Posted by admin on 6th, 2009
First Gall Bladder Symptom-Jaundice the most obvious symptom
When the skin becomes jaundiced(yellow or orange)and the whites of the eye take a yellow colour as well there is most likely an issue with the gall bladder or the liver. Jaundice shows that the liver is not working properly and canât transform the old blood into bile or that there is a blockage in the gall bladder.
Second symptom is the pain
Pains can appear in the upper abdomen or below the ribs on the right side they are rare once in a while. It may be accompanied by nausea and vomiting and may spread in the right shoulder, the attack of pain can be severe and frequent and may have different durations from minutes to hours. Pain in gall bladder may be confused with other types of pains in different diseases: kidney stones, gastric ulcer, heart pains, back problems. Attacks are triggered by chocolate, cheese or pastry and other fatty foods.
Third symptom are the gall stones
There may be silent stones of the existence of which people donât know and are found accidently from X-rays. These stones usually do not require treatment. Other symptoms are: abdominal pain, nausea, vomiting, indigestion, fatty food intolerance, gas, biliary colic, belching, abdominal bloating.
Symptoms that require immediate attention and medical intervention are: fever, sweating, jaundice, persistent pain, chills, pale stools.
Fourth symptoms-gall bladder attack symptoms
May occur any time at night or after a fatty meal, attacks last for 1-2 hours, may cause nausea and vomiting and severe pain in the back between the shoulders. After a true attack occurs, subsequent attacks are more frequent.
Remember that the following are gall bladder attack symptom:
Upper abdominal pain, back pain, pain - between the shoulder blades, nausea, vomiting, steady severe pain that increases rapidly and lasts up to 40 minutes each 2-3 hours with nausea, vomiting, pain - between the shoulder blades.
During the night gall bladder attack symptoms follow after fatty meals and manifest with: colic, bleching, gas, indigestion, abdominal bloating, recurring intolerance of fatty foods. As a treatment: it is treated with antibiotics and in urgent cases emergency surgery is required to remove the gallbladder.
Painful attacks are to be treated with painkillers. Keeping a low fat diet and placing something warm on the pain spot are also helpful methods. Gallbladder disease affects mostly women. Those symptoms are not to be dismissed because they suggest if the state of health is changing and how is this happening.
It is important to intervene with the treatment as soon as possible before becoming too late and dangerous with its complications for the patientâs life.The treatment may be surgical or alternative treatment.
For more resources about gall bladder please review http://www.gall-bladder-guide.com/gall-bladder-removal.htm or even http://www.gall-bladder-guide.com/gall-bladder-symptoms.htm
Posted by admin on 5th, 2009
11 weeks, 2 days pregnant. Experiencing bad sharp lower abdominal pain on one side. No cramping, nor bleeding. Just that sharp irritating pain.
If she has had an ultrasound and they know the pregnancy is in the uterus than it is likely just muscles & ligaments stretching. If she has not had an ultrasound she should probably see the doctor to be sure. At any rate it never hurts to call and ask that is what they are there for:)
Posted by admin on 4th, 2009
Picture this. Your 9-year old daughter staggers to the breakfast table; hands on head, and moans plaintively, “I can’t go to school today. I have a headache.”
“Nonsense,” you say. You give her an aspirin with breakfast and say, “Off you go. You’ll feel better when your history test is over.”
But what if this happens every few weeks? Might it be migraine? Is there such a thing as migraine in children?
Betsy’s Migraines - a true story
My introduction to the possibility of migraine in children came when I was teaching fourth grade in Massachusetts. That’s when I met 9-year old Betsy. Betsy was a pretty child, but headaches kept her from making either friends or academic progress. Betsy claimed to experience regular bouts of migraine in children. Her doting mother vowed that Betsy’s attacks were real, but I was skeptical, since they always coincided with things Betsy disliked.
Even more suspicious was Betsy’s behavior during attacks. She began with plausible head-holding and tears. She begged for her mother to come and get her. Then, her act always went over the top. Looking around the room to be sure she had attention, Betsy shook her head violently from side to side. “You have to do this when you have migraine,” she announced loudly. She hit her head, and turned on the waterworks - always keeping a shrewd eye on her audience. When her mother arrived, Betsy abruptly stopped shaking her head, and moaned piteously. The curtain fell as her mother wrapped Betsy in her arms and ushered her from the room.
True Migraine in Children
While I never received professional confirmation that Betsy suffered migraine in children, I did learn that the condition is authentic. Its name is “migraine in children”, even when it refers to only one child.
Facts about Migraine in Children
Migraine affects people of all ages, social classes, races, and cultures. It is most prevalent between ages 20 and 50, but migraine in children hits younger generations. Often misdiagnosed initially as a “headache excuse” to avoid unpleasant tasks, migraine in children is real. Let me give you seven facts.
* Migraine often runs in families.
* Young babies and preschoolers can suffer migraine in children.
* Migraine in children begins earlier in boys than in girls.
* Up to 6 years, boys are affected equally or slightly more than girls.
* At elementary school level, 10 percent suffer migraine in children.
* The prevalence of migraines increases during secondary school.
* 20-30% of young women and 10-20% of young men experience migraines.
Migraine in children attacks every age from birth to age 20.
Symptoms of Migraine in Children
So, since your young daughter may be suffering migraine in children, and not simply avoiding a test, we need to look for signs. What are the symptoms of migraine in children?
1. PAIN: First of all, migraine in children is very painful, with severe throbbing in the head. Your daughter will probably report pain in the forehead, or the middle of the head, rather than just one side.
2. PALLOR: Typically, migraine in children will cause sufferers to appear ill and pale. There may be dark rings around the eyes.
3. QUIETNESS: A child suffering migraine in children will be very quiet. You may have trouble getting your child to say more than, “My head hurts.” He or she will choose to sit or lie in aching silence.
4. STILLNESS: Unlike Betsy in the schoolroom, children with migraines do not want to move any part of their bodies. They certainly do not want to shake their heads. If a headache complaint is followed by a running off to play, do not suspect migraine in children.
5. NAUSEA: For those taking notes, we’re on the fifth symptom now. Your child may complain of feeling sick in the stomach. He or she may not want to eat anything, and may vomit.
6. ABDOMINAL PAIN: In very young children, the main symptoms of migraine in children are abdominal pain accompanied by nausea and vomiting.
7. VISUAL DISTURBANCES: Some children experience changes in vision during an attack of migraine in children. They may have blurry vision, see flashes of light, or describe zigzag patterns in front of their eyes.
8. PHOTOPHOBIA: Your child may complain of light being too bright, and may want to go to a dark room. For those who like to sound knowledgeable, this light sensitivity is known as photophobia.
9. PHONOPHOBIA: Moving to the eighth symptom, migraine in children may cause them to hold their ears, or complain that you’re talking too loudly. Instead of turning up the television volume, they turn it down or off. This is sound sensitivity, also known as phonophobia.
10. OSMOPHOBIA: Migraine in children will sometimes cause sensitivity to smells. Even if you aren’t cooking liver-and-onions, your child may complain that dinner smells awful. For those who want the technical term, smell sensitivity is known as osmophobia.
11. MOTION SICKNESS: Those who suffer migraine in children have a tendency toward travel sickness. Even when not in a vehicle, a sufferer may complain of dizziness.
12. CONFUSION: Finally, and this is the last symptom we will look at, if your son or daughter is suffering migraine in children, he or she is likely to exhibit confusion and trouble concentrating. You might tell your teenager, “You aren’t thinking straight.”
Is It Migraine in Children?
There you have 12 symptoms. Some will exhibit all - others will exhibit a few. Some will have authentic migraine in children - some will not. How do you tell?
PATTERN: First, note whether your child’s attacks follow a regular, intermittent pattern. Migraine in children comes back again and again, following a pattern. Look for headaches that are very severe, lasting a few hours, and followed by an interval of no symptoms. Days or weeks later, a similar attack occurs, followed by another symptom-free interval. Migraine in children has a rhythm.
FAMILY HISTORY: Check to see if there is a history of migraine in your family. There may be a tendency toward migraine in children.
PHYSICIAN: Ask your doctor. A doctor will focus on ruling out other serious diseases or underlying conditions. If there are none, you will have the doctor’s reassurance, and a plan for effective treatment. I am not a professional, and my information must always be checked with your health care professional.
If your child’s attacks are migraine in children, you can provide relief.
Relief of Migraine in Children
* SLEEP: Sleep is the most important factor when it comes to migraine in children. In many cases, several hours of sleep in a dark, quiet room is all that is required.
* ICE PACK: Try placing a cold compress on your child’s head as he or she lies in a dark, quiet room.
* OTC: With your physician’s approval, use over-the-counter medications such as aspirin, ibuprofen, or acetaminophen.
* PRECRIPTION: Your physician may want to prescribe a medication for recurring attacks of migraine in children.
* WARM BATH: A hot Epsom salt bath may help an older child or teenager.
The most effective of these is usually sleep.
How Migraine Affects Your Children
In closing, I’d like to tell you about Thomas.
Thomas was a mischievous, high-maintenance little boy. From the time he could toddle, Thomas was on the go. Morning to night, he seemed never to stop. He talked incessantly, played loudly. Everything Thomas did was at top speed and volume.
Then, one bright autumn day in his eighth year, Thomas didn’t want to eat breakfast. Pale and listless, he lay on the couch, eyes closed. When his buddy called that the school bus was coming, Thomas covered his ears and moaned. When Mother opened the curtains to let in sunshine, Thomas covered his eyes. It was his first migraine.
Thomas lost that day. He missed the introduction of multiplication at school. He missed a film in history class. He missed an afternoon hayride with his cub scout pack.
Thomas lost many days after that. He lost days to migraine in children, and he lost symptom-free days out of fear. He began moving more quietly, more slowly. As additional migraines came and went, his bubbly laughter was gradually replaced by sadness and worry.
Thomas’ story is fictional, but it describes the experience of many who suffer migraine in children.
If you think your son or daughter may have migraine in children, I urge you to take him or her to your family doctor. Check for underlying problems, and discuss treatment possibilities.
Whatever you do, don’t ignore migraine in children. Appropriate diagnosis and treatment can greatly improve their quality of life.
Posted by admin on 3rd, 2009
The most frequent and important symptom of appendix inflammation in children especially male ones are vague abdominal pains. Most often this sign stands for appendicitis in male subjects with an increased incidence in older children and teenagers. The risk of vague abdominal pain suggesting appendicitis is the surgical intervention often discovering a normal healthy appendix; this occurs frequently at this particular age due to an imprecise diagnose. The other possible mistake and complication in children below six is the appendix perforation due to a late intervention.
The frequent complications regarding misdiagnose of appendicitis concerns surgeons all over the globe and strongly recommends an early and accurate analysis of medical history, physical exams and preliminary investigations. A precise recognition of appendicitis highly decreases the risk of morbidity and mortality of children accusing abdominal pain.
A highly competent diagnose must be based on both obvious clinical signs and an accurate histopathological examination to prove the existence of an appendix inflammation. Long lasting abdominal pain is no particular mark for the presence of appendicitis as must be associated with the migration of the pains to the right iliac fossa or the right lower quadrant of the abdomen. This particular localization of the painful symptoms is strongly connected to a successful positive appendicitis diagnose. Vomiting is a frequent additional symptom in appendicitis and increases the chances of a right diagnose when present.
Other important accompaniment symptoms in appendicitis are rebound tenderness in the iliac fossa and even percussion tenderness; in severe cases of perforation, these signs stretch through the entire abdomen. In acute appendicitis, guarding and rigidity in the lower abdominal quadrant are also signs of certainty.
An important Para clinical investigation in appendicitis suspicion is the blood analysis; an increased rate of the white blood cells especially over 15000 permm3 recommends a positive diagnose while a low number of leucocytes often means no appendicitis. The ultrasonography can also certain the presence of an appendix inflammation in children with classical symptoms, but can mislead diagnosis when the signs are very weak or very strong.
Computer tomography can sometimes be a good additional investigation in appendicitis suspicion but its value is low in cases with too low or too strong accompaniment symptoms.
As a conclusion it is likely to establish a right positive appendicitis diagnose in presence of vomiting, pains in the lower abdominal quadrant, tenderness and rebound tenderness, abdominal guarding and an elevated number of white blood cells. In more vague and unclear illness symptoms and signs-cases the experience of the surgeon and its intuition will always play the most important role.
For more information about appendicitis please review http://www.appendicitis-center.com/treatment-for-appendicitis.htm or http://www.appendicitis-center.com/acute-appendicitis.htm
Posted by admin on 2nd, 2009
am a 15 year old female who has been expieriancing severe abdominal pain for about the past two weeks. It keeps getting worse and worse. It is mainly on the left side, but my entire abdomin is in pain and slightly swollen. I also within the past 2-4 days have been expieriancing a great amount of blood in my stool. Does anyone know what could be going on?
I feel that I should go to the ER, the pain is EXTREMLY severe, but my mom wont take me…what to do?
I have been going through the same type of problem myself through the last couple of weeks myself. I know that it is really painful. I went to the emergency because the pain that I am experiencing, I could barely lie down, or lie on my side, and I could barely walk around. The pains were like contraction like pains as if you were giving birth to a baby. You should go to the emergency to get checked out. This is extremely important, as you need to make sure that you get thoroughly checked. You will be asked to provide an urine sample, and also get blood drawn as well. You will also have to likely get an ultrasound to figure out what is going on, and the doctor will also want to press on your abdomen to feel what is going on. Depending on what they find, they might also do a pelvic examination to rule out other problems.
Posted by admin on 1st, 2009
Ulcer is a disease that unfortunately makes more and more victims each year, because modern lifestyle helps this disease to appear and advance. Ulcer is caused by a bacteria called Heliobacter Pylori, which billions of people are carrying. If a person that carries this bacteria lives a stressful life and eats a lot of spicy food (factors that help the bacteria quickly evolve) then he/she will most likely suffer from one of the many forms of ulcer. Ulcer occurs because this bacteria slowly eats the protective membrane around the lining of the stomach and exposes the sensitive tissue beneath it to the dangerous gastric acids inside the stomach. Therefore, ulcer causes an open wound in the stomach, esophagus or duodenum.
If someone has discovered that he or she is suffering from ulcer then the treatment must start as soon as possible because if the disease is left untreated severe complications can appear. The treatment is simple, the patient is prescribed a series of medication depending on the type of ulcer and how advanced it is.
But what happens if a person is not aware that ulcer is affecting him/her or if he/she simply leaves the disease untreated? Well an untreated ulcer can turn into a much worse form of ulcer – bleeding ulcer. It’s called bleeding ulcer because loss of blood occurs due to the fact that H pylori keeps eating the tissue until it reaches the blood vessels and blood starts to enter the digestive track.
Someone that has bleeding ulcer will start vomiting blood, have black, loose stools, will start to experience pain in the abdominal area and indigestions will often follow a meal. In extreme cases, if nothing is done about the ulcer it will eventually lead to death, so bleeding ulcer must be treated immediately after it’s discovered or its consequences will be felt in the entire body. Bleeding ulcer is treated through surgery in most cases, but surgery is not required if the illness is detected early. It is hoped that in the near future ulcer and bleeding ulcer treatment will be much easier because new medical tehniquies are researched intensively every day, since this disease affects more and more people and the situation is becoming alarming.
In conclusion, if you suspect that you have ulcer or bleeding ulcer pay a visit to the local doctor and ask for his advice as soon as you can, because in the early stages both ulcer and bleeding ulcer are treated with just a few pills, which is of course much better that going through surgery and suffering life-threatening complications.
More information about ulcer or about ulcer Symptoms can be found on this website http://www.ulcer-center.com/
Posted by admin on 31st, 2008
Wilson’s disease is a genetic disorder, which is fatal unless early detected and treated. It is a rare condition, where excess copper builds up in the body causing copper poisoning. Wilsonâs disease is quite uncommon and affects 1 in 30,000 people. It is named after Dr Samual Wilson, who first described the disorder in 1912.
Copper is a ‘trace metal,’ which is found in many foods. Some amount of copper intake is necessarily required to remain healthy. Normally, the body automatically gets rid of the excess copper, but a person suffering from Wilson disease is not able to naturally excrete the excess copper. This result in gradual deposition of the excess copper in the vital organs such as the liver, brain, cornea and kidneys â and if not treated on time, can prove to be potentially fatal.
Generally, the first part of the body to be affected by copper deposits is the liver. In about half of Wilson’s disease suffering patients, the liver is the only affected organ. Too much copper in the liver cells (the hepatocytes) is harmful and leads to liver damage.
Excess copper also damages the brain tissue in an area called the lenticular nucleus. Hence, Wilson’s disease is also called ‘Hepato-lenticular Degeneration’. If left untreated, the damage may become severe and eventually fatal.
What is the cause of Wilsonâs disease?
The basic underlying deficiency in Wilson disease is not known. It may be related to the body’s inability to produce sufficient levels of ceruloplasmin, an enzyme in the fluid portion of the blood that binds to copper and is involved in its transport and regulation. Other scientists believe that reduced production of ceruloplasmin may be the result of a defect in the liver’s ability to break down copper. The correlation between reduced ceruloplasmin levels and excessive copper accumulation is not fully understood. In addition, there is also evidence of impaired excretion of copper by the biliary system.
How does one get Wilson’s Disease?
Wilsonâs disease is quite a rare disease. It is mostly genetically related; therefore, most people inherit it from their parents. It is also quite possible for the mutation to occur spontaneously. One out of 40,000 people inherit Wilson’s disease from their parents, and 1/120,000 (one out of four Wilson’s disease sufferers) get the disease from a spontaneous mutation.
What are the problems related to Wilson’s disease?
Although the genetic defect is already present at birth, it takes years for the excess copper to build up to the toxic level where it is fatally damaging.
Symptoms of the disease typically start to develop between the ages of 6 and 20, most commonly in the teenage years. However, you can also develop symptoms in middle age.
The most characteristic sign of this disease is the Kayser-Fleischer ring - a rusty brown ring around the cornea of the eye that can be seen only through an eye exam. Other signs depend on whether the damage occurs in the liver, blood, central nervous system, urinary system, or the musculoskeletal system.
1. Liver problems â
Symptoms of liver disorders often are the first to develop. The toxic effect on the liver cells can cause hepatitis (inflammation of the liver) leading jaundice, abdominal pain and vomiting. If left untreated, damage to liver cells can cause scarring of the liver (cirrhosis). Eventually severe cirrhosis and liver failure develop in untreated cases causing severe problems.
2. Brain problems â
As copper gets deposited in the brain, it can cause various symptoms:
⢠Physical symptoms such as an odd type of tremor in the arms, slowness of movement, difficulty with speech (dysphagia), writing problems, difficulty swallowing, a wobbly gait, headaches, seizures.
⢠Psychological symptoms such as depression, mood swings, bizarre and inappropriate behaviour, depression accompanied by suicidal thoughts, neurosis, or psychosis, inability to concentrate. Affected people may become very aggressive and sentimental; and may exhibit a ‘change in personality.â
If Wilsonâs disease is left untreated, the accumulation of copper in the brain can lead to severe problems such as severe muscular weakness, stiffness in the body, and dementia.
3. Other problems â
Copper may build up in the cornea of the eye. This causes a characteristic feature called Kayser-Fleischer rings - a brownish pigmentation of the cornea. Other features that may develop include anaemia, kidney damage, heart problems, pancreatitis (inflammation of the pancreas), menstrual problems and repeated miscarriage in women, and premature osteoporosis (thinning of the bones).
Wilsonâs disease is diagnosed with tests that measure the amount of copper in the blood, urine, and liver.
How is Wilson’s disease diagnosed?
If Wilson’s disease is suspected, it is diagnosed by tests such as -
⢠A blood test to measure ceruloplasmin - a protein that binds copper in the bloodstream.
⢠A urine test to measure the amount of copper in the urine.
⢠An examination of the cornea may show the Kayser-Fleischer rings if they have developed.
⢠A biopsy of the liver
If Wilson’s disease gets confirmed in a person, then brothers and sisters should also be tested to see if they have the condition. Siblings of a person with Wilson’s disease have a 1/ 4 chance of having the condition.
Is there a cure for Wilson’s Disease?
Cure for Wilson’s disease involves a liver transplant, which is performed if necessary to save the person’s life. The person will still have the genetic defect, and initial damage to the nervous system will not go, but may improve.
How is Wilson’s disease treated?
The goal of drug therapy in individuals with Wilson disease is to remove excess copper from the body and prevent ongoing copper accumulation and deposition. Therefore, drug therapy must be continued throughout life. The earlier treatment is started, the better the chance of preventing long-term permanent damage to the liver or brain.
Posted by admin on 30th, 2008
I have abdominal pain that is centered in the navel area and mildly radiates to the left side and when my cat (who weighs 14 pounds, and yes kitty is overweight and currently on diet food supervised by a vet) sits on my abdomen the pain goes away. Does anyone have any idea of what may be causing this pain?? Does anyone out there experience the same thing??
Well generally, pain which is relieved by pressure suggests a peritonits. That is, inflammation of the peritoneum, or 'membrane', that covers your abdominal wall and internal organs. When the peritoneum is inflamed, it is highly sensitive to any pressure or irritation. When you push down on the abdomen, this pushes a bit of organ away from the peritoneum, relieving the pressure. A sign doctors look for is 'rebound tenderness' when the pain is elicited when removing the pressure. The doctor pushes on the abdomen, which may not be painful, the doctor then takes their hand away, the organ (which had been depressed) when released, moves back and scrapes along the inflammed peritoneum causing intense pain.
The key question for you is, is the pain worse when kitty jumps off?
This is the most important diagnosis a doctor would consider as patients with peritonitis are quite seriously ill. If you are unwell (temperature, vomiting) go see a doctor.
There are other possible reasons however, pain could be simple constipation. The pressure may have helped move the compacted faeces along and thus relieved the pain. If you are otherwise well I would suspect this is the case.
Posted by admin on 28th, 2008
Ulcer is a very common and known disease that each one of us has heard of. But what many don’t know is what are the true causes of the ulcer disease. Until some time ago everybody believed that ulcer is caused by hot and spicy food and also by stress at work. In fact, a bacteria is responsible for ulcer and it can affect people no matter what age or sex they are.
What exactly is peptic ulcer?
Well peptic ulcer occurs when a small opening, or wound, appears in the inside of the stomach, in it’s lining to be more precise. This open wound situated inside the stomach will cause pain because the gastric acid that can be found there will hurt the tissue that is exposed by the tear.
There are more types of peptic ulcer. The one mentioned above, represented by an open wound in the stomach is called gastric ulcer. If the wound is located in the upper part of the duodenum (small intestine) than the peptic ulcer is called duodenal ulcer, and if it appears inside the lower part of the esophagus then it’s called esophageal ulcer.
The bacteria that has been discovered to cause ulcer is called Heliobacter Pylori and you can get infected with it by simply drinking water or eating food that contains it, but it only starts to manifest once its bearer has reached a certain age. In most cases this age was discovered to be 60. It is known that billions of people are carrying H. pylori.
The bacteria starts to ‘eat’ the protective membrane that protects the stomach lining or the duodenum and lets the damaging acids pass through, causing more trouble and eventually leading to the appearance of peptic ulcer. Certain spicy foods and a stressful lifestyle can amplify the ulcer’s effects, but they don’t cause it. Anyway, it’s more likely that a person who has been eating junk-food all his/her life has a more advanced and severe ulcer than someone who has been eating healthy food.
The symptoms that peptic ulcer presents vary from patient to patient, but the most common ones are indigestions, abdominal burning, and of course pain inside, where the ulcer is located. The signs are more visible after a meal because the stomach starts working and releasing acid.
If you feel pain after eating and you’re experiencing indigestion, visit a doctor, and if you’re diagnosed with ulcer start the treatment soon, before things get worse. Treatments consist of different types of medication and a healthy diet.
Because junk-food and stress are a common thing in modern society more and more people are suffering from peptic ulcer each year, but hopefully medicine will find a very efficient treatment soon. Until this happens the only thing you can do is stay away from the dangerous types of food.
More information about Duodenal ulcer or about Gastric ulcer can be found on this website http://www.ulcer-center.com/
Posted by admin on 27th, 2008
I've had upper abdominal pain, and my doc diagnosed me as having a mild case of pancreatitis (no tests were done). I've had a numbness on and off in my left thigh and left arm, back pain on the same side. I also have a "floater" in my vision sometimes. I think I could have diabetes (my brother has it who is 37, I'm 30). Does anyone think these are all signs of diabetes?
Where is the pain exactly in your upper abdomen?
I'm not saying that no tests need to be done, but pancreatitis is very distinct in where the pain is, and what it feels like…
It could be a sign of diabetes, go get a test kit and find out… they're only like 15 bucks from rite aid, get a cheap one… they all tell you the same thing…
I'm diabetic, from having pancreatitis… And when you're having an onset of pancreatitis, it's not uncommon to have a fluctuation in your blood sugar… Your pancreas is what creates your insulin…
I had half of my pancreas removed, because of tissue necrosis, worst pain ever… Be glad you have a mild case… It's interesting that your doc didn't admit you to the hospital and stop any intake, of anything…. Pancreatitis can easily get worse…. What i'd recommend (i'm not a doctor, but i almost died from it, and i'm in nursing school), is not to eat for a few days… Thats what they'd normally do in the hospital, that and give you pain meds…
I've never seen anyone admitted to the hospital with pancreatitis, that they didn't starve for a few days. Of course, they usually have IV Nutrition… But hey… I've done it to myself during small bouts when I didn't have the time to sit in the hospital for a few days…
Any food stimulates the pancreas to create enzymes… Stimulation of an already inflamed (-itis) pancreas (pancreat/o-) can make it worse… Think about it, would you jump on a broken leg?
As for the diabetes… You'll know when you have it, get a test monitor, and check your glucose readings (AFTER you're done with pancreatitis, you'll get false readings if your pancreas is out of whack)… You'll know, the first major sign is urinating like, every 5 min… seriously, every 5 min…
I know why you're probably paranoid about numbness… Because diabetics are known for loss of sensation in their extremities.. But, you're only 30, and honestly… I doubt you'd be experiencing any of that by now, but… I guess it's possible… You wouldn't have been looked over for that long, for you to be having numbness…
