National Native HIV/AIDS Awareness Day

Courtesy:  Indian Country Today

It was just few days ago when I learned that March was designated as Women’s History Month.  Well, today, an identical thing happened to me which prompted me to put this post together in a hurry.  I found out just a few minutes ago that today is National Native HIV/AIDS Awareness Day.  I also discovered that my ignorance of the day is not surprising given that it is a little known observance day.  NNHAAD is a day geared toward drawing attention to and building support for HIV prevention, testing, treatment and care among American Indian, Alaska Native, and Native Hawaiian populations.  Here are some facts, according to the Centers for Disease Control (CDC):

• Among American Indians and Alaska Natives (AI/AN), women account for 29% of the HIV/AIDS diagnoses. 
• For Native Hawaiian and Pacific Islander (NH/PI) populations given a diagnosis, 78% were men, 21% were women, and 1% were children (under 13 years of age) in 2005.
• From 2007 to 2010, new HIV infections among AI/NA populations increased by 8.7% (CDC).

While these percentages may seem low, one must remember to take into account the size of these populations compared to more populous races and ethnicities in the U.S. For example, according to the CDC, in 2005 American Indians and Alaska Natives ranked 3rd in rates of HIV/AIDS diagnosis, following blacks and Hispanics. To put this into numbers, the rate of new HIV/AIDS infections in 2008 per 100,000 persons were:

• 73.7 Black/African American
• 25.0 Hispanic/Latinos
• 22.85 Native Hawaiians and Pacific Islanders 
• 11.9 American Indian and Alaska Native 
• 8.2 Whites
• 7.2 Asians

Given that many of these populations live in rural areas, access to health care services can be difficult. Not to mention other roadblocks to obtaining needed services such as language and cultural barriers. Native communities have some of the shortest survival times after diagnosis of HIV/AIDS of all race and ethnicity groups in the U.S.

The report also showed that Native communities are not accessing the much needed care and attention after being diagnosed with HIV.  I also learned that about 26% are living with HIV and don’t even know it.  So, this means that since they don’t know that they have it, they wouldn’t seek medical help.  On the other hand, those who know that they have it, take steps to protect their health and take action to prevent spreading the virus to others.

Thankfully, there are public services like the IHS (Indian Health Service), an agency whose mission is to raise the physical, mental, social, and spiritual health of American Indians and Alaska Natives to the highest level.  Our goal is to assure that comprehensive, culturally acceptable personal and public health services are available and accessible to American Indian and Alaska Native people.  The IHS operates within Department of Health and Human Services.

The IHS National HIV/AIDS Program is committed to partnering with communities to create lasting change in the HIV/AIDS epidemic. We provide programs to assist individuals, families, communities, and health care providers to:

• Understand how HIV is spread, and share knowledge about HIV with others
• Get tested for HIV
• Put policies and procedures in place to offer a HIV testing as a routine part of all health care
• Improve access to care, treatment, and prevention services needed by people living with HIV and AIDS

IHS providers throughout the country are offering screening more often, collaborating with communities to increase education, and offering care or referrals where direct care is not available. We can all help to reduce the stigma within our culture and among health care providers regarding HIV/AIDS.

I was shocked to learn that March 20, 2016 was the tenth anniversary of this annual awareness day.  I wonder how many people out there who even know that it exists.  Awareness, education and access are key.  And I applaud the many dedicated organizations that are currently working hard within the Indigenous communities to break down barriers and to promote HIV/AIDS prevention and treatment.   

The theme for 2016 was:  “Hear Indigenous Voices: Uniting the Bold Voices of American Indians/Alaska Natives (AI/AN) and Native Hawaiian/Other Pacific Islanders.” Last year’s was:  theme is “Unity in CommUnity, Stand Strong to Prevent HIV.” On this day, we recognize the impact of HIV/AIDS on American Indian, Alaska Native, and Native Hawaiian communities.  The theme this year is “Unity in CommUNITY: Stand Strong for HIV Prevention.”

It is my hope and prayer that long after this year’s National Native HIV/AIDS Awareness Day passes, that more people will find ways to stand strong for the Native communities.  We have heard the Indigenous voices, stood with them as we recognized that they are impacted by HIV/AIDS and now we must stand strong for prevention.  We have heard the voices, now it is time to be united in the fight to change the tide in this epidemic which discriminates against no one.  The HIV/AIDs is not one group’s or community’s fight but everyone’s fight.

Sources:  Humanitas Global Development; Indian Country Today; Indian Health Service

Women and Mental Health

May 1-7 has been Mental Health awareness week.

One in three Americans struggles with mental illness but the rate is much higher in women.  Research shows that women are 40% more likely to develop depression than men.  It is not clear why mental illness is more common among women but doctors have come up with a number of possibilities.

Discrimination, Trauma and stressful life experiences

Trauma is common among women with half of them experiencing some form of trauma in their lifetime.  One in four women have faced an attempted or a completed sexual assault.  Reportedly, one in three are abused by a domestic partner.  Gender discrimination, violence and mistreatment undermine a woman’s mental health.  Stress is a predictor of mental illness.  Women juggle housework, kids even while working fulltime.  They report that they have to work harder to get the same credit as men and worry about the gender wage gap.  They have to deal with sexual harassment and discrimination in workplaces where these are commonplace.  These challenges can significantly affect a woman’s ability to cope and her self-esteem.

Hormonal Issues

Women produce lower quantities of serotonin than men due to differences in hormone levels and this deficiency can lead to mental health issues such as depression and anxiety.

Pregnancy, Birth and Parenting

41% or women suffer from some form of postpartum depression.  Some of them are overwhelmed by the demands of parenting, especially in the early days.  I remember that there were times when I felt that I was drowning–in over my head.  Once I even cried out while I was holding my toddler.  Thankfully I had God and a very supportive partner.  It helped when he came home and I had an adult to talk to. Not all women are as blessed.  Research shows that women who don’t have supportive partners, experience traumatic births, live in poverty or a highly stressed will most likely develop postpartum depression.  

Gender bias is another problem women face.  Some research suggests that doctors tend to label women’s symptoms as emotional while taking the men’s symptoms more seriously.  So, a woman who reports that she is experiencing chronic pain to her doctor might be labeled as depressed.  This happens because we live in a world where gender discrimination exists and women are seen as more emotional and less rational.  

In many countries, the way health workers spoke to the women made it difficult for them to disclose their psychological and emotional distress.  And when they worked up the courage to disclose their problems, they were either over-treated or under treated by many of the health workers.

I read in an article in The Globe And Mail that women are getting the prescription that is available more often than the treatment they need.  They are getting medication to solve their problems even when science finds that treatments such as psychotherapy is equally or in some cases more effective without the side effects.  Bias in mental health care is a hindrance to women, preventing them from getting the proper help they need.  Not much effort goes into researching how drugs affect female patients.  While drug companies like to bombard women with their pills, most of their clinical trials have been dominated by men.  And the ironic thing is that the disorders most commonly diagnosed in women such as depression, anxiety and insomnia are the ones most likely to respond to therapy.  Most women are likely to prefer therapy over drugs.  

According to Dr. Marina Morrow, a Simon Fraser University psychologist who studies gender and mental health, “Women aren’t getting access to the range of care they need.”  She believes that an effective approach to this would be to include medication when necessary but in also offer therapy, peer support and pinpoint what social circumstances lead to the illness.

It has been argued that therapy is the safer, more effective and cheaper choice.  The authors of a 2015 study by Canadian and U.S. researchers concluded that, “There remains no sound justification to prescribe drugs without first trying therapy.  Dr. Cara Tannenbaum, scientific director of the CIHR Institute of Gender and Health, believes that “the way we fund therapies in Canada does not make sense right now.”  She wrote a letter to Quebec’s health minister to make the point that even if 20 per cent of seniors with insomnia received Cognitive Behavioral Therapy (CBT) with is used to treat insomnia, the cost-savings to the system could be in the hundreds of millions, based on the potential falls that would be avoided.  Therapy saves on costly and debilitating falls and hip fractures.  

We live in a country where medication is favored over psychotherapy and women are more likely than men to be prescribed antidepressants and sedatives as seniors and as a result they are at a higher risk of suffering from adverse effects.  Hopefully more women and those in the medical profession will speak out against the bias that is prevalent in the mental health care.  Doctors and those in the health care system need to give women more choices when it comes to treatment.  It’s their health so they should have the right to determine how they want to proceed once they have been diagnosed.

Mental Health Crisis in India

More than 50 million people in India suffer from a mental illness.  In 2011, India recorded the highest rate of major depression in the world at 36 per cent.  According to doctors, roughly 10 per cent of India’s population suffers from depression – MGMH

 

Women with mental illness are treated as less than human.  They are dumped, abandoned and abused.  If there are any signs of mental illness, a woman is put in a mental hospital with no chance of getting out.  Men can go back home while women are there for life.  In the following video, we meet a woman whose husband had her institutionalized although she had no history of mental illness.  Here’s a story of a mentally ill woman whose husband built a case against her so that he could get custody of their children after divorcing her.

It is not surprising that women suffer from depression at higher rates than men.  They have to deal with gender inequality, violence, lack of paid employment, lack of education, excessive spousal alcohol use and poverty.  Mothers are blamed for the birth of a female child and many face pressure to have male children.  Women are diagnosed with schizophrenia later in life, oftentimes, following the birth of their children.  The children are often removed from the ill mother’s care and this results in further distress for her. Indian women have higher rates of suicide than women in most developed countries and a higher rate of suicide compared to men in India.  Depression is one of the most common reasons for suicide among Indian women.

Mental health in India carries with it a stigma, especially if the person suffering from mental illness is a woman.  According to MGMH (Movement for Global Mental Health), in rural India, it is common to see people taking their children to temples and faith-healers instead of hospitals and doctors, especially in cases of mental health.  Mental health was something that was talked about in hushed tones.  Thankfully, it is no longer being swept under the rug.  People are coming forward.  Deepika Padukone stunned her fans last year when she admitted that she suffered from anxiety and depression.

At the time the news broke, she was one of the most sought after actresses in Bollywood. It took tremendous courage for her to disclose her illness, especially since people diagnosed with mental illness face discrimination.  Deepika has since launched the Live Love Laugh Foundation to raise awareness about mental health issues and as a result many celebrities were inspired to come out in the open and address the need to talk about mental health.  Varun Dhawan admitted that he was depressed during the making of Badlapur and Honey Singh revealed that he has been undergoing therapy for bipolar disorder.

Sadly, those living with mental illness are victims of a cruel fate.  They are often locked away and stripped of their basic human rights in state-run institutions that are under-staffed. In an article, titled Mentally Ill Suffer a Horrible Fate in India posted on the site for Deutsche Welle (DW), most state run mental hospitals are in deplorable conditions. The National Human Rights Commission (NHRC) reported that out of the 43 government mental hospitals in India, less than half a dozen are in a “livable” condition”.

There are doctors in charge of these hospitals who have no business being there.  “These doctors don’t understand the intricacies of a psychiatric illnesses and the comprehensive care the patients require,” said a psychiatrist working in a state-run mental hospital in Uttar Pradesh.

And in the midst of the crisis of hospitals not providing the conditions and care the patients need, are quack healers who are profiting from this.  According to a study by Dr. Shiv Gautam, former superintendent of Jaipur Mental Hospital, 68 per cent of the mentally ill are taken to faith healers before a psychiatrist.  “The reason, besides superstition, is that most general medicine doctors fail to diagnose psychiatric illness,” Gautam said. “A mentally ill patient displays symptoms which superstitious people believe are paranormal,” he added. “Such patients are tortured, chained and used for extracting money from their families.”  Hema, who was suffering from Schizophrenia was believed to have an evil spirit.  Her family took her to Datar Sharif Dargah where she spent a year locked up.  It wasn’t until her condition deteriorated that she was brought to Dr. Gautam.  In 15 days, she began to improve and a month later she was normal.

In other cases, the mentally ill are subjected to one of these horrific ordeals:  whipping, caning, inhaling burnt chili smoke, having their eyes smeared with chili paste or having their eyes branded with red, hot coins.  There are laws banning this practice, however, many dargahs and temples keep the patients chained.  Some of them spend the rest of their lives like this.  In 2001, 26 patients perished in a fire at a dargah in a coastal village because they couldn’t escape the blaze since they were chained.  What a horrific and senseless tragedy.

Families of mentally ill people opt for dumping them.  This means that they are dumped into an asylum where the conditions are not fit for a human.  When an illegal asylum was raided, they found thirty-five men and six boys living in inhuman conditions.  The stench from their unwashed bodies and the excrement drove neighbors to alert the health department.  Naked and chained inmates were discovered, dumped there by their families after they paid the asylum owner.  Some of these poor souls were found crawling in their excrement, some even consuming it.  On their bodies were marks of torture.  Some had surgical scars on their backs, leading to allegations that the asylum had links to kidney theft.  78 patients had entered the asylum but only 41 were found during the raid.

Other patients are dumped in jungles or forests ranges.  Their families pay lorry drivers to drop them.  Women and children are among these victims and in some cases, the females are raped by the drivers before being dumped.  Social activist Murugan S. who has rescued countless mentally ill people from the streets, cautions us not to judge the families by calling them cruel.  Instead we are to examine what forced them to take such extreme measures.  He believes that system needs to change.

Part of the solution is raising awareness.  The suffering of the mentally ill has been brought to our attention. It is out in the open.  The next thing that needs to be done is to show the superstitious and fearful society that mental illness is nothing to run away from or to be ashamed of.  The person suffering from mental illness needs love, support and most importantly, proper care so that he or she can live a normal life.

The government needs to put something place to ensure that patients are placed in reputable, sanitary facilities that will provide the care that they need and to ban the operation of illegal asylums and the practice of dumping.  Quack healers should be banned from profiting from other people’s suffering.  Husbands should not be allowed to institutionalize their wives if there is no record that they have mental illness.

No one wants to be mentally ill but it is a reality for many people and what they need is to know that they have a platform where they can talk about what is happening with them. Here in Canada, we have Bell Let’s Talk, a wide-reaching, multi-year program designed to break the silence around mental illness and support mental health all across the country. It has done so much to fight the stigma of mental illness and encourage people to get involved in educating themselves and others.

It is my sincere hope and prayer that something will be put in place in India so that attitudes toward mental illness would change and those suffering from it will have a platform where they would not be judged, dumped, abandoned or discriminated but supported and be treated with dignity and open minds.  In the meantime, let’s keep talking and raising awareness.

Talking is the best way to start breaking down the barriers associated with mental illness – Bell, Let’s Talk

 

Sources:  Vice News; Movement of Global Mental Health; Wikipedia; Deutsche Welle

World Leprosy Day

Tens of thousands of people in the world suffer from leprosy, a bacterial infection which affects the skin and destroys nerves.  Since the disease affects the nervous system, the affected areas become numb. People suffering from leprosy cannot feel pain and can easily hurt or injure themselves.  These injuries can become infected and result in tissue loss.  I remember reading about a missionary who put one of his feet in a pan of boiling water and didn’t even feel any pain.  It was then that he realized that he had leprosy.

The stigma that comes from having leprosy can be worse than the disease itself.  People with leprosy are outcasts. Their relatives believe that they are cursed.  Their lives are filled with loneliness and pain. People avoid them.  This happened to Balwant.  He was in his 30s when he discovered that he had leprosy.  He had white patches on his leg that itched and then became numb.  

Leprosy, if left untreated, can cause serious damage and leave a person disfigured.  Balwant and others like him feel ostracized and humiliated.  They are denied access to common wells or prevented from participating in festivals because people are afraid of the risk of contagion.  Family members reject them because they don’t want to catch the disease or be socially rejected because of those affected.  Some people even believe that when a person has leprosy he or she is being punished by the gods for past sins.  So, they avoid those who are affected because they don’t want to the wrath of the gods to fall upon them.

Balwant ended up losing his leg because the disease had progressed severely.  The doctors had to amputate his leg at the knee.  This left him weak and unable to work.  To make matters worse, he couldn’t afford to pay for the medical treatments he needed to treat his high blood pressure and diabetes which he had developed.  All of these things began to take a toll on Balwant and he decided that death was the only way out.  It would relieve him of his suffering, take away his shame and lift the burden that caring for him placed on his family.  He thought of hanging himself but he had no strength in his hands or leg.  He decided that he would jump into the well near his house.

It was at this moment of despair, resignation and hopelessness that God intervened in Balwant’s life.  He sent a Gospel for Asia supported pastor and three Sisters of Compassion, specialized women missionaries to Balwant’s community.  After hearing about Jesus and how compassionate He is, Balwant, moved by this, opened up to the pastor and the missionaries and told them all that he was going through and his plan to end it all.

Pastor Daha and the sisters prayed for Balwant and used God’s Word to encourage him.  They prayed for him for many days and his health began to improve.  He felt a peace that was beyond comprehension–the peace only Jesus can offer.  Balwant began to see his life through God’s eyes–precious.

Pastor Daha and the missionaries visited Balwant and his wife regularly.  They showed the love of Christ through simple acts such as fetching water, chopping vegetables and even trimming Balwant’s nails, something he couldn’t do for himself.  Their care and Jesus’ love made Balwant want to live. “I was emotionally weak and thought to end my life,” he testified, “but I found Jesus in the right time.  I thank God that He loves me.”

Sadly, a few months after Balwant found Jesus, he fell ill with jaundice and died.  He was right.  He found Jesus at the right time and one day he will be among the resurrected dead who will spend eternity with the Lord.  On that glorious day when Jesus returns, Balwant will have a new and incorruptible body (1 Corinthians 15:52-54).

Every year, there are nearly 230,000 new cases of people diagnosed with leprosy. About 60 percent of those cases concern people living in India alone. While leprosy is a curable disease, many men, women and even children find themselves abandoned and scorned because of it. Like Balwant, they live with shame and hopelessness as their constant companions. But God is using His servants to give these precious people hope and new life in Him—and you can help – Gospel for Asia

Pray for those who are living with leprosy.  Their world is filled with so much shame and hopelessness. They are abandoned and scorned by relatives, friends and neighbors.  They are lonely and suffer from physical and emotional pain.  Help Gospel for Asia’s Leprosy ministry to bring love and hope filled life to these people.

Pray that, like Balwant, they will come to know Jesus who loves them and longs to heal them just as He did when He was here on earth.  He healed this man who had leprosy on his hands.  His big smile and perfectly fine hands testify that the Lord is still in the business of healing.  Read about how He also healed Radhika, a 19 year old leprosy patient whose husband left her.

You can help the GFA Leprosy Ministry by praying for:

• the healing of leprosy patients
• the missionaries who are going and sharing the Gospel with the leprosy patients
• more medical personnel to care for and treat the patients
• the children whose parents have leprosy

This year, for World Leprosy Day, let us join Gospel for Asia in raising awareness about the hopelessness and rejection that many leprosy patients face and the hope, love, joy and acceptance they can find in Jesus Christ.

Brain Aneurysm

A few moments ago I read the news about Lisa Colagrossi, the WABC Eyewitness News reporter who died from a brain aneurysm.  She was only 49 years old.  She had just finished from covering a story Thursday morning when she realized that something was wrong.

As I read this story, I was alarmed.  She was just one year older than me.  And she was a wife and mother.  I had to find out more about brain aneurysms and here’s what I learned:

What causes a brain aneurysm?

A person may inherit the tendency to form aneurysms, or aneurysms may develop because of hardening of the arteries (atherosclerosis) and aging. Some risk factors that can lead to brain aneurysms can be controlled, and others can’t. The following risk factors may increase your risk for an aneurysm or, if you already have an aneurysm, may increase your risk of it rupturing:

• Family history. People who have a family history of brain aneurysms are more likely to have an aneurysm than those who don’t.
• Previous aneurysm. People who have had a brain aneurysm are more likely to have another.
• Gender. Women are more likely to develop a brain aneurysm or to suffer a subarachnoid hemorrhage.
• Race. African Americans are more likely than whites to have a subarachnoid hemorrhage.
• High blood pressure. The risk of subarachnoid hemorrhage is greater in people who have a history of high blood pressure.
• Smoking. In addition to being a cause of high blood pressure, the use of cigarettes may greatly increase the chances of a brain aneurysm rupturing.

What are the symptoms?

Most brain aneurysms cause no symptoms and may only be discovered during tests for another, usually unrelated, condition. In other cases, an unruptured aneurysm will cause problems by pressing on areas in the brain. When this happens, the person may suffer from severe headaches, blurred vision, changes in speech, and neck pain, depending on what areas of the brain are affected and how bad the aneurysm is.

Symptoms of a ruptured brain aneurysm often come on suddenly. If you have any of the following symptoms or notice them in someone you know, call 911 or other emergency services right away:

• A sudden, severe headache that is different from past headaches.
• Neck pain.
• Nausea and vomiting.
• Sensitivity to light.
• Fainting or loss of consciousness.
• Seizures.

If you want to find out how Brain Aneurysms are diagnosed and treated, visit this link.  You cannot prevent a brain aneurysm but you can reduce your risks.  Read here to find out how.

Notes to Women‘s thoughts and prayers are with Lisa Colagrossi’s husband, Todd and their two sons, Davis and Evan.

Source:  WebMD

The Oscars Highlights

As usual, after promising myself that I wouldn’t watch it, I ended up watching the Oscars Red Carpet show and the last hour and a half of the Oscars.  I enjoyed the show more in the past.  Nowadays, it seems anything goes.  I didn’t appreciate Sean Penn’s remark when Birdman won for the Best Picture and I am thankful that I missed Neil Patrick Harris in his underwear.  I wonder if he will be invited back next year.  I think Billy Crystal was by far the best host.

The highlights were seeing Tara Kyle, the widow of Chris Kyle, author of the autobiography The American Sniper, Oscar nominee for best picture.  Chris was killed at a shooting range in Texas in February 2013.  Tara was at the 87th Academy Awards ceremony to represent him.  She is a an American author, veteran family activist and advocate for women and families who have lost family members while serving in the war.  She travels around the country speaking about Chris and others like him.  In August 2013, the state of Texas passed the Chris Kyle Law (SB162) which was created to “expand the effort to help ease employment challenges for active duty military members and their spouses”

Tara founded Chris Kyle Frog Foundation.  A frog’s skeleton is a symbol of a fallen Navy Seal.  The foundation’s mission is is to “serve those who serve us by providing meaningful interactive experiences that enrich family relationships”^.

The other highlight was Julianne Moore.  I haven’t seen the movie, Still Alice, but the clip they showed of the movie when the announcement for Actress in a leading role, convinced me that she deserved the honor.  The scene was short but very powerful.  It was of a woman desperately looking for her keys and refusing to take her husband’s advice to wait until the morning.  It’s as if she could feel herself slipping away and was struggling to hold on.  It’s a movie on a disease that affects everyone–those diagnosed with it and their loved ones.  Alice described it as her brain dying.

“Alice: I miss myself.
John: I miss you too, Ali, so much.”
― Lisa Genova, Still Alice

“In the ladies’ room, Alice studied her image in the mirror. The reflected older woman’s face didn’t quite match the picture that she had of herself in her mind’s eye.” p 35”
― Lisa Genova, Still Alice

Women are more likely to get Alzheimer’s partly because they live longer than men.  Genetics are also a factor.  In the movie, Still Alice, Alice looked young, not the typical person you would expect to have Alzheimer’s.  It is no longer a disease of old age.  In fact, many people with early onset are in their 40s and 50s. They have families, careers or are even caregivers themselves when the disease strikes.

In her acceptance speech, Julianne said, “I’m so happy, I’m thrilled that we were able to shine a light on Alzheimer’s disease,” Moore said. “So many people who have this disease feel marginalized. People who have Alzheimer’s disease deserve to be seen so we can find a cure.”  She poured her heart into this role.  She spent four months researching for her role, talking to women with the disease, doctors and visiting a long-term care facility.  This was well earned Oscar win.  Congratulations, Julianne for bringing to life and light a disease that affects so many.  Thank you for raising awareness and helping those who live with the disease not to feel like they are alone.

Initially, when I heard that Lady Gaga was going to sing a medley from The Sound of Music, I was very skeptical.  I didn’t think she had it in her but I was pleasantly surprised.  I found myself wondering why the medley and then, Dame Julie Andrews steps out on the stage to the delight and surprise of the audience.  You could see that Lady Gaga was a bit emotional. With her usual gracefulness, Dame Julie said, “Dear Lady Gaga, thank you for that wonderful tribute.”

Seeing Dame Julie Andrews step out on the stage was the biggest highlight of the night for me.  She looked terrific as usual.  She was there to hand out the Oscar for the Best Original Score and also in honor of the movie, The Sound of Music which celebrates its 50th anniversary.  It will always be one of my favorite musicals.

I was thrilled when the song, “Glory” won for Best Original Song.  It was a moving tribute to the civil rights’ movement.   The cast and some in the audience were in tears.  Congratulations to Common and John Legend for their much deserved win.

In his acceptance speech, John Legend said, “We wrote this song for a film that was based on events that were 50 years ago, but we say that Selma is now because the struggle for justice is right now.  We live in the most incarcerated country in the world. There are more black men under correctional control today than were under slavery in 1850. When people are marching with our song, we want to tell you, ‘We are with you. We see you. We love you. And march on.'”

Congratulations to Patricia Arquette and Eddie Redmayne.  It was touching the way he dedicated his Best Actor Oscar to “all of those people around the world” battling motor neurone disease – the illness that left Professor Hawking in a wheelchair.  Redmayne thanked the Hawking family and his wife, Hannah, telling her,  “I love you so much. We’ve got a new fella coming to share our apartment!” His acceptance speech was refreshing and sweet at the same time.

Notes to Women wish to congratulate all the Academy Award winners for 2015.

Sources:  http://en.wikipedia.org/wiki/Taya_Kyle;

http://www.alzinfo.org/articles/why-women-may-be-more-likely-to-get-alzheimers/; http://www.alz.org/alzheimers_disease_early_onset.asp;

http://abcnews.go.com/Entertainment/wireStory/julianne-moore-wins-oscar-best-actress-29153141

http://www.rollingstone.com/movies/news/glory-wins-best-original-song-at-oscars-brings-cast-to-tears-20150222

http://www.telegraph.co.uk/culture/film/oscars/11428940/Oscars-2015-Watch-Eddie-Redmaynes-adorable-Best-Actor-acceptance-speech.html

http://www.mirror.co.uk/3am/celebrity-news/stephen-hawking-praises-eddie-redmaynes-5213165

Kishori’s Story

“Today, the diagnosis and treatment of leprosy is easy and most endemic countries are striving to fully integrate leprosy services into existing general health services. This is especially important for those under-served and marginalised communities most at risk from leprosy, often the poorest of the poor” (WHO:  Leprosy Today).

I learned about leprosy from reading the Bible and watching the movie “Ben Hur” but always believed that it was a disease of those times.  After watching Leprosy Mission, I realize that it is very much a reality.  I never saw how disfiguring it was until I watched the faces of men, women and children who were living with it.

I was touched when I read the story of Kishori, a woman who was diagnosed with leprosy during her second pregnancy.  Unable to take medications that would restrict the sickness from spreading she watched as the disease disfigured her arms and legs.

For years the leprosy racked her body with pain.  The medication she took hardly reduced her symptoms and the one hour walk to the hospital where she hoped to find relief took four hours because of the excruciating pain in her feet.  The treatment she received brought some relief but the pain returned when the sores did and Kishori found herself sinking into emotional despair.

Kishori was not abandoned by her husband, Manit but their neighbors were cruel and unfeeling and demanded to know why he kept her with him and didn’t send her home to her parents.  Manit insisted that he would not abandon Kishori and reaffirmed his love for her even though she sided with the neighbors and told him that she would go and live with her parents.  She wondered why he was still married to her.  The words of her neighbors cut her deeply and she shied away from being with others.  She lived in emotional and physical agony, feeling neglected and unwanted.

After decades of living the emotional and physical pain of leprosy, Kishori found relief in an most unexpected way.  Visitors came to her door and offered to clean her sores.  She gladly received Pastor Jiva and another missionary into her home and she saw them everyday as they returned to minister to her.  Her feet and arms soon began to heal.

Kishori and her family listened as the missionaries shared how Jesus could completely heal her.  No doubt they shared the story of the leper who went to Jesus and imploring Him, kneeling down to Him and saying to Him, “If You are willing, You can make me clean.”  Then Jesus, moved with compassion, stretched out His hand and touched him, and said to him, “I am willing; be cleansed.”  As soon as He had spoken, immediately the leprosy left him, and he was cleansed (Mark 1:40-42).

After years, decades of pain and despair, hope became alive in Kishori.  She learned about Jesus who could heal her.  She was encouraged to pray for healing.  She received kindness from Pastor Jiva and the missionaries who continued to visit her and clean her sores. They assured her of Jesus’ love.  As a result of this outpouring of love and compassion, Kishori placed her hope in God.  She and her family are now attending a local church.

This story ends on a very positive note.  Kishori is completely healed of leprosy because of the God in who she had placed her hope and the Jesus whom she had trusted to heal her.  God continues to care for her through the Gospel for Asia’s Leprosy Ministry.  Thanks to this ministry Kishori has received a pair of shoes specially designed for her and other gifts such as mosquito nets, blankets and daily meals.  Life is better for Kishori now.  She is able to care for her family instead of begging on the streets for help.  Her home which was once a place where she hid from society and life, is now filled with laughter and love.

God healed Kishori in body and mind.  He brought hope, love and healing into the life of a recluse.  He showed Kishori that there is a God who cares for her.  Just as her husband could not abandon her because he loved her, God did not abandon her because He loved her.  He sent Pastor Jiva and the missionaries to care for her.

Kishori’s story inspires me.  It reminds me that God cares.  He cares for the neglected and unwanted.  And no matter how long it takes, He will always come through for us.

Help Gospel For Asia to bring hope and God’s healing to another person living with leprosy by visiting their Leprosy Ministry webpage at:  http://www.gfa.org/leprosy.

Sources:  http://www.who.int/lep/en/; http://www.gfa.org/news/articles/healing-for-the-sores-on-her-soul/