Showing posts with label Media. Show all posts
Showing posts with label Media. Show all posts

Thursday, July 22, 2010

One More "Impossible" Disease Reversed By Repair Stem Cells---NOT Embryonic Stem Cells


Last Sunday we were contacted by our local NBC affiliate, KNDU reporter Hilary Whittier who asked how Mailia was doing and if she could come out to do a follow up story about Mailia’s Stem Cell procedure. We were thrilled to see Hilary and it was truly wonderful and humbling to be able to tell another soul…all about Mailia’s incredible journey.

It has been six weeks since her lungs accepted all her own adult stem cells and we are thrilled and truly blessed to see Mailia thriving and healing…every single day.

We owe so much gratitude to everyone for their help and prayers and hope that it is evident in the miracle they have chosen to support.

Today we were also blessed with seeing a wonderful post on Don Margolis’s web site which I have copied below and I also encourage folks to visit his web site from time to time to learn all they can about Adult Stem Cell Therapy and people’s stories…and speaking of which, I encourage EVERYONE who is part of “the family” or “club” who has received and benefited from Adult Stem Cells to send Don Margolis an email or letter telling him of their journey so as to help inspire others.

Here is the post from DonMargolis.com:

If you ask your pulmonologist if stem cells can help your lung disease (COPD, emphysema, pulmonary fibrosis, etc. etc.) he/she will tell you “No---stem cells are snake oil.” That is what we hear from almost every lung patient who comes to us trying to get out of the medical prison imposed by all lung conditions. We know that stem cells have helped dozens treated in Latin America and Europe, but a disease almost no one has heard of?
Ten years ago, one teen in the state of Washington was told she only had months to live, but today, 16-year-old Mailia Goforth has defied the odds and continues to surprise doctors.

At the age of 3, Mailia was diagnosed with Eisenmenger's Syndrome. It's a heart defect that causes high blood pressure in her lungs and doesn't allow her to breathe on her own.

But recently, Mailia and her family took a trip across the country for a special procedure using stem cells. The hope, to fix her lungs and be one step closer to closing up a hole in her heart.

After more than a month of recovery, Mailia says the $50,000 operation worked, and she's getting stronger everyday.


She can now take out her breathing tube and even find enough energy to play outside. She tells me, after a few more operations she could be able to run, jump and do everything most 16-year-olds can do.

"It feels amazing," she said. "I know I'll be able to do everything I've always wanted to do without having to get sick anymore... just to be free at last."

Free at last from the worry and stress of her disease is what the family is wishing for. To get there, she still needs her lungs to get stronger from the stem cell surgery. Once the lung pressure goes down she will be able to have heart surgery.

The video is HERE.

To follow Mailia's progress or donate to her cause go to http://mailiasmiracle.com/

Thank you Don. Thank you Dr. Grekos and Regenocyte. Thank you God and everyone for your help and prayers once again…all our gratitude!

Max, Andrea and Mailia

Thursday, June 17, 2010

A Miracle For Mailia - Tri City Herald Article by Michelle Dupler June 7, 2010


Mailia Goforth, center, prepares to undergo an experimental stem cell procedure in the Dominican Republic. Doctors hope stem cells from her own blood will help heal high blood pressure in her lungs so she can have a life-saving heart surgery. Nurses Amie Ryan, left, and Emily Storrer, right, from RADY Children’s Hospital in San Diego, observed the procedure while volunteering in the area.
Pasco teen begins experimental stem cell treatment

By Michelle Dupler, Herald staff writer

PASCO — Once upon a time, Mailia Goforth was a young girl dreaming of a miracle that would break the curse cast over her as a child.


She waited 12 years for someone to fix her heart, which while full of love has a defect that makes her weak and steals the breath from her lungs.

Last year, a wizard entered the tale holding in his hands an almost magical treatment using her own blood, but it appeared it might take more time than Mailia had for her parents to find the money to pay.

Max and Andrea Goforth wished for a miracle for their daughter, but Mailia grew weaker and her parents grew more afraid, even though they never gave up hope.

But across the land, a fairy godmother heard of Mailia's curse and waved a wand to grant her dearest wish -- a chance at life free from the curse that has bound her.

Mailia Goforth on Wednesday became one of a handful of people in the U.S. to get an experimental stem cell treatment that could end up not only saving her life, but allow her to live the normal one she's never been able to experience.

Mailia, 16, has Eisenmenger syndrome, a condition that affects the blood flow to the heart that in her case is caused by a hole in her heart's wall.

She also suffers from secondary pulmonary hypertension, or high blood pressure in her lungs. Her blood pressure is high because the hole in her heart allows too much blood to flow from her heart to her lungs, causing her blood vessels to constrict and stiffen and strain her heart. The pressure also stops surgeons from closing the hole.

That in turn means not enough blood flows into her lungs and she becomes fatigued and short of breath.

She can't walk more than a few steps without tiring, and for seven months of the year -- when temperatures are cool -- she can't venture outdoors because of the strain on her lungs and her susceptibility to viruses.

A double-lung and heart transplant -- the customary treatment for Mailia's condition -- is not an option, as doctors have told the family Mailia would not survive.

Andrea Goforth believed she found an answer to Mailia's problem when she learned about Dr. Zannos Grekos -- Mailia's wizard.

Grekos developed an experimental technique to repair pulmonary hypertension using adult stem cells. In fact, it's so experimental it can't legally be done in the United States because it isn't approved by the Food and Drug Administration, so Grekos flies with patients to the Dominican Republic to perform the procedure.

Because it is experimental, the $64,000 cost of treatment is not covered by the family's insurance.

Blood is drawn from the patient and flown to a lab in Israel where stem cells are extracted and activated with a protein known as a growth factor to cause them to multiply.

Growth factors are produced normally in every person's blood and tell other cells to become brain tissue, heart tissue or liver tissue, Grekos told the Herald in August.

"We use ones that are specific in this instance for blood vessels," he said.

Every person also has stem cells running around in their body like miniature repairmen, and when they can be extracted, multiplied and told what to do, they can repair damaged blood vessels and even make new ones.

The stem cells are flown from Israel to the Dominican Republic, where Mailia would be waiting to have them inserted into her lungs through a small tube. The stem cells would attach to her pulmonary blood vessels and help them regenerate.

For Mailia, that would reduce her blood pressure, making it easier for her to breathe and allow surgeons to give her a pulmonary artery band, which would reduce the blood flow through the hole in her heart.

Once Max and Andrea Goforth knew they wanted Grekos to treat Mailia, they started raising money as fast as they could. They figured they'd need the $64,000 for the stem cell treatment, plus $10,000 for travel and expenses.

They also expect to need the money for a second stem cell treatment in about a year. They hope the surgery to correct Mailia's heart defect will be covered by insurance.

By the end of April, the family had raised $47,000 -- significant progress, but not enough to start Mailia's journey to the Dominican Republic.

Andrea Goforth said she's stayed in constant contact with Dr. Grekos and e-mailed him an update after their last fundraiser in April to tell him how much they'd been able to raise.

In response, she got a surprise she's describing as Mailia's miracle come to life.

Dr. Grekos' staff at his company Regenocyte wrote back to tell Mailia's parents he was willing to take $42,000 of the money they'd raised to perform Mailia's stem cell procedure, and that a nonprofit called the Alliance for Adult Stem Cell Research and Therapy -- Mailia's fairy godmother -- was going to pay the rest.

After they got the news, Max and Andrea Goforth each scheduled a month off from their jobs, got the family's SUV in shape for the more than 4,000-mile, nine-day drive, and set off on a cross-country adventure.

They arrived in Florida about a week ago, where Mailia underwent preliminary tests and her blood was drawn and whisked away to Israel to make stem cells.

She flew to the Dominican Republic a week ago, and on Wednesday had nearly 58 million stem cells pumped into the arteries in her lungs through a catheter.

Within days, she'll be on her way back home.

"This is an adventure," Andrea Goforth said by telephone from Florida. "This is a first for us, as it is for many. I hope Mailia will be able to come back and tell a very positive story about her journey for others."

Grekos has said if the stem cell therapy is successful, Mailia's pulmonary hypertension could be reduced enough that she could have a relatively normal life without an oxygen tank and perhaps even be able to play sports.

Mailia has dreams both simple and lofty -- she'd like to go to the mall like other teenagers and be able to swim like her idol, Michael Phelps. She also envisions one day running her own animal sanctuary in Costa Rica where she'd preserve endangered species.

Right now, Andrea Goforth is focusing her prayers on a successful stem cell procedure that will allow Mailia's heart repair within a matter of months.

But she's also worried about how the family will pay for additional procedures with just $33 left in the Mailia's Miracle fundraising account after the costs of the procedure and trip.

The family plans additional fundraisers when they return home, and has set up a website called mailiasmiracle.com that tells Mailia's story and gives information on how people can donate.

Thursday, May 27, 2010

Mailia's Blood Draw a Success at Regenocyte



Mailia's Stem Cells - The Ultimate Gift
Tuesday morning, we were greeted at Regenocyte by Nancy Trombino and Roxanne Pleva who are patient coordinator's at Regenocyte.  Everyone was so thrilled to finally meet Mailia...a young patient who has traveled so far in hopes of reaching her dream of a miraculous healing.

Mailia was very nervous about the procedure and Dr. Grekos and his incredible team of nurses, Michelene and Felicia, were able to talk to Mailia and give her the necessary dialog on what they would be doing, step by step...in order to draw her blood successfully with minimal stress to her body and psyche.

In speaking with Dr. Grekos about our concerns relating to Mailia's previous blood draws via her arm's and how difficult she is to do in this manner, I asked if he would consider doing her blood draw through a femoral pic line through her groin instead.  He agreed to do this validating that it is the parents that know their kids specifics and he is all about listening and taking these things into account.  Boy...big relief!

They preped Mailia in their catherization lab and lightly sedated her while monitoring her heart rate, blood pressure and oxygen saturations.  Once she settled down...they inserted the line and were able to draw around 30% more blood which for Mailia...means more stem cells we hope.

 

After Mailia's blood draw, we took her for a good meal to replenish her strength and gave her alot of fluids and supplements to replenish her blood.  She did well, and expressed excitement about finally getting her stem cells.  We also had a wonderful interview with Tri City Herald reporter Michelle Dupler who is doing a follow up article on Mailia's Miracle and her journey now to Florida and the Dominican Republic for stem cell therapy.

Today...we needed to replenish her oxygen once again, so headed to LinCare to exchange 20 empty E tanks for 20 full ones which should last her through the weekend, for we will be planning to check out of our hotel here in Bonita Springs, and head in to Miami this coming Suday.  Our flight to Santo Domingo in the Dominican Republic will be Monday May 31st...for her scheduled procedure on June 2nd.

We also spent some time this afternoon at the Regenocyte clinic meeting with Dr. Grekos and discussing Mailia's procedure and the options and opportunities this would present for her.  We also had the chance to meet Howard Linderman, a Regenocyte patient who underwent stem cell therapy two years ago.  To hear his story is one of true inspiration and can be seen by clicking the Regenocyte link.  He offered Mailia so much hope and motivated her to stay positive and believe in herself...and her doctors.  She is now...part of their exclusive club!  He offered to teach Mailia how to scuba dive at some point...she told him she already was an accomplished diver...in her Wii game "Endless Ocean". 


                  Howard Linderman and Mailia

During our visit with Dr. Grekos and Howard, we also were visited by WINK CBS tv reporter Carlos Suarez who I had contacted to see if their station would be interested in doing a story on Mailia's Miracle and Regenocyte.  More on this...shortly.

Saturday, April 17, 2010

Tu Decides News and KNDU TV report on Mailia's Miracle - Night of Hope event


We were thrilled and blessed this week to have been given the opportunity to tell Mailia's story and ask the community for their support.

Correspondent Annagrisel Alvarez from the Tri-Cities Tu Decides bi-lingual newspaper did a wonderful article, both in English and in Spanish, about Mailia's Miracle and the upcoming Night of Hope event on Friday April 23rd at the Shilo Inn, as seen in the below post.  Annagrisel's story can be found by clicking on this LINK for the English version or by clicking this LINK for the Spanish version.

Also, Blanca Torres from Tu Decides reported on KNDU news at 6:00 p.m. about Mailia's Miracle, for which we are truly grateful to her and the KNDU staff of reporters, anchors, producers and technical staff at KNDU news station.  Thank you Chris for meeting with us and giving Mailia the "grand tour" which she so enjoyed and Scott, thank you for your awesome report at 11:00 p.m.!  Thank you too Blanca and Annagrisel!  We appreciate it so very much!

Friday, April 16, 2010

Mailia's Miracle - Night of Hope Benefit Fundraiser


























On Friday April 23rd, 2010 there will be a Benefit Dinner, Dance with the MissyG Band, Live and Silent Auction starting at 6: p.m. at the Shilo Inn located in Richland, Wa.  This event is being spearheaded by our dear friend Jesica Dawsey and her wonderful team of Angels/Volunteers who are planning a very festive and fun evening to be enjoyed by all who can attend the Mailia's Miracle - Night of Hope event.  Please contact Jesica (509)542-0791 for tickets and information on how you too, can help be a part of a great cause and miracle. 

We look forward to seeing everyone and thank you in advance, for your support and prayers in helping to be a part of Mailia's Miracle.

All our gratitude and blessings...

Max, Andrea and Mailia

Monday, March 29, 2010

Fox News in Portland Interviews Dr. Julia Robirds for Mailia's Miracle


On Saturday March 27, 2010, KPTV Fox News did a story about Dr. Julia Robirds from Portland, Oregon who we wrote about in our previous blog post.  Reporter Ronna Sweeney and her crew interviewed Dr. Robirds and quickly ran her story...one so compelling and from the heart.

It really shines a beacon of light on our experience and reminds me, one more time, how truly fortunate we are to have people like Dr. Robirds and her incredible staff giving of their tallent, time and resources to help Mailia.





Sunday, January 31, 2010

EXTRAORDINARY MEASURES - "Don't Hope For A Miracle...Make One"



This past week we went to see the new movie Extraordinary Measures and I sobbed and cried through the entire movie. We thought it was a very powerful story in how they captured the essence of living with a child with disabilities.

Don’t Hope For A Miracle…Make One, is the tagline of CBS films newly released movie Extraordinary Measures, starring Brendan Fraser and Harrison Ford. It is inspired by the story of John Crowley, a father who defied conventional wisdom and great odds and risked his family’s future to pursue a cure for his children’s life threatening disease.

To celebrate the Crowley family’s story, there is a wonderful opportunity to get the word out about a cause that is close to you, and also possibly win some money for them. All you have to do is upload an inspirational video by going to the Inspirational Quilt and click on Upload Your Story. Once the video is uploaded, you will be entered into the sweepstakes for a chance to designate the charity or cause of your choice to receive $10,000! Then share with your friends and contacts to vote to increase your chances of winning.

We hope to get a video compiled soon…on Mailia’s Miracle to add to the Inspirational Quilt.

Anyway...please try to see this...and tell others too as well. Scientists, medical practitioners, parents, students, families and the community must see this exciting movie, not only because the story has proved to save the lives of Pompe-stricken individuals, but the spirit and sunshine it brings to each viewer, because we, as advocates of Mailia's health and healing, and having moved almost heaven and earth to find the cure for Pulmonary Hypertension and congenital heart disease with other parents and adults, we believe this movie lifts viewers to a height that really transcends beyond cinematography and arts. It truly gave us the “Shot in the arm” we really needed now, more than ever!

In gratitude…

The Goforths

Wednesday, December 30, 2009

Recap of 2009 and What 2010 Shall Bring For Mailia's Ongoing Miracle

Greetings everyone…Our apologies for being out of touch relaying updates on Mailia’s blog. We hope that everyone had a wonderful holiday…as we did. We have so much to be grateful for. There have been so many inquiries as to how Mailia is doing. Mailia had been sick with a very strange and severe viral bug she came down with in Nov/Dec. that landed her in the hospital in need of some additional support due to her coughing up blood from the lung bleeds she would experience. Very scary stuff for us, but in light of this…she was able to get through this healing crisis and is now doing much better.

This past year, after starting this blog and Mailia’s Miracle…it was our intention and desire to maintain this web site not only as a means to help Mailia with our fundraising efforts but also for others who would follow, maybe baptized by fire as we were and looking for the means of creating a miracle to save their life or the life of a loved one. It was to be our way of giving back. Through this experience we think Mailia is a pioneer among many…and through her journey, she will be healed through a beautiful miracle and become a great inspiration to many through sharing her story to help champion financial support for others found in need of a life saving stem cell therapy possibly through a non profit designated primarily for adult stem cells.

When we get e-mails or are contacted by folks…even now, searching as we have and continue to do on the internet for anything new in the realms of technology or medical science to help themselves or their children or loved ones, it gives us so much joy and inspiration to know that we could help…that by you being here too…supporting Mailia, that you are also contributing to their miracle. It is huge blessing for all.

We still encourage and would like to remind folks to research adult stem cell therapy. A site we continue to espouse and follow for updates on a weekly basis is called www.donmargolis.com We hope Mailia’s success story will be featured and supported on his site as well this coming year.

So to sum up this past year we would like to say it was a time in which we were full of gratitude….grateful that Mailia has made it this far and continues to blossom into a beautiful young lady despite her challenges…she prefers to be seen as a normal happy child…still a kid at heart. Grateful for the windows of opportunity presented her from her doctors, surgeons and researchers on ground breaking therapies and treatment. Grateful for the opportunity to personally meet Dr. Zannos Grekos and the staff of Regenocyte and to also connect with heart surgeon Dr. Michael Black from San Francisco. Grateful to the news media for capturing and reporting Mailia’s story. Grateful for the outpouring of support from family, friends, folks behind the scenes who were generous with their time and financial resources in helping us raise funds to pay for her future stem cell transplant and therapies. But grateful also in advance…for all the incredible help and resources that are yet to come, in fulfilling Mailia’s desire to be well and live a happy life.

As we look to the new year and what the possibilities are for 2010, we can’t help but be optimistic and will gear back up to our getting Mailia’s Miracle shared with everyone in hopes that her message, story and need will be the catalyst for a beautiful miracle. We are not just praying and asking for this miracle to happen…we are all going to make it happen!

Please check back from time to time during the year, to check our updates to this blog and we humbly and graciously ask for your continued support and prayers for Mailia. There are plans for more fundraising events and requests for assistance in getting Mailias Miracle out to as many folks as possible. But most importantly we wish to share with you the heart warming events that we know and trust will come.

Thanks for being part of Mailia's Miracle! All our love, gratitude and blessings for a prosperous New Year!

The Goforths

Sunday, November 15, 2009

Radio Announcements and Interview with New Northwest Broadcasters for Mailia's Miracle

We would like to acknowledge the folks at New Northwest Broadcasters in Kennewick, WA. for affording us the opportunity to share Mailia's story and journey on several A.M. and F.M. radio stations throughout the Tri Cities. Our heartfelt thanks to Amy LeMasters, Public Service Director and On Air-Personality for her gracious help in putting together a special public service announcement we have included below and secondly, an interview we just did that will run on Sunday in the Tri Cities Forum with a link to the audio below.

AudioLink public service announcement


TriCitiesForumInterview with Amy LeMasters and Andrea Goforth for Mailia's Miracle

Friday, September 18, 2009

Tri City Herald News Story on Mailia's Miracle

Mailia's miracle: Family struggles to pay for teen's experimental surgery
By Michelle Dupler, Herald staff writer



Herald - Andrea Goforth ponders the future of her daughter Mailia, 15, left, who has pulmonary hypertension. Goforth and her husband Max are hoping to raise enough money to take Mailia to the Dominican Republic for an experimental stem cell procedure.

In a country house in Franklin County, surrounded by horse pastures, lives a sheltered young girl who talks to her parrot and animals and dreams of a normal life. But a cloud hangs over her, a curse cast at birth that could claim her life before her dreams are ever realized.


In a way, the story of 15-year-old Mailia Goforth is like a fairy tale — not the cheerful Disney versions full of song, but the darker ones told by the Brothers Grimm. Like Sleeping Beauty — who was sheltered by her parents from the danger of a simple prick from a spindle — Mailia has lived a secluded life, unable to attend school or even have many friends except those she’s found online. But for Mailia, the curse her parents are desperate to protect her from is a hole in the wall of her heart. And her parents have hope it can be lifted if they can find a way to pay the $75,000 fee.

Mailia Goforth suffers from Eisenmenger’s Syndrome, secondary pulmonary hypertension, or high blood pressure in her lungs. Her blood pressure is high because the hole in her heart allows too much blood to flow from her heart to her lungs, causing her blood vessels to constrict and stiffen and strain her heart. The high pressure also stops surgeons from closing the hole.
That in turn means not enough blood flows into her lungs and she becomes fatigued and short of breath.

She can’t walk more than a few steps without tiring. Her carriage is a motorized scooter with a basket on the front for her service dog and an oxygen tank on the back so she can breathe.
For seven months of the year, when temperatures are cool, she can’t venture outdoors because of the strain on her lungs and her susceptibility to viruses.

And time is running out for her. An examination by her cardiologist in Portland in May showed the left side of her heart is collapsing, while the right side is enlarging. A double-lung and heart transplant — the customary treatment for Mailia’s condition — is not an option, as doctors have told the family Mailia would not survive.

At this point in the tale, a wizard enters: Dr. Zannos Grekos, a Miami Cardiologist who has promised the hope of a cure derived from Mailia’s own blood.

Grekos has developed an experimental technique to repair pulmonary hypertension using adult stem cells. In fact, it’s so experimental it can’t legally be done in the United States because it isn’t approved by the Food and Drug Administration, so Grekos flies with patients to the Dominican Republic to perform the procedure. Because it is experimental, the cost of treatment is not covered by the family’s insurance.

Blood is drawn from the patient and flown to a lab in Israel where stem cells are extracted and activated with a protein known as a growth factor to cause them to multiply. Growth factors are produced normally in every person’s blood and tell other cells to become brain tissue, heart tissue or liver tissue, Grekos said. “We use ones that are specific in this instance for blood vessels,” he said.Every person also has stem cells running around in their body like miniature repairmen, and when they can be extracted, multiplied and told what to do, they can repair damaged blood vessels and even make new ones, he said.

The stem cells are flown and hand couriered from Israel to the Dominican Republic where Mailia would be waiting to have them inserted into her lungs through a small tube. The stem cells would attach to her pulmonary blood vessels and help them regenerate, Grekos said.
For Mailia, that would reduce her blood pressure, making it easier for her to breathe and allow surgeons to give her a pulmonary artery band, which would reduce the blood flow through the hole in her heart.

He said the idea came from research into using adult stem cells to build natural bypasses and improve circulation in patients with blocked arteries and poor leg circulation. “We took that information and applied it to patients that had poor circulation of the lungs,” he said. “We found we were able to reduce the pressures in patients after treatment.”

Grekos said he started using adult stem cells to treat heart patients in 2006, and began using the treatment for lung patients about 18 months ago. In that time, he’s successfully treated 20-30 patients with pulmonary hypertension. The procedure isn’t without controversy. Dr. Irving Weissman, a Stanford researcher and president of the International Society for Stem Cell Research, told CNN in July that Grekos’ work has no basis in medicine or science.

But Grekos countered that Weissman, as a researcher focused on use of embryonic stem cells, just doesn’t understand.

“He is not aware of all of the adult stem cell research,” Grekos said.

The Florida Department of Health shows Grekos has been licensed to practice medicine in the state since 1992 with no disciplinary actions on his record.

With no other realistic options for Mailia, Andrea and Max Goforth are putting their faith and trust in Grekos that he can give their daughter the normal life she craves.

“We have been told there is no hope, no cure, that her condition is very rare,” Andrea Goforth said. “I have faith and hope that technology has finally caught up.

Grekos said if the stem cell therapy is successful, Mailia’s pulmonary hypertension could be reduced enough that she could have a relatively normal life without requiring oxygen 24/7 and perhaps even be able to play sports.

Mailia(’s) has dreams both simple and lofty — she’d like to go to the mall like other teenagers and be able to swim like her idol, Michael Phelps. She also envisions one day running her own animal sanctuary in Costa Rica where she’d preserve endangered species.“I see myself without my oxygen just being free and happy,” Mailia said. “Being like a normal person, doing the sports I want to do especially baseball.”

But that will require her parents raising $75,000 for the treatment and the trek to the Dominican Republic. The Goforth’s are grateful and hoping to find the assistance to organize several events, such as a gala night at a local winery or a golf tournament, to raise the money.
The family also has set up a website called Mailia’s Miracle that tells Mailia’s story and gives information on how people can help and donate.

“It has been almost ingrained in us that this is what she needs,” she said. “We want her regenerated and healed. The reversal of this has the potential of her living to a ripe old age ... to actually really experience life physically with no holds barred. What we want is to see her happy, fulfilling her life’s purpose and to help other’s faced with similar circumstances.”

Donations can be made by going into any HAPO Community Credit Union and making a donation to Mailia’s Miracle fund. Information about other ways to donate is at http://www.mailiasmiracle.com/.