I have no cold symptoms and have not had a cold in a very very long time. however, I have a numbness and painful sensation on the left side of the bridge of my nose and it is slightly swollen in appearance. I have gotten a headache three nights in a row, but it goes away in the daytime. Any clues?

Sinusists, go see your doctor about it, you could get infection

Some STDs (such as HIV) may not have symptoms for a long time. if you get HIV, you may not have symptoms for years. The only way to find out if you have any STDs is to get tested. Don't wait until you have symptoms.

tons of STDS and you cant be sure the time the symptoms, but if your questioning this and you had sex and you feel weird "down there", or there is weird discharge you might want to go to a doctor.

Theres many std's out there so its hard to say when or if you ever do get symptoms of the sexual transmitted disease. It just basicallity all depends on the persons immune system and how it affects the blood system.

it depends, however sometimes with an STD like chlamydia you dont get any symptoms at all

some std's have no symptoms,for peace of mind go 2 the doctor

I had a late miscarriage in January. I lost the baby because some sort of tissue has wrapped around the umbilical cord and cut it off. Since the miscarriage I have had light periods, been constantly looking and feeling bloated, and I am very sensitive to touch around where my uterus is. I know I sound crazy but I have been ignoring how I feel for a long time and I just want to know if I have any cause for concern. thanks!

I had suffered from and successfuly got rid of fibroids naturally.
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If i had an std that i contracted over 1-2 months ago wouldnt i have symptoms and stuff till this day? i had unprotected sex with someone and am worried.

Many STDs have no symptoms for a long time after infection. the only way to find out if you have an STD is to get tested. you can check the website hivtest.org to find free testing sites in your area. Just enter your ZIP code.

As a long time Crohn’s patient, I am often sought out for advice on handling the disease by newly diagnosed patients and their families. And while awareness of Crohn’s is much greater than it was twenty years ago, most people really don’t understand much about the disease or the way it impacts a patient’s life. so I’ve decided to write a four-part document that hopefully explains to new Crohn’s patients and the general public what to expect and how to cope. these posts cover the medical symptoms tips for patients living with the disease and tips for people who know someone living with Crohn’s.

In this post, I’ll cover some of the treatment options available and the improvements made since I was first diagnosed. but before deciding on a treatment or treatments, discuss all of these options with your doctor. you may want to read to read the section on symptoms before reading this post, so that you understand why certain treatments are used.

When I was first diagnosed in April 1991, there weren’t any truly effective treatments for Crohn’s Disease. the treatments were either drastic – an ostomy – or did their best to mask the symptoms . Medications included a form of sulfa, antibiotics, oral steroids and anti-diarrhea solutions. Since these medications rarely induced remission of the disease (that is, a significant reduction of symptoms), most of us with Crohn’s were hospitalized often. Between 1991 and 2000, I was hospitalized 18 times for Crohn’s or Crohn’s related symptoms. all told, I spent 318 days in a hospital bed during those ten years.

The principle reason treatments were so ineffective was that so little was understood about the disease or how it functions. Fortunately, great strides have been made over the past ten years. thanks to the work of researchers, current treatments are much more effective. I’ll go through each of these.

Corticosteroids are artificial hormones often given to patients in during “flare-ups” (periods of extreme disease activity). During a flare, what happens is the tissue surrounding the disease inflames, causing the extreme pains for which Crohn’s is noted (I’ve joked that I know what labor pains must feel like – my wife actually agrees!). Corticosteroids such as Prednisone, Prednisolone and Deltasone work by reducing the inflammation. these drugs are artificial replacements for the corticosteroids generated by the human body, but are given in much higher doses than the body normally makes. I’ve received as much as 120mg of prednisone a day, or about 60x the body’s normal production. While they are as close to a miracle drug as any for ending flare-ups, they pose serious risks with extended or frequent use. the first is dependence; when receiving such massive doses the body stops producing its own. this is why they are usually prescribed for short periods and ramped down while prescribed. Prolonged use can also lead to cardiovascular disease, osteoarthritis and cataracts. also, patients taking corticosteroids should note that weight gain and mood changes are common when taking them.

This type of medicine is used to help maintain remission. It’s been used since I was first diagnosed, but the delivery of the active ingredients in sulfonamides has improved greatly in that time – meaning lower and less frequent doses are needed for the same effect. the first medication I was prescribed was Sulfasalazine; I had to ingest three 600mg tablets 4 times a day. if you’re not interested in doing the math, I was taking 7200mg every day, without much positive effect. Today, I take 1200mg of Lialda daily. the most commonly prescribed sulfonamide for Crohn’s today is Asacol (or its generic equivalents, Mesalamine and 5-ASA ), usually at a 800mg dose three times daily. the side effects are relatively minor, such as excessive gas and bloating. in rare cases, it can exacerbate pre-existing heart and lung cases. And some studies link these drugs to reduced fertility in men.

Everyone has bacteria lining their digestive tract. we actually need them to help with proper digestion. but during Crohn’s flare-ups, the bacterial populations literally explode. Nobody is quite sure why, or what the connection may be. regardless, most gastroenterologists will prescribe one or more antibiotics during a flare-up. the most common is flagyl, given intravenously.

The first major advance was in understanding the role an antigen called tumor necrosis factor (or TNF) plays in Crohn’s and the use of anti-TNF drugs in fighting Crohn’s. TNF forms naturally within the body and is one of our immune system’s defense mechanisms against cancer. it works by inflaming the cells around the cancer cells, in essence choking them. Nobody is quite sure why Crohn’s patients suffer this type of inflammation, but studies in the mid and late 1990′s showed that anti-TNF drugs actually reduced the chronic tissue inflammation. Since then, drugs like Imuran or 6-Mercapturine (6-MP) have been introduced. They can’t actually induce remission, but they are effective in maintaining remission once it’s been achieved. the big downside is since they reduce the body’s principle anti-cancer agent, patients taking them are at much higher risk for developing cancers. recent studies show the possibility that Crohn’s patients who have been on one of the anti-TNF medications for extended periods are at substantially higher risk for a type of leukemia.

An offshoot of anti-TNF medications, biologics as used in Crohn’s treatment are designed to essentially “turn-off” the immune system. there are three currently in use: Remicade, Humira and Cimzia. Each has some unique side-effects; ask your doctor about them. in 1998, Remicade was the first of these drugs approved for use in Crohn’s, so it has the longest track record. However, it also has the most common allergic reactions and needs to be administered by IV over a course of several hours. Humira and Cimzia are similar to one another, but whereas a Cimzia injection can last 4 weeks, Humira needs to be injected every other week. Generally speaking, since the immune system is kept in a very depressed state while taking these, the patient is very susceptible to any airborne illness and contracting one can be deadly. if you are planning to take one of these, know the risks and make certain you discuss them with your doctor. I’ve been taking Cimzia for close to a year and it has made a HUGE difference in my quality of life.

Crohn’s patients often require surgical procedures. these can range from the relatively benign (colonoscopy for examining the lower GI tract and removing polyps for closer examination) to a full-blown ostomy. before undergoing any surgical procedure, make certain you discuss all of the implications with your GI doctor and meet the surgical team. you should also try to have a trusted friend or family member with you for these consultations – odds are if you’ve reached this point, the pain has also become nearly unbearable. Whether you’re fighting the pain au natural or with painkillers, you won’t be in the best command of your mental faculties.

For Crohn’s patients, diet is truly a four-letter word. we obviously need to eat, but many foods (including what can seem like most of the yummy ones) will cause an exacerbation of symptoms. Eat too many of them and you may wind up with a full-blown flare. Match that with the fact that as a Crohn’s patient, you need to ensure good nutrition even more so than most people and you stand a good chance of being baffled by your diet – or going insane J. your best bet is to avoid foods that are hard to digest, such as nuts, popcorn and seeds. as for everything else, keep a log of everything you eat and if you experience increased symptoms, then avoid it in the future. Personally, I try not to exclude anything unless I’m in a flare – I just make certain my “avoidance” foods aren’t a constant part of my diet.

Also, you may want to consider nutritional supplements if you find you can’t get enough nutrients from eating. these can range from vitamin supplements to more robust liquid supplement shakes, like Ensure or Boost. in any case, working with a registered nutritionist is always a good idea. And one more thing: most Crohn’s patients find eating large meals tend to make them symptomatic. Try to eat smaller meals and eat more often. for instance, I typically eat 6 times a day – I cover this in more detail in the lifecyle adjustments post.

There are quite a few alternative (or herbal) therapies out there for Crohn’s patients. I do not recommend any of them, although parts of them can be helpful. for instance, I find mint tea can help calm my stomach if I overdue it. regardless, before trying any of them, be sure to check with your doctor and investigate them fully to find out how they can interact with your medications or each other. just because they’re herbal or all-natural doesn’t mean they can’t have side-effects.

Perhaps the most important part of treatment is your ongoing care. your doctor will likely send you for seemingly endless tests. CAT scans, GI studies, barium enemas, X-rays, colonoscopies, blood tests and more are part of the typical “Crohnie’s” regimen. Undergoing these and maintaining your relationship with your doctor are crucial in keeping Crohn’s at bay.

Those one suffer with painful kidney stone, they ever search simple solution for dissolve kidney stones. many of people suffer with chronic kidney disease but they don’t know whenever they don’t get any subtle symptoms. Kidney stone are not the chronic kidney disease but when you avoid it for a long time it may be converting in the chronic disease. the final result of chronic kidney disease is kidney failure.

If you want to take maximum benefit to get better result, then you have to be knowledge about kidney stone symptoms. if you have the sufficient knowledge about kidney stones then you can easily remove it by the natural home based remedy.

If any time you get any kidney stone symptoms then you not need to be worried about it. Just go to the doctor and clarify your doubt. to diagnose the stone doctor will suggest you blood and urine test. many of advance procedure are available to diagnose but blood and urine test is enough to diagnose.

Home remedies for kidney stones are preferred to take your primary action against stone. In a primary action you can start with the water. Drink good quantity of water and also increase the fluid intake. Kidney infection main causes are microorganism and bacteria. Drink the more quantity of water help to flush out such types of germs.

Another reason for kidney stone is taking high consumption of animal protein. the animal proteins are the main cause of chronic urinary infection. due to accumulation of such types of waste material take place in the form of kidney stone.

Lemon is another perfect natural resources to cure your kidney stones. Add the lemon juice to your daily life. Expert suggests it for especially when you are suffering with calcium based kidney stone. its acidic nature make easy to break calcium oxalate kidney stone and help to flush kidney stone.

Tomato juice can also be used as good home remedies. to make your kidney healthy you can take one glass of tomato juice with pinch of salt and pinch of pepper. Dairy product is strictly avoided during kidney stone.

How to natural product are help to dissolve kidney stones. why the natural things easily flush kidney stones. you can also read more about kidney stone remedy.

My sister is undergoing a biposy tomorrow to see if she has cancer.

She's had bone pain in her arm for over one year now. one doctor diagnosed it as an arthritic joint in late 2005. another put her on anti-inflammatories and physical therapy for bursitis/frozen shoulder in October of 2006. the drugs alleviated the bone pain a little bit but the shoulder joint and back and spine remained very achey. She looked uncomfortable and pale all of the time and I kept telling her that maybe she should see another doctor.

She finally went to a different doctor last week when she noticed some swollen lymph nodes in her neck. Her blood tests revealed that she's very anemic.

Do anti-inflammatories delay a correct diagnisis of cancer by masking/reducing bone pain? She's been looking unwell for a long time and unfortunately, her doctors only viewed her as a body part (in this case a shoulder) instead of a whole person who looked quite obviously, unwell. I'm just terribly worried about her

Hey,

What were the rest of her blood test results?

If she is anemic – something is wrong; rest of test should show bigger picture.

She has 2 of the "base symptoms" for a could of different deseases and cancers (such as Myeloma) but it could also be nothing – the pain killers (with long term use) could surpress the HGB and RBC.

Just like looking at one part of the body, the blood test is made up of many sections.

Good luck

Jewells
35 months and still here

Unfortunately the answer is yes…It took 9 months for the docs to diagnose my bone cancer and just told me to take Advil. not until my blood work went to terrible did they decide something was wrong. I was fortunate I lived to tell the tale. I wish you and your family well.

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When I do not go to urinate for a long time, it hurts very much. Something like prostatitis, but it is not. I think it is bladder symptoms, like spasmed.
What possible help you can offer ?

maybe its a sign that you just need to urinate. but i gather this is odd to you (never happened before)

go visit your doctor. dont diagnose yourself

Go the doctor. Now.

Urinary tract. go see a doctor. Urinating rids your body of toxins…if they back up you could lose a kidney.

Does it take 5 min 1 hour 5 days?

You usually die within a year and may show no symptoms for a long time. this is why dog bite victims get tested for rabies and the dog that bit you gets tested as well.