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What do you mean is the line being tapped?

> Postings

>

>

> From: User102241@...

>

> I submitted a report to the Onelist regarding the veterinarians and the

> results of the survey. It never appeared. I don't know where it

> went. Also,

> I haven't received anything today. Is the line being tapped again!?

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  • 1 year later...

Larocque wrote:

>

> From: " Larocque " <rlarocque@...>

>

> What do you mean is the line being tapped?

>

> > Postings

> >

> >

> > From: User102241@...

> >

> > I submitted a report to the Onelist regarding the veterinarians and the

> > results of the survey. It never appeared. I don't know where it

> > went. Also,

> > I haven't received anything today. Is the line being tapped again!?

> SHE MEANS BIG BROTHER IS PLAYING AGAIN, JIM GREEN

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  • 8 years later...

Dear Misty,

I do not take issue with the content of the material you have been posting,

but I do object to your treatment of this list as a bulletin board for the

posting of naked urls.

Stop it.

List moderator

Dr. Saul Pressman

VIDEO: Vaccination: The Hidden Truth (1998)

Comments?

Misty L. Trepke

searching-alternatives

ps- Please check and double check that has not put any spaces in

the link's url.

VIDEO: Vaccination: The Hidden Truth (1998)

http://video.google.com/videoplay?docid=8610554679207090010

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  • 4 years later...

Wow, are our postings getting sophisticated or what.

Once before we tried to pen a " basic " group, but there was

no activity on it.

Are people satisfied with level of discussion now? Sometimes

I think our members know more than non-specialized

oncologists.

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Hi ,

I, for one, am very satisfied. I can ask any

question without feeling " dumb " and appreciate the high

level of discourse in the replies and general discussions.

Best wishes,

Q

wrote:

> Wow, are our postings getting sophisticated or what.

>

> Once before we tried to pen a " basic " group, but there was

> no activity on it.

>

> Are people satisfied with level of discussion now? Sometimes

> I think our members know more than non-specialized

> oncologists.

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This group has been a fountain of knowledge and

encouragement for me. I really appreciate the sharing of

info and experience. By the way, I called MD

about going for a second opinion on treatment options. They

quoted a price for that of $22,500. I almost dropped the phone.

My insurance will not pay because it is out of my service area.

Will be seeing a well-known oncologist-hematologist in Ft. Worth

for a second opinion. Just thought I would share that.

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This list is terrific. And I agree, I do think that many

members know more than their " local " oncologist. We are

blessed to have a knowledgeable one, and one who listens to

us, and is more than eager to work with the real CLL

specialists (we'll be seeing our 3rd CLL specialist in a

couple of weeks because there are even specialists among the

specialists!). But we wouldn't have known to ask and who

knows where we would be now. Thanks to everyone and

especially to the docs who spend (unpaid) time here

answering our questions.

Alice

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Hi Guys -

I want to thank everyone for their caring & sharing on this

list. It has been a BIG help to me.

The discussions here contain excellent CLL information &

commentary. This group (along with CLL Topics,

CLL Updates & CLL Canada) make up my CLL University where I

get my " continuing CLL education. " In the 2 years since my

Dx I have spent considerable time learning about CLL. This

enabled me become an informed CLL patient (which helped me

ask the right questions and then find the right medical team

to monitor my CLL).

It took almost 2 years to find a local hematalogist /

oncologist that welcomed my involvement as an informed CLL

patient. My new local H/O is an excellent doctor (part of

the new UCLA satallite hematology/oncology office in my

area). My CLL expert is Dr. at UCSD (backed up by Dr.

Eradat at UCLA). I also have an excellent local PCP who

looks after me like a mother hen (and is an important part

of my CLL team).

Again, thanks to all of you for your excellent commentary &

sharing. You are a big part of my continuing CLL education.

Warm regards - Patti Kruse

Dx 2009 (w/w), IgVH mutated, 13q (bi-allelic deletion)

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Hi Sylvia.

Thanks for sharing your info about M D . I am

seriously considering going to MDA for a second opinion

which is the closer of CLL specialist for me. I was

shocked at the price you quoted. Do by chance know what that

included?

Thanks,

YuVonna

Sylvia wrote:

I called MD about going for a second opinion on

treatment options. They quoted a price for that of $22,500.

I almost dropped the phone.

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I just joined the listing in Feb. 2011, after my dx in Jan.

2011. I can't even begin to express how much help I have

received from this group. The knowledge of this group is

current and vast. I avoided a way-too-soon FCR treatment by

going to a CLL expert. I have been given hope that I will

see my son's wedding in May 2012 (which I will need to

travel, something I also learned about on this listing) and

maybe will see grandchildren. I have had wonderful email

exchanges from people that have freely shared their

experiences and their philosophies in life...truly an

inspiration... I have gained emotional strength through

this group and, to me, that equals the knowledge I have

gained.

Thanks to all,

Peggy

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I went to MD for a second opinion in May 2010 and

it cost me about $20 dollars. I am on Medicare and have a

supplementary policy that pays 80% of the 20% that Medicare

does not pay. I was not referred by another doctor but

called the number that was online for an appointment with a

cll expert. I was assigned a coordinator who took all my

insurance information and did all the contacting of them.

When it was all approved, he called me back with the

appointment.

I was very satisfied with my appointment and my follow up

appointments with Dr. O`Brien. She put me on Watch and

Wait when a regular oncologist was ready to start treatment

then with Rituxan. Dr. O`Brien has said I have a very slow

developing case and may never need treatment.

I decided to go for the 2nd opinion thanks to this group. I

am so very thankful I did because I have learned so much

about cll and realized if I had done treatment, it would

probably made it worst. All I have is a slightly elevated

white blood cell count with no lymph nodes or organs

involved.

Jean

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I remember those old days , amazing how much good work

you have done during these past years.

It makes me feel so good to see how this educational list

has grown and the quality of the postings and wonderful

people.

Best Regards

Chonette (UK)

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I too would like to add my thanks to everyone involved in

this group! I was dx in Jan 09 and since then have been

learning all I can about CLL. I am in the Natural History

trial at NIH and see my local oncologist quarterly. Since I

was dx I have been at my daughter's wedding, had our first

grandchild and will have our second in February. Even when

I don't understand all the postings in this group it

encourages me to just learn more. Thanks to everyone and

especially to the doctors who are willing to share their

knowledge with us all!!

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,

The group is terrific, I have been a member now for 6 yrs

and you provide a valuable service to us all. I know you put

a lot of time and effort into this group and I for one am

grateful. I hope you are well.

R

Adks NY and AZ

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