Re: help with OB treatment

[Guest guest]

Cooky,

I found a bunch of emails going back to 3/2006. Is this what you are

looking for:

'I receive my photopheresis at the Indianapolis Bone Marrow Treatment

center, IBMT located in St. Francis Hospital, Beech Grove, Indiana.

As chemotherapies go, this is not particularly brutal. You are confined to a

bed with a rather large needle in your arm during the procedure. It takes

approximately 2.5 hours and it is done 2 days in a row, about every 2-3

weeks in the beginning. There is no nausea, no hair loss, I am tired, that's

it!! My understanding is that the risks are a slight risk of infection at

the injection site. So far, so good here. (you do have to " hold it " during

the duration of treatment :>) that is the most difficult for me) I know many

of you have asked me to post regarding my treatment and I apologize for the

delay. With this treatment, DRs say it can take up to 6 months to work. I

wanted to be absolutely certain before I put it out there that the

photopheresis was working. "

El

_____

From: rheumatic [mailto:rheumatic ] On Behalf

Of Cooky Stonkey

Sent: Monday, September 20, 2010 4:26 PM

rheumatic

Subject: rheumatic help with OB treatment

Hi everyone,

I keep a lot of your emails in case I ever need info on something. but for

the life of me I can't find any info sent on OB. I know Debbie Gibson and

O have it but I just can't find the emails on what you are being

treated with.

I am getting Clindy IV's at a local hospital and of course the IV nurse has

a sister who has rheumatoid and questioning further she also has Ob. She has

been to Cleveland clinic and they don't have answers for her.but we do

(teehee)! She is in Delaware and near Baltimore hospital. OK so I copied

antibiotic info for her and I need you guys to write your treatment. I am so

sorry to have to ask. I should be able to find it!! (grrr I get frustrated).

Thanks

cooky

[Guest guest]

Yes El thanks so much. Sometimes when I send something I delete by accident

and maybe that's what I did to these.. I am so glad you have them!

hugs

I found a bunch of emails going back to 3/2006. Is this what you are

looking for:

'I receive my photopheresis at the Indianapolis Bone Marrow Treatment

center, IBMT located in St. Francis Hospital, Beech Grove, Indiana.

As chemotherapies go, this is not particularly brutal. You are confined to a

bed with a rather large needle in your arm during the procedure. It takes

approximately 2.5 hours and it is done 2 days in a row, about every 2-3

weeks in the beginning. There is no nausea, no hair loss, I am tired, that's

it!! My understanding is that the risks are a slight risk of infection at

the injection site. So far, so good here. (you do have to " hold it " during

the duration of treatment :>) that is the most difficult for me) I know many

of you have asked me to post regarding my treatment and I apologize for the

delay. With this treatment, DRs say it can take up to 6 months to work. I

wanted to be absolutely certain before I put it out there that the

photopheresis was working. "

El

[Guest guest]

Cooky,

Is the info below enough or do you want me to forward more of the 2007

messages? El

_____

From: rheumatic [mailto:rheumatic ] On Behalf

Of Cooky Stonkey

Sent: Monday, September 20, 2010 5:22 PM

rheumatic

Subject: RE: rheumatic help with OB treatment

Yes El thanks so much. Sometimes when I send something I delete by accident

and maybe that's what I did to these.. I am so glad you have them!

hugs

I found a bunch of emails going back to 3/2006. Is this what you are

looking for:

'I receive my photopheresis at the Indianapolis Bone Marrow Treatment

center, IBMT located in St. Francis Hospital, Beech Grove, Indiana.

As chemotherapies go, this is not particularly brutal. You are confined to a

bed with a rather large needle in your arm during the procedure. It takes

approximately 2.5 hours and it is done 2 days in a row, about every 2-3

weeks in the beginning. There is no nausea, no hair loss, I am tired, that's

it!! My understanding is that the risks are a slight risk of infection at

the injection site. So far, so good here. (you do have to " hold it " during

the duration of treatment :>) that is the most difficult for me) I know many

of you have asked me to post regarding my treatment and I apologize for the

delay. With this treatment, DRs say it can take up to 6 months to work. I

wanted to be absolutely certain before I put it out there that the

photopheresis was working. "

El

[Guest guest]

HI Cooky, just saw your post and I see that someone has already copied my emails

but I thought I would write, is there anything else you need? There are many

photopheresis centers all over the country...it is done in many places...more

info re photopheresis can be found at Therakos, they actually make the

unit...or...I believe its www.therakos.com it is only approved for G v Host

disease and for T cell lymphoma as far as I know BUT...having said that..if you

have OB, your body is rejecting your lungs, i.e. like G v H disease...and it may

take a while but you can get your ins company to give you a trial..then when it

works...they go ahead and allow it...Another source of info might be Inger at

Yale University, she runs the photopheresis unit there...they have used photo

extensively to treat patients with SD and OB and pulm fibrosis....Inger has

access to the studies, etc...AND the DR who developed photopheresis, Dr. Rick

Edelson is at Yale as well..he is researchable online and I contacted him and he

wrote letters on my behalf regarding my obtaining tx with photopheresis for the

OB...let me know if there is anything I can do.

Right now...I am in the middle of more issues...Having 2 US this week...my

breasts had been veryyyy sore for months...could not find anything..ok, then the

past month, my back has been killing me(2 wks ago my Internist cked my kidneys

and urine, all good there ) and I have had an awful discharge..well, my GYN

today said my estrogen is off the charts...which, due to my age, should not

be..so they are doing an US to ck and see what is going on...and she told me I

am definitely having a biopsy..UGH...sort of figured on the biopsy...so...appts

all week and will know more later...I have felt like I am going to have a

period...for over a month now...since that stopped a few years ago...veryyyy

unexpected...they are not sure of anything yet but gyn said they are looking for

cancer...as they see cancer in autoimmune patients...50% more than the rest of

the population...especially, breast, ovarian and lung...so....always

something....

Let me know if you need anything else re the person you know with OB...does she

have an autoimmune disease or....is it just ideopathic OB? Sometimes OB occurs

in environmental occupations, like anything to do with birds...or with oddly

enough, popcorn factories and flavorings...weird huh?

Have a good Monday eve...Hugs, Debb

RE: rheumatic help with OB treatment

Yes El thanks so much. Sometimes when I send something I delete by accident

and maybe that's what I did to these.. I am so glad you have them!

hugs

I found a bunch of emails going back to 3/2006. Is this what you are

looking for:

'I receive my photopheresis at the Indianapolis Bone Marrow Treatment

center, IBMT located in St. Francis Hospital, Beech Grove, Indiana.

As chemotherapies go, this is not particularly brutal. You are confined to a

bed with a rather large needle in your arm during the procedure. It takes

approximately 2.5 hours and it is done 2 days in a row, about every 2-3

weeks in the beginning. There is no nausea, no hair loss, I am tired, that's

it!! My understanding is that the risks are a slight risk of infection at

the injection site. So far, so good here. (you do have to " hold it " during

the duration of treatment :>) that is the most difficult for me) I know many

of you have asked me to post regarding my treatment and I apologize for the

delay. With this treatment, DRs say it can take up to 6 months to work. I

wanted to be absolutely certain before I put it out there that the

photopheresis was working. "

El

[Guest guest]

Blessings to you Deb,my thoughts and heart are with you. sally

Re: rheumatic help with OB treatment

HI Cooky, just saw your post and I see that someone has already copied my emails

but I thought I would write, is there anything else you need? There are many

photopheresis centers all over the country...it is done in many places...more

info re photopheresis can be found at Therakos, they actually make the

unit...or...I believe its www.therakos.com it is only approved for G v Host

disease and for T cell lymphoma as far as I know BUT...having said that..if you

have OB, your body is rejecting your lungs, i.e. like G v H disease...and it may

take a while but you can get your ins company to give you a trial..then when it

works...they go ahead and allow it...Another source of info might be Inger at

Yale University, she runs the photopheresis unit there...they have used photo

extensively to treat patients with SD and OB and pulm fibrosis....Inger has

access to the studies, etc...AND the DR who developed photopheresis, Dr. Rick

Edelson is at Yale as well..he is researchable online and I contacted him and he

wrote letters on my behalf regarding my obtaining tx with photopheresis for the

OB...let me know if there is anything I can do.

Right now...I am in the middle of more issues...Having 2 US this week...my

breasts had been veryyyy sore for months...could not find anything..ok, then the

past month, my back has been killing me(2 wks ago my Internist cked my kidneys

and urine, all good there ) and I have had an awful discharge..well, my GYN

today said my estrogen is off the charts...which, due to my age, should not

be..so they are doing an US to ck and see what is going on...and she told me I

am definitely having a biopsy..UGH...sort of figured on the biopsy...so...appts

all week and will know more later...I have felt like I am going to have a

period...for over a month now...since that stopped a few years ago...veryyyy

unexpected...they are not sure of anything yet but gyn said they are looking for

cancer...as they see cancer in autoimmune patients...50% more than the rest of

the population...especially, breast, ovarian and lung...so....always

something....

Let me know if you need anything else re the person you know with OB...does she

have an autoimmune disease or....is it just ideopathic OB? Sometimes OB occurs

in environmental occupations, like anything to do with birds...or with oddly

enough, popcorn factories and flavorings...weird huh?

Have a good Monday eve...Hugs, Debb

RE: rheumatic help with OB treatment

Yes El thanks so much. Sometimes when I send something I delete by accident

and maybe that's what I did to these.. I am so glad you have them!

hugs

I found a bunch of emails going back to 3/2006. Is this what you are

looking for:

'I receive my photopheresis at the Indianapolis Bone Marrow Treatment

center, IBMT located in St. Francis Hospital, Beech Grove, Indiana.

As chemotherapies go, this is not particularly brutal. You are confined to a

bed with a rather large needle in your arm during the procedure. It takes

approximately 2.5 hours and it is done 2 days in a row, about every 2-3

weeks in the beginning. There is no nausea, no hair loss, I am tired, that's

it!! My understanding is that the risks are a slight risk of infection at

the injection site. So far, so good here. (you do have to " hold it " during

the duration of treatment :>) that is the most difficult for me) I know many

of you have asked me to post regarding my treatment and I apologize for the

delay. With this treatment, DRs say it can take up to 6 months to work. I

wanted to be absolutely certain before I put it out there that the

photopheresis was working. "

El

[Guest guest]

From

HI Cooky, just saw your post and I see that someone has already copied my

emails but I thought I would write, is there anything else you need? There

are many photopheresis centers all over the country...it is done in many

places...more info re photopheresis can be found at Therakos, they actually

make the unit...or...I believe its www.therakos.com it is only approved for

G v Host disease and for T cell lymphoma as far as I know BUT...having said

that..if you have OB, your body is rejecting your lungs, i.e. like G v H

disease...and it may take a while but you can get your ins company to give

you a trial..then when it works...they go ahead and allow it...Another

source of info might be Inger at Yale University, she runs the photopheresis

unit there...they have used photo extensively to treat patients with SD and

OB and pulm fibrosis....Inger has access to the studies, etc...AND the DR

who developed photopheresis, Dr. Rick Edelson is at Yale as well..he is

researchable online and I contacted him and he wrote letters on my behalf

regarding my obtaining tx with photopheresis for the OB...let me know if

there is anything I can do. Thank you so much Deb.I think I have enough now.

I really don't know a whole lot about this person.only what I wrote.

Right now...I am in the middle of more issues...Having 2 US this week...my

breasts had been veryyyy sore for months...could not find anything..ok, then

the past month, my back has been killing me(2 wks ago my Internist cked my

kidneys and urine, all good there ) and I have had an awful discharge..well,

my GYN today said my estrogen is off the charts...which, due to my age,

should not be..so they are doing an US to ck and see what is going on...and

she told me I am definitely having a biopsy..UGH...sort of figured on the

biopsy...so...appts all week and will know more later...I have felt like I

am going to have a period...for over a month now...since that stopped a few

years ago...veryyyy unexpected...they are not sure of anything yet but gyn

said they are looking for cancer...as they see cancer in autoimmune

patients...50% more than the rest of the population...especially, breast,

ovarian and lung...so....always something....Deb hopefull this is not

cancer. It may just be vaginosis Lots of the symptoms you have sound like

it. I need to add you to my nightly prayers so far the prayers for my #1

hope is doing good. You will too.

Let me know if you need anything else re the person you know with OB...does

she have an autoimmune disease or....is it just ideopathic OB? Yes she has

rheumatoidSometimes OB occurs in environmental occupations, like anything to

do with birds...or with oddly enough, popcorn factories and

flavorings...weird huh?Not really look at all the stuff that goes into your

lungs in these places.!!

Have a good Monday eve...Hugs, Deb

You have a great evening and blessings too.

,___

[Guest guest]

Thanks EL I think I have enough for now. I can always depend on you.

Love and hugs

cooky

From: rheumatic [mailto:rheumatic ] On Behalf

Of ehgooding

Sent: Monday, September 20, 2010 5:25 PM

rheumatic

Subject: RE: rheumatic help with OB treatment

Cooky,

Is the info below enough or do you want me to forward more of the 2007

messages? El

[Guest guest]

Well it looks like my attempt to write back in Green didn't work (grr) so

here are my writings shortened..Sooo sorry

OB and pulm fibrosis....Inger has access to the studies, etc...AND the DR

who developed photopheresis, Dr. Rick Edelson is at Yale as well..he is

researchable online and I contacted him and he wrote letters on my behalf

regarding my obtaining tx with photopheresis for the OB...let me know if

there is anything I can do.

Thank you so much Deb.I think I have enough now.

I really don't know a whole lot about this person.only what I wrote.

Right now...I am in the middle of more issues...Having 2 US this week...my

breasts had been veryyyy sore for months...could not find anything..ok, then

the past month, my back has been killing me(2 wks ago my Internist cked my

kidneys and urine, all good there ) and I have had an awful discharge..well,

my GYN today said my estrogen is off the charts...which, due to my age,

should not be..so they are doing an US to ck and see what is going on...and

she told me I am definitely having a biopsy..UGH...sort of figured on the

biopsy...so...appts all week and will know more later...I have felt like I

am going to have a period...for over a month now...since that stopped a few

years ago...veryyyy unexpected...they are not sure of anything yet but gyn

said they are looking for cancer...as they see cancer in autoimmune

patients...50% more than the rest of the population...especially, breast,

ovarian and lung...so....always something...

..Deb hopefull this is not

cancer. It may just be vaginosis Lots of the symptoms you have sound like

it. I need to add you to my nightly prayers. so far the prayers for my #1

hope is doing good. You will too.

Let me know if you need anything else re the person you know with OB...does

she have an autoimmune disease or....is it just ideopathic OB? Yes she has

rheumatoidSometimes OB occurs in environmental occupations, like anything to

do with birds...or with oddly enough, popcorn factories and

flavorings...weird huh?

Not really look at all the stuff that goes into your

lungs in these places.!!

You have a great evening and blessings too.

,___

[Guest guest]

Hey Cooky, thanks for your prayers, always appreciate those...my gyn tested me

for vaginosis and for yeast today..nope...it was estrogen discharge...eck...ah

well, will keep you posted...I see one gyn Tues for an US and then my friend for

an US on Wed at the hosp...their US is much better than the office one but hubby

insists I let my other GYN do one so I will go on Tues..the more info the

better...

What a game yesterday...Troy had another interception and a Qb sack..woo hoo...I

was soooo proud of him...sooo much fun to watch..

Talk to you soon, let me know what you need, I have contact numbers and emails

for everyone...you know it! Hugs, D

RE: rheumatic help with OB treatment

Well it looks like my attempt to write back in Green didn't work (grr) so

here are my writings shortened..Sooo sorry

OB and pulm fibrosis....Inger has access to the studies, etc...AND the DR

who developed photopheresis, Dr. Rick Edelson is at Yale as well..he is

researchable online and I contacted him and he wrote letters on my behalf

regarding my obtaining tx with photopheresis for the OB...let me know if

there is anything I can do.

Thank you so much Deb.I think I have enough now.

I really don't know a whole lot about this person.only what I wrote.

Right now...I am in the middle of more issues...Having 2 US this week...my

breasts had been veryyyy sore for months...could not find anything..ok, then

the past month, my back has been killing me(2 wks ago my Internist cked my

kidneys and urine, all good there ) and I have had an awful discharge..well,

my GYN today said my estrogen is off the charts...which, due to my age,

should not be..so they are doing an US to ck and see what is going on...and

she told me I am definitely having a biopsy..UGH...sort of figured on the

biopsy...so...appts all week and will know more later...I have felt like I

am going to have a period...for over a month now...since that stopped a few

years ago...veryyyy unexpected...they are not sure of anything yet but gyn

said they are looking for cancer...as they see cancer in autoimmune

patients...50% more than the rest of the population...especially, breast,

ovarian and lung...so....always something...

.Deb hopefull this is not

cancer. It may just be vaginosis Lots of the symptoms you have sound like

it. I need to add you to my nightly prayers. so far the prayers for my #1

hope is doing good. You will too.

Let me know if you need anything else re the person you know with OB...does

she have an autoimmune disease or....is it just ideopathic OB? Yes she has

rheumatoidSometimes OB occurs in environmental occupations, like anything to

do with birds...or with oddly enough, popcorn factories and

flavorings...weird huh?

Not really look at all the stuff that goes into your

lungs in these places.!!

You have a great evening and blessings too.

,___

[Guest guest]

Thanks Sally, always appreciate prayers! Hugs, Debb

RE: rheumatic help with OB treatment

Yes El thanks so much. Sometimes when I send something I delete by accident

and maybe that's what I did to these.. I am so glad you have them!

hugs

I found a bunch of emails going back to 3/2006. Is this what you are

looking for:

'I receive my photopheresis at the Indianapolis Bone Marrow Treatment

center, IBMT located in St. Francis Hospital, Beech Grove, Indiana.

As chemotherapies go, this is not particularly brutal. You are confined to a

bed with a rather large needle in your arm during the procedure. It takes

approximately 2.5 hours and it is done 2 days in a row, about every 2-3

weeks in the beginning. There is no nausea, no hair loss, I am tired, that's

it!! My understanding is that the risks are a slight risk of infection at

the injection site. So far, so good here. (you do have to " hold it " during

the duration of treatment :>) that is the most difficult for me) I know many

of you have asked me to post regarding my treatment and I apologize for the

delay. With this treatment, DRs say it can take up to 6 months to work. I

wanted to be absolutely certain before I put it out there that the

photopheresis was working. "

El

[Guest guest]

OK Deb.gotta keep those gyne's in business! Try is amazing just like you.

Blessings and hugs

cooky

From: rheumatic [mailto:rheumatic ] On Behalf

Of DEBBIE GIBSON

Sent: Monday, September 20, 2010 7:41 PM

rheumatic

Subject: Re: rheumatic help with OB treatment

Hey Cooky, thanks for your prayers, always appreciate those...my gyn tested

me for vaginosis and for yeast today..nope...it was estrogen

discharge...eck...ah well, will keep you posted...I see one gyn Tues for an

US and then my friend for an US on Wed at the hosp...their US is much better

than the office one but hubby insists I let my other GYN do one so I will go

on Tues..the more info the better...

What a game yesterday...Troy had another interception and a Qb sack..woo

hoo...I was soooo proud of him...sooo much fun to watch..

Talk to you soon, let me know what you need, I have contact numbers and

emails for everyone...you know it! Hugs, D

[Guest guest]

Hi, Cooky. I just saw your post and see that you have the info you need. Just to

say I had to stop the Mino and substitute, Doxy, because of the breathing issue,

result of taking the abx. But Dr. Sinnott has me on Azithromycin. It is good

(but not as good as Mino) and so am on a plateau for now with that. But so far

no allergic reaction. He agrees with several of you that posted, that one can

develop supersensitivities, which he thinks I did to the Mino. I hope your

friend does not have OB. I will be going for tests today and (hopefully) find

out more conclusively.

Debbie, I am so, so sorry to hear of your issues. I will be thinking of you and

wishing you the best. It is amazing how destructive this disease can be. Hang in

there.

I have been diligent in following the earlier rec's and getting health and

other issues attended to. Now that the Zithro is controlling the RA I have been

able to deal with the other issues. I am to be admitted to the hospital today

re: the heart and lung issues. Lots of tests...so this may be the last post I

get in for a while. Hope to follow you guys..Debbie - I also saw in reading up

on the heart issues...rheumatic disease sufferers are also 50% more likely to

have heart complications. =<

o

>

> Hi everyone,

>

>

>

> I keep a lot of your emails in case I ever need info on something. but for

> the life of me I can't find any info sent on OB. I know Debbie Gibson and

> O have it but I just can't find the emails on what you are being

> treated with.

>

>

>

> I am getting Clindy IV's at a local hospital and of course the IV nurse has

> a sister who has rheumatoid and questioning further she also has Ob. She has

> been to Cleveland clinic and they don't have answers for her.but we do

> (teehee)! She is in Delaware and near Baltimore hospital. OK so I copied

> antibiotic info for her and I need you guys to write your treatment. I am so

> sorry to have to ask. I should be able to find it!! (grrr I get frustrated).

>

>

>

> Thanks

>

>

>

> cooky

>

>

>

>

[Guest guest]

Hi, Debbie. Have you done any hormone testing ? Many times the sore breasts can

be related to lack of enough progesterone..? Best wishes....Troy who?

>

> Hey Cooky, thanks for your prayers, always appreciate those...my gyn tested me

for vaginosis and for yeast today..nope...it was estrogen discharge...eck...ah

well, will keep you posted...I see one gyn Tues for an US and then my friend for

an US on Wed at the hosp...their US is much better than the office one but hubby

insists I let my other GYN do one so I will go on Tues..the more info the

better...

> What a game yesterday...Troy had another interception and a Qb sack..woo

hoo...I was soooo proud of him...sooo much fun to watch..

> Talk to you soon, let me know what you need, I have contact numbers and emails

for everyone...you know it! Hugs, D

> RE: rheumatic help with OB treatment

>

>

>

> Well it looks like my attempt to write back in Green didn't work (grr) so

> here are my writings shortened..Sooo sorry

>

> OB and pulm fibrosis....Inger has access to the studies, etc...AND the DR

> who developed photopheresis, Dr. Rick Edelson is at Yale as well..he is

> researchable online and I contacted him and he wrote letters on my behalf

> regarding my obtaining tx with photopheresis for the OB...let me know if

> there is anything I can do.

>

> Thank you so much Deb.I think I have enough now.

> I really don't know a whole lot about this person.only what I wrote.

>

> Right now...I am in the middle of more issues...Having 2 US this week...my

> breasts had been veryyyy sore for months...could not find anything..ok, then

> the past month, my back has been killing me(2 wks ago my Internist cked my

> kidneys and urine, all good there ) and I have had an awful discharge..well,

> my GYN today said my estrogen is off the charts...which, due to my age,

> should not be..so they are doing an US to ck and see what is going on...and

> she told me I am definitely having a biopsy..UGH...sort of figured on the

> biopsy...so...appts all week and will know more later...I have felt like I

> am going to have a period...for over a month now...since that stopped a few

> years ago...veryyyy unexpected...they are not sure of anything yet but gyn

> said they are looking for cancer...as they see cancer in autoimmune

> patients...50% more than the rest of the population...especially, breast,

> ovarian and lung...so....always something...

>

> .Deb hopefull this is not

> cancer. It may just be vaginosis Lots of the symptoms you have sound like

> it. I need to add you to my nightly prayers. so far the prayers for my #1

> hope is doing good. You will too.

>

> Let me know if you need anything else re the person you know with OB...does

> she have an autoimmune disease or....is it just ideopathic OB? Yes she has

> rheumatoidSometimes OB occurs in environmental occupations, like anything to

> do with birds...or with oddly enough, popcorn factories and

> flavorings...weird huh?

>

> Not really look at all the stuff that goes into your

> lungs in these places.!!

>

>

> You have a great evening and blessings too.

>

> ,___

>

>

[Guest guest]

Thanks Cooky! Will know more today.

Yes, Troy is amazing...he is such a great person and a terrific football

player..and oh, sooo easy on the eyes...Hugs, Debb

Re: rheumatic help with OB treatment

Hey Cooky, thanks for your prayers, always appreciate those...my gyn tested

me for vaginosis and for yeast today..nope...it was estrogen

discharge...eck...ah well, will keep you posted...I see one gyn Tues for an

US and then my friend for an US on Wed at the hosp...their US is much better

than the office one but hubby insists I let my other GYN do one so I will go

on Tues..the more info the better...

What a game yesterday...Troy had another interception and a Qb sack..woo

hoo...I was soooo proud of him...sooo much fun to watch..

Talk to you soon, let me know what you need, I have contact numbers and

emails for everyone...you know it! Hugs, D

[Guest guest]

yes, do please tell the rest of us about Troy! sally

Re: rheumatic help with OB treatment

Thanks Cooky! Will know more today.

Yes, Troy is amazing...he is such a great person and a terrific football

player..and oh, sooo easy on the eyes...Hugs, Debb

Re: rheumatic help with OB treatment

Hey Cooky, thanks for your prayers, always appreciate those...my gyn tested

me for vaginosis and for yeast today..nope...it was estrogen

discharge...eck...ah well, will keep you posted...I see one gyn Tues for an

US and then my friend for an US on Wed at the hosp...their US is much better

than the office one but hubby insists I let my other GYN do one so I will go

on Tues..the more info the better...

What a game yesterday...Troy had another interception and a Qb sack..woo

hoo...I was soooo proud of him...sooo much fun to watch..

Talk to you soon, let me know what you need, I have contact numbers and

emails for everyone...you know it! Hugs, D