Friday, December 14, 2012

While I’ve been here over the past month I’ve dwelled a lot on the parts of life here that are not so exciting or inspiring.  I’ve felt frustrated over the loss of much of the autonomy I had back home.  My choices of how I spend my time, where I spend my time, what I eat, where I eat, etc. have all been very limited here.  On a day to day bases life is basically the same-old same-old as a Mercy Ships crewmate, so it’s been hard to see the important things that have been going on here.  I’ve been overlooking what Mercy Ships really does for people.

  As an example, for the past month the hospital has designated an entire ward to treating women with vesico-vaginal fistulas (VVF).  You may not know what this is.  I didn’t until I got here.  A VVF is a hole that develops through the wall of a woman’s vagina during child birth.  This doesn’t happen to just any woman.  It is caused by both circumstantial and physical factors.  These women have little to no access to health care.  They mostly live in rural communities that are several days journey away from a hospital.  They have no health professionals nearby to aid in the delivery of their child.  Often these women are married at a young age, like 14, and have not fully developed.  The other women that are older may have poor nutrition and have not grown to their full stature.  These women that are small do not have pelvises that are large enough to deliver a child through their birth canal.  As a result of these factors when these women become pregnant they often times have difficulty delivering the baby.  The baby is unable to pass through birth canal, and can be stuck for several days.  While the baby’s head is stuck it is blocking off the blood supply to the wall of the birth canal.  Without blood supply the tissue dies and a hole is left behind.   In almost all cases the baby is lost.  In addition to the immense amount of emotional damage, these women are left with physical damage too.  The holes that are created run right through into the bladder and/or the rectum and therefore these women become permanently incontinent without medical treatment.
  The thing that grabs my attention the most about these women is the social stigma they face.  The incontinence is what pushes them out of their homes, families, and villages.  Because of the holes in their vagina they can’t control their urine and feces, so they constantly leak.  With constant leaking comes constant smell.  People don’t want to be around smelly people.  They are often rejected by their family and community because of their inability to function in normal life. 
  Mercy Ships tries to locate as many VVF women as they can when they arrive in the country.  They sent a screening crew into the interior of Guinea to evaluate women with incontinence problems.  Once enough women were screened and selected to fill-out the surgery list they were scheduled to be admitted to the hospital.  They arrived over a month ago.  When first they arrived they came in clothing that had been soaked in their own waste.  The smell was so strong that it permeated through the whole hospital.  I wasn’t even involved in caring for them, but I could still smell their presence.  It was hard not to be bothered by it.  I was challenged to remember that it’s not the fault of these women that they smell.  After showering and having their clothes laundered the smell was a lot more controlled.
   The surgeries have been going on for about a month now, and while there have been many challenges fixing these women, some have been healed and are now continent.  The amazing thing about these women is their joy and appreciation for being loved and treated like a normal person by the Mercy Ships crew.   Another extraordinary thing is that they have now found other women who have the same problem and have faced the same challenges.  Not only is the hospital a place for physical healing, it’s a place for emotional healing too.  Even if they’re not fixed yet you can tell that they are happy. 
  I have not personally cared for these women, except for one shift when I got floated to that ward, but from what I’ve learned about them I find a challenge for myself when come back home.  My challenge is to not be one of the many people that reject or ignore people with unsightly or unpleasant physical disabilities.  I think a common thing I do is blame people for their problem.  I think, “Why can’t they clean up better?” Or “Why would they let themselves be that way?”  It’s a strange human impulse to blame people for their diseases.  If only I had the wisdom to always consider that they may have no fault in their physical or mental disabilities.
  If you’re interested in learning more about VVF and the emotional struggle women go through with this disease you should check out the documentary “A Walk to Beautiful”  It’s very good.

Weekend out in Kindia


Wednesday, December 5, 2012

I have a week and a half left on the ship.  Crazy.  When I started 4 months ago I couldn't imagine there ever being an end.  Now it's just up ahead, almost in view.   As I mentioned in my previous post, things are really changing here.  Even more people left in the past week.   Our evening Dutch Blitz game crew is getting pretty sparse.  It's harder to find people to sit with at meals.  Those of us who remain have stuck together, but soon I will be another one to jump ship.  Over the holidays the crew (especially hospital crew) will be quite small because there will be no surgeries performed for a couple weeks.  All the patients will be combined to one ward.  Once the holidays have passed a new influx of crew will come to the ship.  I imagine this place will breath new life in January.
  Despite all the sadness of saying good-bye every other day the holidays have made ship-life fun.  This past weekend people put Christmas decorations up all around the ship.  There are Christmas trees, wreaths, ornaments, Christmas lights, and garland everywhere.  The international lounge where we have our church services is so nicely decorated that it almost made me want to cry.  It's amazing to be able to celebrate such an important holiday with Christians from around the world.  I'm grateful for not being in America right now.  There are too many distractions from the the true purpose of the holiday back home.  There's no talk of sales, toys, or new gadgets on the ship.  I think Americans could learn a thing of two from the Dutch.  They celebrate the Santa Claus part of Christmas on a different day than the celebration of Christ's birth. Today is Sinterklaas.  The day when the Dutch celebrate Saint Nick bringing gifts to the children of Holland.  I put my shoe outside my door last night and this morning I had a carrot in it.  I think the carrot was for Sinterklaas' horses, so it should have been what I put in my shoe last night. Oh well, at least I didn't get any coal.  Tonight Sinterklaas will even come to the ship. That should be fun.  Later this month on December 25th the Dutch will Celebrate Christ's birth.  I think this makes more sense that what we do in our country.
  Work is going well for the most part.  I only have 6 more shifts.  Hopefully they're fun and worthwhile.  There is one patient who has been with us since the hospital opened.  He has not been doing well.  About a week ago he developed meningitis as a complication of his surgery, and while he's mostly recovered from the meningitis he has a long road ahead.  His name is Abou and he's 16 years old.  He was born with a myelomeningocele (look it up) and the surgeons thought they could help him by removing it.  The surgery site took very long to heal.  He was leaking CSF for a long time and now he has a CSF drain to control his leaking.  The drain is only a temporary fix.  What he really needs is a shunt.  It would drain the extra spinal fluid into his abdominal cavity.  The surgery can probably be done on the ship, but it again would only be a temporary fix.  The shunts get clogged occasionally and can sometimes get infected.  The ship leaves Guinea in June and probably won't be coming back for several years, so there be no chance of us offering follow-up care for him if he has complications.  It's a sad situation all together, because he may not get past this.  His mother said this week that she didn't think she would see him leaving the ship.  We've had several 24-hour prayer days for him and it seems that God's answer is not to let him be healed at this time.  The crew is still earnestly praying for him and hoping that we can see healing on his body.  It'll hard for me to leave and not know his outcome.
  Other than those updates there's not much more to say.  Hopefully I'll get one more blog entry in before I leave the ship.

A picture of Bintou and me.  She's back home now and I miss her.

Some of the HOPE Center crew.  I can only visit this place a few more times.  Hard to believe.