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I would check with the child's doctor before giving him anything.
Euphorbia Hirta is NOT a homeopathic remedy. It is a plant. You have to boil the plant leaves for a minute and drink the water.
It is supposed to stimulate PAF and produces platelets very quickly...often within 2-3 days, platelet becomes normal.
Google Euphorbia Hirta for more and see its photos.
Patti:
Suggesting that someone ask their doctor is a very acceptable response. In my opinion, it sure beats your approval. I am not against alternative treatments, but just because you say it is okay does not mean it is.
I have studied the subject. You are not the first person here to discuss homeopathy. The thing is, every single person who believes in homeopathy seems to detest doctors. The rest of us do not detest homeopathy, only the arguments it seems to spark because you think you know it all. I've been with the PDSA for 12 years and believe me, I've seen and heard it all. I do not have a problem with alternative treatment discussions and they are obviously encouraged here. I do have a problem with you telling people what to do based on your very limited experience with ITP.
I've never once had to say this, but I am the Administrator and will decide what is acceptable here and what is not.
Patti:
You are missing some key points along the way. You are stating that Bendryl should not be used for someone with ITP based on your experience. I have had two suspected platelet drops after taking Amoxicillin, but I have not discouraged any one from using it. Two reasons: 1) it may not affect them as it did me, and 2) my experience could have been a coincidence and there is no way to prove that it caused counts to drop. I would not blindly state that a certain drug could cause harm to everyone because it may have happened to me. I also would not state that Rituxan is a cure and everyone should use it because it has caused a 6 year remission for me. Am I cured? That is what you are saying with your treatment regimine; that it is a cure for ITP.
Patti:
What I really don't understand, is people who have been sick for years not even being willing to try something that might, just might, heal them. It's cheap, it's easy, it doesn't ruin the body. And yet people can just toss it aside because they don't understand it. It just blows me away. I'd be standing in line saying, "fix me, please." If it worked, I'd be praising God. If it didn't, I'd be out a couple of hundred dollars as opposed to the many thousands many of us have sucked out the window to the medical community. THAT is what I don't understand. We're all entitled to trust who we want to. But to brush off people and a mode of healing that has CURED people, is unfair to others who are still looking.
Perhaps the reason so many of us seem to misunderstand you, then, is because, in fact, you have made "broad statements here," such as each of the following:I'm not making broad statements here. I'm suggesting people use some wisdom in using a drug known (especially because it is a pre-med so often) to aggravate the very problem they're trying to treat. You seem to be missing this point.
My 10yr old DS was dx with ITP on May 6th. His platelet count was 1000 at the time. I'm not new to blood diseases so I understood all of the ramifications of that. We tried IVIG, against our better judgment, twice and it didn't work either time. We tried prednisone for 4 days and he bled like a stuck pig. We didn't check to see until after we tried it that bleeding is one of the known side effects. So we are 2 1/2 months out on a watch and wait. He's been 0-2000 for just over two weeks. We use a lot of natural stuff so his cell integrity is good and he has little to no petichaie. Everything I've read online says it can take 4-6 months to heal from this. Everyone I'm reading about here has had it for years. I'm just wondering, do you know anyone who has gotten through this????? Our son has had immune suppression since his MMR shot at 14 months. He has a TON of food allergies that we know contributed to this (also caused by shots). We are slowly getting his immune system into check. I wonder, will this go away? Right now, he does live somewhat in a bubble because he is so low. Around 10k we let him walk around more and not be down much. I guess I'm just wanting to hear of anyone's child his age that actually got over this thing.
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