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Post by Baraka Obam on Oct 12, 2012 23:05:24 GMT -5
This is what most people imagine when they think of leprosy, but there is quite a range of affliction, some is not noticable.
In fact people will manifest issues much quicker because of poor health and eating habits.
So lets say a person from a good home would not show all this fingers and toes falling off.
We have alot going on with our hands and arms legs and feet, same as the lepers.
I also saw a leper colony movie and one of the men had the deep lines in the skin, just like many here including me have spoken about.
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Post by itchin4answers on Nov 2, 2012 2:19:48 GMT -5
Bonnie treated and transformedOctober 31, 2012, 6:18 pm Mark Gibson Today Tonight Bonnie Burns, a young woman struck down by Lyme disease after being bitten by a tick, was forced to seek treatment overseas, like so many other Australians. tinyurl.com/bwy3penIt is a great story, especially to see young Bonnie looking so much better. The other lady in the story looks so very ill and it is heart breaking because I know exactly how she feels. My resent grows stronger by the day for the Australian Government and the medical profession, actually it is HATRED. No person should be put in a position of being denied health care. Baraka, you will find this story interesting regarding Bonnie's treatment - "Ozone" is involved. Thank you itchin.
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Post by Baraka Obam on Nov 2, 2012 10:10:13 GMT -5
I was thinking about doing this ozone of the blood in Thailand, there is one problem with the idea for me. The fact of the matter is they treat alot of HIV and AIDS patients with this machine, the problem is, I really have to wonder how safe it is after treating a person with these issues. It supposedly is like dialysis, I posted the treatment on MDR years ago. www.o3center.org/Clinics/WorldWide/Thailand.htmlau.news.yahoo.com/today-tonight/health/article/-/15267188/bonnie-treated-and-transformedI do not know how actually the machines work still there is always some sort of risk when blood is taken out and re infused into the body. There is also a site that is saying this form of therapy kills, the people that searched this form of treatment and died in their list mostly had cancer. Then you have to also imagine how many people die after the first treatment of Chemo therapy. I knew a 32 year old man that this happened to. Here is the site of the deaths, seems quite small com paired to the 50,000 doctors in America kill every year from negligence and drugs. When you look at that woman's change after ozone therapy it seems litter ally amazing. whatstheharm.net/ozonetherapy.htmlThanks Itchin!
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Post by itchin4answers on Nov 23, 2012 0:27:01 GMT -5
Hi Folks,
There is a Lyme Protest happening right NOW as I type in Brisbane Queensland. My friend, sheredelight is there and I know she will give it all she's got, go girl friend!!!
I will be back with any further updates.
Thank you itchin
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Post by itchin4answers on Nov 24, 2012 22:52:39 GMT -5
Hi folks, Me again, have to make this quick only 10 min internet at the library today. I have NO news to report on the rally, sorry. Apparently, this is via an sms from sheredelight, there was NO TV media at the rally. What a surprise As for how I'm doing - my liver function tests were through the roof. I may have to slow my treatment down, still waiting word from the doctor. Helllooooo doctor I'm a waiting.... Anyway, must fly, miss my internet soo much coz I get lonely. Love you all itchin
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Post by Baraka Obam on Nov 25, 2012 8:36:22 GMT -5
Hello Itchin, what treatment are you doing?
Be very careful of treatments by doctors that send your readings through the roof, some times, many times they cause more harm than good.
I am personally dealing with just such a case right now, a lifelong friend did the new treatment for hep C.
His platelets took a hike, twice now
His stomach swelled to a huge size and now he has a baseball size growth and growing on his liver.
The doctors will tell you the good, they seldom tell you the risks.
This fellow was doing just fine before this, now he can barley walk and moans all day and all night.
The doctors suggest all this stupidity to a person operating at 80% and now he does not operate at all, its sleeping, blood transfusions and hospital stays for him.
I am not trying to scare anyone, it was just such thoughtless thing to do, the risks not worth the reward, this man would continue taking treatment untill he died on the doctors mouthing what he assumes.
Be careful, we are no more then test subjects to these white coat killers.
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Post by itchin4answers on Nov 25, 2012 20:12:21 GMT -5
Hello Itchin, what treatment are you doing? Be very careful of treatments by doctors that send your readings through the roof, some times, many times they cause more harm than good. I am personally dealing with just such a case right now, a lifelong friend did the new treatment for hep C. His platelets took a hike, twice now His stomach swelled to a huge size and now he has a baseball size growth and growing on his liver. The doctors will tell you the good, they seldom tell you the risks. This fellow was doing just fine before this, now he can barley walk and moans all day and all night. The doctors suggest all this stupidity to a person operating at 80% and now he does not operate at all, its sleeping, blood transfusions and hospital stays for him. I am not trying to scare anyone, it was just such thoughtless thing to do, the risks not worth the reward, this man would continue taking treatment untill he died on the doctors mouthing what he assumes. Be careful, we are no more then test subjects to these white coat killers. Hi Baraka, Thank you for sharing about your friend, that is truly terrible to hear and I can only imagine how you must feel to witness this happening. You make a VERY valid point. I will first say I am grateful to have a Lyme doctor (even if he is interstate) that BELIEVES me. In saying that, yes I totally agree with you that at times the treatment can kill. I experienced that in 2006 having IV treatment and the doctor back then admitted I was dying, so perhaps we stop the IV!! Ok, my current treatment for BARTONELLA HENSELAE is Rifampicin 600mg a day. Doxycycline 4 tablets a day (I think they are 100mg tablets) and I know that the 4 tablets a day is the highest dose. Also Plaquenil 1/2 a tablet twice a day. A friend of mine is about 7 weeks ahead of me with treatment, he weighs 105kg and he struggled. I am around 56kg - so I'm almost taking an elephant dose. Things have got rather confusing and I did say on another thread about menopause. Well I borrowed a book from the Library and bingo I have been perimenopausal for years. The white coat killers chose ANTIPSYCHOTIC injections via a court order for me. Didn't believe in LYME and they sure DID NOT BELIEVE IN MY HORMONES. These ding bats all suffer from "the world is flat syndrome". I mean, how would it be to pull a big fat pay cheque every week and all you've done is confuse the public (patients) and contributed to destroying peoples lives!! That is how I see it, because that is exactly what has happened to me. So, yeah as I was saying perimenopausal for years, and I was passed off as a nut case, AS WELL as having Lyme and our good friend Morgellons!!!! So I'm here - change of life, and boy I'm HOT and not as in sexy...LOL and my sleep well I'm thumping myself with Endep (antidepressant) for sleep issues, but then I wake 4 hours later walking the house all hot and bothered popping Valium in a desperate attempt for more sleep. One becomes obsessed with sleep (naturally) when sleep is very disturbed. I will endeavour to find a clinic that deals with Women's health as my GP was less than sympathetic and said "you're lacking Oestrogen, basically no big deal"...huh?... Thanks for listening. itchin
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Post by itchin4answers on Nov 27, 2012 17:23:18 GMT -5
Here it is!!! the video from the Lyme Disease Protest Brisbane.
QLD's FIRST LYME DISEASE PROTEST - NOV 2012- BRISBANE- BEC MILLS
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Post by Lynn on Nov 27, 2012 23:22:55 GMT -5
Hi Itchen
I watched the video earlier today and then had to run and wanted to try and finish it but want to thank you for posting this. Hope it gets more recruits or positive action with the medical community.
In Light Lynn/TorpedoLynn
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Post by itchin4answers on Nov 28, 2012 18:14:18 GMT -5
Hi Itchen I watched the video earlier today and then had to run and wanted to try and finish it but want to thank you for posting this. Hope it gets more recruits or positive action with the medical community. In Light Lynn/TorpedoLynn Hi Lynn, When I posted the video I'd only watched the first 5 minutes and had to run to an appointment. I watched it all in full last night, came down to the Library after tea. I had to hold my tears back. The video is excellent, the cold hard truth and when I get a moment I will try to find out who the heck the CDA or whatever they call themselves are. I reckon the Government are making up new "bodies" of so called people to keep fobbing us off. Dr Ladhams, what an absolute gentleman, my friends Lyme doctor and he is getting her well! I so wish other doctors Australia wide jump on board, please doctors you have too because I would hate to see this happen to your child. Thanks itchin
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Post by itchin4answers on Nov 28, 2012 18:54:57 GMT -5
Hi Itchen I watched the video earlier today and then had to run and wanted to try and finish it but want to thank you for posting this. Hope it gets more recruits or positive action with the medical community. In Light Lynn/TorpedoLynn Hi Lynn, When I posted the video I'd only watched the first 5 minutes and had to run to an appointment. I watched it all in full last night, came down to the Library after tea. I had to hold my tears back. The video is excellent, the cold hard truth and when I get a moment I will try to find out who the heck the CDA or whatever they call themselves are. I reckon the Government are making up new "bodies" of so called people to keep fobbing us off. Dr Ladhams, what an absolute gentleman, my friends Lyme doctor and he is getting her well! I so wish other doctors Australia wide jump on board, please doctors you have too because I would hate to see this happen to your child. Thanks itchin This is the only CDA I could find in Google. www.cda.org.au/aboutI would think one shouldn't have to research too hard if this "CDA" that is mentioned on the Lyme video are such a powerful group of people. So in saying what I just said this link may possibly have NOTHING to do with LYME. Hope I haven't confused anyone there and I would welcome someone else doing a search for "CDA and Queensland (Brisbane) and Government". Cheers itchin
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Post by Lynn on Nov 28, 2012 20:08:46 GMT -5
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Post by itchin4answers on Nov 28, 2012 23:56:41 GMT -5
Hi Lynn,
Thank's a bunch for finding that.
I'm not feeling very happy right now, was having a good day up until my GP appointment. My Lyme doctor is not concerned with my Liver function levels, he wants me tested for Hep B & C. Immunised againist Hep B back in the 90's working in the Hospital. As for Hep C, oh dear, sexually transmittable. I am concerned to say the least.
itchin
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Post by itchin4answers on Dec 3, 2012 2:49:22 GMT -5
I would like to share my good news, I do not have hepatitis B or C. The GP said it is the treatment effecting my liver. Not sure what will happen from here. I did tweak the medication prior to my blood tests and my liver function had normalised.
I was right about my hormones too, good thing someone is consistent - ME! - HRT here I come and NO doctor is going to screw this one up. I've suffered way too long due to their neglect and mismanagement.
Thanks itchin
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Post by Lynn on Dec 3, 2012 10:48:41 GMT -5
Hi Itchen
Glad they found out part of what is wrong. Hope you get well from that.
In Light Lynn/TorpedoLynn
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Post by itchin4answers on Dec 4, 2012 18:33:56 GMT -5
I just wanted to share a quick note I sent off to the Communicable Diseases Network. I will blame my girlfriend for getting me all worked up! I personally believe the more we post on the internet the lack of support from the Government and their replies the more people will see no one gives a shite! If I could withdraw my tax file number and never pay tax again I damn well would!! ----------------------------------------------------------------------------------- To whom it may concern; When are you going to recognise Lyme disease? PLEASE do NOT palm me off with the old "The Department of Health and Ageing is aware that some patients in Australia have developed symptoms that are similar to those of Lyme disease". I am very interested what the Government means by "similar to Lyme". I am positive for Lyme disease, which I contracted in 1987 on the NSW Coast whilst holidaying in Merimbula. I am now late stage Lyme and am only 44 years of age. I have co-infections of Mycoplasma Fermentans, Bartonella and Rickettsia. I probably have more co-infections though my lack of finance, due to being on Disability 10years, prevents me from being tested and treated for further co-infections. PLEASE do NOT refer me to the NSW Health Department Website. I have written to the Department of Health and Aggravation since 2008 as well as the Department of Health Protection. I think I can quite comfortably say the Government has not protected the citizens of Australia from infectious disease. My treating Lyme doctor is interstate and it is very difficult for my General Practitioner to support me in my treatment as her words are "I know nothing about Lyme disease"....NOW whose fault is that? I believe the blame is in the lap of the Government and it is high time someone did something. Recognition of Lyme disease is long over due. Once again thousands and thousands of people around Australia will spend Christmas 2012 alone because this useless health system has passed them off as crazy and no one, not even family wants to know them. How would you feel if that were you? I await your urgent reply. With thanks,
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Post by itchin4answers on Dec 4, 2012 18:38:21 GMT -5
Oh look - auto reply - my email address must be red flagged
------------------------------------------------------------------------------
Thank you for your enquiry, the appropriate area of the Department will respond as soon as possible.
Please note that while we endeavour to respond rapidly, complex enquiries may take several weeks for a response.
If you believe your enquiry has taken too long for a response, please contact us through one of the following channels:
Email: enquiries@health.gov.au, or Call: (Australia) 02 6289 5448
Best regards, Department of Health and Ageing
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Post by sheredelight on Dec 5, 2012 20:29:23 GMT -5
Hi itchen,
Very well said, hope they get back to you soon, think I know what they will say.....so sad...I will keep mailing them also, just not today, headache and tired....
Hope you have a good weekend...
Hugs xo
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Post by itchin4answers on Dec 6, 2012 3:09:13 GMT -5
Hi itchen, Very well said, hope they get back to you soon, think I know what they will say.....so sad...I will keep mailing them also, just not today, headache and tired.... Hope you have a good weekend... Hugs xo Hi sheredelight, I'm not bothered if they don't get back to me. The drug companies have got them by the balls and they ain't got the balls to admit it. WE KNOW so stop pissing around, simple. Monster head this morning, pain pills first thing in my gob and then I cry. Back home in the guinea pig wheel I'm given a free sample herbal hormone supplement, oh great - they could work in 8 weeks, that's if I haven't jumped off a cliff, or had a road rage incident. If I stick to maybe meditation 24/7 I could possibly achieve what the doctors think is going on. Honestly, they do not see they are the smiling asassins. Have a lovely weekend sis. Love you itchin
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Post by itchin4answers on Mar 12, 2013 22:00:53 GMT -5
I recently had a SPEC scan of my brain - I think it was the 22nd February. I still don't have my results. Seems my doctor is busy, everyone is busy, though I do matter and I will try again today to contact him. I'm not going to wait on hold for 25 minutes like yesterday, because my phone bill (or should I say) my bank account won't allow big phone bills!
After having a chat to a Lyme girlfriend yesterday I wanted to bring up something that she mentioned to me. I then realised that what I have is the same and I want to know if anyone else has the same issue.
About 6 months ago I could feel and see blackish BRUISES on the backs on my lower calves. These bruises are still there, and if I touch them they kinda feel like a bruise too.
Not so long ago, sat outside in this heatwave I rubbed a bit of coconut oil on these bruises and black specks came out. My girlfriend said these bruises could be like a nest of the Myasis.
As for the medication I've been on for the treatment of Bartonella, the Rifampicin is hard going. After having a flu like illness around the time of my SPEC scan I've had terrible kidney pain and I want to ditch all the pills, feels like they are killing me.
Our inner voice just knows sometimes huh.
Thanks itchin
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