Jump to content
RemedySpot.com

Re: New Rheumatologist

Rate this topic


Guest guest

Recommended Posts

Hi Everyone, Except for a few good Drs. I agree with Mark compleely I really

think these RA drs. are afraid if this works as well as it does, they will

have to find a new field of medicine, Like your regular dr. could give this

treatment. There has to be a reason that it is still takeing this long to

reach more drs. Maybe the AMA or the drug companies make more money, It was

on 20/20 that SOME drs were makeing between 50 to 600 thousand in kick-backs

from the drug companies, by pushing their drugs to us?? Doesn't that make you

warm and fuzzy? Just my view. from Ohio

Link to comment
Share on other sites

--- In rheumaticegroups, " Gloria M. Tate " <MissGloria@j...>

wrote:

> After months of putting off going to the new rheumatologist who is

nearby

> AND on my HMO, I finally went last Weds. I had been trying to wait

until

> the Biaxin was controlling my RA before going, but my HMO finally

made me go

> when the referral was ready to expire.

> I was hoping for a young guy since he is new here, but I got an

old and

> arrogant one.

Are you sure you're not seeing my rheumatologist? LOL Boy, know how

you feel - I've been there (and still am there). They love the

safety of their medical journals and their double blinded studies,

don't they? Keeps them out of law suits, I figure (or they figure).

If he doesn't treat you better soon, give up on him if at all

possible. I don't think anyone needs the stress of some jerk. If I

were getting worse, I wouldn't tolerate my Mr. Arrogant. However,

I'm doing pretty well, so go there basically just to get my

prescriptions refilled. Sort of funny - after 2 1/2 years of

doctors, I realize I could have self treated myself, had I the

ability to get my own prescriptions. I can't see where any doctor

has in reality done anything for me, other than to give me my drugs.

Any talk about stress, family concerns, depression, physical exercise

programs and follow through to make sure they're being taken care

of? HA! They only give lip service to those thoughts, if that.

Do they consult with my family doctor to discuss my progress and form

a plan of action? HA!

I really think medicine, as we know it, is really failing us when it

comes to treating us as " whole " human beings. And I'm not seeing it

get a whole lot better.

Mark

SW VA

metho 12.5mg/week ; Lodine 400mg 1-3x/day

Link to comment
Share on other sites

--- In rheumaticegroups, " Gloria M. Tate " <MissGloria@j...>

wrote:

> After months of putting off going to the new rheumatologist who is

nearby

> AND on my HMO, I finally went last Weds. I had been trying to wait

until

> the Biaxin was controlling my RA before going, but my HMO finally

made me go

> when the referral was ready to expire.

> I was hoping for a young guy since he is new here, but I got an

old and

> arrogant one.

Are you sure you're not seeing my rheumatologist? LOL Boy, know how

you feel - I've been there (and still am there). They love the

safety of their medical journals and their double blinded studies,

don't they? Keeps them out of law suits, I figure (or they figure).

If he doesn't treat you better soon, give up on him if at all

possible. I don't think anyone needs the stress of some jerk. If I

were getting worse, I wouldn't tolerate my Mr. Arrogant. However,

I'm doing pretty well, so go there basically just to get my

prescriptions refilled. Sort of funny - after 2 1/2 years of

doctors, I realize I could have self treated myself, had I the

ability to get my own prescriptions. I can't see where any doctor

has in reality done anything for me, other than to give me my drugs.

Any talk about stress, family concerns, depression, physical exercise

programs and follow through to make sure they're being taken care

of? HA! They only give lip service to those thoughts, if that.

Do they consult with my family doctor to discuss my progress and form

a plan of action? HA!

I really think medicine, as we know it, is really failing us when it

comes to treating us as " whole " human beings. And I'm not seeing it

get a whole lot better.

Mark

SW VA

metho 12.5mg/week ; Lodine 400mg 1-3x/day

Link to comment
Share on other sites

Gloria, remember this! YOU are HIRING this or any doctor. YOU decide whether

to keep or fire him. How 'bout giving him an evaluation??? As any employer,

I'd tell him he's on trial, that you MAY have to fire him if his actions do

not improve.

In fact, after that visit, you might consider firing the jerk already.

There's more where he came from.

Lyn

=============

>After months of putting off going to the new rheumatologist who is nearby

>AND on my HMO, I finally went last Weds. I had been trying to wait until

>the Biaxin was controlling my RA before going, but my HMO finally made me

>go

>when the referral was ready to expire.

> I was hoping for a young guy since he is new here, but I got an old and

>arrogant one. When he read my list of meds, he flipped out. He was so

>rude

>that I stopped him and told him I expected to work with him against my RA

>and that I expected to be treated and talked to as an intelligent equal.

>He replied that he didn't need to do that since he had the education and I

>didn't. When I told him I would not take methotrexate or Enbrel and wanted

>to stick to antibiotics, he wanted me to go away without any treatment. I

>just stayed there and tried to get him to do something and to be

>reasonable.

>He wrongly said that tetracycline and other such drugs only work on new

>disease and so won't work for me. He also said that Tom Brown only

>followed

>his patients for ten years and he wanted to find something that would work

>for forty. Like anyone lives forty years on these immune suppressant

>drugs.

>I pointed out that people have died from Enbrel and he said,

>Well, not that many. " He tried to tell me a lot of facts about drugs and I

>was able to either say 'I know' or to correct him because of this group.

>He

>saw that I had previously taken placquinil and asulfadine, and asked it I

>would consider using asulfadine again to see if it would work again. I

>said

>I would Think about it but only if I could keep my antibiotics. Then he

>finally consented to examine me and to do blood tests and x rays.

>I have to go back this next week for the results. I hope he will be nicer.

>Of course, he kept saying that all of the results of drugs other than the

>cycline family were only anecdotal and not backed by studies. He said it

>was all placebo effect. When I pointed out that my thyroid had gotten

>stronger on minocycline, he said maybe the blood tests were wrong. Talk

>abo

>ut wearing blinders. He acted as it were a personal attack.

>I will let you know what happens.

>love,

>Gloria

>

>

>

>To unsubscribe, email: rheumatic-unsubscribeegroups

>

>

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

Share information about yourself, create your own public profile at

http://profiles.msn.com.

Link to comment
Share on other sites

  • 4 years later...

--- In , " Jim/Terri Hauff " <JimH@t...>

wrote:

> Hi group,

>

> Last Tuesday I drove to Seattle to see a new rheumatologist. She

was recommended to me by my primary doc. I liked her very well.

Great news!

>

> I do think I overdid it this weekend though. I had to supply some

goodies for an auction on Friday night and stood in my kitchen for

about 7 hours baking and preparing food and have been quite sore in

my feet.

I've had that happen, too, and have taken to sitting on a stool while

I'm preparing food. It's a simple solution, but it involves getting

into a new habit.

Sierra

Link to comment
Share on other sites

> Hi group,

>

> Last Tuesday I drove to Seattle to see a new rheumatologist. She

was recommended to me by my primary doc. I liked her very well.

Great news!

>

> I do think I overdid it this weekend though. I had to supply some

goodies for an auction on Friday night and stood in my kitchen for

about 7 hours baking and preparing food and have been quite sore in

my feet.

I've had that happen, too, and have taken to sitting on a stool while

I'm preparing food. It's a simple solution, but it involves getting

into a new habit.

Sierra

Link to comment
Share on other sites

Terri, that is great news!!!!

--- In , " Jim/Terri Hauff " <JimH@t...>

wrote:

> Hi group,

>

> Last Tuesday I drove to Seattle to see a new rheumatologist. She

was recommended to me by my primary doc. I liked her very well. A

lot better than my last one. Did a thorough medical history on me

and then did an exam on me. She said I look good for having RA for

12 years. She could not detect any swelling, redness, or increased

synovial fluid. She is going to continue on the plan that my last

rheumie had me on which is to continue to taper my Arava down. I was

on 2x/wk and now am going to one time per week. She did new set of x-

rays and labs on me. Don't know the results of these and have no

worries that there is anything wrong so will wait to see the results

when I go back again in January. She did say to me in the beginning

when she came into the room that she was there to help me in any

way. She wants me comfortable and in no way does she want to harm

any organs. She also does not want me to be sick in any way. She

seemed more like a concerned friend than a doctor. It was an extreme

change from what I have had.

>

> I do think I overdid it this weekend though. I had to supply some

goodies for an auction on Friday night and stood in my kitchen for

about 7 hours baking and preparing food and have been quite sore in

my feet. Then on Saturday I had a breakfast meeting here at my house

and was up on my feet cooking and preparing the table. On Saturday

evening our family celebrated my mom's birthday here at my house.

Now if I am up on my feet for too long my feet just ache. Also, all

I wanted to do yesterday was just kind of lay around. Hopefully work

won't be too bad, but I know better than that. Currently a work day

is 12 hours long with one 1/2 hour lunch.

>

> Talk to you all again.

>

>

> Terri

>

>

Link to comment
Share on other sites

Terri, that is great news!!!!

> Hi group,

>

> Last Tuesday I drove to Seattle to see a new rheumatologist. She

was recommended to me by my primary doc. I liked her very well. A

lot better than my last one. Did a thorough medical history on me

and then did an exam on me. She said I look good for having RA for

12 years. She could not detect any swelling, redness, or increased

synovial fluid. She is going to continue on the plan that my last

rheumie had me on which is to continue to taper my Arava down. I was

on 2x/wk and now am going to one time per week. She did new set of x-

rays and labs on me. Don't know the results of these and have no

worries that there is anything wrong so will wait to see the results

when I go back again in January. She did say to me in the beginning

when she came into the room that she was there to help me in any

way. She wants me comfortable and in no way does she want to harm

any organs. She also does not want me to be sick in any way. She

seemed more like a concerned friend than a doctor. It was an extreme

change from what I have had.

>

> I do think I overdid it this weekend though. I had to supply some

goodies for an auction on Friday night and stood in my kitchen for

about 7 hours baking and preparing food and have been quite sore in

my feet. Then on Saturday I had a breakfast meeting here at my house

and was up on my feet cooking and preparing the table. On Saturday

evening our family celebrated my mom's birthday here at my house.

Now if I am up on my feet for too long my feet just ache. Also, all

I wanted to do yesterday was just kind of lay around. Hopefully work

won't be too bad, but I know better than that. Currently a work day

is 12 hours long with one 1/2 hour lunch.

>

> Talk to you all again.

>

>

> Terri

>

>

Link to comment
Share on other sites

That is excellent news about your new rheumatologist, Terri! You deserve

no less.

Hope you recover from your weekend partying quickly.

I'll tell you where to go!

Mayo Clinic in Rochester

http://www.mayoclinic.org/rochester

s Hopkins Medicine

http://www.hopkinsmedicine.org

[ ] New rheumatologist

>

> Hi group,

>

> Last Tuesday I drove to Seattle to see a new rheumatologist. She was

recommended to me by my primary doc. I liked her very well. A lot

better than my last one. Did a thorough medical history on me and then

did an exam on me. She said I look good for having RA for 12 years.

She could not detect any swelling, redness, or increased synovial fluid.

She is going to continue on the plan that my last rheumie had me on

which is to continue to taper my Arava down. I was on 2x/wk and now am

going to one time per week. She did new set of x-rays and labs on me.

Don't know the results of these and have no worries that there is

anything wrong so will wait to see the results when I go back again in

January. She did say to me in the beginning when she came into the room

that she was there to help me in any way. She wants me comfortable and

in no way does she want to harm any organs. She also does not want me

to be sick in any way. She seemed more like a concerned friend than a

doctor. It was an extreme change from what I have had.

>

> I do think I overdid it this weekend though. I had to supply some

goodies for an auction on Friday night and stood in my kitchen for about

7 hours baking and preparing food and have been quite sore in my feet.

Then on Saturday I had a breakfast meeting here at my house and was up

on my feet cooking and preparing the table. On Saturday evening our

family celebrated my mom's birthday here at my house. Now if I am up on

my feet for too long my feet just ache. Also, all I wanted to do

yesterday was just kind of lay around. Hopefully work won't be too bad,

but I know better than that. Currently a work day is 12 hours long with

one 1/2 hour lunch.

>

> Talk to you all again.

>

>

> Terri

Link to comment
Share on other sites

Terri, How do yo do it?? I couldn't keep up with the 12 hour days.

I'm glad to here that you have a good rheumatologist. I hope things

work out for you....Blessed Be.....Marina

--- In , " Jim/Terri Hauff " <JimH@t...>

wrote:

> Hi group,

>

> Last Tuesday I drove to Seattle to see a new rheumatologist. She

was recommended to me by my primary doc. I liked her very well. A

lot better than my last one. Did a thorough medical history on me

and then did an exam on me. She said I look good for having RA for

12 years. She could not detect any swelling, redness, or increased

synovial fluid. She is going to continue on the plan that my last

rheumie had me on which is to continue to taper my Arava down. I

was on 2x/wk and now am going to one time per week. She did new set

of x-rays and labs on me. Don't know the results of these and have

no worries that there is anything wrong so will wait to see the

results when I go back again in January. She did say to me in the

beginning when she came into the room that she was there to help me

in any way. She wants me comfortable and in no way does she want to

harm any organs. She also does not want me to be sick in any way.

She seemed more like a concerned friend than a doctor. It was an

extreme change from what I have had.

>

> I do think I overdid it this weekend though. I had to supply some

goodies for an auction on Friday night and stood in my kitchen for

about 7 hours baking and preparing food and have been quite sore in

my feet. Then on Saturday I had a breakfast meeting here at my

house and was up on my feet cooking and preparing the table. On

Saturday evening our family celebrated my mom's birthday here at my

house. Now if I am up on my feet for too long my feet just ache.

Also, all I wanted to do yesterday was just kind of lay around.

Hopefully work won't be too bad, but I know better than that.

Currently a work day is 12 hours long with one 1/2 hour lunch.

>

> Talk to you all again.

>

>

> Terri

>

>

Link to comment
Share on other sites

  • 9 months later...

What do you hope your rheumatologist to accomplish?

--- In , " MollyBloom54 " <jawlaw93@y...>

wrote:

> Please wish me luck on my new rheumatologist. My old rheum. at the

U is not on my new

> insurance. And, she is also a very long drive, which is harder and

harder for me to make.

Link to comment
Share on other sites

I just need to find a new doctor, because my old rheumatologist is not on my new

insurance

plan. I take plaquenil, and need to monitor it.

I also have questions about my diagnoses - My old rheum. wrote on my med records

that I

have fibromyalgia, and lupus. My old doc never mentioned fibro, and I want to

ask about

that.

> > Please wish me luck on my new rheumatologist. My old rheum. at the

> U is not on my new

> > insurance. And, she is also a very long drive, which is harder and

> harder for me to make.

Link to comment
Share on other sites

To answer your question, I hope this rheumatologist is not a pain in the neck.

I have run into those.

> > > Please wish me luck on my new rheumatologist. My old rheum. at the

> > U is not on my new

> > > insurance. And, she is also a very long drive, which is harder and

> > harder for me to make.

Link to comment
Share on other sites

Molly,

I do wish you luck . . . most rheumatologists don't

take implant problems seriously! . . . You might take

some of the information we share with you.

They like to say the the NIH didn't find a problem. If

you can, find out where they get their information. It

seems like they've memorized the same script!

Love,

Rogene

Link to comment
Share on other sites

Oh I know, and I dreaded that, Rogene. At least, this rheumatologist does seem

to believe

that implants do cause problems. That is a good start.

I wished she didn't have such an attitude about lawyers and the settlement (or

any legal

matter). But the important thing is to have someone who seems to believe what

we are

saying -- she said she has seen to many women with implants and autoimmune

problems to

not believe it.

> Molly,

>

> I do wish you luck . . . most rheumatologists don't

> take implant problems seriously! . . . You might take

> some of the information we share with you.

>

> They like to say the the NIH didn't find a problem. If

> you can, find out where they get their information. It

> seems like they've memorized the same script!

>

> Love,

>

> Rogene

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...