Pain is a long-lasting problem for people who have sickle cell disease. Bouts of severe pain can last for hours to days and are difficult to treat. Pain can be exhausting for caregivers as well as for the person in pain. A pain management plan can help a person cope with chronic pain and with pain caused by a sickle cell crisis.
Your doctor or a pain treatment specialist can help you make a pain management plan. This plan includes instructions on how to treat mild pain at home. And it tells you when you need to go to the hospital if your pain gets worse.
The bladder is the hollow organ in the lower abdomen that stores urine. As the bladder fills, muscles in its walls relax so that it can expand. As the bladder empties during urination, the muscles contract to squeeze the urine out through the urethra.
Several different bladder problems can cause pain. The three most common causes of bladder pain are interstitial cystitis, urinary tract infection, and bladder cancer.
Clarifies your and your doctor's preferences ahead of time.
Explains your needs to other health professionals who care for you.
Offers you some predictability and control during times of crisis.
How can you prevent and treat pain at home?
Treatment of pain at home is a way of life for most people with sickle cell disease. Sickle cell pain varies from person to person, from mild to severe, and from occasional to constant. Some people experience numerous sickle cell crises, or painful events, a few times a year. Others experience none.
In many cases, you can treat mild to severe sickle cell pain at home with a combination of pain medicines, plenty of fluids, and comfort measures such as heating pads or hot water bottles. Do not use heating pads with children.
Painful events can become severe and last for days to weeks. Such extreme pain requires aggressive pain medicine that must be monitored in the hospital. If pain is increasing and isn't relieved by treatment at home, call your doctor and seek emergency medical care.
Mild to moderate body pain and some sickle cell crises can be prevented by:
Drinking plenty of water and other fluids, especially before, during, and after exercise or strenuous activity and when you have a fever or infection. Drink enough so that your urine is light yellow or clear like water.