Archive for December, 2010

Stem Cell Success for Parkinson’s Patient

Tuesday, December 28th, 2010

Monday, December 27, 2010 

Stem Cell Parkinson’s Patient, Stan Lahovec advises Doctors in Germany where he received his stem cell treatment that “You gave me back my life.”
[Watch Stan’s Video Below]
My name is Stan Lahovec, I live on the Gold Coast, Queensland Australia.  Originally I come from Slovenia but I’ve been Australian citizen for more than 30 years.

By trade, I am an optical technician and have been working in the industry since March, 1984.  My passion is oil painting, which I had to put on hold because of my disease.

About three years ago, I was diagnosed with Parkinson’s disease.  Nobody in my family has the disease, so it was a complete surprise when the doctor told me the news.

Most disturbing was the knowledge that there is no cure for this debilitating disease as I was told by the doctors.

In April this year, my step daughter Marina told me that Helensvale was hosting an informational evening about Parkinson’s disease.   My wife and I attended the presentation where we learned about adult stem cells and got the information about a clinic in Germany.

Soon thereafter, I contacted Mr. Issam Errahmaoui, the Area Manager at the Center and the “ball started rolling”.

On October 15th, I arrived in Frankfurt where nurse Stefanie from the Centre collected me at the airport and drove me to Cologne, where I met other friendly staff, as well as Mr. Issam.

On Monday October 18th, the bone marrow collection was performed.

Two days later, the transplantation of stem cells was done very professionally.  I hardly felt anything. There was no pain and no bruises.  Doctor gave me some pain killers, but I never needed any.

On Saturday, October 23rd, I boarded the plane on my way to see friends and family in Slovenia, where I spent two wonderful weeks on holidays recovering and where the healing process began.

November the 4th was the day to say goodbye to all my friends and family.  I boarded the plane in Graz to Frankfurt and Marina, my stepdaughter, joined me in Frankfurt for the flight to Singapore.  The journey was smooth and a little boring.

Finally, we arrived in Singapore where we had to disembark.  We waited few hours to board the Sydney-bound plane (Qantas A380).   All went ok.  Marina and I were seated next to the window. At takeoff, the whole plane started to shake like an earthquake.  I thought we`re going to crash but after few long seconds, which seemed like eternity, the plane stabilised and we started to ascend.  Everybody was relieved of the sudden fear.

Marina and I were talking, hoping the journey home will be fine and smooth when suddenly, just after 20 minutes of flying, there was a loud bang and huge flame shot out of the engine number one.  At first I didn`t know what to make of it, then I froze and couldn`t move.  My mind went into high gear. I saw pictures of my life flashing in front of me, then everything went blank. In the distance, I heard screaming and shouting and didn’t understand what it was all about.  Then I turned around and saw panic on other passengers faces around me. I sat still; frozen in my seat.  I wasn’t aware of how long that lasted, when suddenly, I heard loud clapping and cheering.  Then I realized that we had landed safely back in Singapore.

To me the whole thing froze in time. I only snapped back to reality when I felt the wheels touch the ground.  We were safely back from the brink.  Next we got off the plane.  After the fire brigade inspected the damage, we were sent to the hotel overnight, totally exhausted.

The next day, we boarded another plane and safely arrived in Sydney.  We took another plane to Brisbane without much drama.  We got home and two days later I couldn’t move.  It was like I was paralysed and all good work that was done by my stem cells and dedicated doctors in Germany was for nothing.

Only after a couple of weeks passed by, I started to get better and am still getting better by the day.  At first, I was able to shave by myself.  Next, I could eat without help.  Now, I can drive my car and walk straight upright.  I feel like a new man.

Today, I went to see my GP and he was speechless; seeing my transformation.  He thinks I have improved about 80%.  I even took my paintbrush and unfinished pictures and started to paint again; which is making me very happy.

I thank you Mr. Errahmaoui.  Your team of doctors and staff deserve all the gratitude and praise in this world.

You gave me back my life. Forever in your debt.

Stan Lahovec

Watch Stan’s video below: 

Boy Makes Full Recovery From Rare Blood Disorder

Monday, December 27th, 2010

26 December 2010 – As reported in BBC News, UK

Jack Hayhoe    Jack Hayhoe

This article highlights the importance of the Bone Marrow

Wirral mother wants to thank the donor of the bone marrow that she said “saved her son’s life”.

Two years ago, Mandy Hayhoe, 34, did not think she would see her son playing with his Christmas presents like any other happy child.

Her son Jack has Wiskott-Aldrich syndrome, a condition in which he does not produce enough blood platelets.

Now, after a bone marrow transplant and months of specialised after care, Jack is like any other two-year-old.

“I can’t thank the person who donated their bone marrow enough for the new life it has given Jack.

“He has spent much of his life in and out of hospital having blood transfusions and operations, but now he is doing really, really well,” Mrs Hayhoe said.

Before the operation the toddler had just three blood platelets – when he needed between 150 and 450. Without the transplant he may not have lived beyond the age of 10.

Blood platelet shortageWiskott-Aldrich syndrome affects only one in four million people. Their blood may not clot easily, they will be prone to catching severe infections, and will need frequent blood transfusions.

The only hope of a cure is through a bone marrow transplant or by stem cell transplantation from umbilical cord blood that has been banked from baby donors.

Fortunately for the Hayhoe family, who are from Hoylake, within seven months of being on the donor list matching bone marrow was found.

“We couldn’t believe it,” Mrs Hayhoe said, “Some people are on the waiting list for years and some don’t even find a match.

Jack Hayhoe When little Jack was in and out of hospital having transfusions

“We were lucky enough to be offered two. He had the operation back in July last year and it was a success.”

Now Jack is producing 100% donor cells – which means his body is working normally.

Before he had the operation, he had to rely on others donating blood platelets – at a time when there was a shortage.

Back in early 2009, the Hayhoes campaigned to highlight the need for blood platelets. Donors can give their blood platelets as easily as giving blood.

Now they do not have to worry.

“He has been so excited for Christmas Day,” his mother said, “He has spent the past couple of weeks looking out of the window waiting for Father Christmas.”

In January he will be back in hospital, and hopefully, she said, they will be told to come back for an appointment only once a year instead of the routine check-ups.