Talking to your doctor

Bringing a more honest relationship with your doctor to life

Not everyone is the same, and the symptoms of ulcerative colitis (UC) can range in severity from person to person. The important symptoms are the ones that affect you. That is why we have developed this interactive, customized conversation starter. You can choose the topics that are relevant to you, and bring the questions to your appointments.

Embarrassing symptoms

If you are feeling embarrassed about having to go to the bathroom all the time, tell your doctor just
that—you are embarrassed. It will let your doctor know that your symptoms are not under control. It will also tell your doctor to be sensitive to your feelings about your symptoms, without ignoring or minimizing them.

The same goes for rectal bleeding. Of course this may be a symptom you are used to dealing with because of your UC. But it is an important part of your condition that your doctor needs to know about. In fact, your doctor may have just what you need to reduce or stop the bleeding.

Do not be afraid to talk about diarrhea. Even though society doles out bathroom humor in large doses, diarrhea is no laughing matter. It is a serious and often debilitating symptom of ulcerative colitis, and your doctor sees no reason for embarrassment about it. Even if you have gotten really good at handling your flare-ups and accepting your condition, your doctor will only know it is having an impact on your life if you tell him or her about it.

The same goes for symptoms like cramping or gas. If these symptoms are limiting your experience and enjoyment of life, your doctor may be able to help you find a solution. Tell him or her about it. It is the only way your doctor can help.

Diet and exercise

Living with UC, you know more about how your body reacts to what you do or eat. Keeping a daily log of meals and exercise might help reassure you and your doctor, as will asking your doctor questions like the following:

  • Will certain foods or drinks make my symptoms worse?
  • Are there certain foods or drinks that I should try to include in my diet?
  • Are there activities or exercises that will relieve or reduce my symptoms?

Stress

Although stress may not cause UC, anxiety over having the condition may worsen symptoms. In one survey, 82% of patients with UC said their condition made life more stressful.1 See how your doctor can help. Ask:

  • How does stress affect my UC?
  • What can I do to reduce my stress about having flare-ups?
  • How can I feel less stressed about my condition and more in control?

Intimacy

It is not surprising that one study found 75% of people with UC feel that UC disrupts their sexual relations.2 Knowing you are not alone by keeping this fact in mind when you are talking to your doctor might make the topic easier to discuss.

You are probably thinking, "It is hard enough to talk about my symptoms with my doctor. Now you want me to talk about my relationships?" The answer is yes. Having a frank discussion about any limitations brought on by your condition may improve your overall health and how you cope with relationships.

Your doctor knows your symptoms and will not be surprised about any question you ask, including the following:

  • Are there ways to overcome the fatigue or poor self image I feel so I can enjoy being intimate again?
  • Am I taking any medications that could affect my sex drive?
  • When should I tell a person I am in a relationship with about my condition?
  • Are there resources available to help me deal with relationship problems I am experiencing because of UC?

Your doctor has heard it all before. Do not feel embarrassed to ask questions like the following:

  • Do you have any suggestions for how to talk to my partner about my UC and how it affects our relationship?
  • Can you refer me to a therapist or a support group that may be able to help me with this issue?

For whatever reason, if you are too uncomfortable to bring these kinds of things up with your gastroenterologist, it is important to find a doctor you can talk to about it. You might want to try your primary care physician or gynecologist.

Depression

If you are feeling depressed about your UC, your doctor can help you find resources to help you feel good about yourself again. Don't be afraid to ask your doctor point blank:

  • Are there signs of depression I should watch out for?
  • Can you refer me to a counselor who has worked with other UC patients?

Long-term concerns

It is normal to wonder what your condition could mean for your overall health in the long term. Reassure yourself by asking your doctor

  • Should I be worried about taking so much medication for too long?
  • When should I schedule my next appointment?
  • How often should I see a doctor?
  • What types of screenings or tests should I have done to ensure I stay healthy?

Remember, taking UC medications such as once-daily APRISO and working with your doctor might help you manage your UC symptoms with the end result of remission for up to 6 months.3

IMPORTANT SAFETY INFORMATION

APRISO is a locally acting aminosalicylate indicated for the maintenance of remission of ulcerative colitis in patients 18 years and older. APRISO is contraindicated in patients with hypersensitivity to salicylates or aminosalicylates (sulfasalazine) or to any of the components of APRISO capsules. It is recommended that patients have an evaluation of renal function prior to initiation of APRISO therapy and periodically while on therapy. Exercise caution when using APRISO in patients with known renal dysfunction or a history of renal disease. Mesalamine has been associated with an acute intolerance syndrome that may be difficult to distinguish from a flare of inflammatory bowel disease. Symptoms include cramping, acute abdominal pain and bloody diarrhea, sometimes fever, headache, and rash. If acute intolerance syndrome is suspected, promptly discontinue treatment with APRISO. There have been reports of hepatic failure in patients with pre-existing liver disease who have been administered mesalamine. Caution should be exercised when administering APRISO to patients with liver disease. The recommended dose of APRISO is four 0.375-g capsules once daily in the morning (1.5 g/day) with or without food. Because dissolution of the coating of APRISO granules depends on pH, APRISO should not be coadministered with antacids. Patients with phenylketonuria should be aware that APRISO contains aspartame, equivalent to 2.24 mg of phenylalanine per day. In 2 well-controlled clinical trials, the most common treatment-related adverse events occurring in at least 3% of adult patients taking 1.5 g/day of APRISO and at a rate greater than placebo were headache (11% vs 8% for placebo), diarrhea (8% vs 7% for placebo), upper abdominal pain (5% vs 3% for placebo), nausea (4% vs 3% for placebo), nasopharyngitis (4% vs 3% for placebo), influenza and influenza-like illness (4% vs 4% for placebo), and sinusitis (3% vs 3% for placebo).

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/safety/medwatch/ or call
1-800-FDA-1088.

Complete Prescribing InformationPDF

For product information, adverse event reports, and product complaint reports, please contact:
Salix Product Information Call Center
Phone: 1-800-508-0024
Fax: 1-510-595-8183
E-mail: Salix@medcomsol.com

References: 1. Rubin DT, Siegel CA, Kane SV, et al. Impact of ulcerative colitis from patients’ and physicians’ perspectives: results from the UC: NORMAL survey. Inflamm Bowel Dis. 2009;15:581-588. 2. Ulcerative colitis (UC) sufferers find UC quite disruptive to many aspects of daily life. [press release]. Wayne, PA: PRNewswire; May 17, 2007. 3. APRISO [prescribing information]. Morrisville, NC: Salix Pharmaceuticals, Inc; 2008.