sam cleasby ulcerative colitis

Everything you need to know about IBD in one handy place

Information

IBD is Inflammatory Bowel Disease and should not be confused with IBS (Irritable Bowel Syndrome) which is a completely separate condition.  The two main types of IBD are Ulcerative Colitis (UC) and Crohn’s Disease.

Ulcerative Colitis (UC) and Crohn’s Disease are chronic (ongoing) conditions, which are not infectious

The most common age for diagnosis is between 10 and 40 (although diagnosis can occur at any age)

In both UC and Crohn’s there is a higher chance of developing either illness if you have a close relative who has the condition.

UC affects up to 120,000 people in the UK, that’s about 1 in 500

Between 6,000 and 12,000 new cases are diagnosed each year
Crohns Disease affects approximately 60,000 people in the UK, that’s about 1 in 1000

Between 3,000 and 6,000 new cases are diagnosed each year

sam cleasby ulcerative colitis

UC affects the rectum and sometimes the colon (large intestine). Inflammation and many tiny ulcers develop on the inside lining of the colon resulting in urgent and bloody diarrhoea, pain and continual tiredness. The condition varies as to how much of the colon is affected.  In addition, UC can cause inflammation in the eyes, skin and joints.  If the inflammation is only in the rectum it is known as proctitis

Crohn’s Disease can affect anywhere from the mouth to the anus but most commonly affects the small intestine and/or colon. It causes inflammation, deep ulcers and scarring to the wall of the intestine and often occurs in patches.  The main symptoms are pain in the abdomen, urgent diarrhoea, general tiredness and loss of weight. Crohn’s is sometimes associated with other inflammatory conditions affecting the joints, skin and eyes

For both illnesses the severity of the symptoms fluctuates unpredictably over time. Patients are likely to experience flare-ups in between intervals of remission or reduced symptoms.  The cause or causes have not yet been identified in either illness. Both genetic factors and environmental triggers are likely to be involved

For UC most patients will be treated with drugs, including 5-ASA therapies (eg: mesalazine) and steroids, to control or reduce the inflammation. Suppressants of the immune system (eg: azathioprine) are used to maintain remission. Some people need surgery to remove the whole of the colon if their symptoms do not respond to treatment with drugs. If the colon is removed, the small intestine leads to a stoma (opening on the abdomen or ‘tummy area’) for emptying of liquid stool (faeces). Or a replacement colon (ileo-anal pouch) is created by the surgeon reshaping the end of the small intestine

In Crohn’s the drug treatment is similar to that for Ulcerative Colitis. In addition, various antibiotics can be used; and a new range of drugs are being introduced called monoclonal antibodies (eg: infliximab). Crohn’s Disease can also be helped by special liquid feeds which rest the bowel. Surgery may be required to remove narrowed or damaged parts of the intestine.  Smoking has an adverse effect on Crohn’s Disease, so patients are discouraged from smoking

UC and Crohn’s are relapsing, remitting conditions. Most patients remain under hospital follow-up. Urgent consultation or hospital admission may be required for ‘flare-ups’.  There is no cure for UC or Crohn’s at present (except for UC, if the colon is surgically removed), but treatment can control the disease in most cases.

UC and Crohn’s can affect young people during their education or as they become established in their career. Most sufferers can be maintained in remission for most of the time and are able to lead a full working life. However, some who have severe disease do not achieve their educational and career potential.

This information is taken from Crohns and Colitis UK.

A stoma is an opening from either the digestive system digestive system or urinary system . This opening is the exit point for faeces or urine and is formed, surgically, to treat serious, often life threatening, diseases and medical conditions such as bowel or bladder cancer, inflammatory bowel disease (ulcerative colitis or Crohn’s Disease), diverticulitis, congenital abnormalities or injury.

There are 3 types of stoma – colostomy, ileostomy and urostomy.

• Colostomy
A colostomy is the result of an operation where part of the colon (large intestine) is brought out onto the surface on the abdomen.
Food waste exits the body via the colostomy rather than from the anus. This waste is collected in an appliance that is worn on the abdomen, over the colostomy. These appliances are usually referred to as stoma bags.
A colostomy operation might be done because a section of bowel has had to be removed due to bowel cancer, inflammatory bowel disease, or injury.

• Ileostomy
An ileostomy is the result of an operation where part of the ileum (the last section of the small intestine) is brought out onto the surface on the abdomen.
Food waste exits the body via the ileostomy rather than from the anus. This waste is collected in an appliance that is worn on the abdomen, over the ileostomy. These appliances are usually referred to as stoma bags.
An ileostomy operation is done to treat medical conditions such as bowel cancer, ulcerative colitis, Crohn’s disease, Familial Adenomatous Polyposis (FAP) or injury.

• Urostomy
A urostomy is the result of an operation to divert the flow of urine from the usual route. In most cases a urostomy is formed by a section of small bowel being removed from the digestive system, and then attached to the ureters (which are the tubes leading away from the kidneys).  This section of bowel is then brought out onto the surface on the abdomen to form a urostomy.
The urine will then flow from the kidneys, along the ureters, through the section of bowel and out of the urostomy.  As it is passed from the urostomy the urine is collected in an appliance that is worn on the abdomen, over the urostomy. These appliances are usually referred to as stoma bags.
A urostomy operation is done when the bladder has to be removed, or bypassed, due to cancer, congenital or neurological disorders or injury.

This information is taken from Ostomy Lifestyle.

Links

A list of places you can get help and support with Ulcerative Colitis and Crohn’s.  Remember that your first port of call for advice should be your Specialised IBD nurse, consultant or GP.  The internet has a wealth of information but don’t be an ass about it – ask the experts!!

http://www.ulcerativecolitis.org.uk/  Ulcerative Colitis Support and forum

http://www.crohnsandcolitis.org.uk – Crohn’s and Colitis UK aims to improve life for everyone affected by Inflammatory Bowel Disease (IBD), the most common forms being Crohn’s Disease and Ulcerative Colitis.

http://www.meandibd.org/ – Support for young people under 25 with IBD

0845 130 3344 – Crohns and Colitis Support line

http://www.inflamed-and-untamed.com/ – American IBD support blog

Disability Benefits advice – These guides have been specially written for people who have IBD and will help you through the minefield of applying for support.

Radar National Key Scheme – You may not be aware that you can purchase a disabled loo key along with a guide to over 9000 toilets in the UK.

http://www.the-ia.org.uk/ – The ileostomy and internal pouch support group.

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One thought on “Everything you need to know about IBD in one handy place

  1. i have been told I have severe diahhrea and IBD then plain don’t know. I had colon cancer in 2007 with surgery. Before that in 2002 I had gallbladder removed hiatal hernia repaired and wrapped my stomach around my esophagus all at one time. Two weeks later diahhrea set in not bad at first but progressed to very hindering at work. Surgeon this is normal for some people. After my cancer operation the diahhrea was uncontrollable. Bowel movement every 20 minutes while in hospital after surgery. Used all the linen on one floor. Dr gave me a pill but did not give me the name of it. When I was released went home and wore plastic pants and had overflowing issues. Could not leave house was accused of not wanting to leave after being home for three months. Then the colonoscopies began trying to find reason for my situation. I began to lose weight went down to 70 pounds my body began to shut down went to emergency room and was sent back home. Convinced my surgeon to do colonoscopy he and my primary care doctor told me they could not do anymore for me.after colonoscopy and rehab from that I gained weight on a diet of baked chicken breast baked potato 10 slices white bread daily scrambled eggs and water. Four months later they were surprised to see me in their office. Your information helps me not to feel alone. Thanks.

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