think are helping me with

cfs/me/lyme/pain/etc. Then all these words came pouring out of my soul.

I share them with you in peace, empathy and hopefulness.

So here is the email, the exact way it came out. Thank you for sharing and

for being kind.

Here goes:

I think the Valtrex is helping me with lessening fatigue, pain and brain

fog. I'm starting ivig infusion and have hope I will feel better. For the

Lyme I'm now on biaxin with vancocin (prevent c diff). Did iv therapy before.

I have oxy, vicodin, tylenol with cod, xanax, valium, klonopin, etc. but I

found the more I took, the more I needed for pain and the resulting

increased anxiety and depression.

My pain was getting worse and I rarely left my house. Plus I had horrible

side effects, both mental and physical.

In the hospital with diladid (sp?), I developed worsening restless legs. I

wanted to crawl out of my skin. The depression was harrowing.

Pain from Lyme, cfs, fibro, ddd, and an alphabet soup of autoimmune

diseases cause random, intense pain with disabling fatigue.

[Guest guest]

wow i am empowered by your email you have been thru so much and i am so so

proud of you you have the right approuch to klife anf it seerms to be

working for you i am so happy you got out of this opioid rut but dfidnt you

suffer withdrawals? i am on a emoitonal rollalrcoaster but determined to make a

change with vhurcvh and postive people and not let my fmaily effect my

self esteeem. i wish i could drink 12 glassses of water a day with my chronicn

kidney stoneds but i can only get down 4 16.9 bottleds but it is working

for me i will read you email over and over again you really are a

inspriatation

netty

In a message dated 3/21/2012 9:02:27 A.M. Eastern Daylight Time,

lorijkarasek@... writes:

Hi,

I started this email to share about meds I think are helping me with

cfs/me/lyme/pain/etc. Then all these words came pouring out of my soul.

I share them with you in peace, empathy and hopefulness.

So here is the email, the exact way it came out. Thank you for sharing and

for being kind.

Here goes:

I think the Valtrex is helping me with lessening fatigue, pain and brain

fog. I'm starting ivig infusion and have hope I will feel better. For the

Lyme I'm now on biaxin with vancocin (prevent c diff). Did iv therapy before.

I have oxy, vicodin, tylenol with cod, xanax, valium, klonopin, etc. but I

found the more I took, the more I needed for pain and the resulting

increased anxiety and depression.

My pain was getting worse and I rarely left my house. Plus I had horrible

side effects, both mental and physical.

In the hospital with diladid (sp?), I developed worsening restless legs. I

wanted to crawl out of my skin. The depression was harrowing.

Pain from Lyme, cfs, fibro, ddd, and an alphabet soup of autoimmune

diseases cause random, intense pain with disabling fatigue.

[Guest guest]

wow i am empowered by your email you have been thru so much and i am so so

proud of you you have the right approuch to klife anf it seerms to be

working for you i am so happy you got out of this opioid rut but dfidnt you

suffer withdrawals? i am on a emoitonal rollalrcoaster but determined to make a

change with vhurcvh and postive people and not let my fmaily effect my

self esteeem. i wish i could drink 12 glassses of water a day with my chronicn

kidney stoneds but i can only get down 4 16.9 bottleds but it is working

for me i will read you email over and over again you really are a

inspriatation

netty

In a message dated 3/21/2012 9:02:27 A.M. Eastern Daylight Time,

lorijkarasek@... writes:

Hi,

I started this email to share about meds I think are helping me with

cfs/me/lyme/pain/etc. Then all these words came pouring out of my soul.

I share them with you in peace, empathy and hopefulness.

So here is the email, the exact way it came out. Thank you for sharing and

for being kind.

Here goes:

I think the Valtrex is helping me with lessening fatigue, pain and brain

fog. I'm starting ivig infusion and have hope I will feel better. For the

Lyme I'm now on biaxin with vancocin (prevent c diff). Did iv therapy before.

I have oxy, vicodin, tylenol with cod, xanax, valium, klonopin, etc. but I

found the more I took, the more I needed for pain and the resulting

increased anxiety and depression.

My pain was getting worse and I rarely left my house. Plus I had horrible

side effects, both mental and physical.

In the hospital with diladid (sp?), I developed worsening restless legs. I

wanted to crawl out of my skin. The depression was harrowing.

Pain from Lyme, cfs, fibro, ddd, and an alphabet soup of autoimmune

diseases cause random, intense pain with disabling fatigue.