Aloe symptoms and conditions

I have always for years used SPF45 and never had a problem until I decided to change to SPF70 w/helioplex. I love the outdoors and needed more protection. That was a huge mistake. My whole face and neck broke out in a burning rash and ended up with a swollen eye for about 3 days. I would not recommended this product to anyone. It took a lot of aloe to get rid of the rash.

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?

Well I have been on it for about 3 weeks now.. I am taking it for depression along with Citalopram. Was put on it to give me an energy boost considering i feel tired all the time. Well the first week i could not fall asleep.. I'd lay there for 3 hours wide away!!! so the pharmacist told me to take Benadryl.. well i took that still took me awhile to fall asleep but not as long.. then was completely out like a light!!!! would sleep through my alarm!!!!But now.. I ITCH!!!!!!!! Behind the ears, back of my neck, my forearms... I'll break into little bumps on my forearms.... and also itch in between my thighs!!! So hopefully this will eventually go away!!! Have not spoke to the doctor yet about this.. The first couple weeks i felt down all the time.. but now I am feeling a lot better! so for the most part I think it is help.. besides the constant itching!!!!! I found that calamine and clear aloe have been helping some!

I've been sick for 22 days. I was told I have tonsillitis and was given Amoxicillin but did not get better. I had a cough that did not go away. I went back in and was told I had bronchitis even though I had no fever. I was given the 6 pill Z-Pak treatment - 2 pills the first day, and then 1 pill each of the next 4 days. They had me stop the Amoxicillin. Both all day yesterday and all day today I've had diarrhea. Watery and frequent. Not fun. I also have no appetite, not sure if that is from the bronchitis or the drugs. Half a serving of soup all day and I had to stop eating. I recommend the soft wipes with aloe in them, as I am very sore back there. However, I must say, if my bronchitis is gone in 2 or 3 days, then the diarrhea was worth it. I can't stand being sick any longer, and can't stand the congestion that is in my chest!!! I've only taken the Z-Pak once before, a while ago, I forget if there were side effects, but I seem to remember it worked.

While I have taken it before, I don't recall having anything but very mild side effects (maybe a little discomfort in my belly). This time, however, it is different and I am owing it to the beauty of aging. I just took the second of the three pills (and yes, I've had the three pill one before). My bronchitis is clearing but this afternoon I had really bad abdominal pain and I have a continuous headache in the back of my head, where my spinal cord ends. It is not as bad (so far) as the one I had with Biaxin (I refuse to take that). The only bright side is that it made it a really good time to join Weight Watchers because I do not have much appetite. I was able to sleep last night, at least, because my cough decreased. The verdict is still out on whether I would do this again. Problem is, I am allergic to Penicillin.

I started taking Dox. because I lost my baby.. and my doc. prescribed it to me so i wouldn't get an infection. Im only supposed to take it for ten days.. its day seven and I have this burning sensation that is on my hands.. My hands are all red where its burning me.. The odd thing is it started with my knuckles.. and now it has spread. The weird part is that Its only on the tops of my hands..
I talked to my Pharmasist.. and he said that it was a rare side effect..
I have never heard of an ANTIBODIC that would make your hands burn..
I stopped taking it because my hands are litterally on fire..
If anyone else has gone through this please tell me what you have done to get them to stop burning..
I tried Aloe.. and it worked for ten minutes.. cold water makes it worse along with hot water.. putting pressure helps for a few seconds.. the only releif that I have found is blowing cool air on them..