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Newly Diagnosed With Interstitial Cystitis | Forum profile
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Forum profile page for Newly Diagnosed With Interstitial Cystitis on http://www.ic-network.com.
This report page is the aggregated overview from a single forum: Newly Diagnosed With Interstitial Cystitis, located on the Message Board at http://www.ic-network.com.
This forum profile page summarizes the general forum statistics such as: Users Activity, Forum Activity, and Top Authors, which are reported in either a table or graph below for a given reporting time period.
Additional forum profile information for "Newly Diagnosed With Interstitial Cystitis" on the Message Board at http://www.ic-network.com is also shown in the following ways:
1) Latest Active Threads
2) Hot Threads for Last Week
Warning: These statistics are generated using 'best efforts' and can experience delays and reporting errors at times. Please note that such statistics do not constitute a forum's popularity and/or exact posting volumes at any given reporting period.
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Posting activity on Newly Diagnosed With Interstitial Cystitis:
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Newly Diagnosed With Interstitial Cystitis Posting activity graph:
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Top authors during last week:
user's latest post:
Is there anything stronger then...
Published (2009-11-29 05:54:00)
I agree with Donna. I would call on Monday morning her Dr. and see what could be done. I wish her Mother lasts of luck and pain free soon. DIAMIC65
user's latest post:
Hello! *waves* I'm new -...
Published (2009-11-29 18:46:00)
Thank you curlycue,music lover, and statesboro.It's nice to meet you all. I was going to take both Cystoprotek and Elmiron as well but,I read that Cystoprotek has shellfish extract (or something along those lines) and I have a mild allergy to it.I'm probably being overly cautious but,I am scared to try it.I know I probably should just to see if anything happens.
user's latest post:
Amitriptyline Side Effects-Help!
Published (2009-11-29 08:59:00)
Please be carefull when she increases the dose. Get the doctor's OK before doing so. I know what it did to me with only 25 mg's. Used it one time only. That was enough to convince me other wise.
user's latest post:
Hi,please help!! - Page 3 -...
Published (2009-11-28 06:13:00)
Still no diagnosis Two more doctors I've seen,a psychiatrist said that is due to stress and prescibed me cipralex,and another urologist said that I should try oxybutin. Has any of you guys tried either or both together,and if you have what is your opinion and results? thanks, Marios.
user's latest post:
Hello! *waves* I'm new
Published (2009-11-24 14:57:00)
You've found the right place. Have you had a cystoscopy or a hydrodistention? A cystoscopy is when a camera is placed into your bladder via your urethra to look into your bladder to see what is going on. A hydrodistention is when your bladder is filled up with saline solution. While this is going on, this is done under general anasthesia because it is very painful. Blowing up your bladder with the saline solution promotes healing for...
user's latest post:
Is this pain normal?? Bladder or...
Published (2009-11-25 16:20:00)
Hi Bri, It's crazy! I'm going to talk to my uro and give PT a try to loosen those pelvic muscles...the heating pad just isn't enough right now! This aching pain is way worse then the pain I feel while peeing or after! Have you tried any pain meds that have worked? Thanks for confirming this is in fact "normal" haha best wishes, and happy turkey day! xo, kate
user's latest post:
Recently diagnosed with IC, need...
Published (2009-11-24 18:40:00)
Hi Littlewun, I've been on the Elmiron for almost 2 months. Nothing miraculous to report yet. I did try it years ago for 4-5 months with no positive change, but I saw Dr. Parsons back in late July for my sweet little daughter whom he diagnosed with mild IC. He started asking me some questions about my IC and I told him I had been on Elmiron for 4-5 months with no change. He recommended I go back on it and felt that I very well might have...
user's latest post:
Told that I don't have...
Published (2009-11-28 18:22:00)
It can be tested by using a specific urine culture, swab tests, or blood tests. I've been looking into it a lot though and think even if I could get a dr to test me for it it wouldnt be accurate since I've been on ABs in the past two months and am still on them. I asked my uro that says I have IC about it and she said she didn't test for that kind of thing and was kind of like whatever you have PBS lets get this going so I can...
user's latest post:
Thankful for this website
Published (2009-11-28 13:26:00)
You are welcome! I'm sorry you're on the boards. I was diagnosed in October and, since starting meds and the diet I've been much better. Some days, I even feel like my old self again, so don't get too discouraged. I know it is hard especially the very beginning. I did the urodynamics and they cysto/hydro. Made it through both and you will make it too. Don't give up!
user's latest post:
Remembering what it was like as...
Published (2009-11-29 12:23:00)
I think there's some debate about whether the trigger type foods could still be hurting the bladder - even when you're in remission. I've been eating whatever I'd like for several years now with no ill effects at all. (Did NOT start doing that until I was pretty much symptom free - I totally did the IC diet before that.) Depends who you talk to on whether or not they think it's advisable or not. It's very...
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Latest active threads on Newly Diagnosed With Interstitial Cystitis::
Started 1 week ago (2009-11-24 14:37:00)
by Sunflower2707
I'm glad you found us! I am also new here therefore am still figuring out what to do with my (maybe IC). I have good and bad days right now..after my hydro/cysto I have been in a flare and although it's mild it is sill uncomfortable, but I am still positive it is going to go away soon and then I should feel good for a while.
But, there are plenty of people on here that are in remission or...
Started 2 weeks, 6 days ago (2009-11-11 16:56:00)
by Snowden1
Kim,
Thank you so much for that post and thank you so much for staying here to help. I have found you to one of the people I focus on the most because you can actually eat everything ---- I want this too. You guys are the ones who give me hope to continue to search for answers and not give up.
It is good to be reminded that most people find a way to deal with this illness.
I use to...
Started 2 days, 7 hours ago (2009-11-29 10:56:00)
by dyno
Here is another link also that has a wealth of information in it.
http://www.ic-network.com/guestlectures/
Started 1 week, 4 days ago (2009-11-20 09:44:00)
by Glenda2
I am SO Sorry this stuff affected you like this.
People get upset when I tell MY story of what it did to ME.
I lost my complete memory for 10 days.
I was a Catatonic Zombee.
You can search out the other Elavil (Amitryptaline) thread topics and read my replys about this medication.
It has the Potential to be dangerous. Atleast for ME it was !!!
Other's may do just ...
Started 2 days, 14 hours ago (2009-11-29 03:37:00)
by ICNDonna
My suggestion is to have her see a pain management specialist for help. They are specifically trained in pain control and better able to help than most urologists, whose training is in other areas.
Warm hugs,
Donna
Started 3 days, 15 hours ago (2009-11-28 03:00:00)
by nottoc4
I had the PST test done May of 2008.There is no doubt in my mind that I have IC.
Started 3 days, 15 hours ago (2009-11-28 02:56:00)
by Glenda2
Greetings and welcome to the best Board on the Internet for IC.
The information here is fantastic , and so are the members.
I am also quite new to the board.
I was diagnosed with IC on October 12th. Via a Cystoscopy.
Put on Elmiron , it makes me quite ill , so I had to stop taking it.
You will make alot of wonderfull friends here. They are very supportive.
Started 1 month ago (2009-10-29 14:04:00)
by turnaround
Hey Marios,
Glad you found this board.
I know what you mean about coffee, and if you really can't stop drinking it, what about taking Prelief with it. I don't know if you have that in Greece, but google it and maybe you do.
I do know that my cousin, who is male, does not have IC, but his bladder is highly irritated by soda. Once he stopped drinking it, his symptoms subsided.
...
Started 3 years, 2 months ago (2006-10-02 20:28:00)
by trinklebell
thank you so much for this information!!! i just joined this site today. I
was diagnosed with ic two weeks ago, w/ endometriosis over 2 years ago, and
IBS over 5 years ago. i'm sure all of this info will help me alot with
easing my symptoms. thanks again!
-trinklebell
p.s.
if anybody has any advice on how to make following ic dieting rules any
easier, i would greatly appreciate the info. (my ...
Started 6 days, 22 hours ago (2009-11-24 19:39:00)
by Elacey
I definitely know how you feel.I have horrible abdominal and lower back pain.Aching is definitely the word to describe it.I'll think that I have back problems when really it's the IC.I'm pretty sure it's different for everyone but,I definitely feel that way.Now the burning when you urinate,that is a good question because sometimes I feel as though I have a burning sensation but,I chalk it up to ...
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Hot threads for last week on Newly Diagnosed With Interstitial Cystitis::
Started 1 week ago (2009-11-24 14:37:00)
by Sunflower2707
I'm glad you found us! I am also new here therefore am still figuring out what to do with my (maybe IC). I have good and bad days right now..after my hydro/cysto I have been in a flare and although it's mild it is sill uncomfortable, but I am still positive it is going to go away soon and then I should feel good for a while.
But, there are plenty of people on here that are in remission or...
Started 6 days, 22 hours ago (2009-11-24 19:39:00)
by Elacey
I definitely know how you feel.I have horrible abdominal and lower back pain.Aching is definitely the word to describe it.I'll think that I have back problems when really it's the IC.I'm pretty sure it's different for everyone but,I definitely feel that way.Now the burning when you urinate,that is a good question because sometimes I feel as though I have a burning sensation but,I chalk it up to ...
Started 1 month ago (2009-10-29 14:04:00)
by turnaround
Hey Marios,
Glad you found this board.
I know what you mean about coffee, and if you really can't stop drinking it, what about taking Prelief with it. I don't know if you have that in Greece, but google it and maybe you do.
I do know that my cousin, who is male, does not have IC, but his bladder is highly irritated by soda. Once he stopped drinking it, his symptoms subsided.
...
Started 3 days, 15 hours ago (2009-11-28 03:00:00)
by nottoc4
I had the PST test done May of 2008.There is no doubt in my mind that I have IC.
Started 1 week, 1 day ago (2009-11-23 14:25:00)
by jvr
Hi Amylynn,
I'm seeing Dr. Parsons next month. We first saw him in late July and were able to get in early by being on the waiting list. One thing I will tell you is to keep calling his receptionist Peggy and asking her if anything has opened up. She is a sweetheart! He has a great staff. I was checking in every week or two and one day I happened to call and she said that they had just...
Started 1 week, 4 days ago (2009-11-20 09:44:00)
by Glenda2
I am SO Sorry this stuff affected you like this.
People get upset when I tell MY story of what it did to ME.
I lost my complete memory for 10 days.
I was a Catatonic Zombee.
You can search out the other Elavil (Amitryptaline) thread topics and read my replys about this medication.
It has the Potential to be dangerous. Atleast for ME it was !!!
Other's may do just ...
Started 2 weeks, 2 days ago (2009-11-15 10:17:00)
by Pucca
Are you on any meds? Elmiron did that to me, and many other medications can affect you that way.
__________________
**********************
Diagnosed April 24, 2008
Currently taking hydroxyzine, Urocit-K, Urelle
Tried and stopped: Sanctura, Detrol, Ditropan, Vesicare, hyoscyamine (all caused retention), Elmiron and ...
Started 1 week, 6 days ago (2009-11-18 14:18:00)
by Julie B
My daughter has had two laps for endometriosis and they definitely helped. The second one was quite and extensive surgery requiring an overnight stay, but she has been pain free since January.
I wish you luck in your decision.
Gentle hugs,
Started 3 days, 15 hours ago (2009-11-28 02:56:00)
by Glenda2
Greetings and welcome to the best Board on the Internet for IC.
The information here is fantastic , and so are the members.
I am also quite new to the board.
I was diagnosed with IC on October 12th. Via a Cystoscopy.
Put on Elmiron , it makes me quite ill , so I had to stop taking it.
You will make alot of wonderfull friends here. They are very supportive.
Started 2 days, 14 hours ago (2009-11-29 03:37:00)
by ICNDonna
My suggestion is to have her see a pain management specialist for help. They are specifically trained in pain control and better able to help than most urologists, whose training is in other areas.
Warm hugs,
Donna
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