Stories – Arms of Mercy NPC

Posted on 27/09/202327/09/2023 by AOM

Fundraising for Juvan Meyer – Cystic Fibrosis, Bowel Atresia

Juvan`s story:

“Baby Juvan Meyer was born at 30 weeks and 5 days, on the 14th of July 2023. He was 1.66kg and 40.5cm, and he had an enlarged abdomen.

When they started to examine him with X-rays, CT scans and blood work, they found a meconium cyst and he could not pass stool. They also found symptoms of Cystic Fibrosis.

On the 4th of August 2023 he had his first surgery, where they removed the cyst and they discovered that the small bowel had atresia. They had to cut off a piece and attache two colostomy bags, one at the small bowel and one at the colon.

He still can’t pass stool, so they did some more scans and it seems as if the colon also has atresia. They will have to remove that piece as well.

The doctor already told us what to expect. If they are right about the colon, Juvan will have to live with a colostomy bag for a few years, before they can do reconstructive surgery.

His cystic fibrosis (CF) tests also came back positive and he has two rare types of CF.

He is in Bloemfontein Mediclinic and we are from Olifantshoek. It is 420km from where he is. Our expenses to be with him are a lot and we can only go to him every second weekend. We also received a few medical bills already, which the medical aid did not pay. We need all the prayers and help we can get. Please pray for our baby.”

Please open your heart and support our fundraiser for Juvan by purchasing his “Breath is Life” bracelets. All proceeds are donated towards his ongoing medical care and expenses where needed – together we CAN make a difference in this precious boy`s life!

Alternatively, please consider a donation, any and all donations welcome. REF: Juvan Meyer.

Fundraising for Juvan Meyer

Breath is Life Bracelets

The “Breath is Life Bracelets” consist of wooden beads with silver and diamante fillers.

Bracelet Options:
1. White and grey with cross charm.
2. Blue, white and grey with angel charm.
3. Blue and grey with feet charm.

To place an order, contact the agent in your area or shop online.

Breath is Life Bracelets Arms of Mercy NPC — Breath is Life Bracelets

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Posted on 26/09/202326/09/2023 by AOM

Fundraising for Dylan Beukes – Cerebral Palsy

Dylan`s story:

“Baby Dylan was hospitalised with a fever on 13 March 2023 and diagnosed with an adenovirus infection. He was supposed to go home after a few days but that never happened.

The morning he was supposed to be released, something went horribly wrong. Dylan’s face went blue in his mother’s arms, he wasn’t breathing and his heart stopped. It took 3 tries to resuscitate him, during which he went without oxygen for about 30 minutes plus.

After the absolute horror this angel and his family endured, the doctors ruled that Dylan had severe brain damage and was classified as a vegetative state.

Baby Dylan had to get a trachea to assist with breathing because his throat muscles were extremely weak and had no cough and swallow reflexes, he had to get a feeding peck inserted as well.

They had to make specialised compression boots, to stop his leg muscles from pulling in on themselves.

Currently, Dylan is slowly improving but still needs a lot of care and medical support.

After four hospitalizations, Dylan is finally home, and his health care is in need of specific treatments and equipment. The list of medical criteria is growing and changing daily to sustain his medical need in aftercare.

The medical aid doesn’t cover everything Dylan needs for survival due to the classification as a ”special needs child” criteria. The family had to move in with the grandparents due to circumstances, and the level of assistance in Dylan’s daily daycare provision. It’s been hard on them but they’re by Dylan’s side every moment of every day.

Dylan was readmitted to hospital on the 6th of June 2023 due to Covid and pneumonia.”
He has been home now for 14 weeks (at time of publishing this post).

Please open your heart and support our fundraiser for Dylan by purchasing his “Step by Step” bracelets. All proceeds are donated towards his ongoing medical are and expenses – together we CAN make a difference in this baby boy`s life!

Alternatively, please consider a donation, any and all donations welcome. REF: Dylan Beukes.

Fundraising for Dylan Beukes

Step by Step Bracelets

The “Step by Step Bracelets” consist of green, grey and beige wooden beads with silver and diamante fillers.

Charm options:
Hope / Cross / Tree of Life.

To place an order, contact the agent in your area or shop online.

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Posted on 23/08/202323/08/2023 by AOM

Fundraising for Divan Conway – Lissencephaly, Cerebral Palsy, Epilepsy

Divan`s story:

Divan Conway is a 11 year old boy who was diagnosed with Lissencephaly (smooth brain), Cerebral Palsy, and Epilepsy (West Syndrome). He currently weighs 40kg, he can not walk or talk at all, and his mother has to carry him everywhere.

Divan suffers from extreme cerebral palsy therefore he cannot walk or sit on his own nor can he speak. As a result of constantly being in bed he developed chronic lung damage. He will be using nappies for the rest of his life and therefore also linen savers.

Due to his special needs, mom had to leave her job to take care of him.

Divan has epilepsy and has 5/6 fits on a daily basis, and is on six types of medication: Epilim, Keppra, Sabril, Rivotril, Epanutin and Ativan. The epilepsy is extremely challenging to control.

He regularly contracts infection in his lungs due to all the mucus and lack of movement, and has been admitted to hospital repeatedly for Acute Upper Respiratory infection. Mom has to clean his throat and nose with a suction machine to remove all the mucus that he doesn’t swallow. Divan has a feeding tube because he can’t eat and drink, and can only consume milk and water. He also struggles with bladder infections because his bladder does not get rid of all the urine. It is mom`s duty to empty his bladder for him at home using catheters.

Please open your heart and support our fundraiser for Divan by purchasing any of his “Little Soldier” bracelets, “Hope for Divan” bracelets or key ring. All proceeds are donated towards his ongoing medical are and expenses – together we CAN make a difference in their lives!

Alternatively, please consider a donation, any and all donations welcome. REF: Divan Conway.

Fundraising for Divan Conway

Hope for Divan Bracelets Arms of Mercy NPC

Hope for Divan Bracelets:
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Hope for Divan Key Ring Arms of Mercy NPC — Hope for Divan Key Ring

Hope for Divan Key Ring:
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Little Soldier Bracelets © Arms of Mercy NPC — Little Soldier Bracelets

Little Soldier Bracelets:
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Posted on 10/08/202310/08/2023 by AOM

Fundraising for Brody Van Der Schyff – CHARGE Syndrome, Type II Caudal Regression Syndrome

Brody`s story:

“Brody Van Der Schyff, a 2-year-old resident from KZN, South Africa, was diagnosed with an extremely rare disease called CHARGE Syndrome when he was just 1.5 months old in 2021. Brody has spent more than 60% of his life in hospital, fighting life-threatening recurring bacterial infections.

Brody was born with a Horseshoe kidney and Grade IV Vesicoureteral. He had multiple surgeries to try prevent infections and UTI’s. Due to Genital abnormalities, Brody underwent Ureteral reimplantation surgery before he was a year old. At the age of 18 months Brody went into Kidney failure and had his Horseshoe kidney separated and received a Left radical nephrectomy in December 2022.

Over the last 7 months Brody had been living in absolute agony with 7 recurring E.COLI infections and multiple skin infections with constant itching and severe abdominal pain! On the 17th of July 2023 he was admitted for 19 days where they discovered he has a cyst on his right kidney, an inguinal hernia, a neurogenic bladder and multiple issues in his spine. After an MRI was done, he was diagnosed with Type II Caudal Regression Syndrome.

His inguinal hernia repair surgery has provisionally been booked for the 19th of August 2023.

We have been told by a Neurosurgeon that Brody would need spinal cord surgery to assist with the tethered cord as he can lose total control of his lower body. We will now first see a pediatric Neurologist to get a better understanding of what is going on in the spine as there are multiple issues to be looked at, and then we will see a Neurosurgeon to discuss what needs to happen and when. Brody will always have a neurogenic bladder, and this can lead to kidney damage. Due to Brody only having 1 precious Horseshoe Kidney, we need to protect his kidney. Brody has no bladder function control. His bladder does not empty out and this is what is causing the requiring Infections! We have been referred to go see a Pediatric Urologist In Umhlanga on the 24th of August to discuss a way forward for the neurogenic bladder.”

Please open your heart and support our fundraiser for Brody by purchasing one of his bracelets, two, or the whole set of three. All proceeds from the “Brody in Charge Bracelets” are donated towards his ongoing treatment, medical care and expenses. Together we CAN make a positive difference!

Alternatively, please consider a donation; any and all donations welcome. REF: Brody van der Schyff.

Fundraising for Brody Van Der Schyff

Brody in Charge Bracelets

The “Brody in Charge Bracelets” for consist of blue, coffee and white wooden beads with crystal, silver and diamante fillers.

Charm options:
1. Cross
2. Heart
3. Hope-Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Brody in Charge Bracelets - Arms of Mercy NPC

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Posted on 20/04/202325/04/2023 by AOM

Fundraising for Jan-Hendrik Louw – Malignant Neoplasm (Brain Tumour)

Jan-Hendrik`s story:

Jan-Hendrik Louw is an 11-year-old boy from Klerksdorp in the North West Province, who was diagnosed with Malignant Neoplasm at the age of 6. He has a tumour on his brain, which causes neurological problems such as shaking and imbalance.

Sadly, the process of his treatment was slowed down because of Lockdown. The tumour has recently shown growth and the doctors are now starting with radiation to shrink the tumour, as they can’t operate to remove it because of it`s location. Due to the tumour, Jan-Hendrik has a slight speech impairment and is also totally deaf in his right ear.

Please open your heart and support our fundraiser for Jan-Hendrik by purchasing one of his bracelets, two, or the whole set of three. All proceeds from the “Faithful and Worthy Bracelets” are donated towards his ongoing treatment, medical care and expenses. Together we CAN make a positive difference!

Alternatively, please consider a donation; any and all donations welcome. REF: Jan-Hendrik Louw.

Fundraising for Jan-Hendrik Louw

Faithful and Worthy Bracelets

The “Faithful and Worthy Bracelets” for Jan-Hendrik consist of white and grey wooden beads with crystal, silver and diamante fillers.

Charm options:
1. Butterfly
2. Diamante Heart
3. Faith & Hope-Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 03/03/202303/03/2023 by AOM

Fundraising for Mieke van den Berg – Acute Lymphoblastic Leukemia (ALL)

Mieke`s story:

“Mieke Van den Berg is an 8-year-old girl from Rustenburg who was diagnosed in November 2022 with Acute Lymphoblastic Leukemia (ALL), better known as blood and bone marrow cancer. Mieke is not healthy at all and is currently in a critical condition regarding her heart. She can’t walk, she doesn’t want to eat and she is very weak.

Mieke will have to go through to Pretoria for chemo three times a week for the next 24 months. She will also have bone marrow drawn to monitor the cancer, every third week for the next 3 months. Mieke will not be allowed to return to a normal school, because Leukemia affects her immune system and breaks it down completely. Having said that, she is very susceptible to any virus and/or infection. She has to wear masks when we go to town, and we as parents, have to wear gloves every time when she gets chemo.

Within the next two weeks, she will get a Chemo Pod implanted in her chest, which is implanted under her skin with a tube that is inserted directly into her main artery. This device is then used to give her chemo every week, three times a week, instead of inserting a drip every time or going home with a drip.

The chemo she is currently receiving is: Doxorubicin and Vincristin, two very aggressive chemo treatments. Vincristine is injected directly into her spine by means of a lumber punch injection, every fourth week under anesthesia. Doxorubicin is currently given directly through a drip, and from next week she will receive it through the chemo pod. Her white blood cell count is still low, because of the chemo, but her red blood cell count is increasing, very slowly, but it is increasing.

Mieke is currently being treated at Dr George Mukhari Hospital at Ga-Rankuwa.
The Medical Aid is busy to Reinstate so everything is on hold.”

Please open your heart and support our fundraiser for Mieke. All proceeds from the “Miracle for Mieke Bracelets” are donated towards her ongoing medical care and expenses. Together we CAN make a positive difference and help a child in need.

Alternatively, please consider a donation; any and all donations welcome. REF: Mieke van den Berg.

Fundraising for Mieke van den Berg

Miracle for Mieke Bracelets

The “Miracle for Mieke Bracelets” consist of coral and silver wooden beads with silver and diamante fillers.

Charm options:
Butterfly / Filigree Heart / Hope-Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 02/03/202302/03/2023 by AOM

Fundraising for Jasmijn Duvenhage – Rare Disorder IDIC(15) with intractable Epilepsy, Severe Hypotonia, Gastrointestinal Dysmotility, Recurrent Pneumonia

Jasmijn`s story:

“Meet beautiful little Jasmijn Duvenhage. She is our little superhero, fighting, like only a superhero can, since the day that she was born. Jasmijn was born via C/section with low Apgar scores and hypotonia and started choking, then turning blue on day two of life. Initially diagnosed with severe reflux, with temporal lobe epilepsy later confirmed at the age of 4 months. Complicated with West syndrome, diagnosed two months later.

By the Lord’s Mercy and Grace, West syndrome resolved at 10 months of age after battling through four months of very expensive steroid therapy combined with specific anticonvulsants.

Due to her underlying genetic condition (IDIC 15), Jasmijn’s condition was complicated with several different forms of uncontrolled epilepsy requiring yet another multitude of expensive anticonvulsant therapies, which (still to date) has not completely aborted the seizure activity. Little Jasmijn continues to have multiple daily seizures ranging in severity from quick and mild to completely life-threatening.

The ketogenic diet had been added about five months ago with a favourable, but still incomplete effect. This is still being titrated by a Specialist Dietician in the field and there is always hope.

Unfortunately this brave little girl, of whom her parents are very proud, started combatting recurrent viral pneumonia in mid 2022, these requiring admission for non-invasive ventilation leading to prolonged and very complicated hospital stays.

Her mother, despite being a medical professional, has not been able to go back to work since little Jasmijn had been born. She has been needed next to her little girl’s bedside to assist with her complicated therapeutic regime at home, as well as the hospital. This causes extreme financial strain as their home and their future plans were built on two reliable salaries.

To make matters worse, the medical aid has been helpful, but does not cover most of the expenses needed for Jasmijn’s basic care and the family is still in the process of reapplying for PMB cover. They have depleted their savings on their precious daughter’s care, with Jasmijn’s father working full time to support their family.

Thank you for supporting this brave little girl and our fight by purchasing one of these lovely bracelets from Arms of Mercy. Our Lord Jesus Christ bless you.”

Please open your heart and support our fundraiser for Jasmijn. All proceeds from the “Divine Grace Bracelets” are donated towards her ongoing medical care and expenses. Together we CAN make a positive difference and help a child in need.

Alternatively, please consider a donation; any and all donations welcome. REF: Jasmijn Duvenhage.

Fundraising for Jasmijn Duvenhage

Divine Grace Bracelets

The “Divine Grace Bracelets” for Jasmijn consist of wooden beads with silver and diamante fillers.

Colours: Turquoise and Silver mix.

Charm options:
Dragonfly / Star / Flower.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 31/01/202308/02/2023 by AOM

Fundraising for Wyatt Liberty – Acute Lymphocytic Leukemia (ALL) & Autism

Wyatt`s story:

“Our Story begins on the day of 1st of December 2012, when my husband Neil and I got married.

We have a baby girl named Ava Eliza Liberty. Ava was born on 03 April 2016. She is a talkative, inquisitive and a stunning rising star.

When Ava was 9 months old, we received our miracle surprise blessing who made his presence known. A healthy baby boy, Wyatt Ethan Liberty made our family complete on the 26 February 2018. A very active boy with an amazing wonderful imagination. Always playing, a typical boy that loved any game that includes a ball made him happy. Apart from the occasional seasonal allergies and cold he was always a very healthy boy.

Exciting times for our family, we started potty training Wyatt – he was doing so well, and was on his way to be fully potty trained until it all suddenly changed.

On the 13th of April 2022 he started suffering from constipation over the long weekend. With the fact that he was potty training it didn’t alarm us too much. We got him some medication at the local pharmacy. By Tuesday we took him to the doctor. On the 19th April 2022 the doctor advised that he is pale and that we should take him for blood work. The GP contacted us the same night and advised that we need to come and collect a referral letter for Karl Bremmer hospital as he has a septic blood infection. Karl Bremmer transferred us to Tygerberg hospital at 00:00 hours -observations and blood works were done. The next day, Wyatt received platelets and red blood cells (blood transfusion).

Due to the fact that Wyatt is 4years of age and not speaking, they advised that he should be tested for Autism. His hearing test was perfect, and they made an appointment for us to see the speech therapist and Occupational therapist.

From the 19th until the 24th of April they completed constant testing and on the 3rd of May 2022 they drew blood, discharged us and advised that they will contact us in a week to advise on the blood results.

On the 19th of May I was contacted at work and was told that the blood works are perfect and that he is discharged. They confirmed that it was a very bad viral infection.

Sadly, on the 16th of May, Wyatt started developing bumps on his head and what looks like spider bites on his legs that made him lose feeling in his leg. Because Wyatt doesn’t speak, we took him to the GP and we thought he had mumps, so the GP advised just for safety and with his history, to get blood work done.

The same day the GP contacted us and advised that his blood works are low and referred us to the hospital, this time to Tygerberg hospital directly and recommended that they complete a bone marrow extraction for testing. The hospital advised that due to his recent blood transfusion they would rather give it 2weeks and get the blood tested again. In the interim while we are at home, we should monitor him closely and see if the bumps increase in size or if he develops a fever or shortness of breath. They gave us a date to return back to hospital on the 6th of June 2022.

On the 23rd of May we took Wyatt into hospital as the bumps increased and started to become inflamed. They drew blood and on the 24th of May 2022, Wyatt was diagnosed with ALL (Acute Lymphocytic Leukemia).

He received his first chemotherapy on the same day as he was in a favorable stage and they wanted to start with the treatment as soon as possible. Friday the 27th of May they did a lumber punch.

Wyatt then received Chemotherapy every 2nd day. On the 3rd of June they completed his 2nd lumber punch. He then completed his 10-day trial of the 1st chemotherapy.

On the 13th of June we received the news that stronger chemotherapy needs to be administered as the 1st round of chemo did not kill any cancer cells.

On the day of my only son’s diagnosis, our entire world and life was turned upside down where nothing makes sense anymore. The only thing that keeps us sane and strong is our faith in the Lord Jesus Christ, and believing that our story will be a story of surviving, victory and grace. A true testimony of a miracle working God.

Wyatt was also diagnosed with Autism on 19 June 2022.

The mere fact that my son shows so much power and endurance and through all of this still smiles and laughs gives us strength to carry on fighting with him every single day.

We have maxed our credit cards. Bank balance is in overdraft that is maxed. My amazing husband gave up his job to be with my son in hospital for treatment and we are surviving on personal loans that have been maxed. But the grace of God has carried us this far and he will never forsake us.”

All things are possible – (I can endure all these things through the power of the ONE who gives me strength – Philippians 4:13).

Please open your heart to Wyatt and his family today and support our fundraiser. All the proceeds from the “Life is Beautiful Bracelets” are donated towards his ongoing medical care, treatment and therapy. Together we CAN make a positive difference in his life!

Alternatively, please consider a donation; any and all donations welcome. REF: Wyatt Liberty.

Fundraising for Wyatt Liberty

Life is Beautiful Bracelets

The “Life is Beautiful Bracelets” for Wyatt consist of wooden beads with silver and diamante fillers.

Colours: Blue, Pink, Pearl, Grey mix.

Charm options:
Faith / Hope / Love.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 25/01/202325/01/2023 by AOM

Fundraising for Zachary de Wet – Hunter Syndrome

Zachary`s story:

“Zachary is happy, incredibly busy, and he loves every moment of life. To Zach, the world is full of possibilities and endless fun, but shortly before his second birthday in March 2021, we got the news that Zach’s life will be nothing like we expected. He was diagnosed with MPSII.

Hunter syndrome is a very rare, inherited genetic disorder caused by a missing or malfunctioning enzyme. In Hunter syndrome, the body doesn’t have enough of the enzyme iduronate 2-sulfatase. This enzyme’s job is to break down certain complex molecules, and without enough of this enzyme, the molecules build up in harmful amounts. The buildup of massive amounts of these harmful substances eventually causes permanent, progressive damage affecting appearance, mental development, organ function and physical abilities.

Hunter syndrome occurs in 1 in 120 000 to 170 000 boys. There’s no cure for Hunter syndrome.

Treatment involves managing symptoms and complications through weekly Enzyme Replacement Therapy. This is an extremely expensive treatment but absolutely life changing and life saving. With treatment, life expectancy is much higher, meaning Zachary can live well into adulthood and live a healthy long life. Without treatment the disease will progress and life expectation is 12 to 18 years.

Signs and symptoms include:

• Reduced endurance
• Vision problems
• Reduced field of vision
• Optic nerve damage
• Glaucoma
• Enlarged liver and spleen (hepatosplenomegaly)
• Umbilical and inguinal hernias
• Abnormal facial features (such as flat face, flat and depressed nasal bridge, slightly bulging eyes, enlarged tongue, thick lips)
• Large head (macrocephaly)
• Short stature
• Lung problems
• Reduced lung function
• Frequent, recurrent lung infections
• Sleep apnea
• Potential developmental delays (some may have normal intelligence)
• Potential slowing of mental development
• Carpal tunnel syndrome
• Fluid in the brain (hydrocephalus)
• Compression of the cervical spinal cord
• Thick lips
• Enlarged tongue (macroglossia)
• Abnormal teeth (widely spaced and very thin enamel)
• Frequent ear infections (otitis media)
• Hearing loss
• Frequent and recurrent sinus infections (sinusitis)
• Heart valve disease, especially aortic valve
• Abnormal heart muscle (cardiomyopathy)
• Irregular heartbeat (arrhythmia)
• Angina
• High blood pressure (hypertension)
• Poor circulation
• Joint stiffness
• Skeletal abnormalities (dysostosis multiplex)
• Abnormal hip formation (hip dysplasia)
• Bone deformities in the spine (scoliosis, gibbus, kyphosis), or knees (knock-knees or genu valgum).

Zachary suffers from a wide variety of these symptoms, he therefore has an extensive medical team comprising of the following specialists monitoring and taking care of him: Paediatrician, Pulmonologist, Cardiologist, Ophthalmologist, Ear Nose & Throat Specialist, Neurologist, Occupational Therapist, and a Speech Therapist.

Unfortunately treatments and Specialists are extremely costly and medical aid does not cover all of this. We are continually in need of funds for those additional expenses.”

Please open your heart to Zachary and his family today and support our fundraiser. All the proceeds from his “Amazing Grace Bracelets” are donated towards his ongoing medical care, treatment and therapy. Together we CAN make a positive difference in his life!

Alternatively, please consider a donation; any and all donations welcome. REF: Zachary de Wet.

Fundraising for Zachary de Wet

Amazing Grace Bracelets – Ladies

The “Amazing Grace Bracelets” for Zachary consist of turquoise and black wooden beads with silver and diamante fillers.

Charm options:
Believe/ Feather / Cross / Hope-Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Shop Online

Amazing Grace Bracelet – For Men

The “Amazing Grace Men`s Bracelet” for Zachary consist of turquoise and black wooden beads with silver fillers.

Colour Options:
Black & Turquoise Mix
or Plain Black.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 07/11/202208/11/2022 by AOM

Fundraising for Lenè Grobler – Prader-Willi Syndrome, ADHD, Intellectual Developmental Delays

Lenè`s story:

“Lenè was born a bit early at 36.5 weeks but she was a normal healthy baby as far as the eye could see. When she turned 1 years old I started to worry because she was far behind her cousin who was 2 months older than her. We stayed in a small town with no therapists and doctors, and my father said we must be patient with her as she might just be a bit slow.

When she turned 19 months old she started to lift herself and at 21 months she was walking, but not that well. We moved back to Klerksdorp when she was about 2.5 years old. I was still worried at this stage as she was still on nappies and did not talk. We took her to the Potch University – Care2Kids program to get her assessed and see if there is maybe something wrong. After this I finally got a school that had the time to care for her as the special needs school had her for 1 week and asked us to rather take her out as there is something seriously wrong with her.

In February 2022 she was assessed by Dr J.C.K Strauss who found her to have an intellectual disability as well as a serious communication delay. We started looking around for a Paediatric Neurologist to assess Lenè as we need assistance with treatment and advise on the way forward. In May 2022 she went to see Dr C Erasmus in Pretoria who diagnosed her with Prader Willi Syndrome and ADHD among a list of things. She has a wide range of symptoms and we are eager to find answers so that we can help her have a better quality life.

Lenè turns 5 years old in February 2023. She is currently on 2ml Risperdal a day. This alone is R1900.00 a month. The day to day from our medical covers it but this will soon be depleted. Thereafter, all medicine must be paid in cash. School costs R1850.00 a month and then nappies work out to R165.00 a week. I cannot look for better employment as I need to take off a lot, when she gets sick or is too difficult, so I only get commission on cases completed… no work, no pay.”

Please open your heart to Lenè and support our fundraiser for this family in need – all proceeds from the “Uplifted in Faith” bracelets are donated towards her ongoing medical care and expenses. Together we CAN make a difference!

Alternatively, please consider making a donation. Any and all donations welcome. REF: Lenè Grobler.

Fundraising for Lenè Grobler

Uplifted in Faith Bracelets

The “Uplifted in Faith Bracelets” consist of grey and white wooden beads with crystal, silver and diamante fillers.

Charm options:
Heart / Faith / Butterfly.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 13/07/202213/07/2022 by AOM

Fundraising for Amoré De Wet – 18Q Deletion Syndrome

Amoré`s story:

“Amoré is a tenacious 7-year-old with 18Q Deletion Syndrome. She was diagnosed at six weeks old. 18Q Deletion Syndrome is a rare chromosomal disorder affecting the 18th chromosome. One in 40,000 newborns is affected by this chromosome disorder. There is no cure for her condition.

Symptoms range largely from case to case. Some features include low muscle tone, hearing loss, sight problems, heart defects, kidney problems and features of autism.

Amoré had open heart surgery at 6 months old and sees her cardiologist every 2nd year. She has been diagnosed with Nystagmus and Strabismus and wears glasses to help with these conditions.

There is currently no PMB for her condition and therefore all of her specialist consultations and therapy i.e. Occupational therapy, Speech therapy sessions are paid from their medical aid savings account which is generally exhausted within the first three months of the year. Most of her specialists are also not contracted in with the medical aid and therefore they need to pay cash for their visits. She is non-verbal but they pray for an augmentative and alternative communication device, which the medical aid does not pay for.”

By supporting our fundraiser for Amoré you can make a positive difference in her life – all proceeds from the “Never Give Up” bracelets are donated towards her ongoing medical care and expenses. Together we CAN change the world and help a child in need!

Alternatively, please consider making a donation. Any and all donations welcome. REF: Amoré De Wet.

Fundraising for Amoré De Wet

Never Give Up Bracelets

The “Never Give Up Bracelets” for Amoré consist of white, blue and silver wooden beads with silver and diamante fillers.

Charm options:
Angel / Cross / Hope-Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Never Give Up Bracelets © Arms of Mercy NPC — Never Give Up Bracelets

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Posted on 06/04/202228/02/2023 by AOM

Fundraising for Kian Ludick – Nephroblastoma, Wilms Tumor

Kian`s story:

“Kian had been having a lot of ear infections in the beginning of 2021. Our GP referred us to the nose, ear, and throat Specialist as well as a speech therapist, because he has not begun to speak and was nearing the age of 2 and they suspected that he has autism. On the date of his appointment he did not give his co-operation with the speech therapist and they decided to make arrangements with a Pediatrician to put him under local anesthetics while they conduct the ear test, and because he was not well, the pediatrician decided to do a full exam also while he was under. He discovered something hard on the left side of his tummy. We were sent for a sonar where they discovered the enlarged kidney. They did a CT scan where they saw the abnormal tissue on both kidneys.

Kian was diagnosed with Nephroblastoma on both kidneys, 26 March 2021, as well as an enlarged left kidney. He has been having monthly MRI scans and blood work in Johannesburg where he is treated by Prof Janet Poole. On the 12th of December 2021, he had his 3rd scan and they discovered the Wilms tumor that developed on the left kidney. He started with his weekly pre-operative chemo on 31 January 2021 in Kimberley, which he gets once a week for 6 weeks. On week 5 and 6 they will do a scan and reassess, he will also be having maintenance chemo after surgery.

The chemo has affected him worse than what we expected. He was admitted 4 days after his 1st session, and has been put on a double dose of blood pressure medication. He had moisture on his lungs when his oxygen levels dropped to 65 and had to be put on oxygen. He had an allergic reaction to morphine, and had a seizure because of nausea medication. He also has a feeding tube. On the 17th of February 2022 he developed a fever and was admitted where they did blood work and discovered he had 2 viruses and his blood counts were extremely low.

He finished his last round of chemo on 21 March 2022. He was admitted and had a blood transfusion and platelets because it was too low. He also had an MRI but we have not received his report or any update when and if they will be operating. Kian is seeing a dietician as well as a speech- and occupational therapist because of signs of autism.”

Update 28/02/2023:

“Kian had an operation on 12 April 2022 where half of his left kidney was removed. The surgery was successful and he was discharged on 18 April 2022.

He started with 27 weeks of weekly chemo on 25 April 2022. We had to drive from Kuruman to Kimberley every Monday. He was sick most of the time, could not eat at all and they had to give him a feeding tube. Kian is now on chronic hypertension medication. Sometimes he could not get the chemo because his neutrophil levels were too low. He also got occupational therapy, speech therapy and physio weekly because of the autism, and he lost mobility in his legs. He finished his treatment on the 28 November 2022 and had an MRI scan, they were happy with his progress, however he still needs maintenance chemo as the nephroblastomatosis are still on both kidneys in order to suppress any more tumors from developing, and to save what is left of his kidneys.

He started with his maintenance chemo on the 11th of January 2023. They have adjusted one of the chemo treatments because it is affecting his mobility and that is a concern for them. The physio therapist said she has spoken with an orthopedic specialist and suggested that a tension release operation should be done. The pediatric oncologist agrees with us that the cause of his immobility is not a sensory thing but a result of the negative effects of the chemo treatment. Will be consulting with them again on 07.03.2023 when we are in Kimberley for treatment.”

By supporting our fundraiser for Kian you can be directly involved in making a positive difference in his life. All proceeds from the “Love and Faith” bracelets are donated towards his ongoing medical care and expenses. Together we CAN change the world, and help a child in need!

Alternatively, please consider a donation; any and all donations welcome. REF: Kian Ludick.

Fundraising for Kian Ludick

Love and Faith Bracelets

The “Love and Faith” bracelets for Kian consist of wooden beads with crystal, silver and diamante fillers.

Colour Options:
1. white & blue
2. grey and blue
3. white, grey, blue mix

Charm Options:
1. faith & cross
2. love you heart
3. believe and hope

To place an order, contact the agent in your area or shop online.

Love and Faith Bracelets © Arms of Mercy NPC

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Posted on 09/03/202217/06/2022 by AOM

Fundraising for Lirie van der Merwe – Paraplegia, Respiratory inability, Osteopenia, Epilepsy

Lirie`s story:

Lirie van der Merwe is 10 months old and has paraplegia from the chest-line down, respiratory inability, multi-lobar lung collapse, osteopenia, and epilepsy.

Lirie was born at 32 weeks. After 4 weeks in the NICU she suffered a neck injury that led to paraplegia from the chest-line down. Due to this, her diaphragm is paralyzed and she is unable to breathe on her own and is on a home ventilator to breathe for her. She also suffered from a femur break due to her bones being so brittle.

Lirie is currently at home but her home-care is R28 000.00 per month. She gets her feeds through a feeding tube and she is suctioned regularly. She also has a cough assist to get her secretions loose and keep her lungs from collapsing. She has a vigorous daily medical and mediation routine that needs to be followed. The Medical aid is depleted, and Lirie needs her physio and speech therapy sessions.

By supporting our fundraising efforts you can be directly involved in making a positive difference in Lirie`s life. All proceeds from the “Shine Your Light” bracelets are donated towards her ongoing medical care and expenses. Together we CAN change the world, and help a child in need!

Alternatively, please consider a donation; any and all donations welcome. REF: Lirie van der Merwe.

Fundraising for Lirie van der Merwe

Shine Your Light Bracelets

The “Shine Your Light” bracelets for Lirie consist of pink wooden beads with crystal, silver and diamante fillers.

Charm Options: Diamante Cross / Diamante Crown / Diamante Bird.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 27/01/202226/04/2023 by AOM

Fundraising for Miliah Prinsloo – Rare Genetic Disorder

Miliah`s story:

Miliah is just over 3 years old and has an incredibly rare genetic disorder, 16q11.2q21 duplication – which was discovered only recently after years of tests and doctors’ visits. She struggles through global developmental delay, speech impairment, seizures, a heart defect, self-harming issues, obesity and other ailments.

Miliah has already gone through:

3 MRI’s; ECG Tests; Ph7 Test; Tube feedings; Biopsy; 2 Berium Swallows; 2 Metabolic Tests; 2 Geneticist consultation;
Physio since 8 months and needs to continue; Speech therapist, she had every two weeks; Grommets put in; CT Scan;
Xrays; Sonars; Scopes done; Occupational therapy; Correctional shoes (for a year – which hasn’t helped, hence why she will now need to undergo surgery).

Miliah was also diagnosed with chronic sinusitis, which means she’s sick most of the time, with chronic reflux and dysmotility.

There is not much information on her chromosome genetic disorder as it is so rare, which causes a lot of uncertainty, even for some Drs.

Miliah needs ongoing therapy (speech, OT, PT), frequent neurological check-ups, testing and medications, Specialists for her stomach and immune system, as well as many others.

She had surgery on the 18th of January 2022 in order to correct her metatarsus adductus to help her jump, run and walk normally. The bones had to be broken and placed correctly, and Miliah is due back in theatre in 3 weeks. Recovery will take longer than expected (around 6 months to a year) and she won’t be able to go to school for the next 5 to 6 months. During these first 3 weeks Miliah will not be able to walk at all and her legs need to stay elevated, either at home in bed, or on the couch, or in a wheelchair when walking around the complex or anything.

Her mommy works part-time to be there for all her go-to therapies, hospital check-ups and specialist visits, but she had to stop all forms of therapy due to financial constraints.

Please open your heart and support our fundraising efforts for Miliah – all proceeds from the “Crown of Hope” and the “Incredibly Precious” bracelets are donated towards her ongoing medical care and expenses. Together we CAN make a positive difference and help a child in need. Together we can change her world!

Alternatively, please consider a donation; any and all donations welcome. REF: Miliah Prinsloo.

Follow her Facebook Page – Helping Miliah – for live updates on her journey.

Fundraising for Miliah Prinsloo

Crown of Hope Bracelets

The “Crown of Hope Bracelets” consist of wooden beads with crystal, silver and diamante fillers.

Colour options: Pink / Beige / Grey.
Charm options: Diamante Crown / Diamante Flower / Hope-Awareness Ribbon.

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Incredibly Precious Bracelets

The “Incredibly Precious Bracelets” consist of turquoise wooden beads with silver and diamante fillers.

Charm options: Dragonfly / Feather / Cross.

Incredibly Precious Bracelets © Arms of Mercy NPC — Incredibly Precious Bracelets

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Posted on 06/09/202115/09/2023 by AOM

Fundraising for Esmae Peters – Acute Lymphoblastic Leukemia (ALL)

Esmae`s story:

On the 13th of July, Esmae Peters (3 yr.) was diagnosed with cancer. It was quite a progressive stage by then as she battled for about 2 months prior to receiving the diagnosis. She has had a few lumbar punctures and completed about 9 chemotherapy treatments .

Unfortunately she recently contracted a blood infection together with Neutropenic colitis and Pancytopenia, which are 2 life-threatening conditions on their own … she was transferred from the Cancer ward to ICU high care. She has had enlarged liver and spleen about 4cm each, distended bowel, numerous bruises and blood clots on her skin and gums, oral sores and also blood and platelet transfusions.

Her medical needs include Physiotherapy, Psychology, Speech therapy, Occupational therapy, optometry as well as dental as required.

Update from mommy, Magdalene Peters, 27/02/2023:

“Esmae is on day 593 in her journey thus far and she’s just completed chemo dose 158!!! True hero style! She remains in Remission 5 months to date and we are so grateful for the repeated breakthroughs and miracles the Lord has been faithful in granting her.

Still a long way to go until the end of treatment which is assumed to only be June 2025. The thought of it is just heartbreaking for all that this Braveheart girl off mine has to further endure, but we believe that God goes before her in all things and she’s gonna carry her Cross gracefully to the end.

Expected are…
29 consecutive months off hospital visits,
11 lumbar punctures,
Countless blood draws n tests,
116 more chemotherapy doses,
Bone marrow tests as required,
And whatever else comes up in this long term maintenance cycle she’s on.

Thank you so much to everyone who thinks of, and prays for us, we truly are grateful and appreciate your support and love. As we totally surrender this season of our lives to Jesus, we believe that He will grant us supernatural ableness and strength to reach the finish line reigning Victorious.”

We ask you to please open your heart and help us to carry the heavy financial burden by ordering Esmae`s special “Crowned in God`s Love Bracelets”, “Grow in Grace Bracelets” and Bath Bombs – all proceeds are donated towards her ongoing expenses where needed. Together we CAN make a difference and help a child in need.

Alternatively, please consider a donation; any and all donations welcome. REF: Esmae Peters.

Fundraising for Esmae Peters

Crowned in God`s Love Bracelets

The Crowned in God`s Love Bracelets consist of wooden beads/crystal beads with silver and diamante fillers.

Bracelet Options:
1) Silver and pink crystal beads with diamante heart charm.
2) Dusty pink and grey wooden beads with diamante crown charm.

To place an order, contact the agent in your area or shop online.

Crowned by Glory Bracelets Arms of Mercy NPC

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Grow in Grace Bracelets

The “Grow in Grace Bracelets” consist of wooden beads/crystal beads with silver and diamante fillers.

Bracelet Options:
1) Silver, clear & gold crystal beads with Unicorn charm.
2) Silver, white & gold wooden beads with Cross charm.
3) White & gold wooden beads with Flower & diamante Butterfly, and diamante Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Grow in Grace Bracelets © Arms of Mercy NPC

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Bath Bombs

These Bath bombs are made from 100% natural ingredients and promise to smell amazing. Bath bombs are perfect as a gift or just for yourself, to enjoy some down time..

Choose from the following fragrances: Rose, Rooibos, Spearmint, Mango, Vanilla, Lavender, Geranium, Lemon Grass. Shop Online

Posted on 23/08/202105/09/2022 by AOM

Fundraising for Aldrich Kruger – Stage II Metastatic Papillary Thyroid Carcinoma Cancer

Aldrich`s story:

Aldrich Kruger is a young boy from Mossel Bay who was diagnosed with Stage IV Papillary Thyroid Cancer in March 2020, which already spread to his lungs. His thyroid and lymph nodes had to be removed.

He receives Radio active Iodine treatment at the Red Cross Hospital; not chemo nor radiation works for this type of cancer. Aldrich receives treatment every 6 months, and goes into isolation whilst the treatment is given.

He has always been a very active boy, and loves sport and dancing. This has been difficult for him and his family, as he has to fight, and also go through a world pandemic.

Aldrich was recently re-diagnosed with Stage II Metastatic Papillary Thyroid Carcinoma Cancer.

He will be chronic on eltroxin for the rest of his life.
He also struggles with eczema and requires medication for that too.

You can help us to lessen the financial burden by ordering his special “Hope and Faith” Bracelets – all proceeds are donated towards his ongoing medical care and expenses. Together we CAN make a difference and help a child in need.

Alternatively, please consider a donation; any and all donations welcome. REF: Aldrich Kruger .

Follow his Facebook Page for live updates on his progress and journey.

Fundraising for Aldrich Kruger

Hope and Faith Bracelets

The “Hope and Faith Bracelets” for Aldrich consist of Turquoise, Pink and Lilac wooden beads with silver and diamante fillers.

Charm options: Diamante Awareness Ribbon / Cross / Mossie.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 20/05/202117/06/2022 by AOM

Fundraising for Lyza Kennedy – Moebius Syndrome

Lyza`s story:

“Lyza Kennedy was 4 weeks old when she received her first operation as she could not feed on me. They gave her a Foley catheter in her tummy for me to feed her but she cried it out the next day and went back to NICU and theatre where she received a Mickey button. She has had 12 operations up to date. She was 1yr 7 months when they had the genetic assessment and then said it’s Moebius Syndrome.”

Moebius Syndrome is a rare neurological condition that is caused by the absence or underdevelopment of the 6th and 7th cranial nerves, which control eye movement and facial expression. Other cranial nerves may also be affected. There is no cure for Moebius syndrome, but proper care and treatment give many individuals a normal life expectancy. Learn more about Moebius Syndrome

“Lyza is currently on a ResMed machine as she some days forget to breath and loses consciousness. The ResMed machine is a loan product from Red Cross hospital where she received the machine and a back up battery.
She is often seeing a doctor as she is prone to infections.”

By supporting the AOM bracelet initiative you are helping to raise funds to contribute to Lyza`s ongoing medical expenses. Together we can change her world, one bracelet at a time!

Alternatively, please consider a donation; any and all donations welcome. REF: Lyza Kennedy.

Follow Help Lyza Smile on Facebook for live updates on her progress and journey.

Fundraising for Lyza Kennedy

Victorious in Faith Bracelets

The “Victorious in Faith” Bracelets for Lyza consist of purple and white wooden beads with crystal, silver and diamante fillers.

Charm options: Faith / Hope / Flower.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 11/05/202117/06/2022 by AOM

Fundraising for Liané Rossouw – Neuroblastoma Cancer

Liané`s story:

Liané Rossouw (1 yr.) was diagnosed with Neuroblastoma in December 2020 when she was only 8 months old. She was due to start her chemotherapy on the 19th of December, but she stopped breathing that morning. She was resuscitated and rushed to the pediatric ICU, and was on a ventilator for a little over a week.

The resuscitation caused extensive brain damage and has resulted in her losing her vision. The place where the tumour was, was also pressing against her spine causing the nerves in that area of the spine to die, which will never regrow, meaning Liané would never walk.

After the resuscitation, she completed 4 rounds of intensive chemotherapy. The chemo she had completed shrunk the tumour A LOT, but it was still active and still there.

We had a discussion with the doctors and we were given 3 choices:
1. Intensive chemotherapy which might help, but will make her extremely sick.
2. Less invasive chemotherapy which will just keep the tumour under control and slow down the spread.
3. No treatment.

We went with option 2, knowing that this chemotherapy is not designed to “cure” but to give us just a little bit more time.

Liané was scheduled to go for a MiBG scan in February 2021, but she was just too weak, so they canceled it. Since her last round of intensive chemotherapy, she completed 6 rounds of less invasive chemotherapy and she was strong enough to do the MiBG scan.

6 October 2021, we got to do the first part of the MiBG and then the second part the day after. I got to be with her while they did the scan. I asked the radiologist to explain to me what she is seeing on the scans if she can after the second day and she asked me quite a lot of questions regarding treatments, etc.

She could not find ANY tumour in Liané’s body. 12 October 2021, her doctors could confirm Liané was in remission and no active tumour can be seen or found in her body. LIANÉ HAS BEAT CANCER!!!

What do we do now?

Liané still needs to receive physio to improve her strength and movement. She still has the feeding tube. Her eyesight is improving and is reacting to lightness and darkness.

Liané has to go for blood tests to keep an eye on her for the next 6 months. She also has to do urine tests and she might do follow up scans to just keep an eye on it.

By supporting the AOM bracelet initiative you are helping to raise funds to contribute to Liané`s medical expenses. Together we can change the world, one bracelet at a time!

Alternatively, please consider a donation; any and all donations welcome. REF: Liané Rossouw.

Follow Hope for Liané on Facebook for live updates on her progress and journey.

Fundraising for Liané Rossouw

Anchored in Hope Bracelets

The “Anchored in Hope” Bracelets for Liané consist of gold and pink wooden beads with crystal, silver and diamante fillers.

Charm options: Anchor / Hope / Hope-Awareness Ribbon.

To place an order, contact the agent in your area or shop online.

Anchored in Hope Bracelets © Arms of Mercy NPC

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Posted on 05/04/202117/06/2022 by AOM

Fundraising for Mason and Madison Jacobs – Cerebral Palsy

Mason and Madison`s story:

“Mason and Madison Jacobs are twins who were born premature, weighing 1.6kg and 1.8 kg. Mason was in ICU for 3 weeks on a ventilator for oxygen. We realized when they were about 1 and 1/2years old that they were a bit slower with sitting and crawling than other kids. We also noticed that Mason`s left side is different and started with physio for the last 2 and 1/2 years.

Other problems started like chronic constipation that lead to a CT scan and lead to hemiplegia cerebral palsy, so we took them to a Specialist where we learned that both, Mason and Madison, has CP. They have gone for an MRI, hearing tests, EEG scan, botox injections, and still have to go to an Eye Specialist. They are going for physical therapy once a week. They just turned 4 on the 29th of March 2021 and are still not walking on their own. We are hoping that they will get stronger to walk with all the physio.”

Please support our fundraising efforts for Mason and Madison; all proceeds from the “Miracles and Magic” Bracelets are donated to their ongoing medical care and expenses. Together we CAN make a difference!

Alternatively, please consider a donation; any and all donations welcome. REF: Mason and Madison

Fundraising for Mason and Madison Jacobs

Miracles and Magic Bracelets

The “Miracles and Magic” Bracelets for Mason and Madison consist of pink and turquoise coloured wooden beads with crystal, silver and diamante fillers.

Charm options: Cross / Letter M / Hope.

To place an order, contact the agent in your area or shop online.

Shop Online

Posted on 15/03/202117/06/2022 by AOM

Fundraising for Mikyla Pretorius – Juxtapapillary Retinal Capillary Hemangioma & Hydrocephalus

Mikyla`s story:

Mikyla Pretorius – She epitomizes grit and determination.

Mikyla was unknowingly born with a condition called Acute Hydrocephalus 16 years ago, but has never let this stop her from attending mainstream schooling and achieving good marks in her grades. She is currently a 10th grade student at Goudveld High School in Welkom.

Late last year during the final exams of grade 9, Mikyla told her parents she is experiencing difficulty studying because something was disturbing her vision. After consulting a local optometrist and ophthalmologist, her parents Johan and Claudene decided to consult with Dr. Lynette Venter in Bloemfontein for further testing of the eyes and possible treatment options. Mikyla was diagnosed with Juxtapapillary retinal capillary hemangioma — a rare eye condition. On Dr. Venter’s recommendation, Mikyla also had an MRI scan of her brain where it was discovered by Dr. Dan Hugo that she had Acute Hydrocephalus.

With both these conditions comes a great deal of difficulty in her life, and several operations will be required to get things back to a sense of normalcy. In order for her to have these though, a substantial amount of money will need to be raised, which is where your help is desperately needed.

After the eye condition was first discovered, Dr. Venter recommended that Mikyla receive a series of Avastin injections into both her eyes due to bleeding behind her left eye and the risk in her right eye. Mikyla returned to Dr Venter in March for her check-up and further tests were conducted. However, there was only a slight change in both eyes. Dr Venter recommended further treatment, namely laser treatment followed by eye surgery. She also discovered that there was a certain amount of new bleeding behind the left eye.

Mikyla has to put an enormous amount of effort into completing her school work, often working late into the night and early morning. She is prone to headaches, migraines and nausea and lately is feeling immense pressure in her brain. Both Dr. Venter and Dr. Hugo have been extremely accommodating and they have arranged that if sufficient money can be raised, the laser eye treatment will take place on the 18th of March and the brain operation will take place in late May this year.

In between, Mikyla hopes to continue her education as classes are very important to her. To add to all their woes, Johan lost his job in June 2020 and is working alongside his wife in Web Development from home. In the hope of raising some of the funds, he is arranging a Charity Golf Day with the support of Brand Mashie Golf Course. The date will be advised. All previous costs, in excess of R50,000, have been covered with the help of family, friends, a local church in Odendaalsrus, and by the Grace of God.

For the next two operations, they need to raise a minimum of R220,000 for the operations to take place. If YOU can help with any donation they will be eternally grateful. They have already arranged with an Advocate in Pretoria that if they manage to raise any additional funds, these funds will be used for other young people with the same type of conditions.

Please open you heart and support our fundraising initiative; all proceeds are donated to Mikyla`s ongoing medical care and expenses. Together we can change the world, one bracelet at a time!

Alternatively, please consider a donation; any and all donations welcome. REF: Mikyla Pretorius.

Follow Mikyla Hulpfonds on Facebook for live updates on her progress and journey.

Fundraising for Mikyla Pretorius

See God`s Beauty Bracelets

The “See God`s Beauty” Bracelets for Mikyla consist of coloured wooden beads with silver and diamante fillers. Bracelet options:
1) White with Hope charm
2) Dark purple with love charm
3) White, purple & black mix with diamante flower

To place an order, contact the agent in your area or shop online.

Shop Online

Fundraising for Juvan Meyer

Fundraising for Dylan Beukes

Fundraising for Divan Conway

Fundraising for Brody Van Der Schyff

Fundraising for Jan-Hendrik Louw

Fundraising for Mieke van den Berg

Fundraising for Jasmijn Duvenhage

Fundraising for Wyatt Liberty

Fundraising for Zachary de Wet

Fundraising for Lenè Grobler

Fundraising for Amoré De Wet

Fundraising for Kian Ludick

Fundraising for Lirie van der Merwe

Fundraising for Miliah Prinsloo

Fundraising for Esmae Peters

Fundraising for Aldrich Kruger

Fundraising for Lyza Kennedy

Fundraising for Liané Rossouw

Fundraising for Mason and Madison Jacobs

Fundraising for Mikyla Pretorius

Charm a Child