Information On Hedge Apple For Cancer Treatment?
Dec 4, 2013
I’m trying to find any information about Hedge apple use for treating cancer patients. So far it's really hard to decide whether to try this or not mainly because most information I found were more focused on discussing if you can eat the plant or not, then on the issue of it being used for treating cancer. Basically it seems like it wouldn't do any harm to try this, but I don't know how long or even how should Hedge apple be used for cancer treatment. Some people say they just eat it, but also, I didn't see any rel info on how effective this plant be in either preventing remissions (which I hope), or cancer.
Please, if anyone has any info on Hedge apple use for cancer treatment, especially breast cancer treatment, share.
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I am a 19 year old male in the u.s. who has had molluscum contagiosum for a couple of years. i have not sought treatment because like many of you, doctors had told me that they would go away (not to mention they didn't even tell me what the bumps were or that they were contagious) they haven't gone away on their own and today i decided to take matters into my own hands
From what i found on the web it seems that putting some apple cider vinegar on the skin will help, as this is the easiest and cheapest treatment i am going to give this a try and keep you updated on whether or not this works.
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As far as I know, there is not ETD cure, yet. I am interested in finding one. I am a Caucasian 34 year old man living in Santa Clara, CA. I have a BA in Psychology and work in a Neuroscience Lab. I was diagnosed with ETD a year ago. I have been suffering from it for 17 years. 13 years ago I had a bought of Bulimia that lasted for about a year. I had Anorexia Nervosa as an adolescent. I was given the maximum dose of testosterone to boost me through puberty since Anorexia was preventing it. Soon after I abused alcohol, marijuana, tobacco, and various other drugs until 2005. I believe all these factors have contributed to my ETD. I was diagnosed with OCD and Generalized Anxiety Disorder two years ago and have been taking Effexor (Venlafaxine) to cope. An Ear, Nose, Throat doctor (currently called Head and Neck surgeon in US) prescribed me Flunisolide (corticosteroid) to reduce ETD inflammation. It seems to help a little, but it is certainly not a cure, even when used for a significant period of time (i.e. 3 weeks).
My ETD has been recently aggravated by my attempts to remove pimples and skin tags, which may be a symptom of OCD. Has anyone else experienced this situation? Numerous doctors say there is no connection between the skin abrasions and ETD, but they obviously don't have ETD.
Primarily, I am asking for information regarding ETD. I need to know the statistics of ETD so that I can develop a valid research proposal. Health organizations neglect to respond to my questions. It seems that most biological research is involved in diseases such as cancer and heart disease, which is great. But, as I am sure that anyone reading this knows, Eustachian Tube Dysfunction is a debilitating disease that hinders one's ability to live to their fullest potential. As I have recently graduated with a Bachelors degree. I am researching what my next step will be. I am strongly leaning towards statistics and data mining, since that is a much needed position in all research fields.
I am looking for information on the number of people with ETD worldwide and specific to certain regions. A timeline of ETD cases in these regions. Research groups, Academic and Professional, that are researching ETD. Research groups that are investigating ETD from the Neuroscience and/or Ear, Nose, Throat (Head and Neck surgery) perspective. Any other information is helpful as well, especially your own personal accounts of ETD. Please share your history, as much as you care to disclose, so that I can begin to develop an etiology of ETD.
I have read many of the other discussions on ETD and recognize that many of you are suffering and I certainly empathize with you all. I am still trying to decide if my anxiety disorders are the result of ETD, my ETD the result of my anxiety disorders, if they are mutually intertwined, and/or if something else is going on. I very much hope to hear from you so that we may begin to develop a cure for ETD so that we may not be hindered by this ruthless malfunction.
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I have just been copied in on a letter from the Consultant Urologist to my GP giving an update on the appointment I attended following an MRI.
it says:- "Mr "Sailor Sam" was reviewed today. He is a known case of prostate cancer on active surveillance. His PSA has been slowly creeping up suggesting that he is progressing on a biochemical level. In view of this , radical treatment was discussed but "Sailor Sam" is not keen on this for fear of side-effects. His preference is to continue with active surveillance and therefore he will be seen in clinic in 3 months time"
Now on the letter it says Diagnosis:- Gleason 6 adenocarcinoma of the prostate diagnosed in 2012. Latest PSA 3.3
MRI Scan shows T2 N0 - prostate cancer in 43cc prostate gland.
Staging is small volume. A small low signal foucs at the junction of peripheral and transitional zones on the left lateral aspect at the base does show restricted diffusion and is likely to represent a small focus of prostate carcinoma. It is organ defined. No further focus suspicious for prostate carinoma. The seminal vesicles show normal appearance.
The MDT 17.9.15 concensus of opinion - OFFER RADICAL TREATMENT.
So what I would like to hear is what people think about this? My Psa resutls have been May 2013 2.4
Aug 2013 1.5
Mar 2014 1.7
Aug 2014 1.7
Jul 2015 3.2
Sep 201 3.3
I know there are some very knowledgeable people on this site but am I missing something? Offering radical treatment to a 52 year old man with this history? Is that right? I am a Mental Health Nurse myself and work as part of a Multi-Disciplinary Team which is why I am having trouble coming to terms with their conclusion.
Could I ask for the MDT decision to be reviewed by a different MDT? would it make a difference?
Or are they the "experts" who arrive at this decision following a certain protocol. Not sure if there are any NICE guidelines for offering treatment for example.
I know I will need treatment and I recognise we are lucky that we live in a society that has a health service that can help us so much, but is this a case of over-treatment which I've come to hear more and more about
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I received my PSA blood test score today of 1.5. This is 14 months after Proton Treatment at Loma Linda. My Gleason score was 4+3 seven. My highest PSA pre treatment was 8.0
I had great numbers my first two tests.
!.3 after three months and six months later it was 0.50 in July of this year. I was not planning another PSA test until January but my GP did one as part of a normal physical. Was expecting a number lower than 0.50.
Appreciate any feedback. I know its the trend that counts, not one individual test but still it is disconcerting to not see a drop and even more disconcerting to see this significant an increase.
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I just had a kidney scan and this time they scanned my bladder as well. The Scanner man asked me was i taking hormones for my prostrate, i said no as i was not. I had a very full bladder at the time, thought i would throw that in. I gets home and Googled hormones and prostate and it said it was a treatment for early stages of prostate cancer ....
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How long after a stage 0 lumpectomy , can you wait befor you receive Radiation treatments !! mine is held up due to my HMO Ins. I didnt need Chemotherapy!
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I've recently started suffering from a series of sore throats and tongue Ulcers. This is strange, as I am healthy mid 20's male - i run 4/5 times a week, i have a very healthy diet, and I don't smoke, drink, or do drugs. It got worse last week when i developed a little under 30 ulcers on my tongue, and had an exceptionally sore throat. It died away almost as soon as it started, some 24 hours later. I went to the doctor, but beyond the usual reasons (stress, stopping smoking, acidic food) he could think of no reason for them.This afternoon, I had a drink of apple juice, and within 10 minutes, my throat was closing and felt really sore. It occurred to me that over the past two weeks, I could link all of my outbreaks/worst days to days when i had drunk fresh fruit juice that may have contained apple juice - I usually drink a fruit juice with two or three fruits in it, and they use apple juice to thin the mix of pulpier fruits (such as mango, banana, papaya etc), or to make juice go further (cranberry, raspberry or pomegranate for example). I think i'm fine with orange based fruit drinks, or at least i don't recall Is it possible to be allergic to apple juice?
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I had a sudden swollen lymph node under my right side of my neck near my adam's apple. you can see its swollen to look at and is about the size of a cream egg it gets really painful sometimes when i eat especially crisps and things what make my tastebuds go, i have been on antibiotics for 3 days now but it only seems to feels painless when im sleeping but as soon as i eat swallow talk throughout the day it becomes more painful, i do feel run down some days and iv'e been taking co codamol for the pain as antibiotics don't take away the pain, iv'e just started to have cramps in my stomach this morning and diarrhea which maybe because of the tablets iv'e been taking. but im worried that the lymph node is never going to go down as it feels constant in my neck and i get the odd twinge around the area in pain and am just worried, could anyone give me an insight of when i should see my gp again if this doesn't die down in the coming days please?
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I have just found a pea size lump above my adams apple, it doesn't hurt and I can move it. I have never noticed this before and I'm really worried. I can't get a doctors appointment for nearly 2 weeks so am really worrying now. I'm only 20 but do smoke.
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I would like to know if Apple Cider Vinegar is good for you and what it's good for. Also Pure Aloe Vera juice. Is it good for you and what is it good for?
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I'm looking for advice. My 60 year old father (who has had HCV for more than 10 years; previously treated with Interferon but bad side effects) finished his 12 week Sofosbuvir+Daclatasvir (considered same as Harvoni) treatment a month ago. Already first tests after 2 weeks showed virus was Undetected, but yesterday he received his most recent results and he has a relapse of the virus. He is genotype 1, fibroscan result 4 (close to final stage). He is based in Poland and I'm not sure if our doctors are fully informed of the new generation medications and HCV itself.
Is anyone able to give us any advice? We are pretty desperate and my dad is just so depressed as he thought he finally got rid of the virus (he got infected while on an operation in a public hospital) and now it is back...
Are there any specialists that you are aware of I could possibly get in contact with?
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A few weeks ago my bf noticed some bumps in his pubic area. He went to the dermatologist and was diagnosed with molluscum contagiosum, which is thankfully not that big of a deal! He got his treated with cryotherapy. Around this time I noticed a few bumps and because of the area they were in, went to an OBGYN for treatment so my bf and I don't keep spreading it to each other. The OB GYN agreed that they were also MC bumps and lightly scraped each one, then applied an acid treatment. That was a few days ago and while the bumps are mostly gone, the skin surrounding each one is dark and almost looks like a scab in color. Is this normal post acid treatment?
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Does anyone here relapse after harvoni treatment?
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I and other volunteers see a lot of posts regarding symptoms after an exposure. Some are minor such as a rash or a swollen node to "HIV like" such as a cluster of fever, sore throat, sores and body aches. Keep this in mind that as humans we are covered or exposed to germs, common viruses, and fungus which we all carry. This is called the "the biome" which is the invisible part of our environment. When we have sexual contact with somebody or their body fluids we expose each other to these organisms and our body reacts accordingly to fend off these invaders sometimes making us feel ill or display manifestations of symptoms. Stress and anxiety post exposure contribute to this since chronic stress decreases the immune system and makes us more susceptible to common infections. But what about the rashes? One may ask. Stress and anxiety causes the "fight or flight" response in our bodies causing release of cortisol which causes itchy rashes on the skin. Cortisol rashes are also called "hives" can be be similar to rashes found in STDs and can be frightening when they occur, (Ive been there). Allergic reactions also play a part. Also, sometimes the timing of exposure and illness is purely coincedental. Finally, if you have had a high risk exposure- when in doubt, test out.
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I was on Nortriptyline for a year for migraine prevention. I found it was making me extremely tired and my heart race. I unfortunately stopped it two weeks ago abruptly. Does anyone know how long withdrawal symptoms last for. Still feel jumpy, brain zaps, insomnia and headache.
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I had a doctor appointment today and I tested over so I might have gestational diabetes I have to go into another clinic to get a 3 hour test for it..it makes me nervous but my mom is a nurse and says you mainly just have to maintain your sugar levels...does anyone have information on gestational diabetes?
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I am in a bit of a quandary is there anyone out there that has had their prostrate removed with the use of a robotic arm,I need to find out as much information as possible as I am thinking this may be the lesser of the two evils that they say I need. I would like to find out everything about the op and how it impacts on your life after, how long does it take to heal, how long do you wear a bag, how long before you can have sex or is that part of your life just a memory
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Anyone out there have any information on central pontine myelinolysis , my 26yr old son has been diagnosed with this condition. He has been in hospital for 6 weeks and spent the last 4 weeks in intensive care, he went into hospital on Christmas eve after having seizures to do with alcohol withdrawal the first couple of days he was doing fine then things started to go wrong. He started to loose his balance he started slurring his speech and was getting very confused. He then lost his ability to swallow then started to slip into a coma at which point intensive care induced him into a coma and we were told not to expect him to survive. A week later he started to come round and could breath for himself but could only use his eyes,3 weeks later and he can communicate by blinking his eyes can squeeze my hand with both hands can wiggle his toes and can understand everything we say to him. We know we have a long way to go and don't know what the long term recovery is but would be grateful for any info from anyone who has come through this condition.
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Just wondered if anyone has had these injections, can't seem to find out any information about them. Already had tvt surgery which was unsuccessful so really want more information before I have another procedure.
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I am looking to have a left flat foot reconstruction in The Fall of 2014 at HSS.
I am trying to get as much information as I can in regards to making the right decision. Currently I can still exercise but have pain when walking a distance or being on my feet all day. Also my foot is starting to turn in and affecting my knee.
I want to hear how did you know when it was time for you to get this surgery done. How bad was your foot before you considered this surgery. Could you walk at in orthotics without pain or were you in constant pain all the time.
From what I hear this is a horrible surgery and I don't want to be worse off than I am now. I have already had 4 opinions with different OS and they all recommend close to the same thing just different ways of doing it.
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