Re: WOW.

[Guest guest]

Hi

I only just saw your message.

I'm also on Facebook and run a group called 'Michelangelo'S Angels' there. I'll

be happy to be in contact on Facebook too.

'What we do in life, echoes through eternity.'

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: saint19662005@...

Date: Wed, 20 Apr 2011 03:41:14 -0700

Subject: Re: WOW.

Hi

The group generally will respond when it receives a comment like yours.

[Guest guest]

Anger - no. Initially I was angry that MS was about to change my life. As MS

is usually quite a slow illness, there has been time to get used to the changes

over the 15 years I've had it. If 15 years ago I was told that I'd be in a

wheelchair now it would have surely made me angry. As it is, it was a slow

progression and I see my chair as my friend that helps me do things I otherwise

couldn't. I have learnt to readjust and actually like the situation I am in and

no longer feel any anger. I concentrate on the things I can still do not on

those that I can't.

I've also had CCSVI treatment which gives me hope that I'll get out of this

chair.

Janet

PS I'm on facebook.

To: mscured

From: vbooth@...

Date: Wed, 20 Apr 2011 04:28:39 +0000

Subject: WOW.

This group has slowed waaaaay down.... I was hoping to get some answers about if

others have anger problems? I have melt downs here and there. Mainly because of

things falling around me, but I am wondering if others have experienced this. I

really hate feeling so hateful sometimes....

Hugs to all,

P.S. who s on facebook here? I am on facebook......

[Guest guest]

Don't throw the baby out with the bathwater. Depression isn't necessarily only

situational; it can be organic and MS-related.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC149791/

Martha

[Guest guest]

>

> This group has slowed waaaaay down.... I was hoping to get some answers about

if others have anger problems? I have melt downs here and there.

>

I had some meltdowns even prior to MS, so I can't be sure that it's the root

cause. However, I do remember reading somewhere that some people with MS have

auditory symptoms. One of the things that I noticed before I got my symptoms

under control was that I had a lot less patience with my kids, especially the

noise. I do think that my lower tolerance for that was part of my symptoms.

One thing I also realized after I started BBD and got better was that I had been

feeling the fatigue and brain fog for a long time before the optic neuritis came

on. So it's quite possible that some of the less common symptoms, like auditory

issues/depression/anger were part of the condition and just manifested way

before the more obvious neurological stuff.

Crystal

[Guest guest]

Hey ,

I was diagnosed last summer/fall and I have noticed a big change in my moods. 

Some days I am perfectly fine, others I will get annoyed/irritated with the

slightest thing.  The BBD has helped me " control " these, but they still

happen.  My patience can be very small some times and there is nothing I can do

to change it, even when I realize that there is no reason to act like that.  I

noticed the biggest difference when my voodoo witch doctor did the pressure

points for plutonium.  I noticed the change as soon as I left his office; I had

no road rage going back to work.  Since then, and even more since the plant in

Japan has been destroyed, I can tell when there is " too much " plutonium in my

system because I am very short with people and get annoyed and the smallest

things.  If you see a natropath (sp?) ask them if you have plutonium, or other

metals, in your system and see if they can help.

Yes, I am on facebook.  Let me know where you are and I will find you.

Subject: WOW.

To: mscured

Date: Tuesday, April 19, 2011, 9:28 PM

 

This group has slowed waaaaay down.... I was hoping to get some answers

about if others have anger problems? I have melt downs here and there. Mainly

because of things falling around me, but I am wondering if others have

experienced this. I really hate feeling so hateful sometimes....

Hugs to all,

P.S. who s on facebook here? I am on facebook......

[Guest guest]

hi crystal, well first time i have heard that having ms is a blessing, surely

you would rather be without 'it'

 

me no vitamins, supplements, no special diet, blah, blah, just ldn since 02

december

 

there is no cure so pleased your feel blessed you have ms, i'm not

 

still trying to understand why there is a group called 'mscured' in copy

 

rgds/peter/london/ppms

To: mscured

Sent: Sunday, 24 April 2011, 3:42

Subject: Re: WOW.

 

I think that I'm able to say it because I was fortunate enough to get a very

early start on kicking MS's butt. I've suffered no permanent disability, which I

would think makes it a bit harder to say that MS is a blessing. In my case,

though, I'm healthier and in better shape than I've ever been in my life. That

is thanks to the MS coming along and forcing me to make the choices that have

made me healthier. I had been into alternative medicine and healing for some

time before that, so it was my chance to put my money where my mouth is. It

also helped me realize something that is often said on this group...what works

for one doesn't necessarily work for all. I thought I had a healthy lifestyle

prior to the attack of optic neuritis. Turns out that my vegetarian life, which

included *a lot* of gluten and beans/legumes, was not the way to go for me

personally! That doesn't mean that others can't thrive on it though.

Crystal

>

>

> I am amazed when people see it as a 'gift' or as something great!

> I think it's terriffic for those that do, but my goodness gracious, that is

something which I can never say. lol

> I'm over being angry at it, but will NEVER welcome CCSVI or 'MS' into my life!

>