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THALASSEMIA N ME Official Website

Thalassemia Major Sufferer from inherited blood disease, determined and try to live a better quality of life.

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Henry Ng

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Sin●●●ore , Singapore, 349316

SG

65.9●●●●4299
he●●●@verzdesign.com

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Verz Consulting Pte Ltd

Henry Ng

81 Ubi Avenue 4,●●●●●●●●●●●●●●●●Singapore 408830

Sin●●●ore , Singapore, 349316

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65.9●●●●4299
he●●●@verzdesign.com

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THALASSEMIA N ME Official Website | thalassemianme.org Reviews
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Thalassemia Major Sufferer from inherited blood disease, determined and try to live a better quality of life.
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1 Thalassemianme
2 Thalassemia
3 Thalassaemia official Website
4 Living a Better Life
5 Inheribated Blood
6 Disorder Disease
7 Genetic Minor
8 Intermedia Major Anemia Patients
9 Cure Treatment Transfusion Sufferer Prevention Supplements Chelater Chelation Life Span Expectancy Oral Iron Overload Desferal Deferoxamine Ferrirpox Deferirpone L1
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THALASSEMIA N ME Official Website | thalassemianme.org Reviews

https://thalassemianme.org

Thalassemia Major Sufferer from inherited blood disease, determined and try to live a better quality of life.

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1

What Is Thalassemia | THALASSEMIA N ME Official Website

http://www.thalassemianme.org/what-is-thalassemia

Hp: 65 9820 6703. Raquo; What Is Thalassemia. WHAT ACTUALLY IS THALASSEMIA? In severe form of Thalassemia (known as Thalassemia Major),the person will require a lifetime monthly blood transfusions. This is a painful and traumatic treatment regime that imposes an enormous financial and emotional strain on the patient, and also on his or her family. Thalassemia intermedia is more difficult to prevent and diagnose by screening before birth. As most Thalassemia intermedia patients only began to have symp...

2

Announcement | THALASSEMIA N ME Official Website

http://www.thalassemianme.org/announcement

Hp: 65 9820 6703. Just received a mail saying the 2nd Singapore Thalassaemia had been postponed, might be due to not enough patients and family attending that’s what I am. On behalf of Mr Derrick Lim, President of Thalassaemia Society (Singapore), we regret to inform you that due to unforseen circumstances, the 2nd Singapore Thalassaemia Conference for Asia originally planned to be held from 2-4 September 2011, has been postponed to the 2nd quarter of 2012. 2-4 September 2011, Singapore.

3

About Me | THALASSEMIA N ME Official Website

http://www.thalassemianme.org/about-me

Hp: 65 9820 6703. Raquo; About Me. About THALASSEMIA N ME. Goh Chun Hui is a Sufferer of this inheribated blood disorder known as Thalassemia Major. Despite being born with such a condition, he insists on living a normal life. He is also fully aware that this condition puts him and other like him at a disadvantage. It is precisely for this reason that he takes it upon himself to educate and inspire them, not only by Thalassemia world. Hoping you and me will Impact the Mission together.

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LINKS TO THIS WEBSITE

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME

http://thalassemianme.blogspot.com/2013/12/blog-post_30.html

Get paid to share your links! Monday, December 30, 2013. Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME

http://thalassemianme.blogspot.com/2014/07/mr-marc-wong-left-and-goh-chun-hui.html

Get paid to share your links! Friday, July 4, 2014. Mr Marc Wong (Left) and Goh Chun Hui (Right), two regular blood recipients who has Thalassemia Major condition. They are well alive today owing to the many selfless contributions from blood donors. Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME

http://thalassemianme.blogspot.com/2014/01/blog-post.html

Get paid to share your links! Monday, January 6, 2014. Disclaimer: This video is make just for entertainment purpose, not mentioning thalassemia are different or lazy for work. It's just a scene, I am trying to being out and related based on my own experience. Thalassemia patients do feel tried more easily and might sleep more due to their lower hemoglobin level. Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME

http://thalassemianme.blogspot.com/2013/12/blog-post_31.html

Get paid to share your links! Tuesday, December 31, 2013. Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME: Say Haze!

http://thalassemianme.blogspot.com/2014/03/blog-post.html

Get paid to share your links! Tuesday, March 11, 2014. Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME

http://thalassemianme.blogspot.com/2014/06/an-powerpoint-presentation-video-in.html

Get paid to share your links! Wednesday, June 11, 2014. An PowerPoint Presentation video in collaboration with the World Blood Donor Day 2014! Without them we wouldn't be here. Thank you! Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

thalassemianme.blogspot.com thalassemianme.blogspot.com

THALASSEMIA N ME

http://thalassemianme.blogspot.com/2014/01/biogen-idec-forges-320m-gene-editing.html

Get paid to share your links! Saturday, January 11, 2014. Biogen Idec forges a $320M gene editing deal aimed at curing inherited blood disorders. Http:/ www.fiercebiotech.com/story/biogen-idec-forges-320m-gene-editing-deal-aimed-curing-inherited-blood-diso/2014-01-09. Http:/ www.sangamo.com/. Posted by THALASSEMIA N ME. Subscribe to: Post Comments (Atom).

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THALASSEMIA N ME

Get paid to share your links! Friday, July 4, 2014. Mr Marc Wong (Left) and Goh Chun Hui (Right), two regular blood recipients who has Thalassemia Major condition. They are well alive today owing to the many selfless contributions from blood donors. Posted by THALASSEMIA N ME. Wednesday, June 11, 2014. An PowerPoint Presentation video in collaboration with the World Blood Donor Day 2014! Without them we wouldn't be here. Thank you! Posted by THALASSEMIA N ME. Tuesday, March 11, 2014.

thalassemianme.com thalassemianme.com

Home - THALASSEMIA N ME

Contact Me - Message. HemoThal Heros Blog Post. List of Blog post. 2nd Pan-Asian Conference on Haemoglobinopathies. Date of Event: 25 - 27 September 2015. Venue: Hanoi, Vietnam . World Thalassaemia Awareness Day and Blood Donation Drive 2015. Date of Event: 08 May 2015. Time: 10.00am - 4.00pm. Venue: KKH Auditorium Foyer (Training Centre), Level 1, Women's Tower. BLOOD: THE GREATEST TREASURE OF LIFE. Date of Event: 07 June 2014. Time: 10.00am - 6.00pm. Venue: Sentosa, Port of Lost Wonder*. New Contact Me...

thalassemianme.org thalassemianme.org

THALASSEMIA N ME Official Website

Hp: 65 9820 6703. Goh Chun Hui is a Sufferer of this inherited blood disease known as Thalassemia Major. Despite being born with such a condition, he insists on living a normal life. THALASSEMIA N ME was setup to share with everyone, the life of living withThalassemia Major Condition. Spreading hope and awareness through my website, blog, Facebook, Twiiter and YouTube. Reproduction without permission prohibited.

thalassemians.com thalassemians.com

Thalassemians.com

thalassemiapatientsandfriends.com thalassemiapatientsandfriends.com

Thalassemia Patients and Friends - Index

August 14, 2015, 08:18:12 AM. Tell everyone they can now find this site by typing this into their browser:. Click to visit us on Facebook. If you have any problems registering or signing in, please send an email to: andy@thalpal.com. Please do not send questions about thalassemia to this address. Thalassemia Patients and Friends and thalpal A. Battaglia 2015. Thalassemia Patients and Friends. Tribute to Lisa Cammilleri (1970-2004). Lisa touched many lives. How did she touch yours? Last post on Yesterday.

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thalassemiasociety.org thalassemiasociety.org

index

Welcome on the web site of the Thalassemia Society of Mauritius. Which is an NGO. Non-Governmental Organisation) dedicated to the well being of Mauritians who are. Touched with Thalassemia which is a genetic blood disorder. The Thalassemia Society of Mauritius is an NGO duly registered with The Registrar of. Associations on 01 October 2009 bearing Registration No: 11194. Provide moral support to all persons with thalassaemia and their families to overcome their. Emotional and psychological problems.