Dear Mrs Zenaida Stoenescu,
We are the parents of the little girl Maria-Laura, aged 1 year and 8 months, still under the strong impression of the miracle you brought for us.
Let us present the facts though:
When out daughter was born, maternity paediatrician found with the stethoscope the presence of a accentuated systolic murmur, a situation confirmed by the family doctor few days after discharge.
We were recommended to perform an echocardiography at the Paediatric Clinic of “M.S. Curie” Hospital in Bucharest, but not immediately, but few months from birth, because nothing could be done anyway to alleviate the situation (i.e. removal of systolic murmur).
When Maria has reached the age of 9 months, this echocardiography was performed by a reputed cardiologist MD who found that there wasn’t a simple systolic murmur, but a very serious heart condition, i.e. perimembranous VSD (ventricular septal defect) – i.e. the existence of a gap between atrium and left ventricle of the heart with a diameter of 8 mm.
After this finding, the physician explained to us that, usually, in case there is a common systolic murmur, that gap is 1-2 mm and is closed by the time a child turns 1, and even it is not closed, keeping 1 mm in diameter – the child and future adult may live all his/her life without particular problems and, in the case of our daughter, the gap is very large and will not be closed.
Therefore, by the age of 4, unless other complications occur meanwhile requiring emergency surgery, surgery is required consisting in performing a 8 mm diameter wall, to impede blood flow be strongly pumped into the lungs, and after age 4 – as the child develops and heart force increases – failure to perform operation causes death in a predictable time period.
We were advised to go, by that age, to medical control every 6 months and take blood fluidization medicines, prescribed in accordance with the echocardiography examination bulletin attached to this letter.
Being so desperate, as finding this diagnosis struck us like a lightning, although we knew that said doctor is an excellent specialist, we looked for another examination in another hospital, through a paediatrician, who was also a specialist in this medical area.
When performing the check, that doctor confirmed the first diagnosis, saying to us that there was no other way than surgery, highlighting that there are risks in such interventions, and also the discomfort for the child as an incision is performed on a long stretch of the body which involves cutting the sternum.
We started treatment with medicines prescribed, but, obviously we did not reconcile with the thought of such complicated surgery of the heart of our only child.
We went for medical check after 6 months (i.e. on 31-10-2003) to the same doctor who initially examined our daughter and who told us that the situation evolves within same parameters and we should return after other 6 months or so.
Meanwhile, haphazardly, in December 2003, we found out that you were a bioenergotherapist with remarkable results.
We contacted your office and we were appointed on February 16, 2004.
From the beginning you welcomed us with warmth and attention and to our amazement you said that Maria’s condition could be cured without surgery, however through a long therapy and that the gap inside the heart would be closed by body’s regenerative system.
After sessions with specific therapies performed by you during 2 and a half months (by the end of April 2004), you told us that you felt an obvious improvement and it was required to performed a echocardiography to see the current status of the ventricular septal defect.
On May 11, 2004, Maria-Laura was subjected to new examination (date corresponding to the 6 months period from the last medical check), and we had once again the occasion to be amazed, as the cardiologist MD told us that a very rare thing happened, i.e. the tissue in that heart area started working, there being an agglutination tendency of the defective valve between the two cavities of the heart which closes the opening between the atrium and left ventricle, giving the diagnosis: “Agglutination tendency of the defective tricuspid septal valve with SIV aneurysm formation “
He told us that the situation is even rarer, as such closings, if happened, take place at ages between 8 and 12 months not after 11/2 years and especially at diameters of 8 mm.
He also told us that the gap diameter was reduced to 6 mm and if it was reduced in the next period up to 2 mm, surgery was no longer required.
Considering that the whole history of the affection of our daughter, the spectacular evolution of the disease, we thank you from the bottom of our hearts for the invaluable help you gave us until now and kindly please make us an emergency appointment, to the extent possible, to continue our therapy.
In this regard we send you the medical certificates set we mentioned above.
May God give you good health and energy and help you bring joy to lots of families.
Anca and Octavian Popescu