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Archive for May, 2012

Bernards: Azemeraw

Azemeraw is heavy on my heart.  He is 14 years old. He has cerebral palsy and autism.  He’s never stood straight, never walked, never spoke, until he came to CURE.  Now his legs are straight, and we hope he will learn to walk with braces. Best of all, he has found his voice. I often hear him singing during the day, his voice carrying all the way from the inpatient ward to the operating room. He is loud and clear and so joyful. His voice has been awakened as he feels love for the first time – from our staff, as they share God’s love with him.

His family was unhappy to shoulder the burden of his care.  It can be so difficult to survive here, let alone care for someone with special needs.   Because of this, he was neglected.  They said he has never spoken.  They have left him at CURE, and won’t respond to our calls to come and care for their son or to be ready to bring him home.   Whenever I pass by Azemeraw, he is quick to greet me and hold my hand.  He always asks how I am doing and says he is doing well.  The nurses are obviously very fond of him. He sits by the nurses’ station often, basking in their company.  I worry what will happen when it is time for him to leave the loving environment of CURE.  Please join me in prayer for him, as we seek for a place for him.  I pray it will be a place where he will thrive.  He is so ready to love and be loved.

Originally posted at: http://ethiopia.thebernards.org/2012/05/24/asmerew/.

The value of additional information

My wife’s sister spent a semester abroad when she was a junior in college.  Ann minored in French and she lived and studied in Besançon, a town south of Paris.  During the months Ann was there, first her parents and then my wife and I visited her.  During our visit, Ann took us to a restaurant that she had been to during the visit with her parents.  Because I could not read French, Ann helped me navigate the menu.  She pointed out an appetizer that her dad had gotten which I decided to try.

When the first round of food was delivered to our table, my selection for an appetizer looked like a 5″x5″ cube of Vaseline with an egg, pieces of ham, celery, and other items suspended within the translucent cube.  I decided to try it, and it tasted an awful lot like… a cube of Vaseline with an egg, pieces of ham, celery, and other items.  Trying not to show visible signs of disdain, I said, “Boy, Ann, this really does not taste that good.”  She then replied, “Yeah, my dad didn’t like it either.”

That is when I learned the value of additional information obtained from a good follow-up question: after finding out what my father-in-law had ordered, I should have asked if he had liked it. Read the rest of this entry »

Josh & Julie Korn: CCW in Niger

A baby with clubfoot at the Dosso hospital.

A few days ago, I had the opportunity to go and visit one of the CURE Clubfoot Wordwide clinics in the town of Dosso, 140 km. away from Niamey. It was in the regional hospital of Dosso, and we met with the surgeon, the physical therapist, and the counselor (as well as a few others). It was really great to talk with them a bit,  hear some of the challenges they face, and see them in action.

I met them before, when they came to the CURE hospital in Niamey for a training, but that was when we first got here, so it was good to see them again. They told us that before the training they had no way of treating clubfoot, so whenever they saw clubfoot cases they always referred them to the National hospital in Niamey. Obviously, this was not an option for many families because of the distance and the cost(s) of the trip. But now, they can treat them right there in Dosso, and it is paid for.

One of the patient we saw being treated was Al-Moustapha. He is only three months old. He came in for a recasting, his third one. With the Ponseti Method of treating clubfoot, a series of casts are used to set the feet back in place, which is great because it avoids surgery (at least most of the time; sometimes small surgical procedures are needed). But it is a long and drawn out process, and it involves a lot of visits to the hospital. Al-Moustapha was at the hospital the week before, and now he was back again, getting new casts on both of his legs. It is hard for the families to come to the hospital so often, especially when they don’t live nearby. Some of the families are from villages that are far away, and they often come the night before and spend the night at the hospital so they can be there in the morning to see the doctor. It goes without saying that they don’t spend the night in a bed (most of the patients don’t even have beds). They sleep on a mat on the dirt floor. But that is enough for them; they are just happy to be able to get treatment for their children.

When it was time for the recasting to begin, they first soaked Al-Moustapha’s legs in a bucket of water to loosen up the plaster, and then they just peeled it off. They didn’t use an electric saw to cut off the casts (the power went out while we were at the hospital, so this probably wouldn’t be the best choice even if they did have a saw). All they needed was a bucket and water. I remember when I broke my leg as a kid and they used a saw to take the cast off. That was the most painful part of the process, and it was scary with the saw buzzing right next to my leg. Why didn’t they just do it this way?

 

Next they massaged Al-Moustapha’s feet and legs, and stretched them out. He didn’t like this part very much.

Finally, they put new casts on Al-Moustapha’s legs, and it was done quickly and done well. Al-Mopustapha (“Al-Mou” to his close friends and family – seriously) almost slept through this part.

Since the program started not too long ago, they still do not have a ton of patients coming in to Dosso. A lot of them still go to Niamey because they don’t know that they can be treated in Dosso. It takes time for that kind of information to really sink in, but while we were there a young couple came in with their baby. The future for this program looks bright, and it is exciting to see the progress.

Short-term missions: what it’s really like

We’ve told you a lot about our wonderful volunteers and how their time and talents are a blessing to each of the hospitals they visit, but have you ever wondered what it’s really like to volunteer at a CURE hospital?

If you think traveling to a foreign country, meeting lots of new people, and partnering in the work of changing the lives of children and their families sounds pretty fun and adventurous, your right! Our goal in the GO department is that our volunteers not only help kids, experience new cultures, and have a great time, but that these trips would make a permanent impact on their life journey.

For some volunteers, the impact of a short-term trip can manifest itself in a future career in medicine or missions; for others, the trip taught them something about themselves or about God that has changed them forever. Other volunteers will go home to share their story and spread the word about what CURE is doing, becoming a lifetime advocate for our work.

Every trip, like every volunteer is a unique journey that we hope will change our volunteers in a positive way for the rest of their lives, but don’t take my word for it. Learn from these volunteers as they share their own journeys with CURE through their blogs.

Each of these individuals has volunteered or continues to volunteer with CURE and has blessed us by sharing their journey. You will find that each story, like each volunteer, is wonderfully unique and insightful.

Enjoy your peek into the life of a CURE volunteer. Perhaps one of these blogs will inspire you to make a journey of your own!

Pennsylvania high school holds D4K Dance-a-thon

We received the following update from James Buchanan High School in Mercersburg, PA:

Earlier this year, the James Buchanan High School Student Council took the challenge of helping children in need of surgeries in foreign countries with a D4K Dance-a-thon.  The Student Council had always discussed doing a Dance-a-thon and thought it would be a fun thing for the student body to do.  After learning about the “Dance 4 Kids Who Can’t” program from CURE International,  we decided it was a great opportunity.

Planning the unknown was quite the experience, as we had never done anything like the Dance-a-thon and had no idea how many students to plan on for, let alone anything else.  As we planned the event, we successfully got many donations from local businesses, such as 30 gallons of Sweet Tea from Chick-fil-a and many door prizes from other businesses.  We made t-shirts for the event with our technology department’s screen-printing equipment, posted many posters about the Dance-a-thon, had a photobooth, and got a former student to donate his DJ services.

The event turned out to be a fun and successful day, with lots of food, dancing, and games.  As a whole, we raised around $900, $600 of which went directly to CURE.  Looking back on the experience, we learned a lot and raised awareness of the conditions of children in foreign countries.  It’s a great feeling to know that we were able to impact children all over the world and make their lives better.

- Natalie Brant, James Buchanan High School Student Council

 

You can find photos of this event on Pinterest: http://pinterest.com/curekids/dance-for-kids-who-can-t/.  Interested in hosting your own D4K event with your school, group, or organization?  Learn more at http://cure.org/d4k.

Tom and Tim

A photo essay from CURE Zambia.

Meet the Machinko family - Mr. and Mrs. Machinko and their twin sons, Tom and Tim. Mr. Machinko is a landscape contractor that works on the CURE Zambia grounds. He is passionate about doing a good job to keep the hospital looking its best. He is even more passionate about telling people how CURE Zambia transformed the lives of his sons.

Read the rest of this entry »

Josh & Julie Korn: Healing takes time

Kabirou was one of the first patients that we met here at the hospital. I think we met him the second or third day we were in Niger, almost nine months ago. He came to CURE because his foot was totally deformed. When he was four years old, he injured his foot on a rock and wasn’t able to walk on it normally, so he started walking on the outside of his foot. At first he did this because of the pain. But he did this for such a long time that eventually he couldn’t walk on the bottom of his foot, and his foot was permanently deformed. Read the rest of this entry »

CURE In the News: Week of May 13, 2012

CURE Uganda

CURE gives hope to babies” from New Vision

 

CURE Afghanistan

Life and war in Afghanistan” (photo) from the Washington Post

 

CURE International

High School Students Impact Society With Senior Projects” (photo) from Gingham Patch

 

CURE Philippines

Time for Tim” from Philippine Daily Inquirer

 

Bernards: Patience

Tigist is a little girl who is 11 months old. The name Tigist means “patience.” Her mother is a young woman who loves her little girl very much. Her mother was taken by force and “married” illegally, meaning the man took her, raped her, and forced her to stay with him. Eventually she became pregnant. When the pregnancy became obvious to her “husband,” he no longer had use for her and kicked her out. According to the predominant religions of this area, it is not allowed to have sex with a pregnant woman, so she was dismissed.

Read the rest of this entry »

Josh & Julie Korn: Hauoa

Haoua has been at the hospital for a few weeks. She came with her mom, Hadiza, and her little brother, Ganiou. She came to the hospital because she had a big tumor on her leg, and she has had it since she was 5 years old. She is 11 years old now.

Read the rest of this entry »