TESTIMONI DARI PENGGUNA TRANFER FACTOR 4 LIFE.

TESTIMONI DARI PENGGUNA TRANFER FACTOR 4 LIFE.

Hari ini baru lah saya berani untuk berkongsi testimonial saya pada anda semua kerana saya benar2 yakin semput saya 99% sembuh Alhamdulillah

Nama saya Jamilah Abdollah berusia 38 tahun. Saya ingin berkongsi dengan anda semua kerana ini mungkin boleh dijadikan contoh pada kawan2 anda yang masih belum yakin dengan Tranfer Factor dimana ia dapat membantu dari segi kesihatan dan juga FINANCIAL PROBLEM.

Selama 27 tahun saya menderita penyakit semput bole dikata cronic kerana dalam masa 1 bulan hampir 2 atau 3 kali saya harus berjumpa dengan Dr Chan (Family Dr since my age of 11yrs old). Dari umur saya 11 tahun sehingga lah umur saya 38 tahun masih berjumpa dengan Dr Chan untuk mengambil ubat semput ia itu 2 type of tablet ( Dhasolone & Zenmolin ) dan 2 type of spray ( Ventolin Evohaler & Clenil ). Spray harus digunakan 4x sehari dan ubat 2 tablets each hampir setiap hari. Kadang-kala saya harus ke hospital untuk mendapatkan oxigen dan injection and sometime kena warded. Ubat2 ini ada side effect nya 1st tangan saya tak kuat dan ia sentiasa menggigil dan dejupan jantung laju. Apabila diserang semput saya selalu stress , marah2 & sakit kepala sehinggakan urat2 dikepala timbul.

Dalam masa 10 tahun saya mencuba bermacam-macam produk dari yang mahal sehinggalah yang murah tetapi belum ada satupun yang dapat membantu semput saya sehingga lah 5 bulan yang lepas suami saya Shafie telah berjumpa dengan Rosli (my upline) dimana beliau telah mengenalkan tentang Tranfer Factor. Dengan saranan Rosli saya telah mengambil 18 biji for 3 days ( 6 biji sehari ) dan sehingga hari ini semput saya belum attack Alhamdulillah. Saya sudah dapat naik tangga sehingga 4 tingkat , cycling , makan pulut dengan air coke (favorite food & drink) kalau dulu pantang kena sikit aje semput dan berat badan saya bertambah seimbang dengan height saya dan makan lebih selera. Saya bersykur pada Allah kerana akhirnya telah dimakbulkan doa saya.

Now daily taking 1 advance or plus & 1 cardio

Disini sebagai iktibar jangan sekali-kali kita putus asa kerana setiap doa dan usaha yang kita lakukan , lambat atau cepat pasti akan dikurniakan dan yang penting YAKIN akan apa yang kita minta dan buat.

Saya Ab Karim dari Johor. Saya juga mengalami asthma bronchitis lebih kurang 5 tahun dulu, mungkin kerana umur saya dah melebihi 52 tahun. Saya mencuba dua benda, iaitu TF advance 2 biji sehari dan juga preventive spray of Symbicort Turbohaler (sekali spray pagi dan sekali petang), sejak 6 bulan dulu. Setakat ini saya tidak pernah diserang asthma lagi. Saya telah mencadangkan kepada beberapa kawan yang mengalami kesulitan yang sama, dan telah nampak kesan positif nya.Saya telah mendaftar sebagai pengedar 4life TF sejak 5 bulan dulu, tetapi belum diamond lagi.Namun begitu saya akan teruskan, sebagai pengedar, atau lebih sebagai pembekal kepada kawan2 yang tak nak jadi pengedar lagi. Saya menjual pada harga pengedar sahaja kerana nak tolong kawan2 agar sihat. Walaupun begitu secara keseluruhan saya dapatlah RM500 – 600 sebulan dari usaha minimum saya tu. Pengalaman yang saya dapat dari kawan2 yang telah lebih sihat ini saya gunakan untuk mencuba mengedar kepada pelanggan baru. Nampaknya kesan positif yang paling ketara bila menggunakan 4life TF ialah bagi orang2 tua (50-60 tahun, wanita yang sering sakit belakang dan lutut). Terdapat beberapa pak cik dan mak cik yang tak lupa telepon saya setiap kali duit pencen keluar, untuk membuat order bagi bulan berikutnya. Untuk mempastikan saya ada stok setiap kali mereka call, saya order 12 TF for the price of 10, every time, jadi dah ada untung 2 botol. Dan commision nanti adalah dalam RM400.Biasa nya pelanggan tetap saya ni akan beli 16 – 24 botol sebulan, jadi walaupun saya jual pada harga pengedar, saya masih dapat pocket money yang agak lumayan. Downline saya tak banyak, dan kurang active, kerana saya sendiri tak begitu active. Anyway kalau ada sesiapa yang mempunyai pengalaman seperti ini harap dapat kita kongsi bersama.

Anak saya berumur 11 tahun, hari pertama terkena demam campak, bintikbintik keluar di seluruh badan.
Dia merengek dan tidak mahu makan. Saya beri dia 3 biji TF pada hari itu. Hari kedua, dia ada selera makan,
tak merengek lagi, bintik makin banyak… Hari ketiga bintik-bintik kurang, dia ceria macam biasa. Hari ke-empat,
kulit dia licin macam sediakala. Semua jiran saya pelik!
Anak-anak mereka baik selepas satu minggu kena demam campak. Terimakasih Winners4Life dan TF!
– Abdul Jalil, Kulai,JOHOR

TF Hebat!! Pesakit wanita yang menghidap “mild cerebral palsy” mengadu
batuk dan selsema lebih dari 3 bulan, tidak berhasil dengan berbagai
ubatan, tetapi sembuh dalam masa 2 hari dengan hanya 2 biji TF dua kali
sehari. – Doktor Sani, Klinik Adham, Kota Tinggi –
Saya hidap semput sejak 4 tahun lalu. Alhamdulillah, selepas 2 bulan
mengambil TF anjuran Winners4Life, saya bertambah sihat, dapat tidur
malam, dan kurang terkena serangan. – Pn Ah’Esah Ahmad – Jelapang
Road, Singapura

Anak saya, kalau datang bulan, akan kena senggugut teruk sehingga
menangis kesakitan! Sejak makan TF, senggugut tak pernah datang lagi.
Thank you Winners! – Halida, TNB Batu Pahat –
Saya mengidap sakit lumpuh sejak 2 bulan lalu. Dan sebelah anggota
badan tak dapat bergerak. Setelah mengambil TFAdv selama 4 hari sahaja,
5 biji siang, 5 biji malam, saya sudah boleh bergerak dan beransur pulih.
Alhamdulillah. Terima kasih En Nawi dan Winners4Life. Hussein
Deraman – Kuantan Pahang.

Ibu saya mengalami kencing manis selama 15 tahun, dan berada dalam
keadaan yang teruk. Jari-jari tangannya hampir reput dan menanah. Setelah
mengambil TF selama 5 hari, keadaannya telah pulih dengan begitu ketara,
dan kadar gula kembali normal. Dalam 2 minggu, infeksi dan penanahan
menjadi kering. Terima kasih En Akram dan En Zul dari Winners4Life
kerana mengenalkan produk ini kepada saya. Daripada Ahmad Rodzi, Alor
Star.

Pesakit wanita mengidap penyakit jangkitan kulat (keputihan vagina)
selama 6 bulan dan telah dirawat oleh 3 doktor pakar sakit puan, tetapi tidak
berhasil. Selepas mengambil 2 dose TF, 2 biji sehari, keputihannya terus
“clear!” – Daripada Dr Sani, Klinik Adham Kota Tinggi –
Saya amat terkejut dan bersyukur kerana masaalah penyakit “degupan
jantung” saya kembali normal walau baru saja mengambil 4 biji TF
Advanced selama 2 hari. Terima kasih Winners4Life! – Wan Fuziah, JB

Lelaki umur 40 tahun, kena penyakit TB infeksi tenosynovitis hingga kaki
kanannya hampir lumpuh. Setelah saya berikan TF sebanyak 4 biji sehari,
keadaannya pulih selepas 2 hari. Daripada Dr Sani, Klinik Adham Kota
Tinggi –

Lebih 10 tahun saya tidak dapat hamil dan juga sakit thyroid. Tempoh
hari saya diserang demam selsema dan ibu beri saya 10 biji TF. Dalam 2
hari, sakit saya reda, dan selepas 2 bulan, doktor sahkan saya sudah hamil.
Saya cukup gembira. Alhamdulillah. Terima kasih Winners4Life.
Daripada Puan Fazilah, Tampines Singapore,
Sertailah Winner4Life, untuk sama-sama menyebarkan “Transfer Factor” yang juga dikenali sebagai “Molekul Ajaib”. Insyaallah mujarab, maju & berkat.
Selama lebih 10 tahun saya mengidapi migraine yang kronik! Awal
Februari lalu, saya mencuba TF 2 biji pagi dan 2 bji malam. Selepas 3 hari
sahaja, migraine saya terus hilang! Alhamdulillah, dan thank you
Winners4Life! Pn Jamilah, Kulai, Johor –

Sejak mengambil TF, saya telah dapat semula deria bau saya yang hilang
sejak 4 tahun lalu akibat kemalangan jalanraya yang teruk. Saya telah
berbelanja hampir RM50,000 untuk rawatan. TF telah bantu saya bebas
dari bengkak dan infeksi di mata kiri saya sejak kemalangan dulu. TF
banyak membantu saya dapat kembali kekurangan yang saya alami sejak 4
tahun dulu. Terima kasih Transfer Factor dan Winners4Life. Cikgu
Zainordin, Benut, Johor -

Leader Nutrimetic menalifon dan memberitahu saya dia rasa puashati
dengan TF. Dengan hanya 2 biji sahaja, masaalah sakit urat yang dia
hidapi sejak 5 tahun, telah settle. Dia akan join bila balik dari KL nanti.
Chegu Zul, Alor Star –

Kawan saya mengalami sakit lutut hampir 2 tahun. Pelbagai ubat yang
telah doktor berikan, namun tidak dapat menyembuhkan sakit lututnya.
Setelah mengambil TF 2 biji pagi dan 2 biji malam, keadaan lutut kawan
saya telah baik seperti sediakala. Terima kasih En Zul dan Akram Din dari
Winners4Life! Daripada Ahmad Rodzi, Alor Star
Saya sedang mengandung & selalu merasa tidak sihat & mabuk. Saya juga
sudah keguguran sebanyak 5 kali sebelum ini. Sejak memakan TF, saya
rasa sihat, merasakan tenaga seperti sediakala & tidak mengalami mabuk
lagi. Saya kini telah melahirkan dengan selamat. Terima kasih kepada TF
& Winners4Life! Pn Hani, Tampines, Singapore -

Saya sudah mengidap penyakit migraine dan juga buasir selama beberapa
tahun. Kekadang hari saya terpaksa memakai tuala pelekat wanita untuk
mengawal kesan buasir saya. Saya suka bersukan dan ini sangat
memalukan dan sangat menyusahkan saya. Saya amat terkejut apabila saya
mula mengambil TF untuk migraine saya, saya dapati masaalah buasir saya
juga dapat diatasi sekali gus! Terima kasih Winners4Life dan Puan Sheri
Din. Daripada En Ahmad Hussein – Trengganu –

Saya mengalami stroke (angin ahmar) sejak satu setengah tahun lalu.
Sebelah kaki & tangan saya tidak dapat berfungsi & lidah juga menjadi
kelu. Setelah mengambil TF dari Winners4Life selama sebulan setengah,
sebanyak 4 botol, kini saya sudah boleh berjalan & saya juga dapat
bercakap dengan lancar. Alhamdulillah. Terima kasih pada Anna &
Winners4Life kerana menganjurkan penawar hebat ini! Daripada Che
Gayah, Kulai, Johor.

Saya menderita sakit lutut yang sangat berat. Saya tidak dapat duduk
bersila lebih dari 1 tahun & tidak boleh menaiki tangga & juga terpaksa
bersolat duduk. Lutut saya keras dan tidak dapat berbengkok menyebabkan
saya terpaksa merangkak apabila bangun dari duduk berlunjur dilantai.
Selepas 2 bulan memakan TF sebanyak 6 biji sehari, saya kini boleh duduk
bersila, menaiki tangga & solat berdiri. Alhamdulillah! Terima kasih
Winners4Life. Daripada Pn Rugayah, Kulai, Johor.
Saya mempunyai anak yang terencat akal, yang selalu terkena sawan, sejak
dari umur 1 tahun hingga kini 17 tahun. Apabila sawan menyerang, dia
akan jatuh dan cedera. Banyak kali telah luka di muka dan kepala dan
beberapi kali patah di tangan. Alhamdulillah, sejak mula memakan TF 2 biji
sehari, dia tidak diserang sawan lagi. Pn Mahimah, Kuantan –

Ibu mertua saya hidap diabetes (kencing manis) yang kronik sejak 4 tahun
lalu. Ibu jari kakinya luka lebih satu bulan dan tekanan darahnya naik
tinggi. Setelah memakan Transfer Factor 1 minggu, lukanya kering
sepenuhnya dan tekanan darahnya turun. Terima kasih kepada insan yang
mengenalkan Transfer Factor molekul ajaib ini, kepada saya. Daripada En
Azmi Elias, Masai Johor

Saya menghidap kencing manis hampir 10 tahun. Minggu lalu, saya
mula mengambil TF, 2 biji pagi dan 2 biji petang. Badan saya rasa sangat
ringan, tidur lena dan tak perlu bangun malam buang air kecil! Thank you
En Akram dan Winners Group! Daripada Alawdeen Trading & Provision
Shop, Margaret Drive, Singapore.

Suami saya menderita kanser perut, dan perut dia telah “dibuang” melalui
surgery, tetapi dia mengalami pendarahan dan keracunan darah yang teruk.
Dia di ICU buat beberapa waktu dan sudah mula menulis wasiat untuk
keluarga. Harapan untuk terus hidup terlalu tipis, mengikut pandangan
doktor. Dia kemudian dihantar pulang dari hospital tanpa sebiji ubat pun.
Saya amat terharu melihat keadaannya. Dia tidak dapat berjalan, dan
menjadi kurus sehingga tinggal kulit dan tulang sahaja. Saya
mengusahakan berbagai ubatan tradisional tetapi tiada yang memberi kesan
yang dikehendaki. Namun, setelah kami diperkenalkan dengan produk
Transfer Factor dari Winners4Life, keadaan suami saya terus berubah.
Saya memberi dia 9 biji sehari pada permulaan selama 2 minggu dan
kemudian diturunkan 4-6 biji sehari. Alhamdulillah, dia sudah sihat
sekarang. Dia boleh berfungsi seperti biasa. Badannya sudah naik. Selera
makan sudah pulih seperti biasa. Rambutnya tumbuh kembali. Dan tenaga
batinnya kembali normal. Saya amat bersyukur. Saya rasa seperti dia mati
hidup kembali! Terima kasih pada Chegu Azman dan Pn Sheri Din.
Daripada Norbaba, Sandakan, Sabah –

Saya menderita sakit buah pinggang & menjalani dialisis 3 kali seminggu
. Sebelum makan TF anjuran Winners4Life, saya selalu penat, terlalu lesu
& berbaring sahaja. Sekarang tenaga saya sudah pulih & dapat bekerja
kembali untuk mencari nafkah keluarga. Sel darah merah saya juga sudah
bertambah, menurut doktor. Alhamdulillah. Daripada En Khalid, Kulai,
Johor.

Anak saya sudah menghidapi sinus sejak dia berumur setahun, dan
sekarang dia sudah berumur 17 tahun. Setiap pagi bila dia menghembus
hingus, nescaya sinki bilik mandi akan tersumbat kerana terlalu banyak
hingus yang pekat dan hijau. Dia telah menjalani 2 operasi tetapi penyakit
sinus dia tidak juga sembuh. Alhamdulillah, setelah mengambil Transfer
Factor selama 2 minggu, penyakit dia telah sembuh sepenuhnya! Jutaan
terimakasih kepada Chegu Jalil dan Winners. Drpd Pn Zuraidah, Skudai
Johor,

Pada bulan February, volume 3 level saya, hanya 700LP. Pada bulan
March, volume 3 level saya meningkat kepada lebih 6,000LP! Dan saya
berjaya mencapai pangkat Diamond, dengan hanya mengedarkan flyer
“Raja Penawar” dari kumpulan Winners sahaja! Gunakanlah flyer hebat
ini! Insyaallah anda juga akan berjaya! Ida, Singapura/JB

Walaupun belum ramai ahli dibawah kumpulan saya, bonus bulan
pertama saya dalam 4Life Research adalah RM1,418! Ini adalah kerana
produk TF yang cukup berkesan, persen bonus yang tinggi dan sokongan
kumpulan Winners4Life! Terima kasih pada upline saya, Ina dan Man Batu
Pahat dan En Sadik Din. Daripada Johan, Pasir Gudang,

Walaupun saya baru menyertai 4Life dan bergerak selama 2 minggu sahaja,
saya telah terima bonus pertama yang mengejutkan – RM2,368!
Sebelum ini saya biasa sertai banyak MLM tapi tak pernah terima bonus
setinggi ini dalam waktu yang cukup singkat. Dijangkakan bonus saya akan
meningkat lebih RM5,000 pada bulan depan. Terima kasih Winners4Life
kerana memberi saya peluang yang tiada tandingannya ini. Man, Batu
Pahat –

Sebelum menceburi bidang MLM, saya adalah seorang engineer, dan telah
bekerja di luar negeri buat beberapa tahun. Semasa krisis ekonomi melanda
rantau Asia, saya telah kehilangan pekerjaan. Perkara ini membuat saya
menyedari bahwa masa depan saya sebenarnya diluar kawalan saya sendiri.
Walaupun sekiranya saya berjaya mendapatkan pekerjaan yang lain, ini
tidak menjamin yang saya tidak akan dibuang kerja lagi. Maka saya
mencari satu peluang yang mana saya sendiri menentukan masa depan saya,
dan saya tidak bergantung kepada pemerintah, korporat atau boss. Saya
memilih untuk menjadi boss kepada diri saya sendiri. Diwaktu itu, saya
terus menceburi bidang MLM sepenuh masa selama tiga tahun, tetapi
malangnya tidak membuahkah hasil yang saya harapkan. Ini adalah kerana
saya tidak berpengalaman memilih syarikat yang boleh membawa saya ke
mercu kejayaan. Didalam bisnes ini, “timing” memainkan peranan yang
sangat besar. Syarikat yang saya ceburi dulu memasarkan produk kesihatan
biasa seperti vitamin, herba dan mengkudu yang trend nya sudah berlalu.
Tetapi di 4Life, saya memasarkan produk inovatif, unik & hebat yang tiada
persaingan langsung di pasaran global! Dan plan pemasaran 4Life memberi
ganjaran yang hebat kepada ahli sambilan dan ini memberi kestabilan
kepada kumpulan saya. Alhamdulillah, bersama 4Life dan Winners
Group, kini saya telah mula merasai kehebatan MLM yang selama ini saya
impikan. Akram Din, Singapura/Malaysia -

Saya sudah beberapa tahun menerajui kumpulan MLM syarikat
antarabangsa secara fulltime, tetapi tidak pernah terjumpa produk sehebat
Transfer Factor! Disebabkan oleh keajaiban produk ini dalam membantu
ramai orang (dari kanak-kanak kecil sehingga orang-orang tua) mengatasi
bermacam-macam penyakit (termasuk sinus, allergi, gatal-gatal, kencing
manis, darah tinggi, kanser, gout, bisa sendi, gastrik, sakit gigi, migraine,
buasir, demam, selsema, psoriasis, sawan, lemah IQ dan bermacam-macam
lagi!), kumpulan saya iaitu Winners Group telah menjadi kumpulan yang
begitu hebat, cemerlang dan disegani! Alhamdulillah! Plan pemasaran
4Life pula tiada tandingannya di pasaran. Sistem bonus “Unilevel
Compressed” memberi pulangan yang sangat besar untuk semua ahli
termasuk ahli-ahli baru dan ahli-ahli part-time. Dan ahli2 baru juga
berpeluang mendapat bonus perkongsian sedunia – Power Pool dan
package percutian resort 5 bintang!
Terdapat ahli Winners4Life (Pak Yusuf/Kak Ramlah dari Kuala
Terengganu) yang meraih bonus lebih dari RM10,000 sebulan sejak dari
bulan pertama lagi! Rata-rata, ramai ahli-ahli baru, walaupun mereka yang
tidak mempunyai banyak pengalaman didalam bidang MLM, namun
mereka dapat meraih pendapatan RM1,000 – RM3,000 sebulan pada
peringkat awal lagi, dengan bimbingan dan sokongan kumpulan Winners.
Kini Winners telah melahirkan 6 ahli Presidential Diamond iaitu En Sadik
Din, Pak Yusuf/Pn Ramlah, Dr Hadifaar, Dr Tony Liew, En Akram Din
dan En Fadzli Salim. Tiada kumpulan lain di dalam syarikat ForLife
Research setakat ini, yang melahirkan Presidential Diamond Melayu Islam!
Alhamdulillah!! Winners Hebat! Winners Cemerlang! Winners Terus
Maju! Jutaan terima kasih untuk semua leader2 Winners yang luarbiasa
hebat! Salam hormat dari saya Sheri Din, International Diamond, Winners
4Life! –

Berminat untuk mengetahui lebih lanjut peluang KESIHATAN DAN perniagaan 4life ?? hubungi saya di

016- 3153132 PUAN ZAIDAH

MAKLUMAT SEKIRANYA ADA AHLI KELUARGA ANDA MENGIDAPI SWINE FLU/SELSEMA BABI

Background

The novel H1N1 flu virus is causing illness in infected persons in the United States and countries around the world. CDC expects that illnesses may continue for some time. As a result, you or people around you may become ill. If so, you need to recognize the symptoms and know what to do.
Symptoms

Photo of woman with fluThe symptoms of this new H1N1 flu virus in people are similar to the symptoms of seasonal flu and include fever, cough, sore throat, runny or stuffy nose, body aches, headache, chills and fatigue. A significant number of people who have been infected with this new H1N1 virus also have reported diarrhea and vomiting.   The high risk groups for novel H1N1 flu are not known at this time but it’s possible that they may be the same as for seasonal influenza. People at higher risk of serious complications from seasonal flu include people age 65 years and older, children younger than 5 years old, pregnant women, people of any age with chronic medical conditions (such as asthma, diabetes, or heart disease), and people who are immunosuppressed (e.g., taking immunosuppressive medications, infected with HIV).

Avoid Contact With Others

If you are sick, you may be ill for a week or longer. You should stay home and avoid contact with other persons, except to seek medical care. If you leave the house to seek medical care, wear a mask or cover your coughs and sneezes with a tissue. In general you should avoid contact with other people as much as possible to keep from spreading your illness. At the current time, CDC believes that this virus has the same properties in terms of spread as seasonal flu viruses. With seasonal flu, studies have shown that people may be contagious from one day before they develop symptoms to up to 7 days after they get sick. Children, especially younger children, might potentially be contagious for longer periods.
Treatment is Available for Those Who Are Seriously III

It is expected that most people will recover without needing medical care.

If you have severe illness or you are at high risk for flu complications, contact your health care provider or seek medical care. Your health care provider will Photo of sick childdetermine whether flu testing or treatment is needed. Be aware that if the flu becomes wide spread, there will be little need to continue testing people, so your health care provider may decide not to test for the flu virus.

Antiviral drugs can be given to treat those who become severely ill with influenza. These antiviral drugs are prescription medicines (pills, liquid or an inhaler) with activity against influenza viruses, including H1N1 flu virus. These medications must be prescribed by a health care professional.

There are two influenza antiviral medications that are recommended for use against H1N1 flu. The drugs that are used for treating H1N1 flu are called oseltamivir (trade name Tamiflu ®) and zanamivir (Relenza ®). As the H1N1 flu spreads, these antiviral drugs may become in short supply. Therefore, the drugs will be given first to those people who have been hospitalized or are at high risk of complications. The drugs work best if given within 2 days of becoming ill, but may be given later if illness is severe or for those at a high risk for complications.

Aspirin or aspirin-containing products (e.g. bismuth subsalicylate – Pepto Bismol) should not be administered to any confirmed or suspected ill case of novel influenza A (H1N1) virus infection aged 18 years old and younger due to the risk of Reye syndrome. For relief of fever, other anti-pyretic medications are recommended such as acetaminophen or non steroidal anti-inflammatory drugs. For more information about Reye’s syndrome, visit the National Institute of Health website.

* Check ingredient labels on over-the-counter cold and flu medications to see if they contain aspirin.
* Teenagers with the flu can take medicines without aspirin, such as acetaminophen (Tylenol®) and ibuprofen (Advil®, Motrin®, Nuprin®), to relieve symptoms.
* Children younger than 4 years of age should not be given over-the-counter cold medications without first speaking with a healthcare provider.

Emergency Warning Signs

If you become ill and experience any of the following warning signs, seek emergency medical care.

In children emergency warning signs that need urgent medical attention include:

* Fast breathing or trouble breathing
* Bluish or gray skin color
* Not drinking enough fluids
* Severe or persistent vomiting
* Not waking up or not interacting
* Being so irritable that the child does not want to be held
* Flu-like symptoms improve but then return with fever and worse cough

In adults, emergency warning signs that need urgent medical attention include:

* Difficulty breathing or shortness of breath
* Pain or pressure in the chest or abdomen
* Sudden dizziness
* Confusion
* Severe or persistent vomiting
* Flu-like symptoms improve but then return with fever and worse cough

Protect Yourself, Your Family, and Community

* Photo of familyStay informed. Health officials will provide additional information as it becomes available. Visit the CDC H1N1 Flu website.
* Cover your nose and mouth with a tissue when you cough or sneeze. Throw the tissue in the trash after you use it.
* Wash your hands often with soap and water, especially after you cough or sneeze. Alcohol-based hand cleaners are also effective.
* Avoid touching your eyes, nose or mouth. Germs spread this way.
* Try to avoid close contact with sick people.
* If you are sick with a flu-like illness, stay home for 7 days after your symptoms begin or until you have been symptom-free for 24 hours, whichever is longer. Keep away from other household members as much as possible. This is to keep you from infecting others and spreading the virus further.
* Learn more about how to take care of someone who is ill in “Taking Care of a Sick Person in Your Home”
* Follow public health advice regarding school closures, avoiding crowds, and other social distancing measures.
* If you don’t have one yet, consider developing a family emergency plan as a precaution. This should include storing a supply of extra food, medicines, and other essential supplies. Further information can be found in the “Flu Planning Checklist”

CLICK SINI UNTUK INFO PENJAGAAN

APA ITU SELSELMA BABI/SWINE FLU

LANGKAH LANGKAH MEMPERLINDUNGKAN DIRI ANDA DAN KELUARGA DARI SELSEMA BABI/SWINE FLU

4life

Antara langkah langkah awal untuk melindungi kita dari serangan penyakit seperti Selsema Babi,Selsema Burung dan bermacam macam lagi penyakit yang akan wujud adalah memperkasakan sistem imun kita.

Kadang kadang kita ambil remeh berkenaan sistem imun kita walhal,sistem imun adalah pertahanan badan kita yang paling penting melawan penyakit,saya ingin mengesyorkan kepada anda semua yang membaca blog saya untuk mengambil produk Tranfer Factor 4life untuk penjagaan diri dan keluarga anda dari bahaya jangkitan Selsema Babi dan penyakit yang lain,berikut adalah maklumat-maklumat tentang keberkesanan Tranfer Factor 4life dalam penjagaan imun sistem.

BERMINAT UNTUK MENGETAHUI LEBIH LANJUT,SILA HUBUNGI SAYA DI 016-3163132 (ZAIDAH) ATAU EMAIL SAYA DI help_linemy@hotmail.com

Sistem imun melindungi kita dari penceroboh asing seperti virus, bakteria, kulat, protein asing dan sel kanser. Ia adalah satu sistem yang sangat canggih, anugerah Yang Maha Pengasih, yang merupakan perlindungan terbaik dari sebarang penyakit berbahaya. Tiada ubat yang dapat menandingi sistem imun yang sihat. Secara ringkas sistem imun terdiri daripada sel khas, protein, tisu dan organ (nodus limfa, sistem pernafasan, limpa, kulit, apendiks, perut dan usus). Di dalam artikel ini saya akan terangkan serba sedikit mengenai tugas beberapa pemain dalam sistem imun:

Makrofaj (atau fagosit) – Sel darah putih yang berbentuk seperti Pac-Man, merupakan barisan pertahanan pertama sistem imun. Ia dengan cepat menyerang mana-mana penceroboh asing dan menelannya (seperti dalam permainan video Pac-Man). Namun kadangkala makrofaj tidak pasti sama ada yang datang itu penceroboh asing atau kawan. Makrofaj sudah tentu tidak mahu memusnahkan sesuatu yang merupakan sebahagian dari tubuh kita. Untuk membantunya mengenali kawan atau musuh, makrofaj akan meminta bantuan sel T-pembantu.

Sel T-pembantu adalah dari kumpulan sel darah putih yang dikenali sebagai limfosit. Sel T-pembantu akan mendatangi dan melekatkan dirinya dengan makrofaj untuk membantu makrofaj mengenali sama ada yang berada dalam genggamannya itu kawan atau musuh. Sekiranya sel T-pembantu memutuskan ianya adalah musuh, ia akan mengeluarkan hormon yang dikenali sebagai sitokines, yang memberi isyarat kepada sistem imun untuk bertindak dengan pantas. Ini merangsang sel-B untuk bertindak dan menarik lebih banyak makrofaj dan sel T-pembantu untuk datang menyelamat. Sekiranya sel T-pembantu tidak mengenali penceroboh asing tersebut, sistem imun akan menganggapnya sebagai kawan dan membiarkannya. Bayangkan apa yang akan terjadi. Ya, kita akan mendapat penyakit yang berpunca dari penceroboh (mikro-organisma) tersebut. Sebagai contoh virus SARS. Sistem imun kita tidak mengenali mikro-organisma yang kita atau ibu kita belum pernah terdedah kepadanya. [Transfer Factor memainkan peranannya dengan membantu sel T-pembantu mengenali musuh yang datang menyerang].

Sel-B mempunyai kemampuan untuk menembak penceroboh dengan enzim yang dapat menghancurkannya. Sebahagian dari sel-B akan kembali ke nodus limfa untuk membina antibodi bagi melawan penceroboh tadi. Sekiranya penceroboh ini menyerang lagi, sistem imun sudah bersedia mempertahankan diri disebabkan antibodi yang sudah dibina tadi.

Sel pembunuh semula jadi atau sel NK (natural killer) pula memusnahkan apa-apa yang berada di laluannya. Mereka menyemburkan sel yang dijangkiti dengan toksin dan enzim pemusnah, yang akan memusnahkan semua penceroboh asing atau sel yang tumbuh secara tidak normal seperti sel kanser. Apabila sel NK sudah mulai lemah atau tidak aktif dan tidak lagi berupaya memusnahkan sel kanser, disebabkan radikal bebas dan beberapa faktor lain, seseorang itu akan mendapat penyakit kanser. Memperkuatkan sel NK merupakan satu cara yang baik untuk kita memusnahkan sel kanser secara semulajadi (natural). [Transfer Factor Advance Formula dan Transfer Factor Plus Advance ] masing-masing telah disahkan dapat meningkatkan aktiviti sel NK sebanyak 280% dan 430%.

Sel T-penindas boleh diibaratkan sebagai pasukan pengaman yang datang selepas penceroboh asing telah dimusnahkan dan untuk menenangkan gerak balas imun yang beraksi dengan hebat itu. Ia merupakan faktor penting dalam mengawal kerosakan tidak dijangka (collateral damage). Sekiranya gerak balas imun yang begitu aktif tidak dikawal, ia akan menyebabkan kerosakan yang teruk kepada tisu normal di sekelilingnya. Sekiranya sel T-penindas tidur dan tidak dapat mengawal gerak balas tersebut, kita akan mendapat penyakit yang dikategorikan di bawah penyakit autoimun. Terdapat lebih 80 jenis penyakit autoimun, contohnya adalah diabetes jenis 1, artritis reumatoid, psoriasis, sklerosis berganda dan lupus. [Transfer Factor mampu membangkitkan sel T-penindas dari tidur dan mengawal gerak balas imun dari menyerang sel tubuh dan seterusnya menghindar kita dari mendapat penyakit autoimun].

Untuk membolehkan sistem imun melindungi kita seperti yang ditetapkan oleh Yang Maha Pencipta (Al-Khaaliq), kita perlu menjaga kesihatannya. Ia perlukan Vitamin E, Vitamin C, karotenoid, glutation, koenzim Q10, Zink dan antioksidan untuk kekal sihat dan berfungsi pada tahap terbaik. [Transfer Factor RioVida membekalkan antioksidan dan transfer factor yang diperlukan oleh tubuh kita.

BERMINAT UNTUK MENGETAHUI LEBIH LANJUT,SILA HUBUNGI SAYA DI 016-3153132 (ZAIDAH) ATAU EMAIL SAYA DI help_linemy@hotmail.com

more info

http://helplineenterprise.wordpress.com/2008/04/14/ilmu-khas-hanya-untuk-orang-berpenyakit-dan-yang-pentingkan-kesihatan-sahaja/

Aromatherapy and Modern Medicine

What is aromatherapy?
Aromatherapy uses essential oils that are thought to have healing properties. These oils are the concentrated essences taken from the flowers, fruit, seeds, leaves and bark of certain plants. There are about 400 essential oils, but only about 40 are commonly used in aromatherapy.

Aromatherapists believe aromatherapy can boost well being, relieve stress and help to refresh your body.  In other words, aromatherapy may improve your physical and emotional health.  The theory behind aromatherapy is that each essential oil has its own specific health benefit.  For example, lavender is said to help with sleeping problems, and to relieve muscle tension and anxiety.

Essential oils are usually massaged into the body, but they can also be
•    Added to a warm bath  – use up to 6 drops of an essential oil diluted with a carrier oil (or better still, a dispersing bath oil) in your bath
•    Put in a cold compress next to your skin or on a pillow or handkerchief
•    Added to a burner, so they are breathed in from the air
To inhale an essential oil, heat a few drops of the oil, mixed with water, in an oil burner or diffuser. The steam containing the oil will spread through the air in the room.  This is not recommended for people with asthma.

And if you have cancer you should not use any aromatherapy without advice from a qualified aromatherapist. There is more information about using aromatherapy safely further down the page.
How does aromatherapy work?
There are a couple of theories to explain how aromatherapy might work.  The first is that you directly absorb the oils through the skin into your bloodstream.  The oil can then travel through your body and have an effect on a specific organ or function in your body.

Therapists claim that many essential oils have an anti-inflammatory effect, which can help with arthritis and muscular pain.  Other oils may help with breathing problems or prevent or fight off infections by helping boost your immune system.

The second theory relates to your sense of smell.  The nerves used to smell are found high up inside your nose and they connect directly to your brain. Foods, flowers, perfumes and plants all release tiny molecules into the air and stimulate your smell (olfactory) nerve cells.  The cells send a message to your brain to interpret what the smell is. The smell can then set off a reaction in your body, both emotionally and physically.  For example, it might change your heart or breathing rate or make you feel calm or excited. Because essential oils can stimulate your sense of smell, it is thought that this process may play a part in the effects of aromatherapy.

Although we don’t know for sure, any healing effects from aromatherapy are most likely to come from a combination of the physical effects the oils have on the body (smell and absorption into the bloodstream), as well as how they work on your mind and spirit.
Why do people with cancer use aromatherapy?
As with many types of complementary therapies, people with cancer use aromatherapy because it makes them feel good, and is something they can do to help themselves.  Therapists promote aromatherapy as a natural way to help you relax and cope with
•    Anxiety
•    Pain
•    Depression
•    Stress
Generally, aromatherapy can help lift your mood and enhance your wellbeing.  There is some evidence to support these benefits.

Some people also claim that aromatherapy can help to
•    Boost your immune system
•    Fight off colds and bacterial infections
•    Help with period (menstrual) problems
•    Improve circulation and urine output
•    Relieve headaches and digestion problems
There is no scientific evidence to prove any of these claims.
Evidence to support the use of aromatherapy

There is no scientific evidence to prove that aromatherapy can cure or prevent any type of disease, including cancer.  But there are a few studies to suggest that aromatherapy may be a helpful complementary therapy for people with cancer and other types of illness.

An American study published in The Journal of Palliative Medicine in 2004 looked at the use of massage and aromatherapy in 42 people who had advanced cancer.  These people were divided into 3 groups
•    Group 1 were given weekly massages over 4 weeks
•    Group 2 were given massages using lavender oil
•    Group 3 had no massages at all
At the end of the trial, people in groups 1 and 2 were sleeping much better and had less depression than those in group 3.

In 1998 a UK study looked at the effects of aromatherapy in 58 cancer patients.  Most of these patients were women with breast cancer who said that they would like aromatherapy to help them with feelings of stress, anxiety, depression and fear.  Each patient had 6 aromatherapy treatments during the study.  At the end of these treatments all the patients showed a significant improvement in their feelings of anxiety, depression and stress.

In 1999 a study assessed the effects of aromatherapy massage and massage therapy on 103 people with cancer in a palliative care setting.  Some people had massage using only a carrier oil, and some had an aromatherapy massage with the essential oil Roman Chamomile.  People in both groups had lower levels of anxiety.  But those who had Roman Chamomile oil massage did seem to have more improvement in physical and psychological symptoms and in overall quality of life.

Both these studies are small and don’t provide enough evidence to come to any conclusions about the true benefits of aromatherapy massage in people with cancer.

The Cochrane Collaboration carried out a ‘systematic review’ in 2004 of the studies on aromatherapy and cancer.  This means that they looked at the published results of all the trials investigating the effects of aromatherapy massage and massage therapy on people with cancer.  They pull all the information together to draw their conclusions.

This systematic review concluded that massage and aromatherapy massage does improve people’s emotional well being in the short term.  These therapies may also have an effect on physical symptoms.  There was not clear evidence to show that aromatherapy added to the effects of massage.  We need much larger trials, and a longer follow up period after the trials, to know if this is the case.

You can read this Cochrane Review ‘Aromatherapy and massage for symptom relief in patients with cancer’ in full on the Cochrane Collaboration website.

A UK trial in 2007 tested whether adding aromatherapy massage to usual supportive care could reduce anxiety and depression in patients with advanced cancer.  280 patients took part and they all had anxiety or depression.  Half the patients had usual supportive care.  The other half had supportive care plus aromatherapy massage.  The researchers found that patients who had aromatherapy massage were less anxious or depressed for up to 2 to 6 weeks after the massage but there was no difference at 10 weeks.

There have been reports that inhaling the following oils can relieve the sickness caused by the cancer treatments chemotherapy and radiotherapy
•    Peppermint
•    Ginger
•    Cardamom oil
But there is no scientific evidence to prove these reports.

Look at what’s new in complementary and alternative therapy section to find out if there is any current research going on into the use of aromatherapy in people with cancer.
What having aromatherapy involves
This all depends on how you use the essential oils for aromatherapy.  You can
•    Have an aromatherapy massage from a trained therapist (aromatherapist)
•    Use essential oils yourself at home in various ways – in a bath, oil burner, humidifier or diffuser
•    Use beauty products that contain aromatherapy oils
Have an aromatherapy massage from a trained therapist
When massaged into the skin, essential oils are diluted with another oil, usually vegetable oil.  This vegetable oil is called the ‘carrier oil’ because it ‘carries’ the oil to the skin.  Essential oils are very concentrated so must be diluted.  If used neat, they could cause serious skin irritation.
When you have your first aromatherapy massage the therapist will ask you some general questions about your health, lifestyle and medical history.  If they are concerned about anything, they may ask your permission to speak to your GP.  This is just to check that your GP is happy for you to have aromatherapy.  In general, it is rare that the GP will say no.  But there may be situations where your doctor recommends that you don’t use aromatherapy.

The aromatherapist will choose the oils that they feel will treat your symptoms and help you most.  They will massage the oils gently into your body.  An aromatherapy massage session usually lasts between 60 to 90 minutes.  Your therapist might play some relaxing music during your massage.  It is important that you tell the therapist if you feel uncomfortable at any time or want them to stop.  But generally most people say that having an aromatherapy massage is very relaxing and soothing.
Using essential oils yourself at home

You can add essential oils to water and use them in an oil burner at home.  This way you can enjoy their pleasant smells and possible relaxation benefits whenever you like.  Some people say that adding a few drops of certain oils to boiling water and inhaling them helps to relieve symptoms such as breathing problems and a blocked nose.  Others claim that putting a few drops onto your pillow or handkerchief can have the same benefits.

People also add essential oils to a warm bath to help with
•    Relaxation
•    Sleeping problems
•    Clearing up dandruff or acne
It is important not to put too much oil in though as this can cause skin irritation and cystitis in some people.
Using beauty products that contain aromatherapy oils
Aromatherapy products have become a huge part of the beauty industry.  There are now soaps, hair care products, face and body oils, creams and lotions that all claim to be aromatherapy.  However, unless the label of the product specifically states that only pure essential oils are used, it is very likely that the scents are man made (synthetic).  This means that they won’t give you any real aromatherapy benefits. Essential oils should be used carefully, so don’t add them to any beauty products without advice from an aromatherapist.
Possible side effects of aromatherapy

Essential oils are generally safe if you use them in the correct way. Some oils can cause a skin reaction or an allergic reaction. Never use them on skin that is sore, inflamed, or broken.

You should never swallow an essential oil, or put the oil directly inside any other part of the body (eye, ear, nose, anus or vagina).  Oils are sometimes used in this way in France by aromatherapy practitioners but care is needed as they can be poisonous and harmful when taken in this way.
Using aromatherapy safely

For most people, using aromatherapy is safe.  But there are always exceptions.  If you have cancer don’t use aromatherapy without getting advice from a qualified aromatherapist who is experienced in treating people with cancer, and letting your cancer doctor know. This is even more important if you are having treatment or
•    Are pregnant or breastfeeding
•    Are trying to get pregnant
•    Have fits (for example, with epilepsy)
•    Have asthma
•    Have kidney disease
You should also tell your doctor and aromatherapist if you are taking other medicines or homeopathic remedies. Some essential oils could interact and make these drugs or therapies weaker or stronger. Never use essential oils on children unless you have checked first with an aromatherapist.
The cost of aromatherapy treatments

A private aromatherapy massage will usually cost between £20 and £60 for a 60 to 90 minute treatment.  It is very important that you choose a qualified therapist to treat you. There is information about finding a therapist further down this page.

Many cancer centres and hospitals in the UK now offer patients aromatherapy massages free of charge.  So always ask your nurse or doctor if this is available where you are having your treatment.  If not, they may be able to direct you to a voluntary organisation that offers complementary therapy treatments for free or at a reduced cost.  Look in our complementary therapy organisations section for a list of organisations that can give you advice about where to get an aromatherapy massage.

The cost of essential oils varies depending on the quality and quantity you buy.  It is best to buy oils in small quantities as they don’t last very long once you open them.  You should keep essential oils in a cool dark place, or in the fridge, and out of reach of small children.

more info at :

http://aromasutra.wordpress.com/

www.sutraessential.com

AROMATERAPI DAN PRODUK KESIHATAN

Aromaterapi sebagai alternatif perubatan moden.

Tidak ramai yang tahu dan sedar bahawa aromaterapi itu juga dijadikan salah satu alternatif perubatan moden bagi doktor-doktor malah bomoh serta orang-perseorangan untuk menyembuhkan sesuatu penyakit. Bauan aromaterapi itu secara halus pasti memberikan ketenangan kepada si pemakai sekaligus mengimbangi hormonnya dan meredakan kesakitan yang dialaminya. Sebab itu kebanyakkan doktor menggunakan aromaterapi sekiranya tidak dapat menyembuhkan sesuatu penyakit malah ada yang menggunakan aromaterapi beserta dengan ubat-ubatan dengan presipkri yang betul untuk mempercepatkan penyembuhan penyakit itu.

TEKANAN adalah sesuatu yang lumrah dalam kehidupan. Ia terbahagi kepada pelbagai bentuk. Antaranya termasuklah masalah kerjaya, pasangan hidup, kewangan, mental, emosi dan sebagainya.
Justeru, bagi membantu melegakan sesuatu tekanan atau stres dalam kehidupan kita seharian, aromaterapi boleh menjadi salah satu alternatif untuk meredakan masalah yang dihadapi.
Pakar aromaterapi, Krissy Gee yang telah lama terlibat dalam bidang ini menjelaskan, aromaterapi merupakan pilihan rawatan penjagaan kesihatan yang mampu memberi ketenangan pada seseorang individu.
“Secara saintifiknya rawatan aromaterapi boleh meningkatkan kualiti kesihatan manusia kerana ia menggunakan pati organik semula jadi yang diekstrak daripada tumbuh-tumbuhan.
“Penggunaan minyak pati secara sistematik dalam rawatan holistik dipercayai dapat memperbaiki tahap kesihatan fizikal dan emosi seseorang.
“Selain itu, minyak pati juga mampu memberi kesan terapeutik untuk kesihatan dan perlindungan daripada penyakit,”

Aromaterapi adalah rawatan melalui bau yang menggunakan beberapa titisan minyak pati tumbuhan. Ia boleh dilakukan sama ada dengan cara urutan di badan, dimasukkan ke dalam wap air panas untuk dihidu wapnya atau dititis dalam tab atau air mandian untuk mendapatkan keharumannya.Rawatan aromaterapi menggunakan minyak pati tumbuhan tertentu boleh menjadikan seseorang individu awet muda dan melambatkan proses penuaan di samping memberi kesan positif pada emosi dan psikologi mereka.
“Sebagai contoh minyak pati lavender baik untuk merawat kulit kering atau tidak bermaya selain mampu memberi ketenangan minda. Bagi individu berkulit sensitif yang bertindak balas dengan suhu sejuk, haba atau produk kecantikan pula, mereka boleh menggunakan minyak pati chamomile, sandalwood, neroli dan rose.“Sementara itu, khasiat pati tumbuhan lada hitam dan serai wangi boleh melancarkan peredaran darah manakala minyak pati bunga mawar membantu mengimbangi hormon badan khususnya wanita.
“Tidak ketinggalan, minyak pati juga boleh menjauhkan jangkitan virus seperti selesema, asma dan resdung serta meningkatkan sistem ketahanan badan,”

MAKLUMAT LANJUT BOLEH DIDAPATI DI

www.sutraessential.com

www.aromasutra.wordpress.com

APA ITU MELAMIN/MELAMINE DAN RISIKO PADA ANAK ANDA DAN KELUARGA ANDA.

Apakah itu Melamine ?

Melamine ialah bes organik yang terdiri daripada karbon,oksigen dan nitrogen. Bahan kimia ini kali pertama dihasilkan

oleh Justus von Liebig pada 1830 yang kemudiannya dihasilkan secara besar-besaran untuk kegunaan industri.

Seperti yang kita sedia maklum, melamine merupakan bahan yang digunakan untuk membuat pinggan mangkuk

melamine. Selain itu, melamine juga digunakan untuk menyelaputi permukaan plastik dan kayu.

Melamine mempunyai kandungan nitrogen yang tinggi.Oleh itu, dengan mencampurkan bahan kimia ini ke

dalam susu yang dicairkan akan mengaburi bacaan sebenar tahap protein pada susu tersebut. Penambahan

Melamine dalam makanan adalah menyalahi undang¬undang di bawah Akta Makanan 1983 dan

Peraturan¬Peraturan Makanan 1985.

Walaupun melamine sangat larut di dalam air dan mudah disingkarkan melalui urin, buah pinggang manusia tetap

mempunyai hadnya tersendiri. Akibatnya, pada dos melamine yang tinggi, ginjal tidak lagi mampu menyingkirkannya

dari tubuh badan manusia. Oleh itu, kepekatan melamine akan bertambah seterusnya membentuk kristal

yang turut dikenali sebagai batu karang.Pembentukkan batu karang ini akan bertambah saiz dari

semasa ke semasa yang akhirnya menyebabkan kegagalan ginjal yang serius.

Pada Mac 2007 yang lalu, satu kajian oleh pakar toksikologi,Perry Martos dari Universiti University of

Guelph mendapati ada satu lagi bahan kimia yang mendorong kepada pembentukan batu karang akibat

melamine iaitu cyanuric acid. Gabungan kedua-dua bahan kimia ini boleh menyebabkan pembentukan batu

karang yang sekaligus menyebabkan kegagalan ginjal.

Kesan melamine secara langsung mengakibatkan iritasi apabila terhidu dan bersentuhan dengan kulit atau mata.

Pengambilan melamine melalui makanan boleh mengakibatkan

:

•kerosakan pada sistem pembiakan

•pembentukkan batu karang dalam ginjal dan

pundi kencing. Ini boleh mengakibatkan kegagalan ginjal terutamanya kepada bayi

Sebagai langkah proaktif ,semua pihak disarankan agar ibubapa dapat memantau gejala masalah buah pinggang seperti

bayi menangis tanpa sebab ketika kencing, kencing berdarah,dan tekanan darah tinggi pada bayi.

MAKLUMAT LANJUT SILA CLICK DI BAWAH.

melamine

http://en.wikipedia.org/wiki/Melamine

MAKLUMAT LANJUT BERKENAAN TRANSFER FACTOR kebaikan untuk anda.

Transfer factor (TF) is an extract of low molecular weight containing several lymphokine molecules with immunomodulating properties. It has been described for the first time by Lawrence in the early ‘50s. It seems capable of transferring antigen-specific information to T-lymphocytes, and it is present in the lymphocytes of mammals and birds. It has been widely used over the past forty years in the treatment of viral, parasitic, fungal infections and allergic disorders, as well as immunodeficiencies, neoplasias, viz. cancer of the lung and prostate. Encouraging clinical results have also been observed in patients suffering from candidiasis and tuberculosis.

It has been thought that the potential of this compound for answering the challenge of unknown pathogenic agents is considerable as is its preventative potential. Data have shown that antigen-specific TF administered before a viral infection can prevent the onset of the disease, TF acting as a preventative vaccine based on cell mediated immunity.

Its molecular structure has only partially been unravelled. It seems that to a small peptide (ca. 5000 DA) are attached 2-3 ribonucleotides. However, this lack of knowledge did not prevent its clinical use since it is possible to produce large quantities of specific transfer factor in tissue culture or in immunised animals.

The first observations postulating the existence and establishing the concept of transfer factor dates from the early 1950s when H.S. Lawrence showed that delayed type hypersensitivity (DTH) to a given antigen could be transferred from one individual to another via cell-free extracts obtained from the leucocytes of an immunised donor. He assumed that this adoptive transfer of immunity was due to a molecule which he named transfer factor and he surmised that its molecular weight was less than 12,000 Daltons, as it filters through a standard dialysis bag. Since that time, all transfer factor preparations for clinical and experimental studies have been obtained by disrupting lymphocytes, dialysing the lysates and using the dialysed material for in vitro tests or in vivo clinical or animal studies.

Over fifteen hundred reports have confirmed Lawrence’s original observations and established that the dialyzable extracts thus obtained are capable of transferring specific immune information in vitro to naïve lymphocytes or in vivo to patients or experimental animals. This information concerns only cell-mediated but not humoral immunity, no de novo antibody production has ever been elicited by transfer factor, although it has been reported that it may modulate normal antibody production triggered by conventional immunisation.

Since the early 70’s, transfer factor has been used more often than not successfully for the treatment of viral, parasitic, fungal infections, and also as an adjuvant treatment in autoimmune, allergic and malignant disorders. Its apparent success is of no surprise since cell-mediated immunity (CMI) plays a crucial role in the control of infectious, parasitic, and autoimmune diseases, as well as cancer.

Because the TF extract is usually obtained from the total lymphocyte population containing helper and suppressor lymphocytes, it acts as a modulator of the immune system. It boosts the immune defences when required, e.g. in infectious, malignant or genetically impaired immune disorders or it exerts a suppressing effect on a hyperactive immune system when its down-regulation is desirable, e.g. in allergic disorders.

The mechanism of action of TF remains largely unknown, its activity, in addition to the transfer of immune information, is manifested as a non-specific modulation of the immune response. It is known that the dialyzable extract containing the TF molecules also contains other low molecular weight lymphokines e.g. IMREG 1 and 2. Thus, its non-antigen-specific immunomodulating activity, which may also play a role in the regulation of humoral immunity, is due to molecules present in the dialysate, but distinct from those responsible for the transfer of antigen-specific information.

It seems that the total dialysate obtained from peripheral lymphocytes is a cocktail of molecules that provide immunoregulatory activity, in addition to the adoptive transfer of novel antigenic specificities to the immunological memory of the recipient. Hence the qualification of TF as an immunomodulator, i.e. a lymphokine with immunomodulatory activity mediating adoptive immunity, in contrast with so-called active (antibody induction by immunisation with the corresponding antigen) or passive (mediated by antibody injection) immunity.

Nonetheless, and notwithstanding encouraging clinical results, many drawbacks have impeded research in this field and fast advances in understanding the nature and mode of action of this intriguing biological entity.

Until 1974, the only source of transfer factor was pooled leucocytes from blood donors, which limited material supplies, whereas the biological potency and specific activity of the extract varied from one preparation to another. Indeed, the precise antigenic specificity of the various batches of material used was practically unknown, but presumably large, since each batch reflected the collective immune experience of several individuals. For this reason, these preparations were improperly called “non-specific”, indicating multiple but unknown specificities.

Thus, despite several encouraging reports in the early 1970s, the clinical use of transfer factor was curtailed by the dearth of material with standardised and consistent activity. Similarly, biochemical studies were virtually impossible for lack of sufficient raw material for purification. In 1974, Viza and co-workers reported that TF with known specificities could be replicated in tissue culture, using a lymphoblastoid cell line. In the late 1970s, the same group and other investigators presented evidence that specific TF obtained from mammals after immunisation with a given antigen was also active in humans.

Nevertheless, in spite of the resolution of the supply problem, the controversy relating to this molecule was to grow. There are several reasons for this, and they pertain mainly to its unusual characteristics.

Nearly fifty years after Lawrence’s original observations, transfer factor remains an elusive and controversial entity, despite enormous laboratory efforts and several clinical studies with encouraging and sometimes spectacular results. Biochemical studies have already produced evidence that the molecule responsible for the transfer of the antigenic specificity is a small peptide with a molecular weight of approximately 5000 DA, and it has been suggested that two to three ribonucleotides are attached to the peptide. Unfortunately, attempts at sequencing the peptide have failed, because of the presence of a blocked amino terminus.

The transfer of antigen-specific CMI information by this extract is thought provoking, for it apparently contravenes essential tenets of immunology and molecular biology. However, since the experimental evidence supporting the antigen-specific transfer is uncontested, various hypotheses for understanding its mechanism have been proposed, but so far none has proven totally acceptable.

The specificity issue thus remains one of the essential problems. TF dialysates contain non-specific immunoregulatory molecules which can usually enhance and, in certain cases, down-regulate CMI. Two such molecules named IMREG I and IMREG II were identified by Gottlieb and his co-workers. Nevertheless, such moieties could play a role in enhancing a weak response to a ubiquitous antigen and thus provide false evidence of specific transfer. Studies undertaken with such rare antigens as coccidioidin or keyhole limpet haemocyanin (KLH) preclude non-specific enhancement of “lapsed” immunological memory. Several human and animal studies have established that TF is capable of transferring CMI to rare antigens that the recipient is unlikely to have encountered by chance.

The overall picture became more complex when two types of antigen-specific activity were described within the dialysates: a) inducer or helper activity, which is the activity of the conventional transfer factor and b) anti-transfer factor or suppressor activity. The distinctive properties of the two entities are as follows: transfer factor binds to its related antigen, suppressor factor binds to the related antibody (IgG); inducer factor is absorbed by T suppressor cells and macrophages, whereas suppressor factor is absorbed by T-helper cells and macrophages; inducer factor derives from T-helper cells, suppressor factor from T-suppressor cells.

Be that as it may, TF’s characteristics (low molecular weight, undefined chemical structure, unconventional mode of action, protein-like nature but resistant to most proteolytic enzymes) together with its biological properties (non-species specificity, transfer of antigen-specific information) have generated more opponents than supporters. And the frustration resulting from unsuccessful attempts to solve this multi-faceted riddle, especially the failure so far to unravel the molecular structure, apparently due to a blocked amino terminus of the peptide forbidding its sequence by conventional methods, has led scientists to doubt its very existence.

Despite promising results and hundreds of publications, failure to explain TF’s mechanism of action and define its molecular structure aroused doubts about its very existence. And even though recent work by Kirkpatrick has partially determined an amino-acid sequence (LLYAQDLEDN), thus giving some biochemical reality to the elusive moiety, no further publication has confirmed and complemented these data since.

Moreover, the pharmaceutical industry did not pay sufficient attention to this moiety because of the prohibitive costs of bringing a new medicine onto the market and the lack of patent protection (the impossibility of filing patents after decades of published academic work). In addition, the difficulties involved in production made commercialisation unviable. And a compound producing such astounding results as those described in the scientific literature, and which has not been on the market for so many years, gradually begins to lose its credibility. As for the commercial preparations obtained from colostrums and today sold via the internet, they definitely decrease the credibility of the product. Their acclaimed effects have never been tested or confirmed independently, neither in vitro nor in vivo, and the alleged clinical improvements cannot thus be differentiated from a placebo effect.

Even if some clinical reports of the ‘70s are subject to justified criticism, hundreds of studies have established the efficacy of transfer factor in treating several pathologies. Its lack of toxicity and the absence of side effects made the use of this extract appealing. Moreover, despite current scepticism, no publication has ever rejected reported clinical claims. An impressive number of clinical studies have demonstrated the efficacy of transfer factor in treating and even preventing viral infections. For instance, Steele and co-workers were able to protect leukaemic children receiving chemotherapy from varicella zoster virus infections using varicella-zoster-specific transfer factor. In the early 1980s, Viza and Dwyer described significant improvement obtained by the use of herpes-simplex-virus-specific transfer factor in treating patients suffering from recurrent genital and/or labial herpes. The clinical observations were later corroborated by experiments in a mouse model.

Other clinical studies have shown that specific transfer factor may produce a spectacular improvement in acute cytomegalovirus (CMV) infections. Moreover, in Africa, children suffering from Burkitt’s lymphoma (a tumour caused by EBV) treated over a long period with EBV-specific TF showed a significant decrease in the rate of relapses. Other viral infections e.g. hepatitis B respond equally well to specific TF.

Transfer factor treatment has proven to be helpful in several neoplasias. One should cite the pioneering work of Fudenberg and that of Pizza. Osteosarcoma, melanoma, breast, lung, prostate and kidney cancer patients have benefited from TF therapy.

Parasitic infections also respond to TF therapy as the data of Sharma, confirmed by Delgado, in treating cutaneous leishmaniasis suggest. Other parasitic diseases known to respond effectively to TF are schistosomiasis and cryptosporidiosis, and several reports cite positive results obtained in treating patients with mycobacterial infections such as lepromatus leprosy, mycobacterium fortuitum pneumonia refractory to antibiotic therapy and tuberculosis. Chronic mucocutaneous candidiasis, an immunodeficiency characterized by chronically relapsing Candida albicans infections also responds well to TF treatment.

___________________________________________________________________________________________________

A SHORT BIBLIOGRAPHY

Ablashi DV, Levine PH, De Vinci C, Whitman JE Jr, Pizza G, Viza D: Use of anti HHV-6 transfer factor for the treatment of two patients with Chronic Fatigue Syndrome (CFS). Two case reports. Biotherapy 1996; 9: 81-86.

Bilello P, Fishman M, Koch G: Evidence that immune RNA is messenger RNA. Cell Immunol 1976; 23: 309.

Boucheix C, Phillips J, Pizza G, Sartorio C, Viza D: Activity of animal transfer factor in man. Lancet 1977; i: 189-99.

Burger DR, Vandenbark AA, Dunnic W, Kraybill WG, Vetto RM: Properties of human transfer factor from KLH-immunized donors: Dissociation of dermal transfer and proliferation augmenting activities. J Reticuloendothel Soc 1976; 24: 385-402.

Chang Y, Cesarman E, Pessin MS et al.: Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi’s sarcoma. Science 1994; 266: 1865-1869.

Delgado O, Romano EL, Belfort E, Pifano F, Scorza JV, Rojas Z: Dialyzable leukocyte extract therapy in immunodepressed patients with cutaneous leishmaniasis. Clin Immunol Immunopathol 1981; 19: 351-358.

Dwyer JM: The use of antigen-specific transfer factor in the management of infections with herpes viruses. In: C.H. Kirkpatrick et al. (eds.) Immunobiology of Transfer Factor. Academic Press, New York 1983: 233-243.

Fernandez-Ortega C, Dubed M, Ruibal O, Vilarrubia OL, Menendez de San Pedro JC, Navea L, Ojeda M, Arana MJ: Inhibition of in vitro HIV infection by dialysable leucocyte extracts. Biotherapy 1996; 9: 33-40.

Fudenberg HH, Fudenberg HL: Transfer factor: Past, present and future. In E. Jucker (ed.): Annual Review of Pharmacology and Toxicology. Birkhäuser Verlag, Basel, Switzerland 1989: 475-516.

Fudenberg HH, Levin AS, Spitler LE, Wybran J, Byers V: The therapeutic uses of transfer factor. Hosp Pract 1974; 9: 95-104.

Fujisawa T, Yamaguchi Y: Postoperative immunostimulation after complete resection improves survival of patients with stage 1 nonsmall cell lung carcinoma. Cancer 1996; 78: 1892-1898.

Galbraith GMP, Fudenberg HH: Transfer factor. In: J. Stone (ed.) : Dermatologic Immunology and Allergy. Mosby, St. Louis, Mo 1985: 889-98.

Gottlieb AA, Sizemore RC, Gottlieb MS, Kern CH: Rationale and clinical results of using leucocyte-derived immunosupportive therapies in HIV disease. Biotherapy 1996; 9: 27-31.

Griscelli C, Revillard JP, Betuel H, Herzog C, Touraine JL: Transfer factor therapy in immunodeficiencies. Biomedicine 1973; 18: 220-227.

Hastings RC, Morales MJ, Shannon EJ, Jacobson RR: Preliminary results in the safety and efficacy of transfer factor in leprosy. In: M.S. Asher, A.A. Gottlieb, C.H. Kirkpatrick (eds.): Transfer Factor: Basic Properties and Clinical Applications. Academic Press, New York 1976: 465-76.

Kirkpatrick C.H, Transfer Factors: Identification of Conserved Sequences in Transfer Factor Molecules. Mol Med 2000; 6(4): 332-341. Kirkpatrick CH, Greenberg LE: Treatment of chronic mucocutaneaous candidiasis with transfer factor. In: A. Khan, C.H. Kirkpatrick, N.O. Hill (eds.): Immune Regulators in Transfer Factor. Academic Press, New York 1979: 547-62.

Lawrence HS, Borkowsky W: Transfer Factor – Current status and future prospects. Biotherapy 1996; 9: 1-5.

Lawrence HS: The transfer in humans of delayed skin sensitivity to streptococci M substance and to tuberculin with disrupted leukocytes. J Clin Inv 1955; 34: 219-32.

Lesser PG, Margarido L, Bolda W, Sartori SG, Hares WA, Freire CA, Fleury R, Montenegro MR, Leser W, Naspitz CK: Cell-mediated immunity in patients with Virchowian Hanseniasis before and after treatment with transfer factor. Hansenol Int J 1980; 5(1); 3-27-34.

Levin AS, Byers VS, Fudenberg HH et al.: Osteogenic sarcoma: Immunologic parameters before and during immunotherapy with tumor specific transfer factor. J Clin Invest 1975; 55: 487-499.

Levin AS, Spitler LE, Stites DP, Fudenberg HH: Wiskott-Aldrich syndrome, a genetically determined cellular immunologic deficiency: clinical and laboratory response to therapy with transfer factor. PNAS 1970; 67: 821.

Masi M, De Vinci C, Baricordi OR: Transfer factor in chronic mucocutaneaous candidiasis. Biotherapy 1996; 9: 97-103.

McMeeking A, Borkowski W, Klesius PH, Bonk S, Holzman RS, Lawrence HS: A controlled trial of bovine dialyzable leukocyte extract for cryptosporidiosis in patients with AIDS. J Infec Dis 1990; 161: 108-12. Meduri R, Campos E, Scorolli L, De Vinci C, Pizza G, Viza D: Efficacy of transfer factor in treating patients with recurrent ocular herpes infections. Biotherapy 1996; 9: 61-66.

Metcalf JF, John JF Jr, Wilson GB, Fudenberg HH, Harley RA: Mycobacterium-fortuitum pulmonary infection associated with an antigen-selective defect in cellular immunity. Am J Med 1981; 71: 485-491.

Neequaye J, Viza D, Pizza G, Levine PH, De Vinci C, Ablashi DV, Biggar RJ, Nkrumah F: Specific transfer factor with activity against Epstein-Barr virus reduces late relapse in endemic Burkitt’s lymphoma. Anticanc R 1990; 10: 1183-1187.

Nkrumah F, Pizza G, Viza D, Phillips J, De Vinci C, Levine P: Regression of progressive lymphadenopathy in a young child with acute CMV infection following the administration of transfer factor with specific anti-CMV activity. Lymphok Res 1985; 4: 237-241.

Pilotti V, Mastrorilli M, Pizza G, DeVinci C, Busutti L, Palareti A, Gozetti G, Cavallari A: Transfer factor as an adjuvant to non-small cell lung cancer (NSCLC) therapy. Biotherapy 1996; 9: 117-121.

Pizza G, Chiodo F, Colangeli V, Gritti F, Raise E, Fudenberg HH, De Vinci C, Viza D: Preliminary observations using HIV-specific transfer factor in AIDS. Biotherapy 1996; 9: 41-47.

Pizza G, De Vinci C, Cuzzocrea D, Menniti D, Aiello E, Maver P, Corrado G, Romagnoli P, Dragoni E, LoConte G, Riolo U, Palareti A, Zucchelli P, Fornarola V, Viza D: A preliminary report on the use of transfer factor for treating stage D3 hormone-unresponsive metastatic prostate cancer. Biotherapy 1996; 9: 123-132.

Pizza G, Viza D, De Vinci C, Palareti A, Cuzzocrea D, Fornarola V, Baricordi R: Orally administered HSV-specific transfer factor (transfer factor) prevents genital or labial herpes relapses. Biotherapy 1996; 9: 67-72.

Pizza G, Viza D, Roda A, Aldini R, Roda E, Barbara L: Transfer factor for the treatment of chronic active hepatitis. N Eng J Med 1979; 300: 1332.

Prasad U, bin Jalaludin MA, Rajadurai P, Pizza G, De Vinci C, Viza D, Levine PH: Transfer factor with anti-EBV activity as an adjuvant therapy for nasopharyngeal carcinoma: A pilot study. Biotherapy 1996; 9: 109-115.

Rappaport FT, Lawrence HS, Millar JW, Pappagianis D, Smith CE: Transfer of delayed hypersensitivity to coccidioidin in man. J Immunol 1960; 84: 358-67.

Sharma MK, Anaraki F, Ala F: Preliminary results of transfer factor therapy of persistent cutaneous leishmania infection. Clin Immunol Immunopathol 1979; 12: 183-190.

Spitler LE, Levin AS, Stites DP, Fudenberg HH, Pirofsky B, August CS, Stiehm ER, Hitzig WH, Gatti RA: The Wiskott-Aldrich syndrome. Results of transfer factor therapy. J Clin Invest 1972; 51: 3216-24.

Steele WR, Myers MG, Vincent MM: Transfer factor for the prevention of varicella zoster infection in childhood leukaemia. N Eng J Med 1980; 303: 355-59.

Steele WR: Transfer factor and cellular reactivity to varicella zoster antigen in childhood leukaemia. Cell Immun 1980; 50: 202-89.

Vich JM, Viza D: Specific suppressor dialysates from mice. In: C.H. Kirkpatrick, D.R. Burger, H.S. Lawrence (eds.): Immunobiology of Transfer Factor. Academic Press, New York 1983: 197-202.

Vich JM, Garcia JV, Engel P, Garcia PA: Transfer to man of sensitization to Keyhole Limpet Haemocyanin by mouse transfer factor. Lancet 1978; i: 265.

Viza D, Goust JM, Moulias R, Trejdosiewicz LK, Collard A, Müllet-Bérat N: In vitro production of transfer factor by lymphoblastoid cell lines. Transplant 1975; VII (suppl. 1): 329-333.

Viza D, Lefesvre A, Patrasco M, Phillips J et al.: A preliminary report on three AIDS patients treated with anti-HIV specific transfer factor. J Exp Path 1987; 3: 653-659.

Viza D, Vich JM, Minarro A, Ablashi DV, Salahuddin SZ: Soluble extracts from a lymphoblastoid cell line modulate SAIDS evolution. J Virol Met 1988; 21: 241-253.

Viza D, Vich JM, Phillips J, Rosenfeld F, Davies DAL: Specific transfer factor protects mice against lethal challenge with herpes simplex virus. Cell Immun 1986; 100: 555-562.

Viza D, Vich JM, Phillips J, Rosenfeld F: Orally administered specific transfer factor for the treatment of herpes infections. Lymphok Res 1985; 4: 27-30.

Wilson GB, Metcalf JF Jr, Fudenberg HH: Treatment of mycobacterium-fortuitum pulmonary infection with “transfer factor” (TF): New methodology for evaluating TF potency and predicting clinical response. Clin Immunol Immunopathol 1982; 23: 478-483.

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Low Cholesterol Levels Increases Cancer Risk- American College of Cardiology

For years, I’ve been telling my patients that the medical establishment’s obsession with lowering cholesterol to prevent heart disease is causing more harm than good.

If your doctor continues to get you worried about your high cholesterol levels, here’s a bit of news for you…

In fact, your high cholesterol may be protecting you from cancer.

Today, I’ll explain the truth behind the myth of cholesterol, and show you how to achieve heart health naturally.

A new study published in the Journal of the American College of Cardiology revealed that driving down cholesterol levels actually increases the risk of cancer.

Researchers at the Tufts University School of Medicine found that among people taking “statin” drugs – like Lipitor and Zocor – there was a higher rate of cancer. Although the link between the drugs and cancer wasn’t clear, there was no doubt that drastically low cholesterol levels correlated to cancer risk.

The big drug makers continue to sell the notion that the best way to fight heart disease is to lower LDL levels, the so-called “bad” cholesterol.

Yet 75 percent of people who suffer heart attacks have normal cholesterol levels.

It makes sense that low cholesterol levels are linked to cancer because cholesterol is one of your body’s basic building blocks. You need it to produce testosterone, to build and repair cell membranes, and to preserve your nerve cells through the formation of the protective “sheaths” that cover them.

Starving your body of this critical substance will lead to other health problems. We already know that extremely low cholesterol levels result in muscle weakness, fatigue, depression, decreased sex drive, and “brain fog.” This new research shows that there may be even more deadly consequences.

What really matters is not low “bad” cholesterol, but high levels of HDL, the so-called “good” cholesterol. As long as you have a high HDL count – 75 to 80, for example – it doesn’t matter whether your total cholesterol is 150 or 350. A high HDL will always keep your risk of heart disease extremely low.

So why haven’t you heard this already? It may be because there’s no drug that effectively raises good cholesterol levels. You can only effectively do it naturally.

Consume natural fats. Avoid processed or fast foods containing “trans” fats – these man-made substances were never meant for consumption, and your body doesn’t know what to do with them. They wind up clogging your arteries and putting you on the fast track to heart disease.

Instead, get your fat from free-range or grass-fed animals, eggs, nuts, and unprocessed vegetable oils. These are some of the healthiest foods you can eat. (As with all foods, look for organic or minimally processed options whenever possible.)

The health benefit of these natural fats comes from their balance of Omega-3 and Omega-6 fatty acids. Your body needs both but, as with cholesterol, they have to be in balance. Omega-3s are great for your heart. They’ve been shown to prevent irregular heartbeat, reduce clogging of the arteries, lower blood pressure, and decrease inflammation in body tissues.
If you stick to eating natural fats, you’ll automatically get the right ratio of Omega-6 and Omega-3, which is about 2:1. As an added bonus, you’ll automatically raise your “good” cholesterol levels and you’ll reduce your risk of cancer.

To Your Good Health,

Al Sears, MD