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Hi ;

Slow down little one!Panic is about the worst thing you can do to

yourself as it gets the cortisol going and that will cause more problems

disease wise.Whether it is RA or Lupus you may well wait a long time

before the doctors actually figure it out and many of these rheumatic

diseases overlap.You have come here early and will probably get a fair

control but there is so much to learn that it can be mind bogling.My

sister has Lupus and is in remission just by using Doxycycline 50mg 3

times a week.I have systemic Scleroderma and am in remission as well but

it took years to figure things out.We had to find out that we both have

Celiac disease and until we got that controled the AP did not work too

well.It seems like about 70% of people with chronic diseases have Celiac

and you may just find that if you drastically alter your diet you might

feel much better and that allows the AP to work faster.Celiac causes

systemic yeast problems,leaky gut and malabsorbtion of nutrients.

You are in the right place and these wonderful people will guide you

just as they did me.By the way,the doctors had given me less than a year

to live but all my lab results showed normal except for the red and

white blood cells being a tad off.Go figure.Do you have a doctor that is

easy to work with that might write you a prescription for antibiotics?

If not let the folks here know where you live and they will probably

find someone relatively near you. Lynne G.

ktandtm wrote:

> I just found this group and hope you all can help. I went through

> hurricane Katrina while being pregnant. Never had a symptom in the

> world. Then after I had my baby in Sep. I got arthritis pain and

> could hardly do much of anything. Finally went to the doc and was

> told I had lupus. Then moved again and new rheumy said I have RA

> and doesn't think I have lupus. I have inproved some on my own

> before starting methotrexate. I don't feel the MTX is doing much of

> anything and I just want to cry all the time. I am the mother of 7

> and three of my children are under the age of 5. It is so hard to

> take care of them and I am scared and depressed a lot. I really

> thought I would be getting better by now. I am only 37 and just

> can't believe this has happened. Now I am also having symptoms of

> Raynauds and just don't know what to do. C

>

> Can any of you offer any hope other than taking meds upon meds upon

> meds. Seems like when one med doesn't work they just keep adding

> more. I don't want to take all these high risk meds but I dont'

> know what to do! Sorry for writing a book but no one seems to

> understand why I cry all the time. I am normally a strong person

> and have never cried much. Now I am a baby! I just don't

> understand.

>

> Thanks for listening,

>

>

>

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Hi, First congratulations on your new baby. And you've come to the right place.

A lot of people here have been and some still are where you are, including

myself. First thing, stop having any more children. Second, find yourself a

doctor who believes in A/P. That's antibiotic protocol. Get a real diagnosis

if you can. These diseases are known to overlap. Lastly, get prepared to fight

for your life, the rest of your life. These diseases just don't go away

suddenly by themselves or with the changing of drugs. I have S/D, R/A. and

Sarcoidosis. Just got diagnosed for that yesterday. I am and have been on a

drug called Minocin (Minocycline is the generic name.) I understand the brand

name is better. I started slowly at 50 mg MWF, then found a great doc in Boston

who ramped up my dosage to 100mg. twice a day. I have done very well and my

recovery started rapidly and I was elated. Then I started getting tired again

and my heart started to become irregular. I also

developed pulmonary hypertension. There are different types of illnesses, both

outside the body involving the skin only and inside the body where the internal

organs are attacked. The internal ones are harder to treat. Then there is the

MCTD ( mixed connective tissue disease) That's when you have more than one.

You'll have good days, bad days and some so-so days. You've got to learn to ride

the waves. Accept the progress, expect to regress sometimes and other times you

may even forget that you are sick. This is all very difficult not only on

yourself, but also on your little ones. Try to get someone to help you with the

children, housework, laundry etc.so you can rest more often. Nap when the

little ones nap and listen to your body. Get on a good nutrition plan. You

most likely eat on the run with all those babies to take care of. You need

pampering right now. Maybe you can find a young mother's helper who is willing

to do an internship in your house. Try the

churches and schools. Call social services, but definitely you need the extra

help. These diseases can bring the strongest of people down to their knees,

You cannot do this alone, don't even try. There are some good books out there.

Go to the library and get any book by Henry Scammell. Reserve it or you can buy

it new or used on amazon.com at a reduced price. They are not expensive books,

but they tell the whole story. The Methotrexate and such drugs will definitely

have to go. Good Luck~~~~Dolores

ktandtm <ktandtm@...> wrote: I just found this group and hope you all can

help. I went through

hurricane Katrina while being pregnant. Never had a symptom in the

world. Then after I had my baby in Sep. I got arthritis pain and

could hardly do much of anything. Finally went to the doc and was

told I had lupus. Then moved again and new rheumy said I have RA

and doesn't think I have lupus. I have inproved some on my own

before starting methotrexate. I don't feel the MTX is doing much of

anything and I just want to cry all the time. I am the mother of 7

and three of my children are under the age of 5. It is so hard to

take care of them and I am scared and depressed a lot. I really

thought I would be getting better by now. I am only 37 and just

can't believe this has happened. Now I am also having symptoms of

Raynauds and just don't know what to do. C

Can any of you offer any hope other than taking meds upon meds upon

meds. Seems like when one med doesn't work they just keep adding

more. I don't want to take all these high risk meds but I dont'

know what to do! Sorry for writing a book but no one seems to

understand why I cry all the time. I am normally a strong person

and have never cried much. Now I am a baby! I just don't

understand.

Thanks for listening,

To unsubscribe, email: rheumatic-unsubscribeegroups

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ktandtm <ktandtm@...> wrote: I just found this group and hope you

all can help. I went through

hurricane Katrina while being pregnant. Never had a symptom in the

world. Then after I had my baby in Sep. I got arthritis pain and

could hardly do much of anything. Finally went to the doc and was

told I had lupus. Then moved again and new rheumy said I have RA

and doesn't think I have lupus. I have inproved some on my own

before starting methotrexate. I don't feel the MTX is doing much of

anything and I just want to cry all the time. I am the mother of 7

and three of my children are under the age of 5. It is so hard to

take care of them and I am scared and depressed a lot. I really

thought I would be getting better by now. I am only 37 and just

can't believe this has happened. Now I am also having symptoms of

Raynauds and just don't know what to do. C

Can any of you offer any hope other than taking meds upon meds upon

meds. Seems like when one med doesn't work they just keep adding

more. I don't want to take all these high risk meds but I dont'

know what to do! Sorry for writing a book but no one seems to

understand why I cry all the time. I am normally a strong person

and have never cried much. Now I am a baby! I just don't

understand.

Thanks for listening,

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You sound just like me sorry for your pain having no results here either with

all the meds. while I am writing you I am in so much pain, I am going for Acu

Puncture.They say it helps going to try it here. In a lot of pain trying to

type. Good luck with all the children you need help. Sincerly in N.C.

sincer_._,___

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Hi ,

First of all welcome to the group. You have certainly been through a lot

lately. You are definitely not a baby. You have shouldered many things

this past year. Caring for 7 kids deserves a medal all it's own!

I was depressed and tired when I became aware that things weren't right. It

seems to go hand in hand with these diseases. I don't blame you for being

concerned with taking all of the medication. Glad you found us. I have

been taking nothing more than Minocin for years now and I'm doing great. I

have to remind myself I have that I have RA most of the time.

You should read up on the antibiotic therapy from the www.rheumatic.org web

page. There is a section that can be printed off and taken to the doctor if

he us not familiar with this treatment. And of course there is always this

group. This is where you can come for advice and just to vent if you need

to. We know how you feel because we've been there too.

If you want to read it, my story is on the webpage. It will give you a

little insight as to what went on before I got well. Again, welcome. Just

stay as positive as you can be (I know it's hard) do what you can when you

can do it, and try not to sweat the stuff that's really not important. I

wasn't the best housekeeper when I was at my worst but everyone made it

through.

All the Best,

Dee

rheumatic Hi, new and don't know where to turn

I just found this group and hope you all can help. I went through

hurricane Katrina while being pregnant. Never had a symptom in the

world. Then after I had my baby in Sep. I got arthritis pain and

could hardly do much of anything. Finally went to the doc and was

told I had lupus. Then moved again and new rheumy said I have RA

and doesn't think I have lupus. I have inproved some on my own

before starting methotrexate. I don't feel the MTX is doing much of

anything and I just want to cry all the time. I am the mother of 7

and three of my children are under the age of 5. It is so hard to

take care of them and I am scared and depressed a lot. I really

thought I would be getting better by now. I am only 37 and just

can't believe this has happened. Now I am also having symptoms of

Raynauds and just don't know what to do. C

Can any of you offer any hope other than taking meds upon meds upon

meds. Seems like when one med doesn't work they just keep adding

more. I don't want to take all these high risk meds but I dont'

know what to do! Sorry for writing a book but no one seems to

understand why I cry all the time. I am normally a strong person

and have never cried much. Now I am a baby! I just don't

understand.

Thanks for listening,

To unsubscribe, email: rheumatic-unsubscribeegroups

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Hi and welcome. You are in the right place and there is help and support

here for you.

The first thing I recommend you to do is get tested for Lyme's Disease...not

just the standard blood test because it's just too unreliable but the Igenex

Western Blot test. Lyme's could be the underlying cause for all your

miseries. And, this is the good part, the antibiotic Minocin is THE ANSWER

to any and all of what you are told you have (read those words

carefully...what you are TOLD you have...doesn't mean they are right but

they have to give you a label in order to give you some meds and blood tests

are sometimes incorrect). Even if you don't have Lyme's the Minocin is

still the answer. I too was falling apart....Graves Disease (I did NOT

radiate), edema, swollen sausage fingers, Raynauds, Sjogren's, Lupus, RA,

did I miss anything....all confirmed by blood tests....finally they tested

me for Lyme's. The standard test came back negative. The better test

(Igenex) came back with seriously positive. I got on the Minocin a minute

after the blood draw (for the RA) and now amazingly all the symptoms are

going away. I still have issues but at least now I'm thinking I'm going to

live. Before the Lyme's diagnosis and starting Minocin, I primarily dealt

with all my symptoms with vitamins, organic food, rotation diet,

acupuncture, massage, PT, homeopathic, etc ... I did take meds for a very

short time for Graves; maybe for six months or less with ever decreasing

dosages....but none of the other stuff. I have a neighbor just diagnosed

with leukemia...taking chemo...not doing well...just found out yesterday she

has Lymes...Lymes is so clever...it imitates so many conditions (see the

website http://www.hopetoheallyme.com/). I suspect she doesn't have

leukemia but the doctor's had to put a label on her altered white blood

count and it seems leukemia is a new favorite label. It scares the stuffing

out of people too and that makes them even more docile to the doctor's

advice. Before the leukemia she was told she had fibromyalgia...so all that

to say Lyme's is clever and most doctor's aren't. !

My advice is to hang in there, see if you can get the Lyme's test first and

right after they draw your blood start the Minocin. I hope someone else

will post re the methotrexate...I think you need to go off that but

slowly...I may be getting it confused with another med...not my area of

expertise other then don't take anything you don't have to take. And don't

let a doctor scare you that Minocin is harmful....many of us have been on it

for YEARS and expect to be on it for LIFE (on maintenance dosages)....

And again Welcome! You are where you need to be. We have been waiting for

you and others to find us so we can help you. If your internist will not do

this for you someone on this group can help you find someone in your area

that might. I'd be tempted to take all the kids and trap the doctor until

he gives you what you want. Twenty minutes of active kids...I'm thinking

he/she will do anything to send you (all) on your way. That's supposed to

be a joke so I hope you're laughing. Regards, El

Re: rheumatic Hi, new and don't know where to turn

ktandtm <ktandtm@...> wrote: I just found this group and hope

you all can help. I went through

hurricane Katrina while being pregnant. Never had a symptom in the

world. Then after I had my baby in Sep. I got arthritis pain and

could hardly do much of anything. Finally went to the doc and was

told I had lupus. Then moved again and new rheumy said I have RA

and doesn't think I have lupus. I have inproved some on my own

before starting methotrexate. I don't feel the MTX is doing much of

anything and I just want to cry all the time. I am the mother of 7

and three of my children are under the age of 5. It is so hard to

take care of them and I am scared and depressed a lot. I really

thought I would be getting better by now. I am only 37 and just

can't believe this has happened. Now I am also having symptoms of

Raynauds and just don't know what to do. C

Can any of you offer any hope other than taking meds upon meds upon

meds. Seems like when one med doesn't work they just keep adding

more. I don't want to take all these high risk meds but I dont'

know what to do! Sorry for writing a book but no one seems to

understand why I cry all the time. I am normally a strong person

and have never cried much. Now I am a baby! I just don't

understand.

Thanks for listening,

Messages in this topic (1) Reply (via web post) | Start a new topic

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Recent Activity

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New Members

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Beta.

.

You sound just like me sorry for your pain having no results here either

with all the meds. while I am writing you I am in so much pain, I am going

for Acu Puncture.They say it helps going to try it here. In a lot of pain

trying to type. Good luck with all the children you need help. Sincerly

in N.C.

sincer_._,___

---------------------------------

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faster.

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Hi ,

I'm so sorry that you are going through this. It is a very similar experience

that I had when my second child was born. It took so longer for me to be

diagnosed as the doctors kept telling me I must be holding my daughter too much

and that is why I was so stiff and sore. I was originally dx'd with Lupus and

then they added RA later. I refused to take the Methotrexate because my

daughter was still nursing. I actually went into remission on my own for

several years before it hit again. I am now on the AP therapy and have very

high hopes. I'm curious to know if you have RH negative blood type and had a

RhoGam injection after the birth? A doctor told me this is what triggered the

Lupus and I have since come in contact with several other women who have

developed Lupus and/or RA after giving birth. They all had the RhoGam in common

and I thought it was fascinating that there have been no studies done on this

(at least not publicly). I contacted the company that makes the vaccine and

they refused to discuss it with me.

I'm glad you found this forum because there are many people here that will offer

helpful advice. It seems to me that first you need to find a doctor that will

prescribe the antibiotics to you. Do you have anyone around you that can help

with your everyday chores? I know how much energy it requires to properly care

for children. I have 3 and it is a full time job! Try to take a few minutes

each day to breathe deeply and think positive thoughts. Pain does not have to

control you. You will find a way past this!

Maggy

rheumatic Hi, new and don't know where to turn

I just found this group and hope you all can help. I went through

hurricane Katrina while being pregnant. Never had a symptom in the

world. Then after I had my baby in Sep. I got arthritis pain and

could hardly do much of anything. Finally went to the doc and was

told I had lupus. Then moved again and new rheumy said I have RA

and doesn't think I have lupus. I have inproved some on my own

before starting methotrexate. I don't feel the MTX is doing much of

anything and I just want to cry all the time. I am the mother of 7

and three of my children are under the age of 5. It is so hard to

take care of them and I am scared and depressed a lot. I really

thought I would be getting better by now. I am only 37 and just

can't believe this has happened. Now I am also having symptoms of

Raynauds and just don't know what to do. C

Can any of you offer any hope other than taking meds upon meds upon

meds. Seems like when one med doesn't work they just keep adding

more. I don't want to take all these high risk meds but I dont'

know what to do! Sorry for writing a book but no one seems to

understand why I cry all the time. I am normally a strong person

and have never cried much. Now I am a baby! I just don't

understand.

Thanks for listening,

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This is interesting to me as I also had the RhoGam shot and developed arthritis

(still no official diagnosis) after the birth of my first child.

I had wondered about this. You know how you go through every possible thing

that could have triggered your symptoms. This was something I had thought

about. Very interesting!

Maggy Alonso <MaggyAlonso@...> wrote:

Hi ,

I'm so sorry that you are going through this. It is a very similar experience

that I had when my second child was born. It took so longer for me to be

diagnosed as the doctors kept telling me I must be holding my daughter too much

and that is why I was so stiff and sore. I was originally dx'd with Lupus and

then they added RA later. I refused to take the Methotrexate because my daughter

was still nursing. I actually went into remission on my own for several years

before it hit again. I am now on the AP therapy and have very high hopes. I'm

curious to know if you have RH negative blood type and had a RhoGam injection

after the birth? A doctor told me this is what triggered the Lupus and I have

since come in contact with several other women who have developed Lupus and/or

RA after giving birth. They all had the RhoGam in common and I thought it was

fascinating that there have been no studies done on this (at least not

publicly). I contacted the company that makes the vaccine

and they refused to discuss it with me.

I'm glad you found this forum because there are many people here that will offer

helpful advice. It seems to me that first you need to find a doctor that will

prescribe the antibiotics to you. Do you have anyone around you that can help

with your everyday chores? I know how much energy it requires to properly care

for children. I have 3 and it is a full time job! Try to take a few minutes each

day to breathe deeply and think positive thoughts. Pain does not have to control

you. You will find a way past this!

Maggy

rheumatic Hi, new and don't know where to turn

I just found this group and hope you all can help. I went through

hurricane Katrina while being pregnant. Never had a symptom in the

world. Then after I had my baby in Sep. I got arthritis pain and

could hardly do much of anything. Finally went to the doc and was

told I had lupus. Then moved again and new rheumy said I have RA

and doesn't think I have lupus. I have inproved some on my own

before starting methotrexate. I don't feel the MTX is doing much of

anything and I just want to cry all the time. I am the mother of 7

and three of my children are under the age of 5. It is so hard to

take care of them and I am scared and depressed a lot. I really

thought I would be getting better by now. I am only 37 and just

can't believe this has happened. Now I am also having symptoms of

Raynauds and just don't know what to do. C

Can any of you offer any hope other than taking meds upon meds upon

meds. Seems like when one med doesn't work they just keep adding

more. I don't want to take all these high risk meds but I dont'

know what to do! Sorry for writing a book but no one seems to

understand why I cry all the time. I am normally a strong person

and have never cried much. Now I am a baby! I just don't

understand.

Thanks for listening,

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Hi everyone, you all are so great and filled with tons of info. I am

finally excited about going to my new doc on Monday. I am going to

talk about the AP and also see about getting checked for Lyme's. When

you feel like we do you will do anything to make it stop.

Thank you all so much for shedding some light.

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,

Before you go to the doctor, go to www.igenex.com and read what they have to

say about Lyme disease. I just recently sent for a kit to get my blood tested.

The next problem is getting a doctor to treat you right.

My daughter has Lyme and she has to go almost 100 mi to a doctor. Her daughter

(my granddaughter) also has it. They have to fly to Conn. every 3 mo. to a

doctor there. If you have any questions about it you can contact her. Her

email address is: perkys@... Her name is Gretchen.

jan

ktandtm <ktandtm@...> wrote:

Hi everyone, you all are so great and filled with tons of info. I am

finally excited about going to my new doc on Monday. I am going to

talk about the AP and also see about getting checked for Lyme's. When

you feel like we do you will do anything to make it stop.

Thank you all so much for shedding some light.

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I will definitly check into how to be tested for Lyme's. Also I

forgot to mention that I did not get that shot when I was pregnant

like some of you did. I am not RH so that wasn't a connection for

me.

I am in MO close to either Columbia or Kansas City so if any of you

know a doc that does the AP in these areas please let me know. More

than one would be great if you have any since I hope to find one on my

insurance.

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> I am in MO close to either Columbia or Kansas City so if any of you

> know a doc that does the AP in these areas please let me know. More

> than one would be great if you have any since I hope to find one on my

> insurance.

Hi ,

Here is the list of doctors we have in Missouri - as I'm an Aussie, I

don't know how far these doctors are from Columbia or Kansas City.

Chris.

H. Esther, M.D. – RHU – IM – 1976

226 S. Woodsmill Rd.

Chesterfied, MO 63017

P: 314-205-0300

Francisco J. Garriga, M.D. (RHU – IM – 1970)

1120 Shackleford Rd.

Florissant, MO 63031-4369

P: 314-921-4420

F: 314-921-6086

L. Hilburn M.D. (FP-1978) preventive medicine

116 W. Grant St.)

Republic, MO 65738

P: 417-732-1701

ph T. Hilgeman, M.D. (IM – 1988)

Des Peres Internal Medicine

13611 Barrett Office Parkway

Des Peres, MO 63021

P: 314-821-1313

Rand W. Sommer, M.D. (RHU – 1980)

1034 S. Brentwood Blvd. Suite 1060

St. Louis, MO. 63117

P: 314-721-0666

C. Uchiyama, M.D. (RHU – 1980)

224 S. Woods Mill Road Suite 460

Chesterfield, MO 63017

P: 314-576-0933

F. Wiedner, MD

Esse Health

16555 Manchester Rd., Suite 205

Suite 205, Grover, MO 63040.

P: 636-458-4800

Dr. Sutherland - no record found to verify - oral & Iv – works with

Dr. Sinnott

Sutherland Clinic

Paris, MO 65275

P: 660-327-6407

F: 660-427-6217

Nemechek, MD

Nemechek Health Renewal

3404 Broadway St.

Kansas City, MO 64111

P: 816-756-0090

Ralph , DO

1608 East 20th St

Joplin, MO 64804

P: 417-624-4323

Dr. Monika Aplyn

Dr. Christian Wessling, M.D (accepts insurance)

Holistic Doctor Treats Nutritionally & with the AP Protocol

7979 Big Bend Boulevard

Webster Groves, Missouri 63119

314-961-6631

 

Dr. DiValerio - Rheumatoid Arthritis Doctor (accepts insurance)

Office: 314-432-1111

Fax: 432-7317

Missouri Baptist Medical Building B

Suite 100

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Do you happen to have a list of docs in the state of Kansas? That

isn't too far from me either.

>

> > I am in MO close to either Columbia or Kansas City so if any of

you

> > know a doc that does the AP in these areas please let me know.

More

> > than one would be great if you have any since I hope to find one

on my

> > insurance.

>

> Hi ,

>

> Here is the list of doctors we have in Missouri - as I'm an

Aussie, I

> don't know how far these doctors are from Columbia or Kansas City.

> Chris.

>

> H. Esther, M.D. – RHU – IM – 1976

> 226 S. Woodsmill Rd.

> Chesterfied, MO 63017

> P: 314-205-0300

>

> Francisco J. Garriga, M.D. (RHU – IM – 1970)

> 1120 Shackleford Rd.

> Florissant, MO 63031-4369

> P: 314-921-4420

> F: 314-921-6086

>

> L. Hilburn M.D. (FP-1978) preventive medicine

> 116 W. Grant St.)

> Republic, MO 65738

> P: 417-732-1701

>

> ph T. Hilgeman, M.D. (IM – 1988)

> Des Peres Internal Medicine

> 13611 Barrett Office Parkway

> Des Peres, MO 63021

> P: 314-821-1313

>

> Rand W. Sommer, M.D. (RHU – 1980)

> 1034 S. Brentwood Blvd. Suite 1060

> St. Louis, MO. 63117

> P: 314-721-0666

>

> C. Uchiyama, M.D. (RHU – 1980)

> 224 S. Woods Mill Road Suite 460

> Chesterfield, MO 63017

> P: 314-576-0933

>

> F. Wiedner, MD

> Esse Health

> 16555 Manchester Rd., Suite 205

> Suite 205, Grover, MO 63040.

> P: 636-458-4800

>

> Dr. Sutherland - no record found to verify - oral & Iv – works

with

> Dr. Sinnott

> Sutherland Clinic

> Paris, MO 65275

> P: 660-327-6407

> F: 660-427-6217

>

> Nemechek, MD

> Nemechek Health Renewal

> 3404 Broadway St.

> Kansas City, MO 64111

> P: 816-756-0090

>

> Ralph , DO

> 1608 East 20th St

> Joplin, MO 64804

> P: 417-624-4323

>

> Dr. Monika Aplyn

> Dr. Christian Wessling, M.D (accepts insurance)

> Holistic Doctor Treats Nutritionally & with the AP Protocol

> 7979 Big Bend Boulevard

> Webster Groves, Missouri 63119

> 314-961-6631

>  

> Dr. DiValerio - Rheumatoid Arthritis Doctor (accepts

insurance)

> Office: 314-432-1111

> Fax: 432-7317

> Missouri Baptist Medical Building B

> Suite 100

>

>

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Hi ,

Only two in Kansas - I don't know what their experience level is:

Arnold L. Katz, M.D., - RHU 1970

10550 Quivia Ave, #320

ee Mission, KS. 66215

P: 913-888-3231

Jane Murray, MD

5509 Foxridge Dr.

Mission, KS 66202

P: 913-384-2284

F: 913-384-9884

Chris.

> Do you happen to have a list of docs in the state of Kansas? That

> isn't too far from me either.

>

>

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Just in case this is helpful to , and it might be something would

be interested to note. The two addresses listed below are in the Kansas

City, Missouri metropolitan area, and would probably be of interest to

anyone asking for a Missouri referral.

On 8/25/06 8:44 PM, " Adlard " <cadlard@...> wrote:

> Arnold L. Katz, M.D., - RHU 1970

> 10550 Quivia Ave, #320

> ee Mission, KS. 66215

> P: 913-888-3231

>

> Jane Murray, MD

> 5509 Foxridge Dr.

> Mission, KS 66202

> P: 913-384-2284

> F: 913-384-9884

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Actually the addresses are on the Kansas state side but not too far

from the Missouri boarder. I will have to drive 1 1/2 hours to get

there but it will be worth it if they do the ap.

>

> > Arnold L. Katz, M.D., - RHU 1970

> > 10550 Quivia Ave, #320

> > ee Mission, KS. 66215

> > P: 913-888-3231

> >

> > Jane Murray, MD

> > 5509 Foxridge Dr.

> > Mission, KS 66202

> > P: 913-384-2284

> > F: 913-384-9884

>

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Yes, I lived in ee Mission for a few years, but worked in Kansas City,

Mo. They are all the same metropolitan area, even though the metropolitan

area spans the state border, involving 2 states.So, an address in ee

Mission is probably only a few miles (1 to 8) farther for you than one in KC

MO.

KU med center is immediately across the state line, just a stones throw from

the area of KC MO where I worked.

What town are you living in now? I grew up in southwest Mo, now live in

Saint Louis, but I went to college in Warrensburg in the late 70's, lived in

Overland Park in the early 80's have a niece in college now in Columbia.

On 8/26/06 10:59 AM, " ktandtm " <ktandtm@...> wrote:

> Actually the addresses are on the Kansas state side but not too far

> from the Missouri boarder. I will have to drive 1 1/2 hours to get

> there but it will be worth it if they do the ap.

>

>

>

>>

>>> Arnold L. Katz, M.D., - RHU 1970

>>> 10550 Quivia Ave, #320

>>> ee Mission, KS. 66215

>>> P: 913-888-3231

>>>

>>> Jane Murray, MD

>>> 5509 Foxridge Dr.

>>> Mission, KS 66202

>>> P: 913-384-2284

>>> F: 913-384-9884

>>

>

>

>

>

>

>

> To unsubscribe, email: rheumatic-unsubscribeegroups

>

>

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I found this interesting. I am RH negative but did not develop RA until my

middle forties. Anyone have any info on a link between RH negative people

and increases in RA or Lupus rates. I had never heard of the possibility of

the injection making one more susceptible. I had a total of three of these

shots..one with each child. Any info would be welcome. Martha

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