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Tuesday, 25 April 2017

Ulcerated Colitis


 


Just when you think you have a handle on all that life can throw you, I found out I have severe Ulcerated Colitis. 

If like me you didn't know anything about the condition you could be missing the bigger picture I certainly was, having ME you generally suffer with IBS at some point, I mistook my IBD for IBS.
Now the initials sound similar but the medical condition is in my view much worst.

Inflamed Bowel Disease is a disabling condition and limits what a person can do, as they need to be able to "get the seat down" in seconds when out and about it’s a case of going going gone...

I could write a very personal blog on the toilet habits of a UC sufferer but I would only be repeating what thousands of sufferers will tell you, instead I will guide you to the best source of information I could find in the UK below is a bit from a this most excellent source of information on the subject.


Crohn's Disease and Ulcerative Colitis are the two main forms of Inflammatory Bowel Disease, affecting more than 300,000 people in the UK.
Yet it is largely a hidden disease, and one that causes stigma, fear and isolation – it’s thought that many people with the condition go undiagnosed and suffer in silence. It doesn’t have to be like this.
What is Ulcerative Colitis?
Ulcerative Colitis is a condition that causes inflammation and ulceration of the inner lining of the rectum and colon (the large bowel). In UC, tiny ulcers develop on the surface of the lining and these may bleed and produce pus.
The inflammation usually begins in the rectum and lower colon, but it may affect the entire colon. If UC only affects the rectum, it is called proctitis, while if it affects the whole colon it may be called total colitis or pancolitis.
It’s one of the two main forms of Inflammatory Bowel Disease (IBD). The other is Crohn’s Disease.
Ulcerative Colitis is a chronic condition. This means that it is ongoing and life-long, although you may have periods of good health (remission), as well as times when symptoms are more active (relapses or flare-ups).

What are the symptoms?
Ulcerative Colitis is a very individual condition and its symptoms will vary from person to person. They range from mild to severe and may also change over time.
Some people remain well for a long time, while others have frequent flare-ups. However, the most common symptoms are:
• Diarrhoea
• Cramping pains in the abdomen
• Tiredness and fatigue
• Feeling generally unwell or feverish
• Loss of appetite and weight loss
• Anaemia (a reduced level of red blood cells).
Find out more about the symptoms of Ulcerative Colitis
Who gets Ulcerative Colitis?
It’s estimated that UC affects about one in every 420 people in the UK (roughly 146,000 people).
UC is more common in urban areas and in northern developed countries, although we’re starting to see an increase in numbers in developing nations, too.
UC is also more common in white people of European descent, especially those descended from Ashkenazi Jews (those who lived in Eastern Europe and Russia).
It can start at any age, though it often appears for the first time between the ages of 15 and 25. It affects men and women equally.
UC tends to develop more frequently in non-smokers and ex-smokers than in smokers – but health professionals strongly advise against smoking as a way of treating Ulcerative Colitis.  See Smoking and IBD for more information.
Our Ambassadors embody the wide range of people who get Crohn’s Disease. Read their stories.
What are the causes & is there a cure?
Although there has been a lot of research, we still don’t really know what causes Ulcerative Colitis.  However, advances have been made in recent years, particularly in genetics and we now believe that UC is caused by a combination of factors:
- the genes you’re born with
- plus an abnormal reaction of the digestive system to bacteria in the intestine
- along with an unknown 'trigger' that could include viruses, other bacteria, diet, stress, or something else in the environment.
There isn't a cure at the moment but a lot can be done with medication and surgery to help keep symptoms under control.
Read about the research we’re funding into the causes and treatment of Ulcerative Colitis 
What treatments are there for Ulcerative Colitis?
Ulcerative Colitis can often be managed by medication (drug treatment), but surgery can be necessary if symptoms are very bad.
Your treatment will depend on the type and severity of your UC and the choices you make with your doctor.
Find out what treatments are available for Ulcerative Colitis.
Can Ulcerative Colitis have complications?
More than a third of people with UC develop other conditions outside of the digestive system, mainly affecting the joints, eyes and skin.
Inflammation of the joints (arthritis) affects about one out of 10 people with UC. Some people with UC also develop ankylosing spondylitis, a condition in which the joints in the spine and pelvis become inflamed and stiff. Drugs and physiotherapy are used to treat these symptoms.
A variety of other health conditions can be associated with UC, including:
  • skin problems, such as mouth ulcers, blisters and ulcers on the skin, and painful red swellings, usually on the legs
  • inflammation of the eyes
  • thinner and weaker bones
  • liver inflammation
  • blood clots (including deep vein thrombosis)
  • anaemia.
It’s important to stress that Ulcerative Colitis is not a form of cancer. However, if you have had extensive or total colitis (pancolitis) for many years, you have a greater risk than normal of developing cancer in the colon or rectum. For more information about this, see our information sheet Bowel Cancer and IBD
Find out more about complications by downloading our Ulcerative Colitis booklet
What are the challenges of living with the condition?
Living with a chronic condition like Ulcerative Colitis  can have both an emotional and practical impact on your life.  There may be times when you have to make adjustments and take time to recuperate, for example, if you are having a flare-up.  On the other hand, when you are well you may be able to live life to the full. 
Most obviously, you are likely to see your GP and perhaps also your hospital IBD team quite regularly. It’s good to build up a good relationship with them, as that can make seeking and receiving treatment a less stressful process.  See our booklet My Crohn’s and Colitis Care for more information about to work with your IBD team to get the best out of your care.
Flare-ups can be disruptive to relationships and work – sometimes you may need to cancel engagements and take time off when you are feeling unwell.   It can be very helpful if you feel you can open up about your condition to those around you – your family, friends, work colleagues and employers.  Telling particularly family and friends at least something about your illness may make them feel reassured and more able to give you the support you need.
Diet is considered a factor in the appearance and severity of symptoms by many people with Ulcerative Colitis – although research has not produced clear answers on whether diet plays a role in UC.
Generally, the most important thing is to eat a nutritious and balanced diet to maintain your weight and strength, and to drink sufficient fluids to stop you getting dehydrated. 
However, you may find during flare-ups that certain foods affect your symptoms.  Bland, soft foods may cause less discomfort than raw vegetables, spicy and high-fibre foods .
Most women with Ulcerative Colitis can expect a normal pregnancy and a healthy baby. Also, for most women, having a baby does not make their UC worse. But if you do become pregnant during a flare-up, you may be more likely to give birth early or have a baby with a low birth weight. Your doctor should be able to help you to control your symptoms as much as possible, and it may be helpful to discuss your options with them if you are thinking of having a baby.
Around a quarter of people are children or adolescents when they are diagnosed with IBD, and symptoms in young people often appear around the age of 12. Ulcerative Colitis in children tends to be more extensive in children than adults, and consequently more severe.
Download our free information sheet on Staying well with IBD


Hopefully, upon reading this blog page you will have a better understanding of Ulcerative Colitis and I would like to thank chronsandcolitis.org for the information they gave me on their web site when I was first diagnosed in a NHS hospital in my home town.

So why have I chosen to blog about my UC on my Transgender blog site well there is a link.

Taking female hormones as transgender male to female as you have to do, in order to alter loads of incorrect things with your body, the hormones has the effect of increasing the risk for ulcerative colitis (UC), but not Crohn's disease (CD), according to my consultant at the gender clinic I attend. He sees many transgender M2F people discovering they now have UC. It’s not a show stopper as such on the transition side, and lower surgery can still go ahead in most cases but it needs to be under control and not in flair up mode for obvious reasons.

A transgender person’s BMI is taken into account so being on or below your BMI is a good thing as far as lower surgery is concerned so if like me you have UC just watch your diet as my weight yoyos between flair ups quite a bit.

When I have a flair up I tend to reduce my insoluble fibre intake and make more healthy 80% veg 20% fruit juice as meal replacements I live on a modified vegan diet or a heavily modified paleo type of diet, as it reduces my “seat down time” spent going the loo. 

2 comments:

  1. I have had Ulcerative Colitis for half my life and even had my colon surgically removed. I have also been curious lately about crossdressing and what not. I do very much enjoy your blog and hope to maybe stay in touch with you :)

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    Replies
    1. Hi Hendy
      Colitis sucks for sure.
      I'm not sure if my colitis has been brought on due to the female hormones I'm on, I'm currently researching to see if other transgender persons have developed Colitis as a result of transitioning on hormones.
      there are plenty of websites that cover crossdressing so you should have loads to investigate;-) some people start off crossdressing and later discover they are transgender its a spectrum for sure...
      due to my ongoing ill health I have been a tad lax with my blog but rest assured I have several things in the pipe line to blog about. Happy new year
      Nicola.x

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