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I'm with you. " I'm worried about a family-member. He's been diagnosed with a

Physical Illness. He's Physically Ill. "

> Following up on 's post about the therapist & others blaming her - I was

reading another OCD book where it said that OCD is partly blamed on environment,

can be due to stress in the home, related to traumatic life event. Why don't

they ever say that about cancer or diabetes or osteoporosis? If they looked at

other factors as closely for these conditions as they seem to for OCD, they

might identify something similar. It seems pretty unfair to point fingers at the

family just because it's a " mental " illness.

>

> As far as that goes, whoever says they know someone with a " physical illness " ?

All physical illness are given specific names, like above. Why " mental illness " ?

>

> I'm just really upset that my son came down with a " mental illness " rather

than a condition with a name like all the physical illnesses. Can you imagine

NAPI?

>

> Rhonda

>

>

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All of the rest is related to stress. About 97% of cancers are diet and life

style choices, according to docs now treating two of my family members. I have

arthritis and was told stress is a huge factor in pain .... encouraged to try

yoga as was my child for OCD. I don't know about stress and diabetes for sure,

but it is diet related and I have a friend that always travels with snacks cause

her blood sugar levels drop if she is stuck in traffic ... late for work ... so

that sounds stress related to me.

 

This is not about blame and when we were told OCD was related to home life ....

stress and such I didn't take it as blame .... or finger pointing. Is it not

understood by most that behaviors go up when stress goes up?

 

But, helping my child learn to relax, self sooth, deep breathing ... making sure

she gets enough time on the track and in the pool, making sure she eats

correctly, gets enough sleep, learns to talk about things cause her to worry ...

she didn't really like yoga ... it all helps and never will I rely 100% on

medication .... we approach this from many directions.

________________________________

To:

Sent: Saturday, April 14, 2012 12:44 PM

Subject: Re: pet peeve

I'm with you. " I'm worried about a family-member.  He's been diagnosed with a

Physical Illness.  He's Physically Ill. "

> Following up on 's post about the therapist & others blaming her - I was

reading another OCD book where it said that OCD is partly blamed on environment,

can be due to stress in the home, related to traumatic life event. Why don't

they ever say that about cancer or diabetes or osteoporosis? If they looked at

other factors as closely for these conditions as they seem to for OCD, they

might identify something similar. It seems pretty unfair to point fingers at the

family just because it's a " mental " illness.

>

> As far as that goes, whoever says they know someone with a " physical illness " ?

All physical illness are given specific names, like above. Why " mental illness " ?

>

> I'm just really upset that my son came down with a " mental illness " rather

than a condition with a name like all the physical illnesses. Can you imagine

NAPI?

>

> Rhonda

>

>

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OK, I'm tired so maybe not clearly thinking at the moment, but OCD is the name.

It falls under mental illness, but it is the name of your child's condition.

Mental illnesses are given a name. So, not grasping that part....

Stress does play a role in physical illnesses, and can trigger some, cancer

included (from what I've read). Just like OCD can be " there " but not triggered

yet. Something starts OCD, brings it " out. " Can be the same with physical

illnesses and stress/environment/trauma CAN play a part. Bipolar can be " there "

but not triggered (some meds can bring that out!) For me, it's CAN PLAY a part

with the triggering for either, not necessarily the cause for all. Genetics

plays a part with both types too. I also hate when a book says that about

stress/environment if that is all it seems to say as a cause. If that were it,

why only one of my three sons?

OCD in our family, I can look at my mom and say, Yep all from her and her side

of the family, lol. But no blame.

But yeah, people grow more concerned for others who have a physical illness than

a mental one, i.e., friends, relatives....

>

> Following up on 's post about the therapist & others blaming her - I was

reading another OCD book where it said that OCD is partly blamed on environment,

can be due to stress in the home, related to traumatic life event. Why don't

they ever say that about cancer or diabetes or osteoporosis? If they looked at

other factors as closely for these conditions as they seem to for OCD, they

might identify something similar. It seems pretty unfair to point fingers at the

family just because it's a " mental " illness.

>

> As far as that goes, whoever says they know someone with a " physical illness " ?

All physical illness are given specific names, like above. Why " mental illness " ?

>

> I'm just really upset that my son came down with a " mental illness " rather

than a condition with a name like all the physical illnesses. Can you imagine

NAPI?

>

> Rhonda

>

>

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Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

If I could say to Grandma and Grandpa, my son is being treated for glucositis,

they would look concerned and sympathetic, rather than nervous and uneasy. It's

a double burden for folks with OCD to have to cope with the name as well as the

actual condition. Of course I never gave it a thought until my son got it; I was

a finger pointer myself.

In 2010 they finally passed a law mandating " mentally retarded " be changed to

" intellectual disability. " I hope it doesn't take that long with OCD. Meanwhile

I guess I have to learn to live with it!!

Rhonda

Re: pet peeve

OK, I'm tired so maybe not clearly thinking at the moment, but OCD is the

name. It falls under mental illness, but it is the name of your child's

condition. Mental illnesses are given a name. So, not grasping that part....

Stress does play a role in physical illnesses, and can trigger some, cancer

included (from what I've read). Just like OCD can be " there " but not triggered

yet. Something starts OCD, brings it " out. " Can be the same with physical

illnesses and stress/environment/trauma CAN play a part. Bipolar can be " there "

but not triggered (some meds can bring that out!) For me, it's CAN PLAY a part

with the triggering for either, not necessarily the cause for all. Genetics

plays a part with both types too. I also hate when a book says that about

stress/environment if that is all it seems to say as a cause. If that were it,

why only one of my three sons?

OCD in our family, I can look at my mom and say, Yep all from her and her side

of the family, lol. But no blame.

But yeah, people grow more concerned for others who have a physical illness

than a mental one, i.e., friends, relatives....

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How about " neuro-biological condition " . Not a huge improvement, but it does

avoid some stigmatizing words.

> Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for glucositis,

they would look concerned and sympathetic, rather than nervous and uneasy. It's

a double burden for folks with OCD to have to cope with the name as well as the

actual condition. Of course I never gave it a thought until my son got it; I was

a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed to

" intellectual disability. " I hope it doesn't take that long with OCD. Meanwhile

I guess I have to learn to live with it!!

>

> Rhonda

>

> Re: pet peeve

>

> OK, I'm tired so maybe not clearly thinking at the moment, but OCD is the

name. It falls under mental illness, but it is the name of your child's

condition. Mental illnesses are given a name. So, not grasping that part....

>

> Stress does play a role in physical illnesses, and can trigger some, cancer

included (from what I've read). Just like OCD can be " there " but not triggered

yet. Something starts OCD, brings it " out. " Can be the same with physical

illnesses and stress/environment/trauma CAN play a part. Bipolar can be " there "

but not triggered (some meds can bring that out!) For me, it's CAN PLAY a part

with the triggering for either, not necessarily the cause for all. Genetics

plays a part with both types too. I also hate when a book says that about

stress/environment if that is all it seems to say as a cause. If that were it,

why only one of my three sons?

>

> OCD in our family, I can look at my mom and say, Yep all from her and her side

of the family, lol. But no blame.

>

> But yeah, people grow more concerned for others who have a physical illness

than a mental one, i.e., friends, relatives....

>

>

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OCD does have negative connotations, I agree. I appreciate shows like Glee,

who have made effort to change the message. 

-JuLeah

________________________________

To:

Sent: Saturday, April 14, 2012 4:03 PM

Subject: Re: Re: pet peeve

 

Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

If I could say to Grandma and Grandpa, my son is being treated for glucositis,

they would look concerned and sympathetic, rather than nervous and uneasy. It's

a double burden for folks with OCD to have to cope with the name as well as the

actual condition. Of course I never gave it a thought until my son got it; I was

a finger pointer myself.

In 2010 they finally passed a law mandating " mentally retarded " be changed to

" intellectual disability. " I hope it doesn't take that long with OCD. Meanwhile

I guess I have to learn to live with it!!

Rhonda

Re: pet peeve

OK, I'm tired so maybe not clearly thinking at the moment, but OCD is the name.

It falls under mental illness, but it is the name of your child's condition.

Mental illnesses are given a name. So, not grasping that part....

Stress does play a role in physical illnesses, and can trigger some, cancer

included (from what I've read). Just like OCD can be " there " but not triggered

yet. Something starts OCD, brings it " out. " Can be the same with physical

illnesses and stress/environment/trauma CAN play a part. Bipolar can be " there "

but not triggered (some meds can bring that out!) For me, it's CAN PLAY a part

with the triggering for either, not necessarily the cause for all. Genetics

plays a part with both types too. I also hate when a book says that about

stress/environment if that is all it seems to say as a cause. If that were it,

why only one of my three sons?

OCD in our family, I can look at my mom and say, Yep all from her and her side

of the family, lol. But no blame.

But yeah, people grow more concerned for others who have a physical illness than

a mental one, i.e., friends, relatives....

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Ohhh...yeah. Let's see. Like, Grandma, my son is being treated for a

neurological problem...but a name? Neuroocd or neurocd, not sure they would

have a way to pronounce. Neuroc with the " c " sound as a " k " so neurock?

neurocitis?

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

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I like neurocitis! Grandma would be too baffled to say anything! ;-)

Rhonda

Re: pet peeve

Ohhh...yeah. Let's see. Like, Grandma, my son is being treated for a

neurological problem...but a name? Neuroocd or neurocd, not sure they would have

a way to pronounce. Neuroc with the " c " sound as a " k " so neurock? neurocitis?

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I

guess to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

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Hi Rhonda,

You might want to try " brain-based disorder " . I have started using this myself.

It's the physical part of the body that is affected, the brain, which seems to

make people think a bit differently. You could use your part of " brain not

processing properly " too!

I also prefer, mental health, to mental illness.

You might use anxiety disorder instead of OCD, if you don't want to get into an

explanation. Everyone understands what it is to feel anxious.

With intellectual disabilities, I'm familiar with the term developmental delays.

I like the idea that there is a delay, so it is not a disability so much as

something that needs more time to develop. It really is in how you choose to

look at it. Our son has delays, and it helps me to think of them this way.

Instead of limitations I wonder what the possibilities will be, because we

really don't know.

When you develop a comfort level with the OCD, and it becomes just part of your

life, you may find the term doesn't bother you as much. I do know what you mean

though, and the stigma around all mental health issues can be oppressive and

isolating. You will find your way to talk about it, and will start to know who

you can be more open with what.

Our son's grandfather, when we told him our son had OCD, left the room, then

came back and said, " he'll grow out of it! " Both grandparents did not believe

in psychologists/psychiatrists, or have any understanding about OCD. I gave

them some things to read, and I think that made it worse, because then they were

really worried about what kind of life he would have. He did live with them for

a period of time and they learned first hand what OCD looked like! Six years

later they have learned a lot, and accept without understanding fully, because

they love their grandson.

All that to say, sometimes they just need time to come to an understanding.

They will still say unhelpful things, same as everyone else, wanting to help or

give you " the answer " ....that's when forgiveness comes in handy - I learned to

forgive people before they opened their mouths, knowing they just could not

understand.

Maybe your son could come up with a name that describes how the OCD feels to him

that would give his grandparents a better understanding and help them be more

sympathetic - try " brain terrorist " (our son would use this). Humor is a good

way to go :)

The book, Brain Lock, has one of the best explanations of what is going on in

the brain with OCD, and how ERP works. They show brain scans to show the

changes before and after ERP. This might help them to understand better.

Warmly,

Barb

Canada

Son, 20, OCD, PDD-NOS(Delays/LD)

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for glucositis,

they would look concerned and sympathetic, rather than nervous and uneasy. It's

a double burden for folks with OCD to have to cope with the name as well as the

actual condition. Of course I never gave it a thought until my son got it; I was

a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed to

" intellectual disability. " I hope it doesn't take that long with OCD. Meanwhile

I guess I have to learn to live with it!!

>

> Rhonda

>

>

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Hi Rhonda,

You might want to try " brain-based disorder " . I have started using this myself.

It's the physical part of the body that is affected, the brain, which seems to

make people think a bit differently. You could use your part of " brain not

processing properly " too!

I also prefer, mental health, to mental illness.

You might use anxiety disorder instead of OCD, if you don't want to get into an

explanation. Everyone understands what it is to feel anxious.

With intellectual disabilities, I'm familiar with the term developmental delays.

I like the idea that there is a delay, so it is not a disability so much as

something that needs more time to develop. It really is in how you choose to

look at it. Our son has delays, and it helps me to think of them this way.

Instead of limitations I wonder what the possibilities will be, because we

really don't know.

When you develop a comfort level with the OCD, and it becomes just part of your

life, you may find the term doesn't bother you as much. I do know what you mean

though, and the stigma around all mental health issues can be oppressive and

isolating. You will find your way to talk about it, and will start to know who

you can be more open with what.

Our son's grandfather, when we told him our son had OCD, left the room, then

came back and said, " he'll grow out of it! " Both grandparents did not believe

in psychologists/psychiatrists, or have any understanding about OCD. I gave

them some things to read, and I think that made it worse, because then they were

really worried about what kind of life he would have. He did live with them for

a period of time and they learned first hand what OCD looked like! Six years

later they have learned a lot, and accept without understanding fully, because

they love their grandson.

All that to say, sometimes they just need time to come to an understanding.

They will still say unhelpful things, same as everyone else, wanting to help or

give you " the answer " ....that's when forgiveness comes in handy - I learned to

forgive people before they opened their mouths, knowing they just could not

understand.

Maybe your son could come up with a name that describes how the OCD feels to him

that would give his grandparents a better understanding and help them be more

sympathetic - try " brain terrorist " (our son would use this). Humor is a good

way to go :)

The book, Brain Lock, has one of the best explanations of what is going on in

the brain with OCD, and how ERP works. They show brain scans to show the

changes before and after ERP. This might help them to understand better.

Warmly,

Barb

Canada

Son, 20, OCD, PDD-NOS(Delays/LD)

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for glucositis,

they would look concerned and sympathetic, rather than nervous and uneasy. It's

a double burden for folks with OCD to have to cope with the name as well as the

actual condition. Of course I never gave it a thought until my son got it; I was

a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed to

" intellectual disability. " I hope it doesn't take that long with OCD. Meanwhile

I guess I have to learn to live with it!!

>

> Rhonda

>

>

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Hi Rhonda,

You might want to try " brain-based disorder " . I have started using this myself.

It's the physical part of the body that is affected, the brain, which seems to

make people think a bit differently. You could use your part of " brain not

processing properly " too!

I also prefer, mental health, to mental illness.

You might use anxiety disorder instead of OCD, if you don't want to get into an

explanation. Everyone understands what it is to feel anxious.

With intellectual disabilities, I'm familiar with the term developmental delays.

I like the idea that there is a delay, so it is not a disability so much as

something that needs more time to develop. It really is in how you choose to

look at it. Our son has delays, and it helps me to think of them this way.

Instead of limitations I wonder what the possibilities will be, because we

really don't know.

When you develop a comfort level with the OCD, and it becomes just part of your

life, you may find the term doesn't bother you as much. I do know what you mean

though, and the stigma around all mental health issues can be oppressive and

isolating. You will find your way to talk about it, and will start to know who

you can be more open with what.

Our son's grandfather, when we told him our son had OCD, left the room, then

came back and said, " he'll grow out of it! " Both grandparents did not believe

in psychologists/psychiatrists, or have any understanding about OCD. I gave

them some things to read, and I think that made it worse, because then they were

really worried about what kind of life he would have. He did live with them for

a period of time and they learned first hand what OCD looked like! Six years

later they have learned a lot, and accept without understanding fully, because

they love their grandson.

All that to say, sometimes they just need time to come to an understanding.

They will still say unhelpful things, same as everyone else, wanting to help or

give you " the answer " ....that's when forgiveness comes in handy - I learned to

forgive people before they opened their mouths, knowing they just could not

understand.

Maybe your son could come up with a name that describes how the OCD feels to him

that would give his grandparents a better understanding and help them be more

sympathetic - try " brain terrorist " (our son would use this). Humor is a good

way to go :)

The book, Brain Lock, has one of the best explanations of what is going on in

the brain with OCD, and how ERP works. They show brain scans to show the

changes before and after ERP. This might help them to understand better.

Warmly,

Barb

Canada

Son, 20, OCD, PDD-NOS(Delays/LD)

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I guess

to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for glucositis,

they would look concerned and sympathetic, rather than nervous and uneasy. It's

a double burden for folks with OCD to have to cope with the name as well as the

actual condition. Of course I never gave it a thought until my son got it; I was

a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed to

" intellectual disability. " I hope it doesn't take that long with OCD. Meanwhile

I guess I have to learn to live with it!!

>

> Rhonda

>

>

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Hi Barb-

Those are really helpful experiences, not only for what to say, but for my own

thinking. Thanks.

Rhonda

Re: pet peeve

Hi Rhonda,

You might want to try " brain-based disorder " . I have started using this

myself. It's the physical part of the body that is affected, the brain, which

seems to make people think a bit differently. You could use your part of " brain

not processing properly " too!

I also prefer, mental health, to mental illness.

You might use anxiety disorder instead of OCD, if you don't want to get into

an explanation. Everyone understands what it is to feel anxious.

With intellectual disabilities, I'm familiar with the term developmental

delays. I like the idea that there is a delay, so it is not a disability so much

as something that needs more time to develop. It really is in how you choose to

look at it. Our son has delays, and it helps me to think of them this way.

Instead of limitations I wonder what the possibilities will be, because we

really don't know.

When you develop a comfort level with the OCD, and it becomes just part of

your life, you may find the term doesn't bother you as much. I do know what you

mean though, and the stigma around all mental health issues can be oppressive

and isolating. You will find your way to talk about it, and will start to know

who you can be more open with what.

Our son's grandfather, when we told him our son had OCD, left the room, then

came back and said, " he'll grow out of it! " Both grandparents did not believe in

psychologists/psychiatrists, or have any understanding about OCD. I gave them

some things to read, and I think that made it worse, because then they were

really worried about what kind of life he would have. He did live with them for

a period of time and they learned first hand what OCD looked like! Six years

later they have learned a lot, and accept without understanding fully, because

they love their grandson.

All that to say, sometimes they just need time to come to an understanding.

They will still say unhelpful things, same as everyone else, wanting to help or

give you " the answer " ....that's when forgiveness comes in handy - I learned to

forgive people before they opened their mouths, knowing they just could not

understand.

Maybe your son could come up with a name that describes how the OCD feels to

him that would give his grandparents a better understanding and help them be

more sympathetic - try " brain terrorist " (our son would use this). Humor is a

good way to go :)

The book, Brain Lock, has one of the best explanations of what is going on in

the brain with OCD, and how ERP works. They show brain scans to show the changes

before and after ERP. This might help them to understand better.

Warmly,

Barb

Canada

Son, 20, OCD, PDD-NOS(Delays/LD)

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I

guess to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for

glucositis, they would look concerned and sympathetic, rather than nervous and

uneasy. It's a double burden for folks with OCD to have to cope with the name as

well as the actual condition. Of course I never gave it a thought until my son

got it; I was a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed

to " intellectual disability. " I hope it doesn't take that long with OCD.

Meanwhile I guess I have to learn to live with it!!

>

> Rhonda

>

>

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Guest guest

Hi Barb-

Those are really helpful experiences, not only for what to say, but for my own

thinking. Thanks.

Rhonda

Re: pet peeve

Hi Rhonda,

You might want to try " brain-based disorder " . I have started using this

myself. It's the physical part of the body that is affected, the brain, which

seems to make people think a bit differently. You could use your part of " brain

not processing properly " too!

I also prefer, mental health, to mental illness.

You might use anxiety disorder instead of OCD, if you don't want to get into

an explanation. Everyone understands what it is to feel anxious.

With intellectual disabilities, I'm familiar with the term developmental

delays. I like the idea that there is a delay, so it is not a disability so much

as something that needs more time to develop. It really is in how you choose to

look at it. Our son has delays, and it helps me to think of them this way.

Instead of limitations I wonder what the possibilities will be, because we

really don't know.

When you develop a comfort level with the OCD, and it becomes just part of

your life, you may find the term doesn't bother you as much. I do know what you

mean though, and the stigma around all mental health issues can be oppressive

and isolating. You will find your way to talk about it, and will start to know

who you can be more open with what.

Our son's grandfather, when we told him our son had OCD, left the room, then

came back and said, " he'll grow out of it! " Both grandparents did not believe in

psychologists/psychiatrists, or have any understanding about OCD. I gave them

some things to read, and I think that made it worse, because then they were

really worried about what kind of life he would have. He did live with them for

a period of time and they learned first hand what OCD looked like! Six years

later they have learned a lot, and accept without understanding fully, because

they love their grandson.

All that to say, sometimes they just need time to come to an understanding.

They will still say unhelpful things, same as everyone else, wanting to help or

give you " the answer " ....that's when forgiveness comes in handy - I learned to

forgive people before they opened their mouths, knowing they just could not

understand.

Maybe your son could come up with a name that describes how the OCD feels to

him that would give his grandparents a better understanding and help them be

more sympathetic - try " brain terrorist " (our son would use this). Humor is a

good way to go :)

The book, Brain Lock, has one of the best explanations of what is going on in

the brain with OCD, and how ERP works. They show brain scans to show the changes

before and after ERP. This might help them to understand better.

Warmly,

Barb

Canada

Son, 20, OCD, PDD-NOS(Delays/LD)

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I

guess to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for

glucositis, they would look concerned and sympathetic, rather than nervous and

uneasy. It's a double burden for folks with OCD to have to cope with the name as

well as the actual condition. Of course I never gave it a thought until my son

got it; I was a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed

to " intellectual disability. " I hope it doesn't take that long with OCD.

Meanwhile I guess I have to learn to live with it!!

>

> Rhonda

>

>

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Hi Barb-

Those are really helpful experiences, not only for what to say, but for my own

thinking. Thanks.

Rhonda

Re: pet peeve

Hi Rhonda,

You might want to try " brain-based disorder " . I have started using this

myself. It's the physical part of the body that is affected, the brain, which

seems to make people think a bit differently. You could use your part of " brain

not processing properly " too!

I also prefer, mental health, to mental illness.

You might use anxiety disorder instead of OCD, if you don't want to get into

an explanation. Everyone understands what it is to feel anxious.

With intellectual disabilities, I'm familiar with the term developmental

delays. I like the idea that there is a delay, so it is not a disability so much

as something that needs more time to develop. It really is in how you choose to

look at it. Our son has delays, and it helps me to think of them this way.

Instead of limitations I wonder what the possibilities will be, because we

really don't know.

When you develop a comfort level with the OCD, and it becomes just part of

your life, you may find the term doesn't bother you as much. I do know what you

mean though, and the stigma around all mental health issues can be oppressive

and isolating. You will find your way to talk about it, and will start to know

who you can be more open with what.

Our son's grandfather, when we told him our son had OCD, left the room, then

came back and said, " he'll grow out of it! " Both grandparents did not believe in

psychologists/psychiatrists, or have any understanding about OCD. I gave them

some things to read, and I think that made it worse, because then they were

really worried about what kind of life he would have. He did live with them for

a period of time and they learned first hand what OCD looked like! Six years

later they have learned a lot, and accept without understanding fully, because

they love their grandson.

All that to say, sometimes they just need time to come to an understanding.

They will still say unhelpful things, same as everyone else, wanting to help or

give you " the answer " ....that's when forgiveness comes in handy - I learned to

forgive people before they opened their mouths, knowing they just could not

understand.

Maybe your son could come up with a name that describes how the OCD feels to

him that would give his grandparents a better understanding and help them be

more sympathetic - try " brain terrorist " (our son would use this). Humor is a

good way to go :)

The book, Brain Lock, has one of the best explanations of what is going on in

the brain with OCD, and how ERP works. They show brain scans to show the changes

before and after ERP. This might help them to understand better.

Warmly,

Barb

Canada

Son, 20, OCD, PDD-NOS(Delays/LD)

>

> Thanks all for taking my rant about my pet peeve with a grain of salt. I

guess to clarify - I wish OCD had a name like " glucositis " (brain not properly

processing glucose), or " cerebeletus " (cause it's in the brain, right). Both

" obsessive " and " compulsive " are negative words whenever used in other contexts

- so it brings a load of negativity onto the diagnosis. Imagine if diabetes were

called " gluttonous obesitive " - ridiculous!

>

> If I could say to Grandma and Grandpa, my son is being treated for

glucositis, they would look concerned and sympathetic, rather than nervous and

uneasy. It's a double burden for folks with OCD to have to cope with the name as

well as the actual condition. Of course I never gave it a thought until my son

got it; I was a finger pointer myself.

>

> In 2010 they finally passed a law mandating " mentally retarded " be changed

to " intellectual disability. " I hope it doesn't take that long with OCD.

Meanwhile I guess I have to learn to live with it!!

>

> Rhonda

>

>

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