The doctors shared the bad news with the family, They were all in shock. After he delivered the bad news gasps, shouts of “no”, swearing and anger filled the room. The spirit prompted me to pray for peace, quoting Matthew 4, I stated “peace be still” in my prayer. No matter what may be going on around you today, you can still live in peace. Scripture encourages us not to let our hearts be troubled. In other words, don’t meditate on all the negative things in this world to the point that it steals your peace.
Remember, the enemy knows this, and his goal is to steal your peace. He tries to set you up to get you upset. But when you choose to receive God’s peace, then no weapon formed against you shall prosper! Hallelujah!
Today, if you have fear, worry or anxiety about anything, recognize that those feelings aren’t from God, because He has promised to give you a spirit of power, love and a sound mind. There is tremendous power in peace. When you are at peace internally, you can think more clearly. You can hear the voice of God more easily. You’ll make better decisions. Even your physical body responds to peace.
“Peace I leave with you; my peace I give you. I do not give to you as the world gives. Do not let your hearts be troubled and do not be afraid.” (John 14:27, NIV)
Let’s Pray
Yahweh, thank You for Your gift of peace in my life. Father, I choose to receive Your peace in my heart and hold it close to me always. Despite what happens in life, I receive Your Word as truth and life to my heart and soul. God, I ask for Your healing hands upon the prime minister, his family and the thousands of others who have been unwell by this virus. God, I claim and receive Your promise of peace in our lives today, in Christ’s Name! Amen.
Albinism is the “congenital absence of any pigmentation or coloration in a person, animal or plant, resulting in white hair, feathers, scales and skin and pink eyes in mammals, birds, reptiles, amphibians and fish and other small invertebrates as well.”Varied use and interpretation of the terms mean that written reports of albinistic animals can be difficult to verify.
For ages, Judith had a feeling that she would struggle to become pregnant. There wasn’t a medical explanation for this — it was simply a niggling fear.
She and her husband struggled to believe they would ever become parents after years went by without her becoming pregnant. “I found myself getting anxious and desperate,” Judith first wrote on Love What Matters.
“The fear remained no matter how hard I tried to stay positive. However, Eight years down the line, my husband and I decided to go for our second round of IVF. The first of which failed, as well as other various procedures and fertility treatments. Every ultrasound visit after that was horror”
Judith
The couple could hardly contain their joy when that second round of IVF proved successful.
Judith was carrying twins — a boy, Kamis, and a girl, Kachi.
It felt remarkable that after all these years, their aspirations and dreams of a family were about to be real.
However, mum’s joy quickly turned to horror as doctors broke the news that Kachi was “at risk and might not make it”. “Every ultrasound visit after that was a nightmare as Kachi was far behind in growth whiles Kamsi did great.
“Finally, at 37 weeks, I had to be induced immediately because I was told that Kachi had stopped growing..” After the birth Nurses let Judith hold her daughter briefly before she was whisked to the NICU.
“The first time I saw her, I wondered if the nurse was handing me my baby, or someone else’s,” Judith said. “I waited a few seconds for someone to tell me there was a mix-up?” “Soon the joy of seeing them both healthy surpassed any other feeling at that instant.”
“How did I get black and white twins?”
Several days later Judith and her husband were told that their baby girl had albinism.
“I loved my princess like every mother would love her baby but worried about her condition,” Judith said.
“I worried about her future, how society would treat her, how she’ll be accepted.
“Gradually, worry turned to sadness and I started questioning “I envied other black babies and thought, ‘Why me? Why was I the one to have an albino baby?’
“How did I get black and white twins?”
“I threw the braille sheets in the garbage”
Unfortunately, medical professionals were quick to affirm Judith’s worst fears and told her that Kachi would struggle to see and would likely need to learn to read braille.
“I couldn’t imagine Kachi reading with braille and threw the braille sheets in the garbage.” She said
“She’s so smart and has a strong personality. She knows what she wants and will always go for it. “I always tell her how beautiful she is, because she really is.
“I’m not sure she`s aware of her uniqueness at the moment, but eventually she’ll know.”
“It’s my responsibility to educate her and teach her to love herself no matter what.
Albinism
Albinism affects the production of melanin, the pigment that colours skin, hair and eyes. It’s a lifelong condition, but it doesn’t get worse over time.
People with albinism have a reduced amount of melanin, or no melanin at all. This can affect their colouring and their eyesight.
Albinism is caused by faulty genes that a child inherits from their parents.
Symptoms of albinism
Hair and skin colour
People with albinism often have white or very light blonde hair, although some have brown or ginger hair. The exact colour depends on how much melanin their body produces.
Very pale skin that burns easily in the sun and doesn’t usually tan is also typical of albinism.
Eye colour
Someone with albinism can have pale blue, grey or brown eyes. Eye colour depends on the type of albinism and the amount of melanin. People from ethnic groups with darker pigmentation tend to have darker coloured eyes.
Eye problems
The reduced amount of melanin can also cause other eye problems. This is because melanin is involved in the development of the retina, the thin layer of cells at the back of the eye.
astigmatism — where the cornea (clear layer at the front of the eye) isn’t perfectly curved or the lens is an abnormal shape, causing blurred vision
photophobia — where the eyes are sensitive to light
nystagmus — where the eyes move involuntarily from side to side, causing reduced vision; you don’t see the world as “wobbling” because your brain adapts to your eye movement
squint — where the eyes point in different directions
Some young children with albinism may appear clumsy because problems with their eyesight can make it difficult for them to perform certain movements, such as picking up an object. This should improve as they get older.
How albinism is inherited
The two main types of albinism are:
oculocutaneous albinism (OCA) — the most common type, affecting the skin, hair and eyes
ocular albinism (OA) — a rarer type that mainly affects the eyes
Autosomal recessive inheritance
In most cases, including all types of OCA and some types of OA, albinism is passed on in an autosomal recessive inheritance pattern. This means a child has to inherit two copies of the faulty gene (one from each parent) to have the condition.
If both parents carry the gene, there’s a 1 in 4 chance that their child will have albinism and a 1 in 2 chance that their child will be a carrier. Carriers don’t have albinism but can pass on the faulty gene.
X-linked inheritance
Some types of OA are passed on in an X-linked inheritance pattern. This pattern affects boys and girls differently: girls who inherit the faulty gene become carriers and boys who inherit the faulty gene will get albinism.
When a mother is a carrier of an X-linked type of albinism, each of her daughters has a 1 in 2 chance of becoming a carrier and each of her sons has a 1 in 2 chance of having albinism.
When a father has an X-linked type of albinism, his daughters will become carriers, and his sons won’t have albinism and won’t be carriers.
If you have a history of albinism in your family or you have a child with the condition, you may want to talk to your GP about getting a referral for genetic counselling.
A genetic counsellor provides information, support and advice about genetic conditions. For example, you can discuss with them how you inherited albinism and the chances of passing it on.
Albinism is usually obvious from a baby’s appearance when they’re born. Your baby’s hair, skin and eyes may be examined to look for signs of missing pigment.
As albinism can cause a number of eye problems, your baby may be referred to an eye specialist (ophthalmologist) for tests to check for conditions such as nystagmus, squint and astigmatism.
Electrodiagnostic testing is also sometimes used to help diagnose albinism. This is where small electrodes are stuck to the scalp to test the connections of the eyes to the part of the brain that controls vision.
A man called Aranda approached the little boy’s mom at a group at the mall on the 12 of April 2019. Landen mom asked him if they were in his way and should move. Without hesitation or warning the stranger picked up Landen and threw him from the balcony at the Mall of America.
Surprisingly, this isn’t the first time 24-year-old has committed crimes at the mall. Aranda has two prior assault convictions from 2015 and was apparently banned from the the Mall of America for a period of time. He was also instructed to undergo psychological evaluation following those earlier attacks.
Later that day Aranda admitted to throwing the boy off the balcony to Police after they captured on a light rail train leaving the mall. He also told the police that he had attempted to kill somebody the day before (preferably an adult), but it didn’t “work out.”
He is being held in Hennepin County Jail in lieu of $2million bail and is scheduled to appear in court on May 14.
The suspect’s uncle, Francis Aranda, told KSTP that his nephew had displayed violent tendencies since childhood.
‘He has a serious mental problem, he was diagnosed as a child,’ the relative said.
He added: ‘We are going to pray for that baby [Landen] because what happened is so unfortunate, but it’s going to bring light to mental illness, I hope he [Aranda] doesn’t go to jail, he needs help.’
Pastor Mac Hammond (above) at the church Landen Hoffmann’s family attends in Woodbury, Minnesota, updated the congregation on the five-year-old’s condition on Sunday, nine days after he was thrown off a third-story balcony at the Mall of America on April 12
In spite of being thrown off a balcony that could have killed him, doctors have reported that Landen is thankfully doing much better than expected to the point where even the medical staff are chalking it up to nothing but a “miracle.”
This is truly a miracle. It’s like he fell off a bicycle instead of off the third floor of the mall.”
Mac Hammon, the pastor of the family’s church, was contacted by Landen’s grandpa on Sunday during the Easter sermon.
The results were obtained after a 5-hour MRI. “Doctors said they found no brain damage – not even any swelling,” Hammond told church congregants on Easter. “No spinal damage, no nerve damage ”¦ doctors are saying it is truly a miracle.”
Mac Hammon, shared that the boy did suffer many broken bones, including fractures on his arm, leg, and face. He will also need to have his spleen removed.
The GoFundMe page set up for Landen posted this encouraging update a week after the incident:
“The power of prayer is simply amazing. We all have been extremely humbled by the outpouring of support and prayers from everyone. Thank you for showing us there is so much good not only in our community but across the globe. Condition is again similar to previous days, another peaceful night of sleep — small steps towards the healing process. Each new day is a good day. Landen’s recovery is expected to be ongoing for a long time, while it’s hard to estimate costs, this will change everything for their family and require much of their time and focus.”
Over 27,000 people have donated to a GoFundMe campaign that has raised more than $961,000 as of Tuesday morning.
Mental Health Facts, Stats, and Data
Over 44 million American adults have a mental health condition. Since the release of the first State of Mental Health in America report (2015), there has only been a slight decrease in the number of adults who have a mental health condition (from 18.19% to 18.07%)
Rate of youth experiencing a mental health condition continues to rise. Therate of youth with Major Depressive Episode (MDE) increased from 11.93% to 12.63%. There was only a 1.5% decrease in the rate of youth with MDE who did receive treatment. Data showed that 62% of youth with MDE received no treatment.
More Americans are insured and accessing care. We can continue to see the effects of healthcare reform on the rate of Adults who are uninsured. This year there was a 2.5% reduction in the number of Adults with a mental health condition who were uninsured.
…But many Americans experiencing a mental health condition still report having an unmet need. 1 in 5, or 9 million adults reported having an unmet need.
Mental health workforce shortage remains. Many states saw some improvement in their individual to mental health provider ratio. But in states with the lowest workforce there was almost 4 times the number individuals to only 1 mental health provider.
World Leprosy Day: Gospel for Asia-supported workers’ hands-on care for sufferers brings practical help and spiritual hope to those still marginalized by long-feared disease. WILLS POINT, Texas – Gospel for Asia (GFA) is spotlighting its efforts to bridge the historic social gulf caused by the disfiguring disease that leaves sufferers disadvantaged and often despised–one outstretched arm at a time. As Gospel for Asia-supported workers prepare a series of events offering hands-on care to sufferers across Asia, to mark World Leprosy Day, Sunday, Jan. 27, the organization is also publishing a special report on worldwide efforts to eradicate the disease.
A GFA-supported pastor helps a leprosy patient as part of the Reaching Friends Ministry caring for those afflicted by the stigmatizing disease.
The latest in an in-depth series of GFA reports addressing key global issues, “Leprosy: Misunderstandings and Stigma Keep it Alive” examines how leprosy continues to see those infected shunned despite breakthroughs in treatment, and the fact that most people are naturally immune to the disease.
Though there have been significant medical advances, more than 210,000 new cases were diagnosed in 2016–the majority of them in India. Millions more around the world are suspected to be infected but are not yet symptomatic because the disease’s incubation period is so long.
While doctors and scientists continue to work on prevention and treatment, GFA-supported workers are providing practical and emotional help to those affected. Often losing fingers and toes because leprosy’s nerve damage means they are unaware of infection and injury, many sufferers are left physically unable to work, or as a result of being shunned.
Through associated local churches and members of its Sisters of Compassion ministry, specially trained women missionaries, GFA helps provide practical care, from cooking and cleaning to bathing and dressing wounds. As well as providing physical help, these healing touches also seek to tend to emotional wounds by demonstrating to leprosy sufferers that they have not been rejected.
“When we were completely lost and dejected, Christ came to us and lived among us,” said GFA founder Dr. KP Yohannan.
“By serving these precious people who happen to be afflicted with leprosy, we are not doing anything extraordinary or special. We are simply extending the love that was first given to us.”
GFA’s ministry also endeavors to release patients from the guilt many carry because, the report notes, over the centuries many have believed the disease is the result of some great sin of theirs.
“Eliminating discrimination and false conceptions of leprosy is key to eliminating the disease itself,” the reports adds. All too frequent are “the stories of men and women abandoned by their spouses, in-laws, or even kicked out of their homes by their children.”
The World Leprosy Day outreaches are being arranged in addition to GFA’s ongoing ministry to care for patients. GFA-supported workers have reached thousands of leprosy patients since the Reaching Friends Ministry, as it is called, began in 2007. They visit some of the isolated colonies in which many patients are forced to live, often cut off from the rest of the world.
“We thought we would name the ministry differently, where they won’t have to remember their sickness or feel the stigma of it,” said Tarik, the pastor who helped launched the initiative.
“We thought, ‘Let us call them “friends” because they have been created in the image of God, like us. It is only the sickness that keeps them different, but let us not make that a barrier. Let us accept them as friends.’ “
Among the Sisters of Compassion reaching out is Sakshi, a former leprosy sufferer whose story is shared in the report: at one time she considered suicide because of her despair. Receiving treatment and care, and coming to faith through Reaching Friends Ministry, she now offers help and hope to others.
“Nobody wants to love them, hug them or to come near to them to dress them,” said Sakshi. “They have so many inner pains in their heart, because they also are human beings. They also need love, care and encouragement from other people.”
Observed internationally each year on the last Sunday in January, to raise public awareness of the disease, World Leprosy Day is marked on Jan 30 in India, to commemorate the death of leader Mahatma Gandhi, who championed concern and care for sufferers.
To read more news on World Leprosy Day on Missions Box, go here.
Gospel for Asia (GFA, www.gfa.org) and its worldwide affiliates have–for almost 40 years–provided humanitarian assistance and spiritual hope to millions across Asia, especially among those who have yet to hear the Good News. Last year, this included more than 70,000 children, free medical services in over 1,200 villages and remote communities, 4,600 wells drilled, 11,000 water filters installed, Christmas gifts for more than 200,000 needy families, and spiritual teaching available in 110 languages in 14 nations through radio ministry.
Some people would do almost anything to ward off ‘bad luck’ and bring themselves a little good fortune. There was a time in my life that I believed when things happened in my life it was either “lucky,” or “unlucky.”
As I have become a more mature Christian I have realized that there is truly no such thing as luck, luck is just a religion of the lazy and disillusioned. Here’s why.
A psychologist Richard Wiseman surveyed a bunch of people who considered themselves lucky or unlucky, then performed a very interesting test:
“[Wiseman] gave both the “lucky” and the “unlucky” people a newspaper and asked them to look through it and tell him how many photographs were inside. He found that on average the unlucky people took two minutes to count all the photographs, whereas the lucky ones determined the number in a few seconds.”
“How did the “lucky” people do this? Because they found a message on the second page that read, “Stop counting. There are 43 photographs in this newspaper.” So why didn’t the so called unlucky people see it? Because they were so intent on counting all the photographs that they missed the message.”
So what does this mean?
People who we often consider themselves lucky are more relaxed and open to what’s going on around them. Many people either do not see the open doors that God has provided for them or do not even believe that God will ever open a door for them. God is gracious and gives us blessings. I have learned if I can look beyond the raging storm, I can see where God is constantly blessing me and moving in my life.
This week, my primary doctor told me he was moving to another city. I will not deny that I was really sad as a unique doctor/patient relationship had formed. He has been the only doctor so far that has truly kicked open doors for me, validated me, listened to me, and truly cared for me. It is extremely hard to find a great doctor when you have chronic and rare illnesses. I can’t say enough about how much my now old primary doctor has been a blessing to me and my husband. It wasn’t by chance or luck that I got this doctor that only worked in my area for one-year. God placed him in my path. God used him to change every single one of my other doctors and now I have a great team. God used him for a short while to put some pieces together for me. God sent him to help in my journey but as life has it, God changes things up and that’s ok. I haven’t met my new doctor yet but I am very confident that God has once again moved in my best interest and is sending another person to help me get me to another point.
I had a choice this week. I could have had a meltdown and worried about the unknowns of my doctor’s replacement or I could have scurried to find someone else. Instead, I chose to find peace and solitude in my Father. I can trust that he is moving and I am not relying on luck or chance. The biggest part of trusting God is not knowing all of the answers but placing the unknowns directly in his hands and allowing him to move and bless me.
