spinal MRI

[nogo]

I had my hydro today and the doc took two biopsies. I am a bit sore tonight but not intolerably, however I am still going to the BR constantly! He said if this isn't IC, then he is doing a spinal MRI to check for a disc or some other reason that the nerves innervating the bladder are somehow compromised. Has anyone else ever had this procedure? He also said the IBS with constipation is making the urgency worse. I figured that one out myself! Have any of you been tested for nerve disfunction related to the bladder and urgency/frequency? I will get the biopsy results on Monday. Today, he said the bladder looked pretty good inside except for those two spots that bled. Thanks for all your encouragment and hope. I am still having ridiculous frequency, but my daughter said the nurse told her it might be worse for a couple of days. I just want some relief from the incessant trips to the BR with little resultant urine or, sometimes a lot of urine five minutes after going before. ARGHHHHHHHHHH!!!!!!!!!!!!!!!

[Roxie2007]

HI! Have you tried any of the bladder medication?? Azo is over the counter....for quick relief. Elmiron is a prescription to help heal the inside of the bladder. Elavil helps greatly with frequency and urgency. Freeze dried Aloe Vera coats the inside of the bladder and helps with pain (I've been on it for 3 yrs now and love it!)
Has your doctor dealth with IC patients before? It sounds like he hasn't but is doing some hard core testing. I've never heard of anyone having a spinal MRI with symptoms of IC. Have you thought about finding a dr. who is an IC specialist?? I think it would be in your own best interest! Good luck! Roxie

[CarolinTexas]

nogo, I don't know about any of the things you asked except for the spinal MRI. My IC didn't start until I had a spinal fusion due to L5 crushing the nerve bundle out of S1. I firmly believe that IC has many causes and it is smart of the doc to check your spine to see if it is nerve related.

Best of luck to you!
Carol

[Trishann]

Nogo, I do believe IBS and constipation can make the urgency worse. It seems to put more pressure on the bladder. It sounds like you have a very good doctor and your doctor wants to get to the root of the problem. I hope you find out soon what it is so you can get treatment for it and start feeling better.

Take care, Trishann

[nogo]

I will let you know what goes on with the spinal check et al. I too, think that the IBS-C is playing havoc with my bladder and the urgency is just exhausting and so painful. I have no idea how much I have gone today, but I am still stuck at home trying to cope. I really don't have anything else I can do until the doc calls on Monday. This is such a life altering condition as you all know. Whether it is labeled IC or just the symptoms, it is a devastating condition. I can't even imagine relief at this point. I have been looking at relaxation tapes online to order something, ANYTHING that will help me with my bladder issue. I am up most of the night even with Ambien on board, followed by Sonata at about 4 a.m. I just need a break here. Again, I can't imagine how you all do this with such grace. I am afraid my husband is nearly at his wit's end because it always seems to be something wrong with me. Either the IBS, IC symptoms or migraines as a result of the stress from it all. We have no life together since Ijust can't go out to dinner or anything at this point. I hope it will eventually get better. I can't live this way. Thank you for your help.

[Roxie2007]

Nogo, Have you tried dried prunes for the IBS-C? I suffered with that for years and over the years several dr.s told me to eat prunes. It just sounded way to simple to me since I was trying everything else on earth! Finally after having to use enemas I decided to try prunes.....and low and behold....they really do work! I eat 4 or 5 every day......and that is the key.....every day! I haven't had constipation in a cpl years now and continue with the prunes. It's truly fiber, fiber, fiber........it works wonders! Roxie

[nogo]

ROxie, I use prune juice with pulp, about 8 oz. and sometimes it works andothers it doesnt'. Unfortunately, my potassium intake is limited becaues I have oxalate kidney stones. That also rules out most fiber. It is unbelievable...the things that can help me the most are forbidden.

[GoldSeals]

Nogo,I heard of the spinal cord theory that when its damaged it causes ic.There are tests being done to see how the spinal cord is involved.People with back problems seem to have a higher incidence of ic, so they say.More research needs to be done in this field.Maybe your doctor is on to something.I wish it was that simple.Wouldnt it be nice if the cause was a pinched nerve in a disc.
One day hopefully the cause will be found and it can be corrected.
Im sorry to hear your still suffering.Hopefully tomorrow will be a better day for you.Some people have no idea how bad ic is.It really changes your life for sure.
I can go on and on about my stories and about my ic.Somedays I just want to put a sign on my car telling the whole world I have ic.I have to stop so much to go.I feel like wearing a t-shirt that says "I have ic"I have to plan everything around a bathroom.What used to be a simple thing like stand in a line at a grocery store and then try not to panic.Most people do these things everyday.But for an ic person its a real big deal!
GoldSeals

[verdicries]

i had a full mri workup (head/full spine) as i have white matter spots in my brain and a large cyst. i suffer retention so doc wanted to see if a nerve was causing it. found out i have 2 herniated discs (the one in my neck just keeps getting worse despite chiropractic care...i'm dying it hurts so bad i can't MOVE) but they claim nothing is inpinging on a nerve to cause retention. sometimes i wonder. GOOD luck.

[shell]

I also have IBC and have found that getting that somewhat under control did ease the pressure and frequency symptoms from IC. I've been successful with MiraLax to regulate the IBS. Then I'm able to control my IC symptoms with just diet modifications.

I've had about 6 MRIs in the past 3 years, but that was due to a spinal tumor not my IC. Since an IC diagnosis is often a diagnosis of exclusion, it is good that your doctor is checking every possible alternative to your symptoms.

[verdicries]

shell, how often do you take miralax? i USED to have ibs-d but b/c of rectocele/rectal prolapse it's been more like impossible C!!!!!! (actually it's difficult to evacuate my bowels no matter how hard/soft). anyhoo, i'm on miralax but don't want my bowels to become "dependent" on laxatives, that terrifies me. how long have you been on it? every day?

thanks.

[born2swim]

I had a spinal MRI last summer for pain (I was not having any urinary symptoms though). The MRI was not fun. I mean, it wasn't torture, but it was awefully enclosed and loud. I took a CD that they played via headphones for me and I tried to zone out. I got my entire spine checked. I was having right upper quadrant pain that ended up being a sneaky gallbladder problem. But anyways... they did see some compressed disks, degenerated disks, and partial slips in my lower lumbar. It pointed out no nerve damage. So, if there is something going on with you nerve wise, you should be able to see it on the MRI.

Good luck and don't forget a CD! I hope you can play one!

[CarolinTexas]

MRI's are funny. I find that old clanking sound relaxing while it grates on other (most) people's nerves.

The enclosed space was the most difficult thing for me to deal with as I'm claustrophobic anyway. My husband had one on his knee last year and he was able to have it with his head sticking out. Lucky guy!

If you are worried about it, ask your doc for a dose of Xanax or Valium before you get in there. I will ask if I have another - just for the claustrophobia.

[Mishque]

Hi Nogo,

There was a clinic trial done by a Warren Hammer in 1997 I believe. He is a Chiropracter and within the trial he helped quite a few people with IC just by medically untrapping nerves connected to the bladder. I think he has a web site too. Perhaps put his name into google and you might find the piece. I was thinking of saving up for the MRI to be done on myself as they wont pay for it on the NHS in the UK.

Good luck. I hope it goes well.

Best wishes
Mishque:cat:

[nogo]

Thank you for your information. I do hope you can get the MRI and the help you need as well. I will check out the website. I am open to any suggestions to help with this.
It helps so much to know others care, like you. Thank you.

[Mishque]

Hi Nogo,

You are very welcome.

I wish you all the best and hope something good comes out of this for you.

Best wishes
Mishque :cat:

[shell]

verdicries,

I actually take the Miralax every day and have been for quite a few years now, at least four or five. I started at the full dose in 8 oz. of water and have decreased it to about half that now. The GI that presribed it felt it was better for me to be on this long term than to suffer with the symptoms I had. I'm sure there are different opinions out there and that not everyone's symptoms would warrant daily or long-term use.