Re: June Grimes - New Zealand

[Guest guest]

June,

I am sorry to hear you have cerebellar Atrophy. I am also sorry to

hear about the passing of your husband. It sounds like you have had a

lot thrown at you in a short amount of time. You are fortunate to

have alot of support with your family and friends. You have come to a

wonderful place. We are all like family here and are always there for

others. Welcome!

God Bless,

Belinda

> Hello all. I am so glad to have found others with my problem. I

was beginning to think I was the only one diagnosed with cerebellar

atrophy. My name is June Grimes and I live in Auckland, NZ. I have

4 children, none who seem to have been affected (fingers crossed). I

will be 62 this coming July and my husband died last year from cancer

of the lung. My balance is not too good (I walk as if I am drunk) -

not true and my hands tremble at times. I am not on any medication

but take loads of vitamins hoping to hit on the " right " one some

day. I belong to the Motor Neurone Society as it seems to be the

closest thing in this part of the world.

> I am a member of the local Lioness Club and it is the friendship of

the other ladies that keeps me going although I gets lots of support

from my family.

> My mother is in a rest home and I am taking her out tomorrow. She

will be 93 next week and is so fit it makes me sick!! Not really.

>

> Love to you all

> June

[Guest guest]

June,

I am sorry to hear you have cerebellar Atrophy. I am also sorry to

hear about the passing of your husband. It sounds like you have had a

lot thrown at you in a short amount of time. You are fortunate to

have alot of support with your family and friends. You have come to a

wonderful place. We are all like family here and are always there for

others. Welcome!

God Bless,

Belinda

> Hello all. I am so glad to have found others with my problem. I

was beginning to think I was the only one diagnosed with cerebellar

atrophy. My name is June Grimes and I live in Auckland, NZ. I have

4 children, none who seem to have been affected (fingers crossed). I

will be 62 this coming July and my husband died last year from cancer

of the lung. My balance is not too good (I walk as if I am drunk) -

not true and my hands tremble at times. I am not on any medication

but take loads of vitamins hoping to hit on the " right " one some

day. I belong to the Motor Neurone Society as it seems to be the

closest thing in this part of the world.

> I am a member of the local Lioness Club and it is the friendship of

the other ladies that keeps me going although I gets lots of support

from my family.

> My mother is in a rest home and I am taking her out tomorrow. She

will be 93 next week and is so fit it makes me sick!! Not really.

>

> Love to you all

> June

[Guest guest]

June,

I am sorry to hear you have cerebellar Atrophy. I am also sorry to

hear about the passing of your husband. It sounds like you have had a

lot thrown at you in a short amount of time. You are fortunate to

have alot of support with your family and friends. You have come to a

wonderful place. We are all like family here and are always there for

others. Welcome!

God Bless,

Belinda

> Hello all. I am so glad to have found others with my problem. I

was beginning to think I was the only one diagnosed with cerebellar

atrophy. My name is June Grimes and I live in Auckland, NZ. I have

4 children, none who seem to have been affected (fingers crossed). I

will be 62 this coming July and my husband died last year from cancer

of the lung. My balance is not too good (I walk as if I am drunk) -

not true and my hands tremble at times. I am not on any medication

but take loads of vitamins hoping to hit on the " right " one some

day. I belong to the Motor Neurone Society as it seems to be the

closest thing in this part of the world.

> I am a member of the local Lioness Club and it is the friendship of

the other ladies that keeps me going although I gets lots of support

from my family.

> My mother is in a rest home and I am taking her out tomorrow. She

will be 93 next week and is so fit it makes me sick!! Not really.

>

> Love to you all

> June

[Guest guest]

Hello June,

Welcome to the group.

I'm certain you will find answers to lots of questions you now have with these fine folks.

Take care.

Dr. Ray, Las Vegas

-- June Grimes - New Zealand

Hello all. I am so glad to have found others with my problem. I was beginning to think I was the only one diagnosed with cerebellar atrophy. My name is June Grimes and I live in Auckland, NZ. I have 4 children, none who seem to have been affected (fingers crossed). I will be 62 this coming July and my husband died last year from cancer of the lung. My balance is not too good (I walk as if I am drunk) - not true and my hands tremble at times. I am not on any medication but take loads of vitamins hoping to hit on the "right" one some day. I belong to the Motor Neurone Society as it seems to be the closest thing in this part of the world.

I am a member of the local Lioness Club and it is the friendship of the other ladies that keeps me going although I gets lots of support from my family.

My mother is in a rest home and I am taking her out tomorrow. She will be 93 next week and is so fit it makes me sick!! Not really.

Love to you all

JuneIf you do not wish to belong to shydrager, you may unsubscribe by sending a blank email to shydrager-unsubscribe

[Guest guest]

Hello June,

Welcome to the group.

I'm certain you will find answers to lots of questions you now have with these fine folks.

Take care.

Dr. Ray, Las Vegas

-- June Grimes - New Zealand

Hello all. I am so glad to have found others with my problem. I was beginning to think I was the only one diagnosed with cerebellar atrophy. My name is June Grimes and I live in Auckland, NZ. I have 4 children, none who seem to have been affected (fingers crossed). I will be 62 this coming July and my husband died last year from cancer of the lung. My balance is not too good (I walk as if I am drunk) - not true and my hands tremble at times. I am not on any medication but take loads of vitamins hoping to hit on the "right" one some day. I belong to the Motor Neurone Society as it seems to be the closest thing in this part of the world.

I am a member of the local Lioness Club and it is the friendship of the other ladies that keeps me going although I gets lots of support from my family.

My mother is in a rest home and I am taking her out tomorrow. She will be 93 next week and is so fit it makes me sick!! Not really.

Love to you all

JuneIf you do not wish to belong to shydrager, you may unsubscribe by sending a blank email to shydrager-unsubscribe

[Guest guest]

Hello June,

Welcome to the group.

I'm certain you will find answers to lots of questions you now have with these fine folks.

Take care.

Dr. Ray, Las Vegas

-- June Grimes - New Zealand

Hello all. I am so glad to have found others with my problem. I was beginning to think I was the only one diagnosed with cerebellar atrophy. My name is June Grimes and I live in Auckland, NZ. I have 4 children, none who seem to have been affected (fingers crossed). I will be 62 this coming July and my husband died last year from cancer of the lung. My balance is not too good (I walk as if I am drunk) - not true and my hands tremble at times. I am not on any medication but take loads of vitamins hoping to hit on the "right" one some day. I belong to the Motor Neurone Society as it seems to be the closest thing in this part of the world.

I am a member of the local Lioness Club and it is the friendship of the other ladies that keeps me going although I gets lots of support from my family.

My mother is in a rest home and I am taking her out tomorrow. She will be 93 next week and is so fit it makes me sick!! Not really.

Love to you all

JuneIf you do not wish to belong to shydrager, you may unsubscribe by sending a blank email to shydrager-unsubscribe

[Guest guest]

Hi June,

I'll forward your message to the group. The correct email to reach the

entire group is shydrager

Regards,

Pam

June Grimes - New Zealand

Can anyone please enlighten me - did we catch this disease or were we born

with it?

June