Never heard of it???
Well the predominent countries are, India, Pakistan and Iran with millions of sufferers.
Thalassemia minor is an inherited form of hemolytic anemia that is less severe than thalassemia major. This blood smear from an individual with thalassemia shows small, pale, variously-shaped (poikilocytosis) red blood cells.
These small red blood cells (RBCs) are unable to carry the sufficient amount of oxygen required by normal RBCs.Cells require oxygen (O2) to live, because O2 is what our body cells feed off.
Without O2, cells will starve and die. .
When you breath in air you get approximately 21% O2 as you inhale.
Transported to your lungs it hops aboard the fresh blood's haemoglobin in RBCs pumped from your heart.
Via circulation it then gets transported all over your body to feed and revitalize billions of cells to keep you alive.
Treatment for these children is a blood transfusion every month.
Without this treatment the sufferer would die.
And what about the children who's parents cannot afford this??
There is also a cure, but it is an expensive one, and not one that is readily available.
The cure is a Bone Marrow Transplant,
or for some, the Stem Cells from the mother.
Yet this is not a hundred percent success.
It is only for unrelated (donor registries) bone marrow donation that the age limit is much narrower, generally between age 20 and 40.
Money speaks, so donations are desperately needed.
This is a despairing disease and the sadness is.... many die.
Should the Lord place it on your heart to help then your donation would gratefully be appreciated.
http://www.cure2children.org/node/222
"There will always be poor people in the land.
Therefore I command you to be openhanded toward your brothers and toward the poor and needy in your land." Deuteronomy 15:11
Thanks sister---for writing about thalassemia.It's really very necessary to know people about this,espacialy in india and other asian contries.i hope people read this and be aware for this illness.
ReplyDeleteWith Regards.
Hemant
Happy Thursday,
ReplyDeleteGlad to see you in my place.
Take good care.
I value your kindness.
I have a niece who went through so many awful, seemingly endless transfusions. She's okay now by God's grace. I'm glad you posted about this genetic disease. Blessings.
ReplyDeleteYou know Mary, Just knowing that disease and such as this won't be allowed in heaven is going to make heaven just a little sweeter yet.
ReplyDeleteHement, You might like to add the Widget for Save z Children onto your Blog?
ReplyDeleteJungle, what a sweet girl you are...
Rose, Its good to share with others and help with understand.
Covnitkeprf, I have to say, I can't wait to get
there. It will be wonderful...
God bless you all for your visit.
Blessings Crystal ML