Thursday, March 21, 2019

:: Review Filem - Bikers Kental 2 ::



Last weekend ai berpeluang p nonton Bikers Kental 2 kali ni Incik Pinky join (anak-anak pun minat) sebab dia peminat Bikers Kental nih. Kebetulan time kitaorang sampai ada sesi dengan peminat pulak tapi tak sempat nak bergambar sebab masa tu Zizan, Awie & Afdlin dah nak balik.

Mimi siap cakap "Mama..apa Husin Hantu Kak Limah buat kat sini?"
Tergelak besar ai. Hahahaha

Bikers Kental 2. Ceritanya santai sesuai untuk satu family la. Cerita pun straight to the point je tak de kona-kona. Senang faham. Tapi...yang sedehnya awal-awal lagi watak Bront dah dimatikan. Sayangnya....padahal pada pendapat ai dia antara watak yang sangat penting untuk meneruskan kelangsungan BK2 nih tapi tak sure la betul-betul mati ke tak.

Macamana pun BK2 ni tak menghampakan sebab memang boleh buat ai terkekeh-kekeh ketawa. Anak ai pun ketawa maknanya lawak itu sampai even kat budak2 sekali pun. Betul? Ya Betul....!

Selepas Bront mati, BFF Bront la yang meneruskan perjuangan Bront untuk dapatkan balik duit yang Zizan amik masa BK1 dulu.
Kebetulan si Zizan a.k.a Bidin (Bideeeeen) ni masuk Thai balik nak p lamar GF Thai dia tu. Macam biasa si Bidin ni kalau tak buat hal bukan Bidin la kan?

Dah kena kejar balik ngan AL Bukerk (salah eja ni) tu. Dah kena kejar. Abang GF pulak dok jaki je dengan dia. Lepas tu jumpa pulak si Saiya, Saiya ni dah bukak kedai kat Phuket. Dia lak try ejas Bidin. Pulak tu Saiya ni tak seperti Saiya yang dulu...kenapa? Isk isk isk....unsangkerable!!!!

Sudahnya, HERO kena la menang dengan bantuan kawan-kawan Bidin la. Happy ending.

Adid Denyutttttttttttt srooot srooot mmg tak leh blah la lu. Siap bawak gambo "frame" tudung carik jodoh ya?
Hahahahhaa.

Boleh je korang nak pergi tengok. Siapa yang susah nak terhibur akan ada masalah tengok movie nih.

Berapa bintang?
3.9 bintang!

Please sambung p Bangkok pulak ke Pattaya ke Samui ke baru denyutttttttttttttttt lebihhhhhh!



watermark

Tuesday, March 19, 2019

:: Kereta Hello Kitty - Hobiku hias kereta ::




Assalamualaikum/Hi,
Ya selain dari melancong hobi ai adalah hias kereta.
Dah tentu konsep hias kereta tu konsep kegemaran ai - HELLO KITTY!

Siapa yang kenal ai lama tau la tahap kegilaan ai macamana.
Tak de duit kepok-kepok je. Kalau ada....mmg siap bertelinga la kereta ai ni.







Tak semua orang suka kalau kita ni ada hobi.
Kena kecam? Selalu
Keca kecam netizen? Pernah je masa Harian Metro buat coverage tu hari.
Keputusan : Ai don't care..opsssss










Hobi ai ni so far alhamdulillah...memang tak tinggal hobi semata-mata sebab apa?









Sebab hobi tak tinggal hobi. alhamdulillah ada la sikit-sikit jugak pendapatan dari KureSya ai ni.

KureSya?
Ya......naka kereta ai KureSya



Gambar atas masa mula-mula KureSya muncul dalam majalah.







Alhamdulillah sampai sekarang masih ada rezeki KureSya.
Cuma ada sekali hari tu production tu dah janji amik details semua dah sekali dia leh cancel last minute padahal kita dah amik cuti nak hantar KureSya kat set.


Kalau ada sesapa minat nak sewa kereta konsep HELLO KITTY  buat prop birthday ke kawen ke photoshoot apa2 ke leh ke contact ai ye.


Adalah satu drama tu yang pelakon dia ala-ala cinta hati netizen Malaya (katanya).
Sekian.
watermark

Friday, March 15, 2019

:: Neurofibromatosis - Symptom & Cause ::



Overview

Neurofibromatosis is a genetic disorder that causes tumors to form on nerve tissue. These tumors can develop anywhere in your nervous system, including your brain, spinal cord and nerves. Neurofibromatosis is usually diagnosed in childhood or early adulthood.
The tumors are usually noncancerous (benign), but sometimes can become cancerous (malignant). Symptoms are often mild. However, complications of neurofibromatosis can include hearing loss, learning impairment, heart and blood vessel (cardiovascular) problems, loss of vision, and severe pain.
Neurofibromatosis treatment focuses on encouraging healthy growth and development in children affected with the disorder and early management of complications. When neurofibromatosis causes large tumors or tumors that press on a nerve, surgery can reduce symptoms. Some people may benefit from other therapies, such as stereotactic radiosurgery or medications to control pain.

Symptoms

There are three types of neurofibromatosis, each with different signs and symptoms.

Neurofibromatosis 1

Neurofibromatosis 1 (NF1) usually appears in childhood. Signs are often noticeable at birth or shortly afterward, and almost always by age 10. Signs and symptoms are often mild to moderate, but can vary in severity.
Signs and symptoms include:
  • Flat, light brown spots on the skin (cafe au lait spots). These harmless spots are common in many people. Having more than six cafe au lait spots is a strong indication of NF1. They are usually present at birth or appear during the first years of life. After early childhood, new spots stop appearing.
  • Freckling in the armpits or groin area. Freckling usually appears by ages 3 to 5. Freckles are smaller than cafe au lait spots and tend to occur in clusters in skin folds.
  • Tiny bumps on the iris of the eye (Lisch nodules). These harmless nodules can't easily be seen and don't affect vision.
  • Soft, pea-sized bumps on or under the skin (neurofibromas). These benign tumors usually develop in or under the skin, but can also grow inside the body. Sometimes, a growth will involve multiple nerves (plexiform neurofibroma). Plexiform neurofibromas, when located on the face, can cause disfigurement. Neurofibromas may increase with age.
  • Bone deformities. Abnormal bone growth and a deficiency in bone mineral density can cause bone deformities such as a curved spine (scoliosis) or bowed lower leg.
  • Tumor on the optic nerve (optic glioma). These tumors usually appear by age 3, rarely in late childhood and adolescence, and almost never in adults.
  • Learning disabilities. Impaired thinking skills are common in children with NF1 but are usually mild. Often there is a specific learning disability, such as a problem with reading or mathematics. Attention-deficit/hyperactivity disorder (ADHD) also is common.
  • Larger than average head size. Children with NF1 tend to have a larger than average head size due to increased brain volume.
  • Short stature. Children with NF1 often are below average in height.

Neurofibromatosis 2

Neurofibromatosis 2 (NF2) is much less common than NF1. Signs and symptoms of NF2 usually result from the development of benign, slow-growing tumors in both ears (acoustic neuromas), which can cause hearing loss. Also known as vestibular schwannomas, these tumors grow on the nerve that carries sound and balance information from the inner ear to the brain.
Signs and symptoms generally appear in the late teen and early adult years, and can vary in severity. Signs and symptoms can include:
  • Gradual hearing loss
  • Ringing in the ears
  • Poor balance
  • Headaches
Sometimes NF2 can lead to the growth of schwannomas in other nerves of the body, including the cranial, spinal, visual (optic) and peripheral nerves. Signs and symptoms of these schwannomas can include:
  • Numbness and weakness in the arms or legs
  • Pain
  • Balance difficulties
  • Facial drop
  • Vision problems or the development of cataracts

Schwannomatosis

This rare type of neurofibromatosis usually affects people after age 20. On average, symptoms appear between ages 25 and 30. Schwannomatosis causes tumors to develop on the cranial, spinal and peripheral nerves — but rarely on the nerve that carries sound and balance information from the inner ear to the brain. Because tumors don't usually grow on both hearing nerves, schwannomatosis doesn't cause the hearing loss experienced by people with NF2.
Symptoms of schwannomatosis include:
  • Chronic pain, which can occur anywhere in your body and can be disabling
  • Numbness or weakness in various parts of your body
  • Loss of muscle

When to see a doctor

See your doctor if you or your child develops signs or symptoms of neurofibromatosis. The tumors associated with neurofibromatosis are often benign and slow growing. So although it's important to obtain a timely diagnosis, the situation isn't an emergency.
Causes
Neurofibromatosis is caused by genetic defects (mutations) that either are passed on by a parent or occur spontaneously at conception. The specific genes involved depend on the type of neurofibromatosis:
  • NF1. The NF1 gene is located on chromosome 17. This gene produces a protein called neurofibromin that helps regulate cell growth. The mutated gene causes a loss of neurofibromin, which allows cells to grow uncontrolled.
  • NF2. The NF2 gene is located on chromosome 22, and produces a protein called merlin (also called schwannomin), which suppresses tumors. The mutated gene causes a loss of merlin, leading to uncontrolled cell growth.
  • Schwannomatosis. So far, two genes are known to cause schwannomatosis. Mutations of the genes SMARCB1 and LZTR1, which suppress tumors, are associated with this type of neurofibromatosis.

Risk factors

The biggest risk factor for neurofibromatosis is a family history of the disorder. About half of people with NF1 and NF2 inherited the disease from the affected parent. People with NF1 and NF2 that don't have affected relatives likely have a new gene mutation.
NF1 and NF2 are both autosomal dominant disorders, which means that any child of a parent with the disorder has a 50 percent chance of inheriting the genetic mutation.
The inheritance pattern for schwannomatosis is less clear. Researchers currently estimate that the risk of inheriting schwannomatosis from an affected parent is about 15 percent.

Complications

Complications of neurofibromatosis vary, even within the same family. Generally, complications result from tumor growth distorting nerve tissue or pressing on internal organs.

NF1 complications

Complications of NF1 include:
  • Neurological problems. Learning and thinking difficulties are the most common neurological problems associated with NF1. Uncommon complications include epilepsy and the buildup of excess fluid in the brain.
  • Concerns with appearance. Visible signs of neurofibromatosis — such as extensive cafe au lait spots, many neurofibromas in the facial area or large neurofibromas — can cause anxiety and emotional distress, even if they're not medically serious.
  • Skeletal problems. Some children have abnormally formed bones, which can result in bowing of the legs and fractures that sometimes don't heal. NF1 can cause curvature of the spine (scoliosis) that may need bracing or surgery. NF1 is also associated with decreased bone mineral density, which increases the risk of weak bones (osteoporosis).
  • Vision problems. Sometimes a tumor develops in children on the optic nerve (optic glioma), which can affect vision.
  • Problems during times of hormonal change. Hormonal changes associated with puberty or pregnancy might cause an increase in neurofibromas. Most women with NF1 have healthy pregnancies but will likely need monitoring by an obstetrician familiar with the disorder.
  • Cardiovascular problems. People with NF1 have an increased risk of high blood pressure and may develop blood vessel abnormalities.
  • Breathing problems. Rarely, plexiform neurofibromas can put pressure on the airway.
  • Cancer. An estimated 3 to 5 percent of people with NF1 develop cancerous tumors. These usually arise from neurofibromas under the skin or from plexiform neurofibromas. People with NF1 also have a higher risk of other forms of cancer, such as breast cancer, leukemia, colorectal cancer, brain tumors and some types of soft tissue cancer. Women with NF1 should start screening for breast cancer at an earlier age than the general population.
  • Benign adrenal gland tumor (pheochromocytoma). This noncancerous tumor secretes hormones that raise your blood pressure. Surgery is usually needed to remove the pheochromocytoma.

NF2 complications

Complications of NF2 include:
  • Partial or total deafness
  • Facial nerve damage
  • Vision problems
  • Small benign skin tumors (skin schwannomas)
  • Weakness or numbness in the extremities
  • Multiple benign brain tumors or spinal tumors (meningiomas) requiring frequent surgeries

Schwannomatosis complications

The pain caused by schwannomatosis can be debilitating and may require surgical treatment or management by a pain specialist.

this lump, just pop out of nowhere and when i woke up one morning it just there like it was there long ago but it doesn't it become bigger quite quick recently and it is a hard lump.
Hopefully nothing goes wrong down there because it already start fells like..uncomfy.




watermark

Wednesday, March 13, 2019

:: Kebun Bunga Matahari Thailand ::






Assalamualaikum/Hi,
Apa khabar semua hari nih?
Kali ni ai nak cerita tentang perjalanan ai mencari Kebun Bunga Matahari masa ai ke Thailand tempoh hari.





Lopburi antara tempat yang sangat terkenal dengan keindahan ladang bunganya terutama bunga matahari.
Tapi kalau korang nak tahu dekat Satun pun ada satu tempat yang tak berapa besar tapi bila tiba musim bunga mataharinya kembang, memang puas hati jugaklah kalau nak ke sana.
BERBALOI!



Bunga matahari di Satun akan kembang sekitar bulan Februari hingga Mac setiap tahun.
Jadi kalau korang nak melihat bunga matahari yang gemok-gemok yang memang cantik tanpa perlu korang naik flight atau memandu sampai ke Bangkok, bolehlah ke Satun. Memang tak sama dengan yang ada kat Lopburi. Tapi, bolehlah dari tak de.





Cara nak sampai ke kebun bunga matahari ni memang tak susah. Dari Kuala Lumpur sila ke Dannok/Wang Kelian/Ban Prakob (ikut suka korang  nak ikut border yang mana) yang penting korang MESTI menghala ke arah PAK BARA (now...siapa kata Pak Bara ni tak de tempat best?). Kemudian korang bolehlah cari jalan menuju ke arah Rawai beach dan cari Thung Bu Lang.






Thung Bu Lang ni adalah sebuah perkampungan yang ada jauh sedikit dari bandar. Makanya sila berhati-hati ketika memandu. Banyak lorong-lorong kecil keluar masuk kampung.
Yang seronoknya dekat sini waktu BUKAN musim bunga matahari kawasan ni agak sunyi walaupun terdapat tasik yang cantik.
Bila tiba je musim bunga matahari penuh kawasan ni dengan peniaga-peniaga makanan/minuman dan pelancong tak yah kira la. Tak berapa padat - masih seleasa.

Bayaran masuk? TIADA BAYARAN masuk setakat ni yang penting korang tolong parking kereta ditempat yang sesuai tanpa menghalang lalu lintas.






Bukan setakat bunga matahari yang kuning tu je..ada bunga-bunga lain yang KUNING yang sama naik kembang mekar bila tiba musim bunga/panas kat Thailand nih. Tu korang belum tengok pokok Raja Phruek yang menguning kat sepanjang jalan kat Songkhla/Samila Beach. Lawaaaaaaaa~





Penginapan? Korang boleh menginap di sekitar Satun mahupun Pak Bara. Jaraknya dari Pak Bara lebih kurang 30 minit je.
Balik dari Thung Bu Lang ni kalau korang nak singgah amik angin kat Rawai Beach pun boleh atau boleh la jenguk-jenguk Wang Saithong Waterfall (lawa tempat nih. ni ada bayaran masuk ye lebih kurang THB200/pax).

So, memandangkan sekarang pokok bunga mataharinya pun dah kering sebab dah pertengahan Mac pun. Jadinya kena tunggu next year la ye kalau  nak pergi. Dan insyaAllah kalau murah rezeki, memang akan jadi program tahunan ai nanti. Kalau nak ikut next time boleh je. Bawak kereta masing-masing ye.




Ok...sekian!



watermark

Tuesday, March 12, 2019

:: Review : Royal Hill Satun, Pak Bara ::

Pak Bara ni adalah salah satu tempat di selatan Thai. Dan ia adalah hub untuk lompat ke Koh Lipe. Jarang sekali ai tengok orang datang Pak Bara duduk setempat 3-4 hari. Tapi ai suka stay kat Pak Bara sebab tenang!

So hari ni ai nak cerita sikit tentang hotel kegemaran ai. Setiap kali datang Pak Bara MESTI stay dekat sini.

HOTEL ROYAL HILL SATUN.






Taraf : 4 bintang
Harga : Bermula RM180-255 (ikut low season/high season)
Kemudahan : Kolam renang, kareoke, gym, hotel transportation
Kelebihan : Mesra muslim, ada bilik pemandangan laut, bilik luas, pekerja yang semunya mesra pelanggan
Kekurangan : tak berapa sesuai untuk orang tua yg sakit lutut, hotel memang ada lif tapi kalau sebenarnya kena b uat sikit aktiviti mendaki tangga kalau nak ke bilik especially kalau bilik high floor.

Ai suka stay dekat RHS ni sebab ia memang menepati ciri2 hotel kegemaran ai di samping harga yg affordable dengan service yang teramatlah baik.





Hotel bersih, pemandangan cantik. Tak pernahlah kalau mintak apa2 tak diendah. Yang penting anak-anak ai yang suka mandi swimming pool tu dapat mandi swimming pool.





Tempatnya juga sangat dekat dengan Taman Negara Mu Ko Phetra (entry Mu Kho Petra KLIK SINI), dekat dengan Five Colors Beach. Jalan kaki je kat bawah hotel.



(bumbung yang korang nampak tu pintu masuk Mu Kho Petra)


(lepak-lepak kat 5 colors beach)

Pak Bara view point & pasar malam pun tak jauh dari hotel.



Yang bercahaya tu la kawasan view point/pasar malam. Memang boleh nampak dari bilik hotel je.



Sarapan pagi memang disediakan sekali dengan pakej bilik. Makanan memang banyak pilihan. Boleh duduk dari pagi sampai waktu habis makan.
Bilik pulak memang lengkap dengan arah kiblat.











Kalau ikut saiz bilik yang besar tu selain dari kami 4 beranak yg muat katil king. Rasanya tolak tambah boleh muat lagi 4 katil single! Cuma kalau nak tambah katil dalam RM50 satu katil lipat tu.










Maka begitulah ceritanya. hahahhahaa..selamat beristirehat!





watermark

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