Aloe vera symptoms and conditions

After 4 days in the hospital with the colon infection and some antibiotics treatment via I.V. I walked home, I was fine. All I needed was to have 7 x 500mg in coming week.
After three days and 3 of 500mg Levaquin pills very itchy reddish rash developed in a day all over my entire back where I have solid areas , bottom, parts of the arms and upper chest and neck where I have dense spots..
I used the Witch hazel and Aloe Vera Mist (no help) till I’ve got hold of the Triamcinolone Acetonide Cream. No help yet in last 4 hours. I’ll try Calamine lotion next.
Boy it itches I didn’t sleep all night. I never had any allergies before.

I am 39 years old and have been on Omeprazole for 6 years. I have had the worst year ever. I was always a healthy and fit guy until 2008. I had chronic headaches and extreme fogginess which led to me having an MRI and seeing a chiro(all negative). I had chronic chest pain which led to EKG's, stress tests, ER visits, and tons of blood work ranging from cardiac, glucose, liver, renal, thyroid, etc...(all negative). Did gastroscopy and found esophagitis and gastritis. Upped the dosage of Omeprazole. Then I started getting tremors, muscle cramping, muscle pain, fatigue, blotchy red skin, and continued fogginess and lightheaded.

Did I mention i still have constant heartburn despite all the Omeprazole. I have done everything...tilt up head of bed, bland diet, no coffee or alcohol, no eating late evening etc....

Doctor put me on Fluoxetine (Prozac) for all my stress and anxiety from these crazy symptoms. After seeing this site and reading all your testimonies I am now thinking it is from the Omeprazole!!! Scary thought to stop since my chest pain and heartburn can be pretty severe and constant. What do I do? Feel like I'm caught between a rock and a hard place here.

I too have had all the horrible side effects of this dangerous drug.. Yesterday after much research I started taking Aloe Vera gel capsules available at the health food stores.. I stopped the Omeprazole and I fee like a new woman already!!. Many sites recommend the aloe vera capsules not just one site..They work!! Also am eating a bland diet for awhile..applesauce, serial, apple juice..No Citrus, no chocolate, no tomatoes the list goes on.. Bland bland bland is key.

hi i have been on omeprazole for 18months now and have had a lot of chest infections has anyone else had this, also does anyone know of a natural remedy for acid reflux.

My mother was given this drug, Lisinopril, because the doctor decided she had high blood pressure after she went in for a bladder infection (she's had these all her life, every now & then). The doctor also prescribed Nitrofur (please avoid THAT one like the plague - she was on the couch for a week in stomach agony). We didn't put 2 and 2 together on what was really going on until yesterday. She was on Lisinpril for 3 months and every 2-3 weeks had an episode of extreme stomach spasms, bloating and fatigue. These episodes have lasted 3-5 days each, keeping her on the couch in agony. I researched the internet and found out that Lisinopril is made from SNAKE VENOM, can you believe? Turns out lots of people have reactions from this, including coughing. There was one woman who had the exact same things as my mom and wouldn't you know it, stopped using Lisinopril and the episodes went away. Turns out this is an allergic reaction, something they say is rare, BUT I think it depends how long you take it and how sensitive you are. So my mom immediately stopped taking it. What's happening inside is something they call gastrointestinal angioedema (in layman's terms, internal hives). If you experience coughing, the hives are in your throat. If you experience the stomach pains, the hives are all in your intestinal tract and very possible more areas internally. So then I looked up and found an excerpt from "One Earth Herbal Sourcebook" on Google and found the author had experienced something similar, using ayervedic (indian) herbs to fix the problem. I couldn't find where to buy ayervedic herbs, calling Whole Foods Market with no success. Well, all over the world there are healing herbs that do similar things. So I did find 2 that would work. Marshmallow (the herb, not the campfire kind) will help relieve swelling internally. There is another herb called Goldenseal (don't use it if you have very high blood pressure as it can cause a spike) that has antibiotic and anti-inflammatory properties. Anyway, now you know what is going on inside - hives you can't see from snake venom. Take that to the doctors and see what they say. Maybe your just better off like we are to research yourself and find a natural answer from nature. I hope this can help others avoid the hell we've been through.

EVERYONE PLEASE READ!!!! GARDASIL HAS DESTROYED MY LIFE! I am 24 years old and a year and a half ago I was graduating college and planning to be a professional dancer and go to law school...I was perfectly healthy and energetic! In February of 2007 I received my first Gardasil shot. After a few days I started to feel as though I had a Urinary Tract Infection and was also feeling more tired than usual. The doctor gave me an antibiotic and sent me on my way.

In May of 2007 I received my second Gardasil shot and yet again, a few days later I started to feel like I was getting another Urinary Tract Infection. I went to the doctor numerous times between the second and third shot...all for bladder and urinary tract pain. For months I was on different antibiotics and they were not making the pain go away. After visiting a number of urologists, I found out that the urine cultures had all been coming back negative - showing no sign of an infection, so the antibiotics were pointless. All tests that I had run, both blood and urine came back normal. It is not standard procedure for a doctor to call you if your test results come back normal, but there was clearly something wrong, so I searched for a urologist who would believe me that I wasn't making up the pain I was in.

In August 2007, I had a cystoscopy done (they took a scope and went into the bladder to look in the bladder wall) and they concluded that I have an incurable bladder disease called Interstitial Cystitis. This is a condition where there becomes a defect in the bladder wall causing it not to have the protective mucus layer inside of it. The pictures of inside my bladder show red, raw skin, obviously showing the severity of my case of it.

There is no evidence as to what causes Interstitial Cystitis, and there is no proven successful way of treating it. The initial signs are exactly the same as a Urinary Tract Infection (painful bladder spasms, painful urination, body aches and back pain). The main difference is the fact that it is not an infection. There are thousands of people with Interstitial Cystitis who are misdiagnosed as having chronic Urinary Tract Infections.

I received my third Gardasil shot in October of 2007 and that is when EVERYTHING fell apart. The bladder pain became constant and there has not been one minute in a day since that shot I have not been in unbearable pain. This is when everything else in my body began to crash down as well. The other health problems and side effects from the Gardasil that I am having are constant sore throat, vicious migraines, vision changes, back pain, body aches, joint pain, sinus problems, vomiting, constipation, dizziness...I could keep going on forever!

I have tried all of the conventional treatment for Interstitial Cystitis and have gotten NO relief from the pain and other side effects. The doctors didn't know what to do, so they put me on OxyContin and a diet consisting of no acidic foods. That has now posed its own set of problems seeing as now my body is addicted to the narcotic, and I have gone from 5'6'' 125lbs to 100lbs over the course of a year due to the diet. I am extremely malnourished and have to take B12 vitamin shots once a week due to the severe anemia. I am 24 years old, and feel like I am 100. I can not live a normal life, I am going to lose my job from numerous absences, I lost my fiancé and am not able to have an intimate relationship anymore, I am extremely depressed, I have to have my family clean my apartment because I am too sick to do it, I can not do social activities because I am too tired and in pain. This vaccine has DESTROYED my life! I am desperately seeking out someone else who is having bladder problems due to the Gardasil so that I can contact an attorney. This needs to be OFF the market a soon as possible so that it does not run any other lives! Gardasil has caused some deaths, but in my mind, I'd rather die than live with the pain I am having. I did notice there are some posts regarding girls getting urinary tract infections... PLEASE PLEASE PLEASE have your urine cultured because there is a good chance it may be Interstitial Cystitis!

I am desperately looking for someone who is having some of these symptoms so that I can go to a lawyer and get something going before things like this happen: Numerous states are pushing to make it mandatory that girls receive the vaccine before they enter the 6th grade. We can not let this happen! We all need to stick together and somehow fight this and get out lives back!

Let me know if you are IN - and also what you thought about my post!

You can email me at ******

Bless All of You!

*~Amber~*

I am a male of 67 years old. I took Lipitor for a year, and after a few months of taking it, I felt muscle pains in my arms and shoulders, as well as my back. I felt weak and could hardly put my socks on by myself. I told my family doctor that I thought the problem was caused by LIpitor. He said it couldn't be possible, but he couldn't figure out what was wrong, so he sent me to a rheumatologist, who gave me an initial diagnosis of polymyalgia rheumatica. I went back for a checkup, and although the sed rate was normal, the C-reactive protein was elevated. He felt his diagnosis was an accurate one. He prescribed prednisone for me. I had some doubts about it, since I am diabetic, and was concerned about the elevated blood sugar it might cause. Well, it did elevate my blood sugar, and I weaned myself off it within three months. My blood sugar went back to normal, and while the prednisone helped the symptoms of muscle pain and aches, after I stopped it, the pain returned with a vengeance.

About a year passed after discontinuing the prednisone, and I felt worse and worse. Any time I engaged in physical activity, such as yard work, I was almost incapacitated for two or three days. I felt weaker and weaker, and by now, my activity is about ten per cent of what it was three or four years ago. I am unable to do anything physical without paying a heavy price.

I would tell the doctor that I felt the problem was caused by the Lipitor. He would dismiss my comments, saying that the pain should have gone away after discontinuing Lipitor. He sent me back to the rheumatologist with results of recent blood tests. Both the sed rate and C-reactive protein were normal. The rheumatologist touched my back and other areas, which caused me to jump. He said it might be fibromyalgia. I told him again that I thought it was caused by the Lipitor. He said the same thing my GP had said: if it had been the Lipitor, the pain would have gone away when I stopped taking it. I know the Lipitor caused the pain, because I tried red yeast rice for a couple months. The pain increased to almost unbearable, so I discontinued the red yeast rice. If I were not susceptible to the pain from the Lipitor, would the red yeast rice have increased the pain?

So here I am with a fuzzy diagnosis from the rheumatologist, and no clue from my family doctor (that he will verbalize, at any rate). My life has gone steadily downhill. I used to be a strong, active person, but now I can do very little, and my strength is a shadow of what it formerly was. What can I do?

I have been taking nexium for about 3 months and I decided to stop due to the development of severe pain in my heels, hip, shoulder, collar bone, and hands. Now looking for a natural way to heal my ulcers. I was told aloe vera liquid. Not sure about this so I will investagate.

I was diagnosed with Colitis just over two years ago. At the time, I was having severe symptoms and my doctor put me on 40 mg of Prednisone for 3 days, 30 mg for 3 days, 20 mg for 7 and 10mg indefinitely. The 40mg dosage caused me to not sleep at night, severe nevousness and basically feeling like I was on drugs. I felt this way until I got down to 20mg. Initially, I had swollen ankles and overall swollen feeling in my body. After I had been on this drug for more than a few months, I began to notice my hair falling out, my finger nails breaking and a severe tooth sensitivity to cold (never had this before). Over the last two years, I have been on and off of Prednisone and have had the exact same side effects each time. Right now I have been on 20mg for the last 6 months. I am meeting with my doctor this week to discuss some naturopathic solutions to get off of this horrid drug. Any one heard of using ingestible aloe vera as an alternative to Prednisone?