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hi just thought id ask if anybody is having same problems as me and if you are

what your doing about it,you see its like this i cant control my emotions, one

minute im happy next im sad then im angry and so on its realy getting to me ive

had ms for 20 years now and been on ldn for 6 but dont take anything else but

ive got to do something because i cant keep bursting into tears at the drop of a

hat, any ideas?

andy in uk

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Check out your testosterone levels. Men get low too. Try St. 's wart or SAM-E. Make sure you drink green tea and take fish oil. Green tea and fish oil help with your mood. Kathy

[low dose naltrexone] emotional

hi just thought id ask if anybody is having same problems as me and if you are what your doing about it,you see its like this i cant control my emotions, one minute im happy next im sad then im angry and so on its realy getting to me ive had ms for 20 years now and been on ldn for 6 but dont take anything else but ive got to do something because i cant keep bursting into tears at the drop of a hat, any ideas? andy in uk-----------------------------------------Email sent from www.ntlworld.comVirus-checked using McAfee® Software Visit www.ntlworld.com/security for more information

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I saw DLPA mentioned before, but don't know what it is....assume

it is a natural supplement to elevate mood?? Could you tell me what

it is and if many have been helped.

I intend to start LDN this month. I just found out about it a few

weeks ago. This has been my worst year since I was diagnosed in

1990. The MS never got me down for long... til now. That is why I

have decided to try LDN. Maybe I could use the DLPA too???

Also, I saw bits and pieces of some emails that talked about

the " soap thing " ....putting liquid soap on legs and bars of soap in

bed???....sounded like it was for spasms or pain??? Could someone

repeat the whole theory??

thanks, nancy

>

> Hello Andy,

>

> I am exactly the same way that you are describing. Up one minute,

down the next. Its driving me crazy and my boyfriend too! I have

tried all of the anti depressant meds and none seem to help. I am

taking DLPA (must get Solaray brand) only one a day. I can tell a

difference with it, but I think that it truly is also just the

nature of the disease. It is depressing. It is hard to want to do

things so bad, and you can't do them. I am tired of it. I have had

MS for 15 years, and you think I'd be used to it, but it doesn't get

easier. I would love to have a child, I really would but I'm afraid

of bringing someone else into a messy situation. I tried DLPA in

desperation and it did help, I feel much better. But I also think

that my diet has alot to do with it. I am going to go to a

nutritionist. I just have to find a good one.

>

> I am there with you,

>

> [low dose naltrexone] emotional

>

>

> hi just thought id ask if anybody is having same problems as me

and if you are what your doing about it,you see its like this i cant

control my emotions, one minute im happy next im sad then im angry

and so on its realy getting to me ive had ms for 20 years now and

been on ldn for 6 but dont take anything else but ive got to do

something because i cant keep bursting into tears at the drop of a

hat, any ideas?

> andy in uk

>

> -----------------------------------------

> Email sent from www.ntlworld.com

> Virus-checked using McAfee® Software

> Visit www.ntlworld.com/security for more information

>

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>

>

> I saw DLPA mentioned before, but don't know what it is....assume

> it is a natural supplement to elevate mood?? Could you tell me what

> it is and if many have been helped.

> I intend to start LDN this month. I just found out about it a few

> weeks ago. This has been my worst year since I was diagnosed in

> 1990. The MS never got me down for long... til now. That is why I

> have decided to try LDN. Maybe I could use the DLPA too???

> Also, I saw bits and pieces of some emails that talked about

> the " soap thing " ....putting liquid soap on legs and bars of soap in

> bed???....sounded like it was for spasms or pain??? Could someone

> repeat the whole theory??

> thanks, nancy

--

From 's site:

http://ldn.proboards3.com/index.cgi

This is the brand of DL-Phenylalanine I take at 500mg twice per day

(Solaray brand) at Dr. Bihari's recommendation if you do NOT have

high blood pressure. You get it at healthfood stores or order from

the internet, no Drs. script needed. Dr. Bihari says this will keep

your endorphins up throughout the day.

CAUTION: This product NOT intended for use by people with PKU

(Phenylketonuria), or pregnant or lactating women. If you have high

blood pressure or pre-existing pigmented malignant melanoma, use only

under the guidance of a physician. Do NOT take with MAO inhibitor

antidepressant drugs.

DL-Phenylalanine 500mg by Solaray

http://www.affordablesolaray.com/4871.html

Nutraceutical.com / Product Information-Solaray DL-Phenylalanine

500mg caps

http://www.nutraceutical.com/search/view_product.cfm?

product_index=4871

What is DL-Phenylalanine? Here are two great explanations.

DL-Phenylalanine

http://www.internalhealth.com/dl_phenylalanine.htm

DL-Phenylalanine

http://www.vrmed.com/dl-phenylalanine.htm

Sleeping with a bar of soap is supposed to help with body aches and

pains, and it can't be one of those skin moisturizing soaps like Dove

or Dial. Just good old fashioned scrubbing soaps like Ivory. Why it

works, if indeed it does, I don't know.

Artie

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  • 2 years later...

Dear Deanna, I wish I could reach through the computer right now and just hug

you for a long time and cry on your shoulder and you on mine. I am feeling the

exact same way right at this moment and had just moments before checking my

email, wondered if there was ANYONE out there who would understand and just

listen to me for a moment. As soon as I read this, I began to  cry as I had been

on the verge of it ever since I WOKE UP TODAY.. Thanks so much for being there

and writing this today.

God love you Deanna,,,, its again, and as soon as I stop crying, I will

write more to you....

sincerely, in Ga.

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Deanna - yes, I had that problem for the first year or so until we got

the PA under control with DMARDs. It still happens now whenever I

flare. It can be so bad that I won't answer the phone, because I know

the first thing the caller will say is " How are you? " and that question

is enough to trigger a crying jag. I went from a person who could

calmly field computer questions on the radio and regularly spoke before

crowds numbering in the hundreds to a blubbering idiot. Yes, I think

it's the result of chronic pain. The only solution is to get the

disease under control. best regards, sherry z

>

> Does anyone else have trouble controlling their emotions? I have had

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Hi,

Been there -- done that.

I believe for me its fibromyalgia. I describe fibro as permenant

PMS. Hots, cold, sad, happy, crying or laughing.

I really felt like a mess when all this first started. Since I

figured out its the fibro and not really me that is making all of

these emotions come out, I can control it a bit.

I haven't tried much but I know vitamin B 12 and evening primrose oil

can help with moods.

When I get upset about something I try to change the subject somehow.

Just wanted to let you know you're not alone. Good luck and happy

new year.

SD

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Sherry is right that pain can cause your emotions to go haywire. Living with

chronic pain affects all points of your life and it's important to get things

under control.

When I first showed signs of PA I was in a lot of pain and it took almost 6

months to get a diagnosis. In that time period I went from someone who worked

10 to 12 hours a day to barely being able to even drive to work for 3 days a

week and work for only 5 hours. I had trouble concentrating on work and had

absolutely NO tolerance for anyone I worked with. Luckily the girl I worked

closely with knew what was going on and didn't take offense when I snapped at

her. I finally had to stop working between the pain and having to do dialysis

on top of it all I just couldn't function any more and be of any use.

I still have bad days but they are no where near as rotten as they were before I

got a rheumatologist who knew how to treat this.

Celeste

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