thalassemia : A short video in tribute to kiran ashfaq 11 yr old

www.deeplymissed.blogspot.com
please watch this.Its a short video 1 min tribute film about a little 10yr old girl Kiran ashfaq who lost her fight for life after an apparently successful bone marrow transplant to cure her of thalassemia major.After only 5 weeks in hospital and 3days of being discharged from hospital,she was back in hospital.And after 8 months in hospital she died from a host of complications such as gvhd and other multiple infections.During her 8 months of stay in the hospital, every organ in her body damaged and failed ,in the end she passed away in our arms, having her last cuddle.Remembered for ever. r.i.p. WESITE http://thalassaemia-major.blogspot.com/ www.deeplymissed.blogspot.com / www.kiran-ashfaq.blog.co.uk

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• st james's hospital
• thalassaemia
• tribute
• love
• death
• memory
• bone
• marrow
• transplant
• film
• life
• disease
• fun
• watch
• gvhd

[keilaknightxox]

I am so sorry for your loss. As a 20 year old girl with Thalassaemia Major, I hope there will soon be a cure for the children.When I am in the hospital getting treatment and im feeling like I just cant take it anymore.. I will think of Kiran ashfaq, she is my inspiration. ♥

[abukiran]

@keilaknightxox thank you for your kind comments. i know it is hard but you have to carry on and be strong for your self and for your family. take care.

[abukiran]

my deep thanks again to all those who have commented on my dear daughter's video .

[tifosilim]

i feel deeply sadden for this video, am a thal major as well and went tho a BMT b4 but the marrow rejected. well, i am lucky to be still living

[abukiran]

thank you and good luck with the future . i hope you get well and stay well. with GOD GRACE OFF COURSE.

[anamica80]

Words can not express what i feel for the family of this little girl.i am so sorry.remember she is in a better place then this world, in JANNAH.

[abukiran]

thank you for your kind words .

[Cheesewyck]

abukiran, your daughter was such a beautiful princess. Many blessings to you & the rest of your family. For me, I still am trying to figure out why alpha thalassemia is affecting me in my mid 30's and I've never had to go for treatment. Your story makes me shake my head to remember that others still have it harder in life than myself. Thank you for the wake up call on this one! All the best to you.

[ACURachaelH]

What a beautiful girl, and my heartfelt love and thoughts are with you.

[esjayay]

I totally understand your feeling because my 4 year old son is currently undergoing BMT. By Allahs wish the transplant is succesful Alhamdulillah, but he has caught fangal infection and coughing for the past 2 weeks now and so far its been 10 long weeks in the hospital Could you please tell me what type of infection your daughter had because I didnt know BMT was that risky as doctors say theres only 98% chance of a risk.

[101faizan]

shes heaven princess

[vinay10949]

She is in heaven and she is smiling down on you and she wants her dad to be strong.....God bless her soul......lots of love from India........

[atee0011]

i cant tell what i feel. i believe she ll be in heaven, because there everyone willl be rewarded according to ones soul.

Sometimes i think its very unfair that some people born with genetic diseases and congenital anomalies.

[livirae21]

Soo sad