Stem Cell Clinic

Every 13th man has a hair transplant according to Bookimed study – PR Web

BOSTON (PRWEB) November 28, 2019

Aesthetic tourism is especially developed in Thailand, where 20% of all patients are from abroad. Hair transplant is one out 5 of the most popular surgeries and the most frequently performed cosmetic procedures for men.

Hair transplant: facts and figures

Revolutionary methods of hair plantation

High demand gives rise to great discoveries. Doctors around the world are working on the development of new therapies that will help solve the hair loss issue by minimizing risks and reducing treatment time.

Except for the traditional hair transplant methods as FUE (follicular unit extraction) and FUT (follicular unit transplant), specialists apply stem cell hair restoration and robotic operation.

A doctor chooses the most effective treatment method according to your personal features and test results.

Hair transplant market trends

The hair transplant market is one of the fastest-growing health care specialties. The market size of hair plantation has developed by 64% since 2014, according to ISHRS statistics, and accounts for 6.5 billion USD.

Four factors are affecting the surgical hair restoration market:

1. the increasing number of people who suffer from baldness over the world2. the growing interest in self-care procedures within the Asia Pacific region3. development of minimally invasive and painless hair transplant techniques4. changing lifestyles globally.

Because of the high demand, there are a lot of clinics providing this procedure at different prices. According to Bookimed stats, the lowest hair transplant cost is offered in India and Turkey due to the general price policy within the country and residents' living wage. Patients also choose the UAE, Thailand, and South Korea in the interest of the combination of affordable prices and vacation.

About this study

This research is conducted by the Bookimed team and based on:

About Bookimed

Bookimed is a global platform for matching medical facilities over the globe and arranging the medical trip in the shortest term. Over 300,000 users from almost 30 countries request Bookimed to get treatment assistance each month.

Bookimed is a medical tourism provider that cooperates with 340 medical centers to help each patient receive timely and high-quality health care. The services of this platform are free of charge for patients because all the proceeds Bookimed gets from the partner clinics.

For more information, visit The Treatment blog or follow Bookimed on Facebook and Twitter.

Related Linkshttps://bookimed.com/

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Every 13th man has a hair transplant according to Bookimed study - PR Web

253 miles in 4 hours: A Syracuse mans race for a lung transplant, and the angel who helped him – syracuse.com

When the call came, Dimitri Georgiadis would have exactly four hours to hug his two sons, zip up his bag and motor 253 miles from Syracuse to Philadelphia.

If he wasted even 15 minutes, the donated lung would be gone.

Word spread quickly through St. Sophias Greek Orthodox Church community. Does anyone know a pilot?

Ted Limpert immediately said yes. Limpert is a Syracuse city court judge, handling every kind of charge from midnight mishaps to human trafficking.

Before that, he was a part-time fighter pilot one of the first to scramble into action when the planes hit the World Trade Center.

Hes flown 2,200 hours in an F-16 and 750 hours in the A-10 Warthog as a member of the 174th Air National Guard fighter wing.

It was Limpert who flew a jet over Clinton Square, cracking the silence on the first anniversary of the Sept. 11, 2001 attacks.

He has retired from the military, but he still owns an airplane, parked at a small airport in Cortland.

This was the plan: Limpert would collect Georgiadis and his wife Eleni, drive to his plane, fly about an hour to the North Philadelphia airport. They would get a car, even if it meant calling an ambulance, and drive through Philadelphia traffic to Temple University Hospital, where a donated lung would be waiting to replace the ones threatening Georgiadis life.

It would just be another mission, he thought.

We called it TOT, time over target, Limpert said. You can be early, but you cant be late.

Georgiadis, 55, was diagnosed with pulmonary fibrosis in 2006. As he got older, the disease grew more and more aggressive. He worked 18 years at Di Lauros Bakery in Syracuse. Then he went to work in the maintenance department, plowing snow and fixing faucets, for the Onondaga County Parks Department.

Georgiadis went on oxygen and disability. He moved up the list for a lung transplant. It would be done at Temple University Hospital, where he was being treated.

He was planning to drive himself to the hospital. Doctors said the call could come in the middle of the night, when accidents are most likely to claim the lives of donors.

It would be a stretch for a man on oxygen and in shock to make it over the foggy hills of Pennsylvania, through Philadelphia traffic and to the hospital in time.

Eleni Georgiadis started making phone calls.

All summer, I was calling different pilots, she said. Everybody we called, they said they couldnt guarantee me. They said well put you on the list, but we cant guarantee.

Even when she offered to pay, there was no guarantee, she said.

Then, a friend from church asked a friend of Limperts for help. The families were strangers.

He said Absolutely, Eleni Georgiadis said.

For two months, Limpert kept the car gassed up. He constantly checked weather conditions. He carried his phone everywhere, to the bench and to bed.

If he left town, he texted Eleni Georgiadis.

When hed come back, hed say Green Light. Your pilot is here. Ready for call, she said.

On Monday, Nov. 18, Limpert checked the weather one more time before heading for bed. It didnt look good.

At about 9 p.m., the call came.

He had not packed an overnight bag, even though his wife told him to. She handed him a Red Bull and he was out the door.

There was too much fog, they would have to drive to Philadelphia.

Limpert typed the hospitals address into his GPS app. It said the arrival time was 1:06 a.m.

That would be too late.

Limpert, a judge, declined to put a number on his speed down I-81, through Scranton and onto I-76.

I was proceeding with traffic, he said, laughing.

But there was no traffic, he said.

Limpert had thought to consult with police officer friends in advance and he was ready to call in the state police for an escort, if necessary.

In the two months leading up to the call, Limpert got to know the Georgiadises. He invited the couple to the Cortland Airport to introduce them to his airplane.

They climbed into the four-seater Mooney, tried on the headsets, made sure they were up for a noisy and bumpy ride. Other times, they shared Sunday dinner, homemade baklava, calzones and stories. They talked about their Greek heritage and their children.

Heres what Limpert did not say:

He had his own type of transplant last year.

In January 2018, a doctor at the VA Medical Center noticed elevated protein levels during a routine blood check and referred him to an oncologist. The eventual diagnosis: Multiple myeloma.

Limpert did six months of chemotherapy with so few side effects, he kept it a secret from his children and colleagues. By July, he couldnt hide the treatment any longer. He needed a stem cell transplant.

Doctors at Upstate Medical University harvested 17 million cells, then pushed 5 million of them back into his body. He was in the hospital for two weeks. The rest are in the bank for future treatment.

On the late night drive to Philadelphia, Limpert thought about his own illness, the way he relied on others to pull him through.

In the car, he encouraged the couple to focus on the 10-to-12-hour surgery they faced.

I didnt tell them, Limpert said. I thought they needed to focus on their own health issues.

The GPS sent the three on a ride down the Schuylkill Expressway a highway that often functions more like a parking lot. Limpert took the risk.

We pulled in at 12:43 a.m., Limpert said. We still had 15 minutes to spare.

The lung patient, his wife and their fighter pilot took a selfie. The Georgiadises rushed into the hospital.

Limpert looked at the can of Red Bull unopened in his car. He decided to drive back to Syracuse.

Limpert arrived in his office for arraignments by 9 a.m. Every wall in his chamber has a photo or drawing of a fighter jet. There are commendations and photos from the seven times he was deployed to Southwest Asia, starting with Operation Desert Storm and ending with Operation Enduring Freedom.

This was pretty easy, he said.

Georgiadis surgery was a success.

So far, so good, he said in an interview Tuesday from the hospital. He will be in the hospital for at least two months. He expressed a tearful thank you to the donor, whose identity is not known. They will write a letter to the donors family to see if they want to connect and share their stories.

In the past week, they have stayed in constant touch with Limpert, who they now consider family.

He took a huge burden off our shoulder, Dimitri Georgiadis said. The biggest one ever.

In Greek, Theodore means The Gift of God, Eleni Georgiadis said.

We call Ted our angel, she said.

Contact the author: Michelle Breidenbach | mbreidenbach@syracuse.com | 315-470-3186.

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253 miles in 4 hours: A Syracuse mans race for a lung transplant, and the angel who helped him - syracuse.com

Heartbreaking photograph shows the reality of childhood cancer – Yahoo Sports

The mother of a cancer survivor has released a heartbreaking photograph to show the reality of the disease.

Sophia Soto, from Florida, was diagnosed with stage four neuroblastoma at just 14 months old after unusual bruises developed around her eyes.

READ MORE:Girl with neuroblastoma declared cancer-free after pioneering treatment

With doctors dismissing it as just a fall, an eye specialist eventually found tumours behind her eyes were to blame.

The toddler endured 60 rounds of chemo, 20 of radiotherapy and a stem cell transplant over six months. She was snapped just before having treatment.

Sophia, now six, has been in remission for five years and medication-free for the past 24 months.

Now six, Sophia has been off medication for the past two years. [Photo: Caters]

Speaking of her daughters condition, Sophias mother Rosie Soto, 40, said: The picture of Sophia upset really does hone in on the reality of childhood cancer.

She was having a lead put on her chest for her treatment, which she didn't want, hence why Sophia was so upset.

I look back at the picture now and wonder how I did it. It was so hard watching my little girl so ill.

Neuroblastoma is a rare type of cancer that mainly affects babies and young children,according to the NHS.

READ MORE:Childhood Cancer Survivors Are Twice as Likely to Have This Condition

Around 95 youngsters in the UK are diagnosed every year, making up 6% of all childhood-cancer cases,Children with Cancer UK statistics show.

In the US, around 800 are diagnosed annually, also accounting for 6% of all cases,according to the American Cancer Society.

Neuroblastoma develops in specialised nerve cells called neuroblasts, which get left behind during a babys development in the womb.

The disease tends to start in one of the adrenal glands above the kidneys or nerve tissue next to the spinal cord, before spreading.

Sophia's parents Javier and Rosie Soto watched her battle the disease. [Photo: Caters]

Mrs Soto became concerned when her daughter develop bruises around her eyes, with no obvious cause.

I kept taking her to the doctors because the bruising wasn't going away, but they just said it must have been from a bump or something, she said.

Sophia wasn't referred for a scan or biopsy until I went to an eye specialist, who knew straight away it was caused by a tumour.

She was sent for an MRI, where black spots appeared on the scans confirmed the tumours behind her eyes.

Story continues

[A] biopsy found tumours on one of her kidneys as well, which led to her stage four neuroblastoma diagnosis.

Sophia discovered she had the disease in March 2014, aged just 14 months.

After extensive treatment, the youngster has been in remission since that November, but still has check-ups every six months.

The tumours behind her eyes cannot be removed, however, doctors believe they are now benign.

READ MORE: Mom beats breast cancer and then books 'dream' trip

Doctors are reluctant to remove the tumours Sophia has behind her eyes as they've said it would be likely the surgery [would] disfigure her face, Mrs Soto said.

Whilst they are tumours, doctors are reasonably confident they are not cancerous so we have decided to not have the surgery right now, but it may be something she has when she's older.

Over the worst, Sophia loves dancing and dreams of one day becoming a vet.

No one can imagine what she went through looking at her now, she just looks like a normal regular child, Mrs Soto said.

Sophia has her moments when she asks about when she was sick and has questions about her treatment scars, but overall she's a pretty happy girl.

If I was to say anything to other parents with children battling cancer, I'd say to not give up, stay positive.

It's really important not to compare your child's process to anyone else as everyone battles illnesses differently.

We're over the moon Sophia is now doing so well. We're really blessed she's such a fighter.

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Heartbreaking photograph shows the reality of childhood cancer - Yahoo Sports

Exploring the Future of Prostate Cancer with City of Hope – Curetoday.com

Although one in nine men will receive a prostate cancer diagnosis in his lifetime, cutting-edge research has allowed more men to live longer or even be cured.

One such program that sheds light on this cause is City of Hopes NoShaver November. The month-long fundraising and awareness campaign urges participants to forego shaving to start a conversation, encourage testing and raise critical funds to continue leading-edge prostate cancer research and promising new therapies conducted at City of Hope.

CURE recently spoke with Dr.Tanya Dorff, a medical oncologist at City of Hope who specializes in prostate cancer, about the campaign, her current work and where she sees the future of prostate cancer treatment shifting in the coming years.

CURE: What led you to City of Hope? What do you do there?Dorff: City of Hope was attractive to me because I am a clinical and translational researcher. The reason I came here was to work with scientists who share what we are seeing in the clinic and who incorporate the latest insights from the scientific discoveries in our laboratories into patient care. There is a real sense of mission and urgency that binds scientists to clinicians at City of Hope in a way that is unique and gratifyingly productive.First and foremost, I take care of patients who remain my central inspiration and raison detre, but I spend part of my time writing and running clinical trials that have real potential to impact how we treat patients in the future how we can do even better in the future than we do today. I lead the genitourinary cancer program, which includes fostering collaborations between the incredible physicians from urology, radiation oncology, radiology and pathology to work together both clinically and in research projects.You are Grammy-winning songwriter and vocal producer Kuk Harrells physician. Can you tell me what it was like to treat him?Kuk is such an incredible gentleman; it has been a pleasure to be part of his care team. His attitude toward treatment was one of diligence, and he has approached his illness as an opportunity for personal growth and for giving back by promoting prostate cancer awareness through his story. It has been inspiring to see him come through what was a lengthy and involved treatment with so much positive energy.How has the field of prostate cancer treatment evolved in recent years?More and more men with prostate cancer can be cured, and the men who cannot be cured with todays treatments are clearly living longer and better. This is thanks to new drug approvals in advanced, resistant prostate cancer but even more so to the application of more intensive therapy earlier in the course of the disease. This has been the biggest paradigm shift in prostate cancer over the last five years: up-front intensification in metastatic hormone sensitive prostate cancer.The next big shift in prostate cancer treatment is just now upon us molecular selection of therapies to individualize prostate cancer treatment. The most imminent example is olaparib (Lynparza), a PARP inhibitor, which worked better than standard treatment in patients with castration-resistant prostate cancer whose tumors harbor mutations in DNA repair genes. But the ingenious theranostic approach will be close behind where imaging (scans) show us whether a cancer is expressing a certain target (i.e. PSMA) and if so, a radioactive particle linked to that target is applied (i.e. Lu-177 PMSA).

What are you most hopeful for in cancer treatment in the future?I believe immunotherapy will be the way to durable remission or a cure. Here at City of Hope, we are working hard to improve the effectiveness of immunotherapy for patients with metastatic prostate cancer, studying intensive treatments such as CAR-T and bispecific T-cell engaging antibodies, among other approaches. Our scientists are looking at our patients in real time to learn why treatments work or dont work, and how to better engage the immune system. I am very hopeful that these biologic insights will eventually translate into therapeutic success such as we have seen in leukemia with CAR-T and melanoma with immune checkpoint inhibitors.What advice would you offer someone who has just received a cancer diagnosis of their own?One: Play an active role. Ask questions, and if something doesnt sound right or make sense, ask again. It is so important that patients buy into their treatment, understand and feel confident about the treatment plan. No one is perfect, not even the best doctor, and working together as a team will lead to the best success.

Two: Be a squeaky wheel. Patients who communicate symptoms in real time fare better because problems are addressed before they become more serious.

Three: Stay active. Exercise is one of the things that has been shown over and over again to help cancer survivors and cancer patients in various stages. Obviously, a conversation should occur with the treatment physicians to ensure that there are no restrictions but patients who are more active will come through treatment in better shape.

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Exploring the Future of Prostate Cancer with City of Hope - Curetoday.com

South Carolina toddler survives rare cancer and the risky procedure used to treat it – USA TODAY

Hailie Hyman holds her daughter Maci, 1, before an appointment at the Prisma Health Pediatric Hematology Oncology Center Monday, Nov. 4, 2019.(Photo: JOSH MORGAN/Staff)

GREENVILLE, S.C.Hailie and Treylin Hyman saw the bruising on their baby girls leg as a sign that the active 1-year-old was learning to walk.

But as a blood test would later reveal, little Maci was actually suffering from an extremely rare blood cancer that threatened her life without a risky treatment - atreatmentalmost as dangerous as the disease.

In the beginning, it was very scary, Hailie Hyman told The Greenville News.

I couldnt think of anything but the bad things, she confessed. It was all about the statistics. And the statistics arent good.

Terrifying months followed the diagnosis, punctuated by one critical complication after another, leaving the Boiling Springs couple to wonder if Maci would survive.

Somehow, though, the blue-eyed toddler pulled through.And now her family is looking forward to a special Thanksgiving with much to be grateful for.

Alyssa Carson is 18 and has a pilot's license: She wants to be in the crew that colonizes Mars

The Hymans journey began last February atMacis 1-year-old well-child checkup.

We had no idea anything was wrong, her mom said.But they did a routine (blood test) and a couple of hours later, we got a call saying her platelets were very low.

The Hymans were referred to a hematologist who found other abnormalities in Macis blood and scheduled a bone marrow biopsy to investigate further.

Hailie Hyman holds her daughter Maci, 1, before an appointment at the Prisma Health Pediatric Hematology Oncology Center Monday, Nov. 4, 2019.(Photo: JOSH MORGAN/Staff)

During the procedure, the child suffered an aneurysm in an artery and went into cardiac arrest. The team performed CPR on her for 20 minutes before she was stabilized, her mom said.

Later, in the pediatric intensive care unit, she suffered internal bleeding, too.

It was really hard, she said. There were many nights that I would just pray and pray and pray.

Initially believing Maci had leukemia, doctors subsequently determined she had myelodysplastic syndrome, or MDS.

The condition occurs when abnormal cells in the bone marrow leave the patient unable to make enough blood, according to the American Cancer Society.

Its rare, afflicting as few 10,000 Americans a year, though the actual number is unknown.

Maci Hyman, 1, interacts with hospital staff before an appointment at the Prisma Health Pediatric Hematology Oncology Center Monday, Nov. 4, 2019.(Photo: JOSH MORGAN/Staff)

In children, its rarer still. Most people arediagnosed in their 70s.

We were told that just four out of 1 million children get it every year, Hailie Hyman said.

That made the diagnosis elusive at first, said Dr. Nichole Bryant, a pediatric hematologist-oncologist with Prisma Health-Upstate, formerly Greenville Health System.

Shes the only one Ive seen in my career, she said.

Maci had to have regular blood transfusions, antibiotics and other medications to fight the MDS, Bryant said. But the only hope for a cure was a stem cell transplant at the Medical University of South Carolina in Charleston.

When they said that was the only treatment plan for MDS, I of course went to Google, Hailie Hyman said. I read about transplant patients and ...all the complications. It was terrifying. But no matter how many bad things I saw, we had to do it. There is no other option.

The transplantis extremely risky.

Hailie Hyman looks at a fish tank with her daughter Maci, 1, before an appointment at the Prisma Health Pediatric Hematology Oncology Center Monday, Nov. 4, 2019.(Photo: JOSH MORGAN/Staff)

First, high doses of chemotherapy are given to destroy the diseased bone marrow, leaving the patient without an immune system, so fighting infections becomes a challenge. Then healthy donor marrow is infused.

Its also fraught with potentially life-threatening complications, including graft vs. host disease, which occurs when immune cells from the donor attack the patients body, Bryant said. Other complications include permanent kidney damage and gastrointestinal problems.

They have to go to hell and back, she said. But its the only option for long-term survival.

Maci had a really rough start, suffering lots and lots and lots of complications, Bryant said.

Her kidneys failed, so she wound up on dialysis. When she couldnt breathe on her own, she was put on a ventilator. And because she couldnt eat, she had to be tube fed.

Hailie Hyman looks at a fish tank with her daughter Maci, 1, before an appointment at the Prisma Health Pediatric Hematology Oncology Center Monday, Nov. 4, 2019.(Photo: JOSH MORGAN/Staff)

She had blistering sores in her mouth and throughout her GI tract, her mom said. Because her liver wasnt functioning properly, her abdomen filled up with fluid that had to be drained. She was bleeding so profusely in her lungs that one of them collapsed.

Maci, who was sedated through much of it, was put on full life support, she said.

That night we almost lost her, her mom said. We were in the hallway crying our eyes out. We didnt know what do to or think. It was pretty scary for a while.

Somehow, Maci made it.

There were so many times during her first months that it seemed like she would not survive, Bryant said. So the fact that she is here ... is really a miracle.

Macis family found an unrelated donor through the National Marrow Donor Program, enlisting hundreds of other people to join the registry in the process, Bryant said.

Nichole Bryant, M.D.(Photo: Provided)

It was an important part of their journey that maybe didnt directly benefit Maci, she said. But if everybody did that, we wouldnt have difficulty finding a donor for anybody.

Doctors have no explanation for why Maci got MDS. She didnt carry the genetic mutation for it and there is no family history.

She is a rare child - and not in a good way, her mom said, adding,Youve got to laugh sometimes or youre going to cry.

A dying man wanted one last beer with his sons: The moment resonated with thousands

Maci was admitted to MUSC on June 2 and released on Oct. 14.

The Hymans, both 22, spent the entire time in Charlestonwhile Hailies mom cared for their older daughter, Athena, now 2.

Treylins employer held his welding job open for him. And other friends and family members did what they could to help.

We had many, many people very generously donate to us to cover expenses at home and living expenses where we were, Hailie Hyman said.

We are thankful for everyone who helped us through it the cards, the gifts, the donations. Every single cent is greatly appreciated.

Maci's doing well, but recovery from a transplant can take months to years, Bryant said.

Her kidneys are functioning again so she was able to come off dialysis. But she still must take many medications, including anti-rejection drugs that suppress her immune system and leaveher at risk for infection. And she still must be tube fed.

She is miles ahead of where she was two months ago, Bryant said. But she still has a long way to go. Its a long, long road.

Macis mom says she can be up and playing one day and flopped over on the couch another. She still experiences a lot of nausea and vomiting, but is doing well compared to where she was.

Hailie Hyman pulls her daughter Maci, 1, in a wagon in the hallway before an appointment at the Prisma Health Pediatric Hematology Oncology Center Monday, Nov. 4, 2019.(Photo: JOSH MORGAN/Staff)

So as the nation pauses to give thanks this Thanksgiving, she says the family will be countingtheir many blessings family andfriends, Gods mercy, andthe doctors and nurses who saved Macis life.

She has battled a lot and overcome a lot, she said. I have no doubt she will be able to get through.

Want to know more about becoming a marrow donor? Go to bethematch.org.

Follow Liv Osby on Twitter:@livgnews

104-year-old woman bags first buck: 'Never underestimate the power of our senior citizens'

Indiana hospital sued: More than 1,000 patients potentially exposed to HIV or hepatitis

Read or Share this story: https://www.usatoday.com/story/news/health/2019/11/28/south-carolina-toddler-survives-rare-blood-cancer-risky-procedure/4321002002/

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South Carolina toddler survives rare cancer and the risky procedure used to treat it - USA TODAY

Imani Barbarin Coins #PatientsAreNotFaking to Fight Back Against Negative Patient Stereotypes – The Mary Sue

A nurses Tiktok video titled We know when yall are faking went viral on Twitter this weekend for its mocking portrayal of hospital patients. There was immediate backlash, helmed by writer Imani Barbarin (aka Crutches&Spice), who created the hashtag #PatientsAreNotFaking as a response to the video.

The video especially struck a chord with women, bipoc, fat activists, trans and nonbinary folk, and people who live with chronic illness and disabilities. Essentially, any of us who have been disbelieved or ridiculed by doctors due to the inherent medical bias against anyone who isnt a white man. Many of us, myself included, felt compelled to share some of the many instances that doctors and nurses disregarding or disbelieving our symptoms led to extreme medical emergencies.

Of course, because the internet is the internet, D Rose (the nurse at the center of this) has now been doxxed, which forces me to explicitly state that doxxing is bad. Do not doxx. Except maybe Nazis. But really, just please dont. Okay, back to the main issuegetting doctors and nurses to believe us!

This hit especially close to home for me. For ten years I had a fast-growing rash, accompanied by extreme itching and intense nerve pain, encompass almost my entire body. I felt like I was literally on fire 24/7. I spent those ten years (from age 20 to 30, basically my entire adulthood) going from doctor to doctor looking for answers. And while they could tell something was wrong, they refused to believe that I was in as much pain as I said I was in. Instead, they would gather their entire team of nurses and interns into my examination room to gawk at my naked body, whisper to each other that I was some sort of medical marvel, and the shrug and tell me there was nothing they could do. I had to beg for years to get a doctor to even prescribe me something as basic as a high dose cortisone cream.

It wasnt until a large tumor sprouted out of my shoulder/armpit and its subsequent removal and dissection (which even then the surgeon tried to dismiss as a just a keloid) that I finally discovered what was wrongI had a rare form of cutaneous t-cell lymphoma called Mycosis Fungoides. MF is normally a slow-growing easily managed, if incurable, cancer if caught early. Unfortunately because it took a literal decade for my diagnosis, my MF has had time to well, really dig its heels in. Its turned aggressive and resistant to normal methods of treatment. Which means at three years in, and four different clinical trials under my belt, I am now undergoing chemotherapy and a stem cell transplant is in my near-ish future.

Oh, I also have an extreme codeine allergy that doctors and nurses love to ignore which has also almost killed me too! But you get the point. My story, unfortunately, is not uncommon even if my particular type of cancer is.

The hashtag #PatientsAreNotFaking would not have gone viral if it had just been a few bad apples in the medical field ignoring patients. This is a systemic problem and one only made more complicated by the opioid crisisa crisis created by the pharmaceutical companies pushing doctors to overprescribe the highly addictive painkillers, I might add. And while D Rose and others might claim that this was just a joke and a way for nurses to let off steam (dont even get me started on the twerking and her appropriation of black culture, because black women are some of the patients who suffer the most from maltreatment and disbelief by doctors!) its not a laughing matter for the millions of people who have suffered because of this pervasive and harmful stereotype.

(Photo: Robin Marchant/Getty Images for Twitter)

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Imani Barbarin Coins #PatientsAreNotFaking to Fight Back Against Negative Patient Stereotypes - The Mary Sue

Mum shares heart-wrenching photos to show the ‘reality of childhood cancer’ – Mirror Online

The family of a little girl who was diagnosed with cancer at just 14 months old have released a photo of her undergoing treatment to show the devastating effects of childhood cancer.

Sophia Soto was found to have Stage 4 Neuroblastoma shortly after her first birthday when tumours were discovered behind her eyes and on her kidney.

It began a relentless six month period of treatment, during which brave Sophia endured 60 rounds of chemotherapy, 20 rounds of radiation and a stem cell transplant.

Sophia battled through and has now been in remission for five years, unrecognisable from the girl who appears in the heartbreaking images from March 2014.

Her mum, Rosie, says no one could imagine what her six-year-old daughter, and herself as a parent, have been through looking at her now.

"The picture of Sophia upset really does home in on the reality of childhood cancer," she said.

"She was having a lead put on her chest for her treatment - which she didn't want - hence why Sophia was so upset.

"I look back at the picture now and wonder how I did it; it was so hard watching my little girl so ill."

Rosie, from Florida, became concerned about her young daughter after noticing she was developing bruising around her eyes, which she claims doctors dismissed as a result of a bump or fall.

The mum followed her instincts and continued to search for an answer, taking Sophia to an eye specialist who 'knew straight away' the bruising was being caused by tumours.

Rosie continued: "Sophia kept getting bruising on her eyes and I didn't recall her falling over or anything, so I didn't understand where they were coming from.

"I kept taking her to the doctors because the bruising wasn't going away, but they just said it must have been from a bump or something.

"Sophia wasn't referred for a scan or biopsy until I went to see an eye specialist.

"She was sent for an MRI where black spots appeared on the scans confirming the tumours behind her eyes.

"It was then the biopsy which found the tumours on one of her kidneys as well which led to her stage 4 Neuroblastoma diagnosis."

Following half a year of gruelling treatment, Sophia has been in remission since November 2014 and has now been medication free for two years.

The youngster, who loves to dance and has dreams of becoming a vet, isn't yet classified as 'cancer free' and still requires check ups every six months.

The tumours remain behind Sophia's eyes, which cannot be removed due to their placement, but doctors believe they are benign and not causing harm.

"Doctors are reluctant to remove the tumours Sophia currently has behind her eyes as they've said it would be likely the surgery to disfigure her face," said Rosie.

"Whilst they are tumours, doctors are reasonably confident that they are not cancerous so we have decided to not have the surgery right now, but it may be something she has when she's older.

"No one can imagine what she went through looking at her now - she just looks like a normal regular child.

"Sophia has her moments when she asks about when she was sick and has questions about her treatment scars, but overall she's a pretty happy girl.

"If I was to say anything to other parents with children battling cancer, I'd say to them to not give up, stay positive and keep your faith.

"It's really important not to compare your child's process to anyone else as everyone battles illnesses differently as every situation is different.

"We're over the moon that Sophia is now doing so well - we're really blessed that she's such a fighter."

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Mum shares heart-wrenching photos to show the 'reality of childhood cancer' - Mirror Online

Toddler Bravely Cheats Death After He Survived Rare Cancer And Its Treatment – The Digital Weekly

Hailie and Treylin Hyman saw the bruising on their baby girls leg as a symbol that the active 1-year-old was getting to walk.

But as a blood test would following disclose and reveal, little Maci was suffering from an extremely unusual blood cancer that scared her life outwardly a risky treatment a practice nearly as serious as the disease.

At the start, it was very scary, Hailie Hyman told the reports.

Terrifying periods followed the diagnosis, punctuated by one crucial difficulty after another, starting the Boiling Springs couple to wonder if Maci would remain and survive or not.

The Hymans course started last February at Macis 1-year-old well-child checkup.

We had no clue anything was incorrect, her mom told. But they did a normal (blood test) and a few hours later, we attended a call telling her platelets were very low.

The Hymans was transferred to a hematologist who gained other abnormalities in Macis blood and listed a bone marrow biopsy to examine further.

During the treatment, the child endured an aneurysm in an artery and progressed into cardiac arrest. The medical team gave CPR for 20 minutes before she was steadied, her mom told.

Later, in the Emergency room, she underwent internal bleeding, too.

It was difficult, she told. There were many times that I would just pray and pray and pray.

Initially considering Maci had leukemia, doctors finally discovered she had myelodysplastic syndrome or MDS.

The situation occurs when abnormal cells in the bone marrow leave the patient weak and unable to make adequate blood.

In children, its more uncommon still. Most people are diagnosed in their 70s.

Maci had to produce regular blood transfusions, antibiotics, and other medicines to struggle the MDS, Bryant stated. But the only support for a remedy was a stem cell transplant.

The transplant is very risky.

Its also laden with possibly life-threatening difficulties, including graft vs. host disease, which happens when immune cells from the donor strike the patients body, Bryant told. Other difficulties incorporate permanent kidney damage and gastrointestinal problems.

There were so many moments during her initial months that it appeared like she would not survive, Bryant stated. So the fact that she is here is a miracle.

Macis family got an anonymous donor by the National Marrow Donor Program, participating many individuals to register in the process, Bryant told.

Maci was admitted to MUSC on June 5 and discharged on Oct. 14.

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Toddler Bravely Cheats Death After He Survived Rare Cancer And Its Treatment - The Digital Weekly