Re: Repost of Lu's post on Dr. Buckner for those whomissed it.

[Guest guest]

RCColloran@... wrote:

> Hi Everyone,

>

> Dr. Buckner wrote me a letter today. If you want to participate in her

> research. Send me a private e-mail with your name address and phone number. I

> am compiling a list for her from our group.

>

> She was very excited in her letter. She told me she had been able to reach a

> much larger group of RP patients via letters and e-mail.

> The enthusiasm that these individuals have demonstrated has made this a very

> exciting time for her, also the increase has allowed her to expand her RP

> research program.

>

> I'm sure she will send you all this same letter after she gets the names of

> individuals who want to participate. Okay group we need an overwhelming

> response. Also if you have done it before and want to do it again, send me

> your name.

> I just can't express her enthusiasm in the letter. She feels that now she

> will soon be able to identify factors that may contribute to disease severity

> and predict response to therapy.

>

> She wants me to let you know the identity of each patient is kept

> confidential.

>

> The information gathered in all areas will be published in scientific

> journals as they make new discoveries. This fall she will be presenting some

> of her findings on RP at the meeting of American College of Rheumatology.

>

> She plans to expand the work over the next several years. The Virginia Mason

> Research Clinic has moved into new laboratories over the summer allowing her

> to physically expand her work, and she has been able to expand the scope of

> her work through financial support of donations and a grant from the

> arthritis foundation.

>

> She plans to remain in contact with all of the people who donate blood and

> who have already participated in this work. She also sent me a list of the

> research work she has outlined to do.

>

> In the next several weeks they will provide the information about this work

> on their website at www.vmresearch.org.

>

> But if anyone wants to know anything further just e-mail me.

> Please folks send me your name, address, phone number and e-mail address.

> Please send it to Lu1953@...

>

> We want to have a large group that will be willing to contribute their blood

> as an RP patient for research. This will not cost you at all. The donations

> she has received covers the cost.

>

> But we as a foundation want to contribute to her research, we need donations

> to do this. These are tax deductible, please look deep into your hearts, so

> we can send Dr. Buckner funds also. She is really going somewhere now with

> her research. We need to be in on it.

>

> But even more importantly, if you have not joined the Relapsing

> Polychondritis Support & Awareness Foundation, please do so now. WE need your

> help. The money we raise will help further research, it will help print

> brochures for education. Please try to find a way to send in your 15.00

> yearly contribution or a larger amount will be greatly appreciated.

>

> We are all a team working for the same cause. Please be on this team with us!

> We cannot do it alone. We have to get our fundraising programs in action,

> there is so much work to do. Please try to dedicate something of yourself to

> help. To mail donations send them to the

> RP Foundation

> C/O Colloran

> 775 Bounty Place

> Manteca, CA 95337

>

> To volunteer doing other things please send in what you can help do to

> Barbara Angerhofer her e-mail addy is angerhob@...

>

> Remember we are all volunteers, we are here for you. We all want

> answers,remissions, and a wonderful life. But we need all of your help.If any

> of you have any questions please e-mail me and I will try to get the answer

> for you. Or if you have any questions you would like for me to send to Dr.

> Buckner with the list of names, please send them to LU1953@....

>

> Thanks!

> Love to you all!

> Lu

>

>

> DISCLAIMER!!

> WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS RECEIVED

HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR BEFORE TRYING

ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR PHYSICIAN AND ARE

NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND TREATMENT MAYBE DIFFERENT

FOR MANY OF US. THANK YOU

>

>

[Guest guest]

RCColloran@... wrote:

> Hi Everyone,

>

> Dr. Buckner wrote me a letter today. If you want to participate in her

> research. Send me a private e-mail with your name address and phone number. I

> am compiling a list for her from our group.

>

> She was very excited in her letter. She told me she had been able to reach a

> much larger group of RP patients via letters and e-mail.

> The enthusiasm that these individuals have demonstrated has made this a very

> exciting time for her, also the increase has allowed her to expand her RP

> research program.

>

> I'm sure she will send you all this same letter after she gets the names of

> individuals who want to participate. Okay group we need an overwhelming

> response. Also if you have done it before and want to do it again, send me

> your name.

> I just can't express her enthusiasm in the letter. She feels that now she

> will soon be able to identify factors that may contribute to disease severity

> and predict response to therapy.

>

> She wants me to let you know the identity of each patient is kept

> confidential.

>

> The information gathered in all areas will be published in scientific

> journals as they make new discoveries. This fall she will be presenting some

> of her findings on RP at the meeting of American College of Rheumatology.

>

> She plans to expand the work over the next several years. The Virginia Mason

> Research Clinic has moved into new laboratories over the summer allowing her

> to physically expand her work, and she has been able to expand the scope of

> her work through financial support of donations and a grant from the

> arthritis foundation.

>

> She plans to remain in contact with all of the people who donate blood and

> who have already participated in this work. She also sent me a list of the

> research work she has outlined to do.

>

> In the next several weeks they will provide the information about this work

> on their website at www.vmresearch.org.

>

> But if anyone wants to know anything further just e-mail me.

> Please folks send me your name, address, phone number and e-mail address.

> Please send it to Lu1953@...

>

> We want to have a large group that will be willing to contribute their blood

> as an RP patient for research. This will not cost you at all. The donations

> she has received covers the cost.

>

> But we as a foundation want to contribute to her research, we need donations

> to do this. These are tax deductible, please look deep into your hearts, so

> we can send Dr. Buckner funds also. She is really going somewhere now with

> her research. We need to be in on it.

>

> But even more importantly, if you have not joined the Relapsing

> Polychondritis Support & Awareness Foundation, please do so now. WE need your

> help. The money we raise will help further research, it will help print

> brochures for education. Please try to find a way to send in your 15.00

> yearly contribution or a larger amount will be greatly appreciated.

>

> We are all a team working for the same cause. Please be on this team with us!

> We cannot do it alone. We have to get our fundraising programs in action,

> there is so much work to do. Please try to dedicate something of yourself to

> help. To mail donations send them to the

> RP Foundation

> C/O Colloran

> 775 Bounty Place

> Manteca, CA 95337

>

> To volunteer doing other things please send in what you can help do to

> Barbara Angerhofer her e-mail addy is angerhob@...

>

> Remember we are all volunteers, we are here for you. We all want

> answers,remissions, and a wonderful life. But we need all of your help.If any

> of you have any questions please e-mail me and I will try to get the answer

> for you. Or if you have any questions you would like for me to send to Dr.

> Buckner with the list of names, please send them to LU1953@....

>

> Thanks!

> Love to you all!

> Lu

>

>

> DISCLAIMER!!

> WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS RECEIVED

HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR BEFORE TRYING

ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR PHYSICIAN AND ARE

NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND TREATMENT MAYBE DIFFERENT

FOR MANY OF US. THANK YOU

>

>

[Guest guest]

Could someone please re-send Barbara A.'s e-mail address. I have tried the

one that is listed towards the bottom of this e-mail and have tried a couple

of different varieties of it but it won't go through.

Thanks, Kathi

>From: ou82big@...

>Reply-To: Rpolychondritis

>To: Rpolychondritis

>Subject: Re: Repost of Lu's post on Dr. Buckner for those

>whomissed it.

>Date: Tue, 18 Sep 2001 22:27:43 -0500

>

>

>

>RCColloran@... wrote:

>

> > Hi Everyone,

> >

> > Dr. Buckner wrote me a letter today. If you want to participate in her

> > research. Send me a private e-mail with your name address and phone

>number. I

> > am compiling a list for her from our group.

> >

> > She was very excited in her letter. She told me she had been able to

>reach a

> > much larger group of RP patients via letters and e-mail.

> > The enthusiasm that these individuals have demonstrated has made this a

>very

> > exciting time for her, also the increase has allowed her to expand her

>RP

> > research program.

> >

> > I'm sure she will send you all this same letter after she gets the names

>of

> > individuals who want to participate. Okay group we need an overwhelming

> > response. Also if you have done it before and want to do it again, send

>me

> > your name.

> > I just can't express her enthusiasm in the letter. She feels that now

>she

> > will soon be able to identify factors that may contribute to disease

>severity

> > and predict response to therapy.

> >

> > She wants me to let you know the identity of each patient is kept

> > confidential.

> >

> > The information gathered in all areas will be published in scientific

> > journals as they make new discoveries. This fall she will be presenting

>some

> > of her findings on RP at the meeting of American College of

>Rheumatology.

> >

> > She plans to expand the work over the next several years. The Virginia

>Mason

> > Research Clinic has moved into new laboratories over the summer allowing

>her

> > to physically expand her work, and she has been able to expand the scope

>of

> > her work through financial support of donations and a grant from the

> > arthritis foundation.

> >

> > She plans to remain in contact with all of the people who donate blood

>and

> > who have already participated in this work. She also sent me a list of

>the

> > research work she has outlined to do.

> >

> > In the next several weeks they will provide the information about this

>work

> > on their website at www.vmresearch.org.

> >

> > But if anyone wants to know anything further just e-mail me.

> > Please folks send me your name, address, phone number and e-mail

>address.

> > Please send it to Lu1953@...

> >

> > We want to have a large group that will be willing to contribute their

>blood

> > as an RP patient for research. This will not cost you at all. The

>donations

> > she has received covers the cost.

> >

> > But we as a foundation want to contribute to her research, we need

>donations

> > to do this. These are tax deductible, please look deep into your hearts,

>so

> > we can send Dr. Buckner funds also. She is really going somewhere now

>with

> > her research. We need to be in on it.

> >

> > But even more importantly, if you have not joined the Relapsing

> > Polychondritis Support & Awareness Foundation, please do so now. WE need

>your

> > help. The money we raise will help further research, it will help print

> > brochures for education. Please try to find a way to send in your 15.00

> > yearly contribution or a larger amount will be greatly appreciated.

> >

> > We are all a team working for the same cause. Please be on this team

>with us!

> > We cannot do it alone. We have to get our fundraising programs in

>action,

> > there is so much work to do. Please try to dedicate something of

>yourself to

> > help. To mail donations send them to the

> > RP Foundation

> > C/O Colloran

> > 775 Bounty Place

> > Manteca, CA 95337

> >

> > To volunteer doing other things please send in what you can help do to

> > Barbara Angerhofer her e-mail addy is angerhob@...

> >

> > Remember we are all volunteers, we are here for you. We all want

> > answers,remissions, and a wonderful life. But we need all of your

>help.If any

> > of you have any questions please e-mail me and I will try to get the

>answer

> > for you. Or if you have any questions you would like for me to send to

>Dr.

> > Buckner with the list of names, please send them to LU1953@....

> >

> > Thanks!

> > Love to you all!

> > Lu

> >

> >

> > DISCLAIMER!!

> > WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS

>RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR

>BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR

>PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND

>TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

> >

> >

[Guest guest]

Could someone please re-send Barbara A.'s e-mail address. I have tried the

one that is listed towards the bottom of this e-mail and have tried a couple

of different varieties of it but it won't go through.

Thanks, Kathi

>From: ou82big@...

>Reply-To: Rpolychondritis

>To: Rpolychondritis

>Subject: Re: Repost of Lu's post on Dr. Buckner for those

>whomissed it.

>Date: Tue, 18 Sep 2001 22:27:43 -0500

>

>

>

>RCColloran@... wrote:

>

> > Hi Everyone,

> >

> > Dr. Buckner wrote me a letter today. If you want to participate in her

> > research. Send me a private e-mail with your name address and phone

>number. I

> > am compiling a list for her from our group.

> >

> > She was very excited in her letter. She told me she had been able to

>reach a

> > much larger group of RP patients via letters and e-mail.

> > The enthusiasm that these individuals have demonstrated has made this a

>very

> > exciting time for her, also the increase has allowed her to expand her

>RP

> > research program.

> >

> > I'm sure she will send you all this same letter after she gets the names

>of

> > individuals who want to participate. Okay group we need an overwhelming

> > response. Also if you have done it before and want to do it again, send

>me

> > your name.

> > I just can't express her enthusiasm in the letter. She feels that now

>she

> > will soon be able to identify factors that may contribute to disease

>severity

> > and predict response to therapy.

> >

> > She wants me to let you know the identity of each patient is kept

> > confidential.

> >

> > The information gathered in all areas will be published in scientific

> > journals as they make new discoveries. This fall she will be presenting

>some

> > of her findings on RP at the meeting of American College of

>Rheumatology.

> >

> > She plans to expand the work over the next several years. The Virginia

>Mason

> > Research Clinic has moved into new laboratories over the summer allowing

>her

> > to physically expand her work, and she has been able to expand the scope

>of

> > her work through financial support of donations and a grant from the

> > arthritis foundation.

> >

> > She plans to remain in contact with all of the people who donate blood

>and

> > who have already participated in this work. She also sent me a list of

>the

> > research work she has outlined to do.

> >

> > In the next several weeks they will provide the information about this

>work

> > on their website at www.vmresearch.org.

> >

> > But if anyone wants to know anything further just e-mail me.

> > Please folks send me your name, address, phone number and e-mail

>address.

> > Please send it to Lu1953@...

> >

> > We want to have a large group that will be willing to contribute their

>blood

> > as an RP patient for research. This will not cost you at all. The

>donations

> > she has received covers the cost.

> >

> > But we as a foundation want to contribute to her research, we need

>donations

> > to do this. These are tax deductible, please look deep into your hearts,

>so

> > we can send Dr. Buckner funds also. She is really going somewhere now

>with

> > her research. We need to be in on it.

> >

> > But even more importantly, if you have not joined the Relapsing

> > Polychondritis Support & Awareness Foundation, please do so now. WE need

>your

> > help. The money we raise will help further research, it will help print

> > brochures for education. Please try to find a way to send in your 15.00

> > yearly contribution or a larger amount will be greatly appreciated.

> >

> > We are all a team working for the same cause. Please be on this team

>with us!

> > We cannot do it alone. We have to get our fundraising programs in

>action,

> > there is so much work to do. Please try to dedicate something of

>yourself to

> > help. To mail donations send them to the

> > RP Foundation

> > C/O Colloran

> > 775 Bounty Place

> > Manteca, CA 95337

> >

> > To volunteer doing other things please send in what you can help do to

> > Barbara Angerhofer her e-mail addy is angerhob@...

> >

> > Remember we are all volunteers, we are here for you. We all want

> > answers,remissions, and a wonderful life. But we need all of your

>help.If any

> > of you have any questions please e-mail me and I will try to get the

>answer

> > for you. Or if you have any questions you would like for me to send to

>Dr.

> > Buckner with the list of names, please send them to LU1953@....

> >

> > Thanks!

> > Love to you all!

> > Lu

> >

> >

> > DISCLAIMER!!

> > WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS

>RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR

>BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR

>PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND

>TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

> >

> >

[Guest guest]

Kathi Goodwin wrote:

>

> Could someone please re-send Barbara A.'s e-mail address. I have tried the

> one that is listed towards the bottom of this e-mail and have tried a couple

> of different varieties of it but it won't go through.

> Thanks, Kathi

>

> >From: ou82big@...

> >Reply-To: Rpolychondritis

> >To: Rpolychondritis

> >Subject: Re: Repost of Lu's post on Dr. Buckner for those

> >whomissed it.

> >Date: Tue, 18 Sep 2001 22:27:43 -0500

> >

> >

> >

> >RCColloran@... wrote:

> >

> > > Hi Everyone,

> > >

> > > Dr. Buckner wrote me a letter today. If you want to participate in her

> > > research. Send me a private e-mail with your name address and phone

> >number. I

> > > am compiling a list for her from our group.

> > >

> > > She was very excited in her letter. She told me she had been able to

> >reach a

> > > much larger group of RP patients via letters and e-mail.

> > > The enthusiasm that these individuals have demonstrated has made this a

> >very

> > > exciting time for her, also the increase has allowed her to expand her

> >RP

> > > research program.

> > >

> > > I'm sure she will send you all this same letter after she gets the names

> >of

> > > individuals who want to participate. Okay group we need an overwhelming

> > > response. Also if you have done it before and want to do it again, send

> >me

> > > your name.

> > > I just can't express her enthusiasm in the letter. She feels that now

> >she

> > > will soon be able to identify factors that may contribute to disease

> >severity

> > > and predict response to therapy.

> > >

> > > She wants me to let you know the identity of each patient is kept

> > > confidential.

> > >

> > > The information gathered in all areas will be published in scientific

> > > journals as they make new discoveries. This fall she will be presenting

> >some

> > > of her findings on RP at the meeting of American College of

> >Rheumatology.

> > >

> > > She plans to expand the work over the next several years. The Virginia

> >Mason

> > > Research Clinic has moved into new laboratories over the summer allowing

> >her

> > > to physically expand her work, and she has been able to expand the scope

> >of

> > > her work through financial support of donations and a grant from the

> > > arthritis foundation.

> > >

> > > She plans to remain in contact with all of the people who donate blood

> >and

> > > who have already participated in this work. She also sent me a list of

> >the

> > > research work she has outlined to do.

> > >

> > > In the next several weeks they will provide the information about this

> >work

> > > on their website at www.vmresearch.org.

> > >

> > > But if anyone wants to know anything further just e-mail me.

> > > Please folks send me your name, address, phone number and e-mail

> >address.

> > > Please send it to Lu1953@...

> > >

> > > We want to have a large group that will be willing to contribute their

> >blood

> > > as an RP patient for research. This will not cost you at all. The

> >donations

> > > she has received covers the cost.

> > >

> > > But we as a foundation want to contribute to her research, we need

> >donations

> > > to do this. These are tax deductible, please look deep into your hearts,

> >so

> > > we can send Dr. Buckner funds also. She is really going somewhere now

> >with

> > > her research. We need to be in on it.

> > >

> > > But even more importantly, if you have not joined the Relapsing

> > > Polychondritis Support & Awareness Foundation, please do so now. WE need

> >your

> > > help. The money we raise will help further research, it will help print

> > > brochures for education. Please try to find a way to send in your 15.00

> > > yearly contribution or a larger amount will be greatly appreciated.

> > >

> > > We are all a team working for the same cause. Please be on this team

> >with us!

> > > We cannot do it alone. We have to get our fundraising programs in

> >action,

> > > there is so much work to do. Please try to dedicate something of

> >yourself to

> > > help. To mail donations send them to the

> > > RP Foundation

> > > C/O Colloran

> > > 775 Bounty Place

> > > Manteca, CA 95337

> > >

> > > To volunteer doing other things please send in what you can help do to

> > > Barbara Angerhofer her e-mail addy is angerhob@...

> > >

> > > Remember we are all volunteers, we are here for you. We all want

> > > answers,remissions, and a wonderful life. But we need all of your

> >help.If any

> > > of you have any questions please e-mail me and I will try to get the

> >answer

> > > for you. Or if you have any questions you would like for me to send to

> >Dr.

> > > Buckner with the list of names, please send them to LU1953@....

> > >

> > > Thanks!

> > > Love to you all!

> > > Lu

> > >

> > >

> > > DISCLAIMER!!

> > > WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS

> >RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR

> >BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR

> >PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND

> >TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

> > >

> > >

[Guest guest]

Kathi Goodwin wrote:

>

> Could someone please re-send Barbara A.'s e-mail address. I have tried the

> one that is listed towards the bottom of this e-mail and have tried a couple

> of different varieties of it but it won't go through.

> Thanks, Kathi

>

> >From: ou82big@...

> >Reply-To: Rpolychondritis

> >To: Rpolychondritis

> >Subject: Re: Repost of Lu's post on Dr. Buckner for those

> >whomissed it.

> >Date: Tue, 18 Sep 2001 22:27:43 -0500

> >

> >

> >

> >RCColloran@... wrote:

> >

> > > Hi Everyone,

> > >

> > > Dr. Buckner wrote me a letter today. If you want to participate in her

> > > research. Send me a private e-mail with your name address and phone

> >number. I

> > > am compiling a list for her from our group.

> > >

> > > She was very excited in her letter. She told me she had been able to

> >reach a

> > > much larger group of RP patients via letters and e-mail.

> > > The enthusiasm that these individuals have demonstrated has made this a

> >very

> > > exciting time for her, also the increase has allowed her to expand her

> >RP

> > > research program.

> > >

> > > I'm sure she will send you all this same letter after she gets the names

> >of

> > > individuals who want to participate. Okay group we need an overwhelming

> > > response. Also if you have done it before and want to do it again, send

> >me

> > > your name.

> > > I just can't express her enthusiasm in the letter. She feels that now

> >she

> > > will soon be able to identify factors that may contribute to disease

> >severity

> > > and predict response to therapy.

> > >

> > > She wants me to let you know the identity of each patient is kept

> > > confidential.

> > >

> > > The information gathered in all areas will be published in scientific

> > > journals as they make new discoveries. This fall she will be presenting

> >some

> > > of her findings on RP at the meeting of American College of

> >Rheumatology.

> > >

> > > She plans to expand the work over the next several years. The Virginia

> >Mason

> > > Research Clinic has moved into new laboratories over the summer allowing

> >her

> > > to physically expand her work, and she has been able to expand the scope

> >of

> > > her work through financial support of donations and a grant from the

> > > arthritis foundation.

> > >

> > > She plans to remain in contact with all of the people who donate blood

> >and

> > > who have already participated in this work. She also sent me a list of

> >the

> > > research work she has outlined to do.

> > >

> > > In the next several weeks they will provide the information about this

> >work

> > > on their website at www.vmresearch.org.

> > >

> > > But if anyone wants to know anything further just e-mail me.

> > > Please folks send me your name, address, phone number and e-mail

> >address.

> > > Please send it to Lu1953@...

> > >

> > > We want to have a large group that will be willing to contribute their

> >blood

> > > as an RP patient for research. This will not cost you at all. The

> >donations

> > > she has received covers the cost.

> > >

> > > But we as a foundation want to contribute to her research, we need

> >donations

> > > to do this. These are tax deductible, please look deep into your hearts,

> >so

> > > we can send Dr. Buckner funds also. She is really going somewhere now

> >with

> > > her research. We need to be in on it.

> > >

> > > But even more importantly, if you have not joined the Relapsing

> > > Polychondritis Support & Awareness Foundation, please do so now. WE need

> >your

> > > help. The money we raise will help further research, it will help print

> > > brochures for education. Please try to find a way to send in your 15.00

> > > yearly contribution or a larger amount will be greatly appreciated.

> > >

> > > We are all a team working for the same cause. Please be on this team

> >with us!

> > > We cannot do it alone. We have to get our fundraising programs in

> >action,

> > > there is so much work to do. Please try to dedicate something of

> >yourself to

> > > help. To mail donations send them to the

> > > RP Foundation

> > > C/O Colloran

> > > 775 Bounty Place

> > > Manteca, CA 95337

> > >

> > > To volunteer doing other things please send in what you can help do to

> > > Barbara Angerhofer her e-mail addy is angerhob@...

> > >

> > > Remember we are all volunteers, we are here for you. We all want

> > > answers,remissions, and a wonderful life. But we need all of your

> >help.If any

> > > of you have any questions please e-mail me and I will try to get the

> >answer

> > > for you. Or if you have any questions you would like for me to send to

> >Dr.

> > > Buckner with the list of names, please send them to LU1953@....

> > >

> > > Thanks!

> > > Love to you all!

> > > Lu

> > >

> > >

> > > DISCLAIMER!!

> > > WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS

> >RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR

> >BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR

> >PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND

> >TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

> > >

> > >