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they said she had vaginismus from the vvs caused by yeast infection that effected the nerve endings. was going to give her trigger point injections of steroids and lidocaine for the muscles? has anyone had anything like this????

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they said she had vaginismus from the vvs caused by yeast infection that effected the nerve endings. was going to give her trigger point injections of steroids and lidocaine for the muscles? has anyone had anything like this????

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they said she had vaginismus from the vvs caused by yeast infection that effected the nerve endings. was going to give her trigger point injections of steroids and lidocaine for the muscles? has anyone had anything like this????

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They just mentioned vulvar vestibulitis on private practice on abc. They are treating it with injections of lidocaine. a step in the right direction. kara

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I know people on here and my other groups have had trigger point

injections...some got temporary relief, but overall I haven't heard

positive things - it definitely wasn't the cure all that it was for the

girl on the show (she just had the injections and one therapy session).

Hopefully someone who's actually had them will post...

Melinda

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I know people on here and my other groups have had trigger point

injections...some got temporary relief, but overall I haven't heard

positive things - it definitely wasn't the cure all that it was for the

girl on the show (she just had the injections and one therapy session).

Hopefully someone who's actually had them will post...

Melinda

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I know people on here and my other groups have had trigger point

injections...some got temporary relief, but overall I haven't heard

positive things - it definitely wasn't the cure all that it was for the

girl on the show (she just had the injections and one therapy session).

Hopefully someone who's actually had them will post...

Melinda

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Yeah, I had that done. Did absolutely nothing. It's

Charlotte on Sex and the City being magically cured

with Elavil all over again.

--- Carolyn52192@... wrote:

> they said she had vaginismus from the vvs caused by

> yeast infection that

> effected the nerve endings. was going to

> give her trigger point

> injections of steroids and lidocaine for the

> muscles? has anyone had anything like

> this????

>

>

>

>

>

> ************************************** See what's

> new at http://www.aol.com

>

________________________________________________________________________________\

____

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today's economy) at Yahoo! Games.

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Yeah, I had that done. Did absolutely nothing. It's

Charlotte on Sex and the City being magically cured

with Elavil all over again.

--- Carolyn52192@... wrote:

> they said she had vaginismus from the vvs caused by

> yeast infection that

> effected the nerve endings. was going to

> give her trigger point

> injections of steroids and lidocaine for the

> muscles? has anyone had anything like

> this????

>

>

>

>

>

> ************************************** See what's

> new at http://www.aol.com

>

________________________________________________________________________________\

____

Boardwalk for $500? In 2007? Ha! Play Monopoly Here and Now (it's updated for

today's economy) at Yahoo! Games.

http://get.games.yahoo.com/proddesc?gamekey=monopolyherenow

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Molly,

It isn't so much about control, but about listening to the signs

my body gives me to help me figure out which route to take and

right now it looks like another one of my problems for why my

pain is as it is could be related to my bladder. I'm scared to

think that the endometriosis (one of my other medical problems)

could be affecting my bladder now because of a scare I got back

in March. I am going to have to get my bladder checked out

though because of the fact that the symptoms I had in March also

tell me that I could have IC which if I do would confirm the

suspicions that my gyn had 7 years ago. I also had some issues

with my bladder 7 years that caused a great deal of pain.

So from that standpoint I could see where that could come in to

play too as far as causing muscle spasm if it turned out that

they were spasming.

But you have done me a favor hon. Given me a bit more to know

what to look for now when I keep an eye on my bowel too because

when that doctor tried to tell me that I had pelvic floor muscle

spasm she tried to tell me that I had spasm of the muscle area

that Carol said the doctor mentioned the levator ani. I noticed

when I read up on the urogyn in this area that he listed it (and

I've seen it elsewhere too) as levator ani syndrome. Which

means that there is something physically causing this to occur.

I'm going to do some more research on it in relation to fibro

too so that once I rule out all other physical causes that could

be possible then I can try and talk to a physiatrist or go to

that urogyn to have his Nurse Practicioner (just hope she has

handled fibro patients too) look at me and see what can be done

to see what else can be of possible help.

So I may consider PT at some point. And thankfully I did talk

to someone in my area that has a lot of knowledge (talked to her

several years ago) and she told me that if I ever want to try it

that she would respect my wishes to stay external so that's

good.

I will keep you posted on how this turns out but right now it

has to wait because my mom is having surgery for her breast

cancer on Tues.

Thanks for giving me some other thoughts to consider when it

comes to listening to the signals my body gives because

sometimes it can give me new signals too that I need to be aware

of. Which then leads me to more research. I may have some

questions for you at a later date because you mentioned about

what happened to you.

Kristy :)

________________________________________________________________________________\

____

Tonight's top picks. What will you watch tonight? Preview the hottest shows on

Yahoo! TV.

http://tv.yahoo.com/

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Molly,

It isn't so much about control, but about listening to the signs

my body gives me to help me figure out which route to take and

right now it looks like another one of my problems for why my

pain is as it is could be related to my bladder. I'm scared to

think that the endometriosis (one of my other medical problems)

could be affecting my bladder now because of a scare I got back

in March. I am going to have to get my bladder checked out

though because of the fact that the symptoms I had in March also

tell me that I could have IC which if I do would confirm the

suspicions that my gyn had 7 years ago. I also had some issues

with my bladder 7 years that caused a great deal of pain.

So from that standpoint I could see where that could come in to

play too as far as causing muscle spasm if it turned out that

they were spasming.

But you have done me a favor hon. Given me a bit more to know

what to look for now when I keep an eye on my bowel too because

when that doctor tried to tell me that I had pelvic floor muscle

spasm she tried to tell me that I had spasm of the muscle area

that Carol said the doctor mentioned the levator ani. I noticed

when I read up on the urogyn in this area that he listed it (and

I've seen it elsewhere too) as levator ani syndrome. Which

means that there is something physically causing this to occur.

I'm going to do some more research on it in relation to fibro

too so that once I rule out all other physical causes that could

be possible then I can try and talk to a physiatrist or go to

that urogyn to have his Nurse Practicioner (just hope she has

handled fibro patients too) look at me and see what can be done

to see what else can be of possible help.

So I may consider PT at some point. And thankfully I did talk

to someone in my area that has a lot of knowledge (talked to her

several years ago) and she told me that if I ever want to try it

that she would respect my wishes to stay external so that's

good.

I will keep you posted on how this turns out but right now it

has to wait because my mom is having surgery for her breast

cancer on Tues.

Thanks for giving me some other thoughts to consider when it

comes to listening to the signals my body gives because

sometimes it can give me new signals too that I need to be aware

of. Which then leads me to more research. I may have some

questions for you at a later date because you mentioned about

what happened to you.

Kristy :)

________________________________________________________________________________\

____

Tonight's top picks. What will you watch tonight? Preview the hottest shows on

Yahoo! TV.

http://tv.yahoo.com/

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Share on other sites

Molly,

It isn't so much about control, but about listening to the signs

my body gives me to help me figure out which route to take and

right now it looks like another one of my problems for why my

pain is as it is could be related to my bladder. I'm scared to

think that the endometriosis (one of my other medical problems)

could be affecting my bladder now because of a scare I got back

in March. I am going to have to get my bladder checked out

though because of the fact that the symptoms I had in March also

tell me that I could have IC which if I do would confirm the

suspicions that my gyn had 7 years ago. I also had some issues

with my bladder 7 years that caused a great deal of pain.

So from that standpoint I could see where that could come in to

play too as far as causing muscle spasm if it turned out that

they were spasming.

But you have done me a favor hon. Given me a bit more to know

what to look for now when I keep an eye on my bowel too because

when that doctor tried to tell me that I had pelvic floor muscle

spasm she tried to tell me that I had spasm of the muscle area

that Carol said the doctor mentioned the levator ani. I noticed

when I read up on the urogyn in this area that he listed it (and

I've seen it elsewhere too) as levator ani syndrome. Which

means that there is something physically causing this to occur.

I'm going to do some more research on it in relation to fibro

too so that once I rule out all other physical causes that could

be possible then I can try and talk to a physiatrist or go to

that urogyn to have his Nurse Practicioner (just hope she has

handled fibro patients too) look at me and see what can be done

to see what else can be of possible help.

So I may consider PT at some point. And thankfully I did talk

to someone in my area that has a lot of knowledge (talked to her

several years ago) and she told me that if I ever want to try it

that she would respect my wishes to stay external so that's

good.

I will keep you posted on how this turns out but right now it

has to wait because my mom is having surgery for her breast

cancer on Tues.

Thanks for giving me some other thoughts to consider when it

comes to listening to the signals my body gives because

sometimes it can give me new signals too that I need to be aware

of. Which then leads me to more research. I may have some

questions for you at a later date because you mentioned about

what happened to you.

Kristy :)

________________________________________________________________________________\

____

Tonight's top picks. What will you watch tonight? Preview the hottest shows on

Yahoo! TV.

http://tv.yahoo.com/

Link to comment
Share on other sites

I was diagnosed with IC. Did I have IC??? I don't know. Did my bladder hurt??? YES! Was it REALLY my bladder hurting? Yes it was. Was it the muscles that were CAUSING my bladder to hurt? Yes it was. Last year when I had a mini relapse and I was sure just SURE it was my pudendal nerve, was it? NO it was my coccygeus muscle. This from a girl who knows her body and is hyperaware of her pelvic floor after six months of at home biofeedback therapy. I did NOT want to go back to San Fran (a money thing) so I went to three semi local PTs (one one the western slope and two in Denver) who said they were well trained but didn't have a clue. So I

bit the bullet and went back to San Fran (when you've been to the best, what can you do?). So after 30 seconds of exam said "oh, that's your coccygeus muscle, not your PN you'll be fine, just go ahead and work on it.

So what am I trying to say after two glasses of wine? I guess be open minded. was the sixth PT I saw, Dr. Weiss was the 23rd doc. Please just keep on swinging. This is my little niche in life to try to inspire hope to people. I had lost hope. But somehow I kept on trying. I now realize that perhaps I am a perhaps simple case although it didn't seem simple to me. A solid year of horrific, painful, invasive, painful physical therapy. But what choice did I have? I went on a three hour horseback ride yesterday. I am aware every minute, every second of how blessed I am.

So sorry about your mom. I love my mom so much it hurts, she is 79 and I cherish every second. I can't even think about what you're going through.

Keep your chin up and you should join the happypelvis group. People seem to be dissappearing off the group after posting about their improving health - you know why? Because they're getting well!!!

keep your chin up

love, Molly

Re: Private practice

Molly,It isn't so much about control, but about listening to the signsmy body gives me to help me figure out which route to take andright now it looks like another one of my problems for why mypain is as it is could be related to my bladder. I'm scared tothink that the endometriosis (one of my other medical problems)could be affecting my bladder now because of a scare I got backin March. I am going to have to get my bladder checked outthough because of the fact that the symptoms I had in March alsotell me that I could have IC which if I do would confirm thesuspicions that my gyn had 7 years ago. I also had some issueswith my bladder 7 years that caused a great deal of pain.So from that standpoint I could see where that could come in toplay too as far as causing muscle spasm if it turned out thatthey were spasming.But you have done me a favor hon. Given me a bit more to

knowwhat to look for now when I keep an eye on my bowel too becausewhen that doctor tried to tell me that I had pelvic floor musclespasm she tried to tell me that I had spasm of the muscle areathat Carol said the doctor mentioned the levator ani. I noticedwhen I read up on the urogyn in this area that he listed it (andI've seen it elsewhere too) as levator ani syndrome. Whichmeans that there is something physically causing this to occur.I'm going to do some more research on it in relation to fibrotoo so that once I rule out all other physical causes that couldbe possible then I can try and talk to a physiatrist or go tothat urogyn to have his Nurse Practicioner (just hope she hashandled fibro patients too) look at me and see what can be doneto see what else can be of possible help.So I may consider PT at some point. And thankfully I did talkto someone in my area that has a lot of

knowledge (talked to herseveral years ago) and she told me that if I ever want to try itthat she would respect my wishes to stay external so that'sgood.I will keep you posted on how this turns out but right now ithas to wait because my mom is having surgery for her breastcancer on Tues.Thanks for giving me some other thoughts to consider when itcomes to listening to the signals my body gives becausesometimes it can give me new signals too that I need to be awareof. Which then leads me to more research. I may have somequestions for you at a later date because you mentioned aboutwhat happened to you.Kristy :)____________ _________ _________ _________ _________ _________ _Tonight's top picks. What will you watch tonight? Preview the hottest shows on Yahoo! TV.http://tv.yahoo. com/

Shape Yahoo! in your own image. Join our Network Research Panel today!

Link to comment
Share on other sites

I was diagnosed with IC. Did I have IC??? I don't know. Did my bladder hurt??? YES! Was it REALLY my bladder hurting? Yes it was. Was it the muscles that were CAUSING my bladder to hurt? Yes it was. Last year when I had a mini relapse and I was sure just SURE it was my pudendal nerve, was it? NO it was my coccygeus muscle. This from a girl who knows her body and is hyperaware of her pelvic floor after six months of at home biofeedback therapy. I did NOT want to go back to San Fran (a money thing) so I went to three semi local PTs (one one the western slope and two in Denver) who said they were well trained but didn't have a clue. So I

bit the bullet and went back to San Fran (when you've been to the best, what can you do?). So after 30 seconds of exam said "oh, that's your coccygeus muscle, not your PN you'll be fine, just go ahead and work on it.

So what am I trying to say after two glasses of wine? I guess be open minded. was the sixth PT I saw, Dr. Weiss was the 23rd doc. Please just keep on swinging. This is my little niche in life to try to inspire hope to people. I had lost hope. But somehow I kept on trying. I now realize that perhaps I am a perhaps simple case although it didn't seem simple to me. A solid year of horrific, painful, invasive, painful physical therapy. But what choice did I have? I went on a three hour horseback ride yesterday. I am aware every minute, every second of how blessed I am.

So sorry about your mom. I love my mom so much it hurts, she is 79 and I cherish every second. I can't even think about what you're going through.

Keep your chin up and you should join the happypelvis group. People seem to be dissappearing off the group after posting about their improving health - you know why? Because they're getting well!!!

keep your chin up

love, Molly

Re: Private practice

Molly,It isn't so much about control, but about listening to the signsmy body gives me to help me figure out which route to take andright now it looks like another one of my problems for why mypain is as it is could be related to my bladder. I'm scared tothink that the endometriosis (one of my other medical problems)could be affecting my bladder now because of a scare I got backin March. I am going to have to get my bladder checked outthough because of the fact that the symptoms I had in March alsotell me that I could have IC which if I do would confirm thesuspicions that my gyn had 7 years ago. I also had some issueswith my bladder 7 years that caused a great deal of pain.So from that standpoint I could see where that could come in toplay too as far as causing muscle spasm if it turned out thatthey were spasming.But you have done me a favor hon. Given me a bit more to

knowwhat to look for now when I keep an eye on my bowel too becausewhen that doctor tried to tell me that I had pelvic floor musclespasm she tried to tell me that I had spasm of the muscle areathat Carol said the doctor mentioned the levator ani. I noticedwhen I read up on the urogyn in this area that he listed it (andI've seen it elsewhere too) as levator ani syndrome. Whichmeans that there is something physically causing this to occur.I'm going to do some more research on it in relation to fibrotoo so that once I rule out all other physical causes that couldbe possible then I can try and talk to a physiatrist or go tothat urogyn to have his Nurse Practicioner (just hope she hashandled fibro patients too) look at me and see what can be doneto see what else can be of possible help.So I may consider PT at some point. And thankfully I did talkto someone in my area that has a lot of

knowledge (talked to herseveral years ago) and she told me that if I ever want to try itthat she would respect my wishes to stay external so that'sgood.I will keep you posted on how this turns out but right now ithas to wait because my mom is having surgery for her breastcancer on Tues.Thanks for giving me some other thoughts to consider when itcomes to listening to the signals my body gives becausesometimes it can give me new signals too that I need to be awareof. Which then leads me to more research. I may have somequestions for you at a later date because you mentioned aboutwhat happened to you.Kristy :)____________ _________ _________ _________ _________ _________ _Tonight's top picks. What will you watch tonight? Preview the hottest shows on Yahoo! TV.http://tv.yahoo. com/

Shape Yahoo! in your own image. Join our Network Research Panel today!

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Share on other sites

I was diagnosed with IC. Did I have IC??? I don't know. Did my bladder hurt??? YES! Was it REALLY my bladder hurting? Yes it was. Was it the muscles that were CAUSING my bladder to hurt? Yes it was. Last year when I had a mini relapse and I was sure just SURE it was my pudendal nerve, was it? NO it was my coccygeus muscle. This from a girl who knows her body and is hyperaware of her pelvic floor after six months of at home biofeedback therapy. I did NOT want to go back to San Fran (a money thing) so I went to three semi local PTs (one one the western slope and two in Denver) who said they were well trained but didn't have a clue. So I

bit the bullet and went back to San Fran (when you've been to the best, what can you do?). So after 30 seconds of exam said "oh, that's your coccygeus muscle, not your PN you'll be fine, just go ahead and work on it.

So what am I trying to say after two glasses of wine? I guess be open minded. was the sixth PT I saw, Dr. Weiss was the 23rd doc. Please just keep on swinging. This is my little niche in life to try to inspire hope to people. I had lost hope. But somehow I kept on trying. I now realize that perhaps I am a perhaps simple case although it didn't seem simple to me. A solid year of horrific, painful, invasive, painful physical therapy. But what choice did I have? I went on a three hour horseback ride yesterday. I am aware every minute, every second of how blessed I am.

So sorry about your mom. I love my mom so much it hurts, she is 79 and I cherish every second. I can't even think about what you're going through.

Keep your chin up and you should join the happypelvis group. People seem to be dissappearing off the group after posting about their improving health - you know why? Because they're getting well!!!

keep your chin up

love, Molly

Re: Private practice

Molly,It isn't so much about control, but about listening to the signsmy body gives me to help me figure out which route to take andright now it looks like another one of my problems for why mypain is as it is could be related to my bladder. I'm scared tothink that the endometriosis (one of my other medical problems)could be affecting my bladder now because of a scare I got backin March. I am going to have to get my bladder checked outthough because of the fact that the symptoms I had in March alsotell me that I could have IC which if I do would confirm thesuspicions that my gyn had 7 years ago. I also had some issueswith my bladder 7 years that caused a great deal of pain.So from that standpoint I could see where that could come in toplay too as far as causing muscle spasm if it turned out thatthey were spasming.But you have done me a favor hon. Given me a bit more to

knowwhat to look for now when I keep an eye on my bowel too becausewhen that doctor tried to tell me that I had pelvic floor musclespasm she tried to tell me that I had spasm of the muscle areathat Carol said the doctor mentioned the levator ani. I noticedwhen I read up on the urogyn in this area that he listed it (andI've seen it elsewhere too) as levator ani syndrome. Whichmeans that there is something physically causing this to occur.I'm going to do some more research on it in relation to fibrotoo so that once I rule out all other physical causes that couldbe possible then I can try and talk to a physiatrist or go tothat urogyn to have his Nurse Practicioner (just hope she hashandled fibro patients too) look at me and see what can be doneto see what else can be of possible help.So I may consider PT at some point. And thankfully I did talkto someone in my area that has a lot of

knowledge (talked to herseveral years ago) and she told me that if I ever want to try itthat she would respect my wishes to stay external so that'sgood.I will keep you posted on how this turns out but right now ithas to wait because my mom is having surgery for her breastcancer on Tues.Thanks for giving me some other thoughts to consider when itcomes to listening to the signals my body gives becausesometimes it can give me new signals too that I need to be awareof. Which then leads me to more research. I may have somequestions for you at a later date because you mentioned aboutwhat happened to you.Kristy :)____________ _________ _________ _________ _________ _________ _Tonight's top picks. What will you watch tonight? Preview the hottest shows on Yahoo! TV.http://tv.yahoo. com/

Shape Yahoo! in your own image. Join our Network Research Panel today!

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Molly,

My Pain Management doctor who is an osteopathic doctor

discovered at last visit that my sacral area was out of

alignment and did some work on the muscle around that area too

and I felt much better.

In my case though, my bladder really is an issue and how I know

that is because of some symptoms 7 years ago and again back in

March when I had to have an ultrasound done. I just don't know

yet if it's the issue of IC or endo. We'll see after my mom is

fully recovered from her surgery.

Kristy :)

________________________________________________________________________________\

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Sims Stories at Yahoo! Games.

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