Re: Hi (new member) (Holly)

[Guest guest]

Welcome HollyI'm sure everyone will always help answer questions where we can

and give you the (and Rod) the help you might need in making sure reoccurrences

and 'problems' stay minimal.

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

MARCUS AURELIUS (121 - 180 A.D.)

To: mscured

From: hly62@...

Date: Sat, 17 Dec 2011 13:18:27 +0000

Subject: Hi (new member) (Holly)

Hello, my name is Holly, I joined because a few months ago I met a

wonderful man, I fell in love with him and care deeply for him. A few weeks ago

he fell ill while at work, his left side of his body went numb and tingly and

will at times hurt when touched...

[Guest guest]

Hello Holly,

Welcome to the group!

Here is a website Rod may find helpful in treating his MS:

http://tinyurl.com/advice-to-msers

With best wishes,

Dudley Delany

http://profiles.yahoo.com/dudley_delany

[Guest guest]

hi to you both - suggest you wait for the diagnosis of MS then you would get a

lot of support from this and other groups

good luck/peter/london/ppms

________________________________

To: mscured

Sent: Saturday, 17 December 2011, 13:18

Subject: Hi (new member) (Holly)

 

Hello, my name is Holly, I joined because a few months ago I met a wonderful

man, I fell in love with him and care deeply for him. A few weeks ago he fell

ill while at work, his left side of his body went numb and tingly and will at

times hurt when touched.... we went to the doctor and then we're sent to a

bigger hospital. Talked with a nurologist who believes Rod has MS, we are still

waiting for final results which we will know on tuesday of next week if he has

it for sure but with what the nurologist says and what we both see in his

symptoms we are pretty sure he has it. I joined here because I'd like to do

whatever I can to make this mans life as good as I can. I want to learn about

MS so that I am able to help him in anyway I can. I look forward to hearing

what everyone has to say on here, will spend some time looking at past posts to

whats there. Thank you for allowing me to be a part of this group.

Holly (and Rod)

[Guest guest]

Hi Holly,

Fear not...there is a lot that he can do to help if it is MS. Go to

www.thomasbayuk.com If you cannot afford to buy the book send me your mailing

address and I will send to you.

Regards,

Tom Bayuk

Hi (new member) (Holly)

Hello, my name is Holly, I joined because a few months ago I met a wonderful

man, I fell in love with him and care deeply for him. A few weeks ago he fell

ill while at work, his left side of his body went numb and tingly and will at

times hurt when touched.... we went to the doctor and then we're sent to a

bigger hospital. Talked with a nurologist who believes Rod has MS, we are still

waiting for final results which we will know on tuesday of next week if he has

it for sure but with what the nurologist says and what we both see in his

symptoms we are pretty sure he has it. I joined here because I'd like to do

whatever I can to make this mans life as good as I can. I want to learn about MS

so that I am able to help him in anyway I can. I look forward to hearing what

everyone has to say on here, will spend some time looking at past posts to whats

there. Thank you for allowing me to be a part of this group.

Holly (and Rod)

[Guest guest]

Hi Holly (and Rod)I would look into CCSVI treatment which has helped me more

than anything else in the 16 years I've had MS.The Best Bet Diet (BBD) also

helped a fair bit. Exercise, dietary supplement and stress removal too.When

you've looked through the posts here, come back and ask any questions, one of us

will answer.Janet

To: mscured

From: hly62@...

Date: Sat, 17 Dec 2011 13:18:27 +0000

Subject: Hi (new member) (Holly)

Hello, my name is Holly, I joined because a few months ago I met a

wonderful man, I fell in love with him and care deeply for him. A few weeks ago

he fell ill while at work, his left side of his body went numb and tingly and

will at times hurt when touched.... we went to the doctor and then we're sent to

a bigger hospital. Talked with a nurologist who believes Rod has MS, we are

still waiting for final results which we will know on tuesday of next week if he

has it for sure but with what the nurologist says and what we both see in his

symptoms we are pretty sure he has it. I joined here because I'd like to do

whatever I can to make this mans life as good as I can. I want to learn about

MS so that I am able to help him in anyway I can. I look forward to hearing

what everyone has to say on here, will spend some time looking at past posts to

whats there. Thank you for allowing me to be a part of this group.

Holly (and Rod)

[Guest guest]

Hi,

Not sure if you can take out some insurance before you get a definitive

diagnosis but maybe this might just be possible.

You'll get plenty of good advice from the folks on this forum. My wife Sandi,

has MS since 2004. There have been difficult times, but we have struggled

through. The many changes we made in diet and lifestyle have made a difference

but the most significant change was through being treated for CCSVI. However

there is still much to do and I know we must persevere.

Ask questions and research yourself, each MS case is different, so some things

will work for some and others won't. Dont make any rash decisions. It is very

much trial and error I'm afraid.

Cheers,

Pinda

>

> Hello, my name is Holly, I joined because a few months ago I met a wonderful

man, I fell in love with him and care deeply for him. A few weeks ago he fell

ill while at work, his left side of his body went numb and tingly and will at

times hurt when touched.... we went to the doctor and then we're sent to a

bigger hospital. Talked with a nurologist who believes Rod has MS, we are still

waiting for final results which we will know on tuesday of ik if he has it for

sure but with what the nurologist says and what we both see in his symptoms we

are pretty sure he has it. I joined here because I'd like to do whatever I can

to make this mans life as good as I can. I want to learn about MS so that I am

able to help him in anyway I can. I look forward to hearing what everyone has

to say on here, will spend some time looking at past posts to whats there. Thank

you for allowing me to be a part of this group.

> Holly (and Rod)

>

[Guest guest]

Holly,

I had the exact same thing happen to me but @ home and it was my right side.

Over about 4 days my right side arm, then chest, then leg and finally skull/face

went numb. They did all the tests he's gonna get done. For the first 2 yrs after

my MS diagnosis I was relapse free. Three yrs ago my life as I knew it changed

forever. After moving back home w/ my folks at age 32 I embarked on a worsening

spiral that got so bad I ended up in a scooter and homebound. Despite getting

several yearly MRI the md's had no clinical evidence of new or active lesions.

Finally after meeting a person who remarked she had been misdiagnosed with MS

and actually had Lyme Disease I got new hope. Several of her previous Lyme tests

all came back neg. She found a LLMD (lyme literate) who sent her blood to

IgeneX labs and it came back positive for lyme disease. I immediately sched. an

appt. w/ her llmd and was tested. It also came back pos. for Bb lyme disease.

Lyme Disease mimmiks MS in every way. Don't settle for some neurologist and a

few test results to say you have MS. He needs to be his own advocate.

Lyme can be knocked out if you get properly tested and treated in as little as a

month. My Lyme had 5 yrs to get burrowed in my body because I settled for what

the tests and some neurologist said. Now I'm fighting to just walk again all

because the correct tests and the right lab was not used. All the test that were

previously done said MS.

He needs to be sure. Find a llmd that uses IgeneX and get tested for Lyme

Disease. Anyone in here will tell you that living with MS symptom free is very

difficult. Lyme can be cured if caught early enough.

Good Luck...

-M

[Guest guest]

Hi Holly & welcome aboard,

There is a ton of info out there to pick through and many of us are managing and

even curing ourselves without drugs. My advice to you is that there are a

couple things you can start right now, today, while you are going through all

the info. One is a daily megadose of Vitamin D (you need to take calcium with

it). I take 10,000IU in summer and 15,000IU in winter. The other thing is to

pick a diet - Best Bet Diet and Swank are the most common but there are other

options. Get going on those things right away and he'll already be on the way

back. Good luck!

Crystal

> I want to learn about MS so that I am able to help him in anyway I can. I

look forward to hearing what everyone has to say on here, will spend some time

looking at past posts to whats there. Thank you for allowing me to be a part of

this group.

>