Colitis / Crohns ??
Posted , 6 users are following.
Really sorry this may seem a bit long winded!
I was admitted to hospital suddenly 7 days ago because I had severe stomache cramps diarrhea and a lot of blood in my stools aswell as a fever. I had a CT scan which shows thickening of my colon and severe calcium and vitamin D Deficiency in my blood test Im booked in for a colonoscopy a week on Friday but they said thay are sure i have colitis.
I was discharged from hospital last night after having 2 clear das of no bowel movement.
I have been to the toilet today and my stools are now formed and the pain is far less severe although I still have a lot of blood in my stools.
Is this normal for newly diagnosed Colitis can anybody tell me what to expect please?? I hate bothering professionals and dont want to go back to hospital unnecciserally?
0 likes, 21 replies
bustergut1 linda_22361
Posted
let us know how you get on.
linda_22361 bustergut1
Posted
IUnfortunately I have severe heart failure COPD and Type 2 diabetes with insulin and have various meds For my IBD ihave been on IV antibiotics (Flagyl) and Hydrocortosonze doe the last 6 days. I also have an extremely low vitamin D deficiency that showed up and now have to have 20,800 IU daily of Vitamin D & Calcium daily for the next 8 weeks.
Although I do have some pain compared to what it was it has certainly died down as has the diarrhea. Its my first bowel movement in 3 days and I have formed stools without hardly any pain the only thing that remains is the blood so i dont feel ill enough to be in hospital. You were right about the colonoscopy they said my colon needs to settle first before they will carry it out.
I think the reason this hasn't really sank in yet is because until 1 week ago apart from constipation now nd then I have never had any problems with my stomache where as chest problems are second nature. Dont know if age is a differrence but I am 53 and very over weight
pca linda_22361
Posted
Firstly, welcome to the forum. I am sure you will find a lot of advice and support from the members here.
Your message wasn't too longwinded; far from it - just look at the length of this reply!! An important thing to realise is that we are here because we too suffer from IBD and it is a 'messy' complaint, so don't worry about talking about your symptoms/experiences (within obvious limits, clearly!!).
From your post I am assuming that this episode was your first ever, and that up to then you had not had any similar previous experience of IBD? UC is a very individual condition and affects different people in different ways. I was diagnosed with UC in November 2011, after having been passing blood for the previous four months or so. It started with just a few drops on the loo paper (my GP initially thought it was probably haemorrhoids), but it just kept on getting worse and worse until a colonoscopy was ordered; I had to wait 8 weeks for mine, and the diagnosis was UC, a condition about which I hadn't heard much up until then. I'm a bit more clued up on it now!!
UC and Chohn's do share similar symptoms, although the causes of the two are different. As you probably know, Crohn's can affect the whole digestive tract from the mouth to the rectum, whereas UC is a condition specific to the colon, sometimes including the rectum. It can affect all the colon or just a part of it.
The symptoms you have described are pretty much what you would expect of UC. Bloody diarrohea, abdominal pain and cramps. Funnily enough it has only been during a 'fare-up' that my stools have been solid, although flecked with blood.
I think you'll have to wait for the colonoscopy (not nice, but not that bad either - make sure you ask for sedation, if it's not offered; it makes the procedure much more tolerable) to get an accurate diagnosis. The consultant who did my procedure told me immediately of the result and recommended the appropriate medication.
Do not, though, ever worry about troubling the professionals for advice. They are there to help you, and unless I have just been incredibly fortunate, I have had nothing but helpfulness, kindness and understanding from my GP and the gastroenterologists under whose care I have been placed.
Try not to worry too much (dificult at first, I know) and get as much information as you can. Consider reading the various big IBD charities' websites (Crohn's and Colitis UK) and there's a wonderful Scottish-based IBD charity 'Cure Cronh's Colitis' which passes on 100% of its income for research into a cure for these two diseases.
I send you my very, very best wishes.
Peter A
linda_22361 pca
Posted
I also have heart failure and type 2 insulin diabetes not to mention COPD (Think Im dropping to bits) I think the biggest shock at the moment is where did that come from as i never have tummy problems it just happened so quick. Do you know how long it takes to stop bleeding? or is it different for everybody and at least the tummy pains are bearable now Thanks for your reply and support Linda
ann_and_nick linda_22361
Posted
Your D and Ca defficient....suggest the following with your pharmacists OK: sublingual (under the tongue) liquid B12 with folic acid...several drops a day...sublingual or gell type K2...with CHF you want calcium to go to your bones not elsewhere. DHA/EPA 1000 mg or 180 EPA 120mg DHA...(PUFA or omega 3)...please be certain to expalin to your pharmacist your condition...they may have additional or modifications to the above. These are also beneficial for either Crohns or Colitis.
Lastly, probiotics...the combo of discharge volume and frequency plus Flagyl completely modify your digestive flora..and in most cases destroy your good bacteria...(be aware of yeast infections due to flagyl)...put good bacteria back into your system and "often" during the day...for good bacteria to colonize or recolonize takes time..again something to ask your pharmacist as to which productis most suitable.
And if you can tolerate add quality cultured yogurt/kefir along with pure 100% Pomegranate Juice (meaning nothing added C or sugar) and mot a mixture of other juices... (only 2 oz x 2 daily)...PJ should help you A1C. Take 1 hour pre or post your Metformin or other dbt2 meds. relax...lose some weight gradually...but be aggressive...you know well weight goes hand in hand with dbt2 and CHF...and others.
Ann
linda_22361 ann_and_nick
Posted
pca linda_22361
Posted
Many thanks for your generous response. I'm so very sorry you also have to contend with other conditions; it makes coping with potential IBD even more wretched than it might otherwise be.
I believe that in some people flare-ups can come on very quickly, over just a few days whereas for others (such as I) the symptoms develop over a number of weeks or even months.
I had trouble in physically tolerating the original medication (a foam enema containing mesalazine) as it simply wouldn't 'stay in'. My GP swapped it for the same drug, but in tablet form, but at far too low a dose to have any real effect, and it wasn't until I'd seen the consultant in clinic for my initial appointment (some three months after he'd performed the colonoscopy) that I got the proper dosage of mesalazine. After just a few days of taking the higher dose, the bleeding, extreme urgency and the number of loo visits had improved dramatically.
Ann and Nick are far more knowledgable than I about CD, but with the utmost respect to them, were I you I'd wait for the colonoscopy first and if you are as fortunate as I was, you'll get a diagnosis there and then, although you might well find that a few samples are removed and sent away for analysis just to confirm the diagnosis.
If the hospital is right, and you have developed UC, please don't lose heart. You'll almost certainly be well for far more of the time than you will be ill and some people (I pray you are one of them) remain in remission for months if not years - and with few if no real symptoms.
You may wish to know that there is a very promising new probiotic on the market called 'Symprove'; may I suggest you 'google' it see what you think? Possibly ask your consultant/GP if they have any views on it? From what I've seen, independent research has come up with some interesting and encouraging conclusions. It's not cheap, but if you google 'Symprove', it may be something you wish to consider once you know the reality of your situation.
Try to stay positive and not stress unduly. I know that's not easy, but stress is recognised as a condition that can help 'trigger' flare-ups.
I wish you all the very best for your procedure next Friday, and please don't forget to let us know how you get on.
Take care!
Peter A
donclaudio linda_22361
Posted
just looking for an "improvement update" since you stated some improvement in stool form, pain reduction, but yet some blood in stool.
Claudio
linda_22361 donclaudio
Posted
Here's my update so far
I know longer have diarrhea and the pain has certainly subsided to what it was . I have only been to the loo once since my hospital discharge which was still loaded with blood. Every time I do go to the loo there is blood when I wipe myself. The difference in my symptoms is that I now feel constipated all the time and have indigestion and really bloated. I am booked for my colonoscopy a week today and everything for prep is already here lol
Thanks for your interest regards Linda
donclaudio linda_22361
Posted
my concern mirror's Anns...Unfortunately a course of antibiotics can create digestive disorders. And soon the colonoscopy prep will do further insult. What to do? Quickly up your intake of cooked leafy greens...preferably much more than usual put thru a blender. Consider psyllium husk powder (not metamucil) perhaps 1/2 teatspoon with plenty of water. Take with "probiotics"...the psyllium is both a prebiotic as well as a chaperone to probiotics that are "not" acid resistant. Since it contains "inulin"...too much can cause gas...therefore 1/2 teaspoon not a tablespoon....you can gradually increase based on your results.
This particular prebiotic also helps boost the lactobacillus Bif...along with a few others "in your colon".
Would suggest you use "google scholar" to further your understanding of Ann's suggestions... at the search box type in "PUFA's and colitis"...and continue on to the others such as PJ. You'll find that K2 is really very important in your dbt2/heart condition ..simply its the policeman/woman that directs calcium to your bones...you don't want to deal with calcifications...and was your D supplement merely D or D3? Something else to study via google scholar. You seem to be quite savy and yet have difficulty with weight....as does nearly half the world...but you must put the "pedal to the metal" Linda....hope you can......adio Claudio
donclaudio linda_22361
Posted
ann_and_nick donclaudio
Posted
Gracias...Ann
linda_22361 donclaudio
Posted
Thanks for the info there seems to be a lot to take in over a few days. It is my vitamin D3 what is the problem, all I know is my bones have been extrememly painful for sometime and I just put it down to arthritis.
The hospital told me I wasn't digesting food properly therefore not getting the vitamins I need.
As for weight I have struggled with this for the last 10 years since my conditions have deteriorated. I am on the top prescription for Levothyroxone 350mg which they haave reduced in hospital to 250mg.
I have been on and off steroids every other month for the last 20 years due to my Bronchiectasis and COPD. My heart failure became very apparent in February this year when I was diagnonsed with severe left ventricular FS and at the time my lungs had filled up with fluid. I was also put on insulin from February due to my diabetes whicch as yet is still unstable. The consultant gave me a new tablet Alogliptin to go with the insulin and said it should also help with not putting more weight on. To be fair since February I have lost 22lbs but alas I need to lose about another 50lb. I must be the only one I know who spent a week on a drip in hospital and lost no weight whatsoever lol. But hey ho onwards and upwards. Thanks for your support every thing is so new and it seems there are so many possiblitities of what type of colitis I have that I will be glad when I have the results.
donclaudio linda_22361
Posted
Claudio
ann_and_nick linda_22361
Posted
donclaudio linda_22361
Posted
at 500mg daily every two weeks....meaning you cycle...2 weeks on and 2 weeks off?...also do you know why or for what it was prescribed for? this antibiotic can foul up your good digestive flora....usually most good gastro's will suggest supplementing with probiotics durig administratiion of cipro...as well as some other antibiotics...but some do not??...its kinda like kill and replace or take out and put back....hopefully kill the bad guys and put back in the good guys..a reminder that the colonoscopy "prep" too will remove good flora...hope that minimum or no blood via wipes now....
Claudio
linda_22361 donclaudio
Posted
I take the cipro evry two weeks because of my bronchiectasis as a maintainance doze
I am pleased to say I am no longer bleeding stopped 2 days ago at the moment I have quite bad indigestion, really bloated wind and heart burn as well as a burning sensation in my stomache don't know if this is what i should be expecting but i certainly feel better than i did. I keep getting cold sores and pains in my joints. I have managed to lose 7lbs without trying really this week lol I also keep getting constipated and although I am trying to be careful with what I eat the indigestion gets worse. I have to start eating soft food tomorrow in prep for y colonoscopy on Friday. Will they tell me the outcome on Friday?
donclaudio linda_22361
Posted
I don't know what the policy is in your country/clinic/dr...here, once sedation has worn off and your 10 10, RN's advise dr your OK...dr will come by, generally give you "whats what".maybe schedule an office appointment...at least that's how its done here at our Hosptial/endoscopy centers. Our doctors don't like to leave a patient in "limbo"..especially on a Friday giving them time to FRET over a week end. I'm anticipating "good news"..
..colon is healing...if not already, start taking pre biotic (psyllium husk powder) as suggested along with some probiotics...plenty of quality yogurt if tolerated...this ought to get your pain, bloating, and constipation under control...and stay on these indefinitely. Please start yesterday if not already, and let me know quickly how it goes.. Again happy your feeing and doing better...Claudio
linda_22361 donclaudio
Posted
The Dr says there is no signs of crohns or colitis and has took some biopsies. He seems to think it may be my diabetes but hasn't explained anything else. Although my bleeding has stopped I still have severe indigestion every day I have cold sores every other day I have diarrhea and constipation a constant burning in my stomache. Heart burn at night a feeling of urgency but can't go and although I am pleased to have lost weight I have lost 9 lbin 7 days without trying and have no appetite. Is there any other suggestion I'm taking probiotics and living on indigestion remedies.
donclaudio linda_22361
Posted
semprove and vsl 3 are touted probiotics from many patients. give them an immediate trial.also don't dismiss small amount of psyllium husk. you r losing minerals..ask your pharmacist for best replacement drink. cold sores or mouth ulcer? treatment differs ..viral vs bacteria. if viral only ice on
sore..and "Stress" activates the virus from its dormant state. To protect your digestive lining EPA DHA in combo with cold sea water fish
ann_and_nick donclaudio
Posted
biopsy