Back pain

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leighhi27

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HI,

For over a week now I have had such severe back pain that I can hardly move. I have had Crohn's for a while now but I can't remember this symptom before. Do any of ya'll (yes, I'm southern :)) out there have very severe back pain? I have taken all the different types of pain medication that i have and none of it helps very much, a little but not a lot.

Thanks,

Leigh:ybatty:
 
Hi Leigh, I too used to suffer with terrible back pain, it used to take the wind out of me. I had a couple of back xrays and a ct scan and although I was displaying early signs of osteoporosis, that wasn't the cause of the back pain. My pain used to move up and down my back but was most commonly in the shoulder blade area or right across the middle. Does yours happen to be in a particular place?Anyway, my GI told me that my back pain was due to a mixture of a build up in gases and spasms, I still get back pain now if I have had lots of gassy foods or had a couple of glasses of fizzy pop (soda). I was prescribed Mebeverine:

Mebeverine HCI is a musculotropic antispasmodic drug without atropic side-effects whose major therapeutic role is in the treatment of irritable bowel syndrome. It is also indicated for treatment of gastrointestinal spasm secondary to organic disorder. It was first registered in 1965 and manufacture by Solvay Pharmaceuticals.

Mebeverine HCI presented in tablets (100mg or 135mg), capsules (200mg slow release), and liquid (10mg/ml).


Its seems to help me somewhat, but the best way is to avoid gassy things or make sure drinks are soda free. This works for me. This may not be the cause of your problem but its worth investigating. Hope this helps.


Ruth
 
Hi Leigh
I too suffer from severe lower back pain.
Mine is from yrs of having CD and taking Pred.
Now I suffer from osteoporosis and have to take one pill every Monday.It is called Actonal (sp).
I had all kinds of tests done to Ct scan MRI or is it MIR cant remember even seen a specialist (NUROLIGIST) (sp?) and he said just take some pain pills.
In other words not much we can do. Just grin and bear it (slang).
Sorry I wasnt much help.
 
Hi Ruth,

Thanks for your reply. My back pain is in my lower back. I try not to eat much gassy stuff and i limit myself to one carbinated drink a day. I will certainly check out Mebeverine HCI. I have never heard of it. I am so sick of doctors that I want to check here first about the back pain before I made a trip to the doctor. You have an illeostomy? How is that working for you? On March 16 I am having a bowel resection and a repair from my seton surgery that went wrong last Spring and I will have a temporary ostomy. I personally don't know anyone who has had this surgery.

Leigh
 
HI Tammy,
Thanks for your reply. I have lower back pain but I do not have osteoporosis. I just wasn't sure if it was a symptom of Crohn's. I try to grin and bear it but I keep waking up my husband at night when I groan just because I am turning over in bed. He is not getting much sleep.

Leigh
 
leighhi27 said:
Hi Ruth,

Thanks for your reply. My back pain is in my lower back. I try not to eat much gassy stuff and i limit myself to one carbinated drink a day. I will certainly check out Mebeverine HCI. I have never heard of it. I am so sick of doctors that I want to check here first about the back pain before I made a trip to the doctor. You have an illeostomy? How is that working for you? On March 16 I am having a bowel resection and a repair from my seton surgery that went wrong last Spring and I will have a temporary ostomy. I personally don't know anyone who has had this surgery.

Leigh


Hi Leigh, yes I do have an ostomy, a loop ileostomy. I had my surgery back in June last year as I had major problems with fistulas and like you had setons, but they did nothing at all. I had a laparotomy, where they cut from the top of your belly button right down to below the bikini line and the a seperate incision for the stoma. The stoma itself took a little getting used to, I was a little freaked out by it at first, but my stoma nurses were great and I soon got used to it. I was in a lot of pain when I had my surgery, purely because my epidural fell out and I had a stomach drain in as well as the 2 operation marks and then 2 drains in my rectum so as you can imagine, when the pain relief wore off, I was in a lot of pain. Once I was able to control the pain, things were a lot easier. I was in hospital for a week, I should have been in quite a bit longer but I cried for the last 2 days of my stay and begged to go home, so they eventually gave in. I was walking about, I think on my 4th day after surgery, but very slowely and it took a good 4 months before I was totally back to being able to do things again properly. I had got to grips with looking after my stoma within again about 4 days and although in the early days I had quite a few leaks, that didn't put me off. I found a couple of great Ostomy sites and found loads of helpful hints and tips. www.ostomyland.co.uk and www.the-ia.org.uk.

The good thing about having an ostomy is that you have no urgency to go to the loo. I have my reversal soon and to be honest, I'm going to miss that. Not looking forward to loads of D again!!!The other thing is that although you have to avoid a few things that may block your stoma up, you can go back to eating most of the things you stopped eating before you had the op. The crohns symptoms almost disappear and once you heal the pain that you will have had from your fistula will just disappear, its really quite remarkable, how much better you start to feel, well worth the surgery.
As far as clothing goes, I'm only a size 12 (USA 8) and find that some of my tighter fitting stuff I can't wear anymore but I can still wear jeans and dresses and skirts, I just tend to stay away from the tight little tops, I tend to get looser fitting ones, or I wear body tops underneath to hold the bag closer to my body. Theres loads of other stuff I could tell you, but no doubt you have loads of questions in your mind so if you want to know anything ask away, I'll be happy to help, whether its day to day stuff or lady's talk if you know what I mean, just drop me a line.
Hope this helps and good luck with the surgery, you'll be fine.


Ruth
 
Hey Leigh,

Sorry to hear about your back pain - that can't be much fun. I personally had a long period where my back was useless, that was due to Osteoporosis, having been on pred at the age of 10-11. I now don't have any problems.

As a wee add on though, in relation to your ostomy query, I have one, a permanent ileostomy, and have had it since I was 17. I've had it for 13 years now and have no problems whatsoever - undoubtedly the best thing I've ever done. If you've any questions about it, ask away!

Cheers

Moz x
 
Hi
Im so afraid to getan ileasyomy.The Dr. Has been after me for about 2 yrss now. I think that its down to the wire now.
I never experienced so much pain over the past several months.
I too just stopped takin pred was on them striaght for over 10 yrs and it just seems that my hole body aches.
Having 3 fistulas dosnt help the pain situation.
I dont understand why Im having so much lower back pain and my joints and muscles hurt constantly.
I think this is why Ive been moody, bite your head off if someone tries to talk to me.Ive been in a flare-up since Chritmas.
I see the surgeon end of Mar. and I have a preety good idea that hes gonna tell me that I have to have surgery. Im so scared.Ive talked to a few people that have an ileostomy(including Ruth).I dont now what people will think of me if I get one.Especially now while I am single and tring to date.

So If Ive been rude or snippy and not understandable Im SORRY.
Just been trying to deal with to many problems all at once. And my pain level has been at its highest enen still it dosent give me the right to snap at people.
Later :depressed:
 
Thanks very much all of you,

I can't imagine having Crohn's for as long as Tammy and Mozam. I am a bit scared about the surgery. The doctors told me that the ostomy may end up being permanent if I do well with it. That is not what I want. This flare-up has been going on since the end of November and I am sick of it. I do not like taking steroids because they make me mean.

As you mentioned, Ruth, I do worry about the bag under my clothes. I don't really wear tight clothes but I am a USA size 2 or 4 and it seems that most of the clothes in this size are tighter for some reason. I am a bit of a clothes horse and I worry about having to give up my normal, everyday clothes. I guess that is vanity. :-(

Mozam, you sound very positive and that makes me feel good. Do you ever have flare-ups anymore? And if so, what are your symptoms?

I was scheduled for March 16th for the surgery but it has since been changed to March 13th.

Tammy, I understand everything you are saying. It can be very depressing and the pain is horrible. Fistulas are awful too. No one will think anything if you have an ileostomy. If you are dating someone and your date gets discusted or turned off by it, then that is not the right person for you. I will be nervous with my husband about it at first, of course, but I know that he loves me and it won't bother him. He will adjust. I am moody and mean to my husband quite a bit ( I am assuming it is from the steroids) and he understands, so I am sure your friends and family will understand what you are going through too and not be offended.

Anyway, thanks so much all of you!!

At least tomorrow is going to be a fun day. We are going to see Spamalot at the Fox Theater in Atlanta, GA. We actually saw it last weekend too and it is GREAT!!! Very funny!! So, if you are feeling bad, put on "Monty Python and the Holy Grail". That will make you laugh.
 
Hey Leigh,

I am very positive, or at least I try to be. That's not to say that I think everyone should be, because I know it's hard - I've been there, and not just with Crohns. I've been on the bones of my arse (literally), and it's not fun - everything seems dark.

Regarding flare ups, then no, I don't have any. I've had my stoma for almost 15 years and can count on two fingers the amount of flares I've had - even then, they were put right with blood transfusions, no need for long courses of meds etc. I realise that I have been very fortunate with my crohns history, especially after reading some of the truly heartbreaking stories on here from people who have had things so much worse than me. All you guys on here, you are an inspiration - every last one of you.

Any time you need to ask anything or fancy a chat Leigh, then fire away.

Moz x
 

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