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Medical Cases

Anca & Octavian Popescu


10.07.2009

We, the parents of the young girl Popescu Maria-Laura, diagnosed with VSD (Perimembranous ventricular septal defect), have kept the record of the investigations made, have continued the treatments with you, but we have not let you know the results. This was because for a longer period of time, the evolution of the growth of the membrane (the tricuspid valve) in Maria’s heart was quite slow, as you have told us and as the doctor who was in charge of performing the echocardiographic investigations every 6-12 months also remarked.

He mentioned that, as it is growing, the membrane is subject to the pressure of blood flow and in the final stages of growth, the process is different.
You have told us that in various stages of the evolution of the membrane, the growth will stop, but you will continue to consolidate its wall, through specialized therapies so that the valve (the membrane) could resist the pressure from blood flow, in the conditions in which the construction began between the auricle and left ventricle of the heart, from one side, making rapid progress in 13 months, up until the half of the opening diameter (3.3 mm) which initially was 8 mm.

Thus, during October 8, 2004 – July 9, 2009, the situation evolved as follows:
In July 23, 2004 – November 22, 2005 (16 months) the membrane diameter grew to 4.2 mm – i.e. only 0.9 mm.
In the following 6 months there was another 1 mm growth, as the membrane reached 5.2 mm (May 30, 2006) – the medical analysis bulletin indicated a diameter of the blood flow of around 2.8 mm (that is what was left to grow out of the 8 mm of the opening).

During the following 5 investigations between May 30 2006 and July 21 2008 (26 months) – the membrane diameter grew by only 0.8 mm – still reaching a total diameter of 6 mm (the diameter of residual blood flow was of about 2 mm).

In the meantime, during this 4 year period, you changed the treatment twice, so as to consolidate the membrane walls and to overall strengthen our girl’s organism.

Once again, we were able to confirm your recommendation that, in the case of complicated and serious afflictions it takes a lot of patience, perseverance and trust in God.

During the last year, as Maria began first grade, we continued a relaxing therapy mostly at home, but with products recommended by you and on July 9, 2009 (almost a year after the last investigation, as indicated by the specialized doctor) the pediatric cardiologist told us that the evolution is quite good, the membrane as measured electronically is practically closed (the opening is now the size of a pore) which is an exceptional fact. The child is practically cured.

Maria will be able to take part in the Physical Training classes, as all other pupils without any restrictions.
I know that thousands of people have come to you with the most various and serious diseases (afflictions of the thyroid gland, ulcer, afflictions of the nervous system, liver, leukemia, afflictions of the prostate and the spine etc.)

The treatments you applied – including in the case of our child – with energetic paces, herbal tea combinations, compresses and herbal salves prepared following arcane recipes, sometimes requiring even longer periods of time, have proven their efficiency and more. We will recommend you and your therapies to those who are suffering, every time we get the chance to do so.

Thank you

26.07.2004

Dear Mrs Zenaida,
We, the parents of Maria-Laura, the girl diagnosed with VSD (ventricular septal defect) planned to keep a diary about the evolution of the disease and it seems natural to me that every time something significant occurs regarding the outcomes, we should inform you immediately to have yourself a written evidence of what you have done for us.

Specifically, you have scheduled us to continue therapy in 17-05-2004 and on that date, after you welcomed us with concern and love for out child (the closeness between you and Maria-Laura becoming more and more accentuated in these months of treatment), you said that reducing the gap between auricle and ventricle of the heart of our daughter up to 2 mm, for us not having to undergo surgery, is possible through long therapy we must seriously follow.

You also said to us that the gap might even close totally, but then again you advise we had patience, saying you would relax the treatment in the next period, considering that our child is little.

However, even with this slightly lighter treatment, you still sent us, after 2 and a half months or so, to make a echocardiography – performed to our daughter on 23-07-2004 and, as there was a significant outcome, we send it to you. The gap was reduced to a diameter of 4.7 mm compared to 8 mm it had at the beginning of the treatment period – i.e. February 2004.

In this respect we enclose the medical certificate dated 23-07-2004.
We thank you once again and we apply for a new appointment to continue therapy.

At the same time we think that, if at the end of December 2003 we would have not bought a supplement of “Libertatea” newspaper where an article about you was inserted, maybe we wouldn’t have learned now about your amazing therapies.

It would be desirable that more people of all ages, with various ailments, often serious and very serious, find out what you managed to accomplish.

Sincerely Yours,
Anca and Octavian Popescu

12.05.2004

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

10.07.2009

Biz, Popescu Maria-Laura kizi ebeveyler, sistolik ufurum yerinde kalbin agir bir hastaligi olan DVS (ventrikuler septal defekt perimembranos), yapilan muayenelerin sayisi tutuk , sizin kabinede tedavileri devam ettik ama sonuclari size iletilmedik, cunku uzun bir zamanda Marianin kalbineki membran buyume hatti evrimi(tricuspid valv) siz soylediginize gore cok yavas devam etti ve control yapan hakim de bunu gormus, 6-12 ayda yapilan ekokardiyolijide.
Bu, membrane buyudu zmaaninda, kan jetin basincina dayaniyor e son buyutme etaplarda surec zor oluyor.
Siz, membrane buyume etaplarda bazen durdurulacak ama bunun duvar konsolide icin ellinde gelenler yapacaksiniz , ozel tedavilerde valf( mambran) kan jetinde dayanamak icin , yapi sol aurikul ve ventrikul arasi baslayan sartlarda, bir tarafta ve son 13 ayda cok hizli genislenmis, yani delik cai 3.3 mm a kadar oldu , ve baslangictan 8 mm olduguna.

Boylece, 8 ekim 2004 -9 temuz 2009 tarihler arasi, saglik durumu soyledir;
23 temus 2004- 22 kasim 2005 tarihler arasi ( 16 ay), membrane tedavisi 4,2 ,, a kadar buyudu – yani sagdece 0,9 mm
Gelecek 6 ay 1 mm daha fazla buyutu, membrane 5,2 mm ( 30 mayis 2006)- tahlil bulteni kan jeti capi ≈2,8 mm( yani deligi o 8 mm den bu kadar buyurmesi gerekiyor).
Geldigin son 5 kontrollerde, 30 mayis 2006 ve 21 vtemuz 2008 ( 26 ay) arasi- o delik capi 0,8 mm buyutu, toplam 6 mm apida oldu( kalan kan jeti capi ≈ 2mm)
Zamanda, 4 yil donemin icinde, membrak duvari konsolide icin ve kizin vucutun genel guclendirmek icin tedavi iki deva degistirdiniz.

Sizing oneriler yeniden konfirme edilmis, ve ciddi ve karmasik hastalari durumundan cok sabir, azim ve Allhtan inanmak gerekiyor.
Son yildan, Maria okul I.nci siniftan basladi icin evde bir rahatlatici tedavi basladi, ama sizing taafindan onerilen urunleri ile ve 9 temuz 2009 ( sonkontrol de yaklasin bir yil sonra, uzman doktorun onerilen gibi) , cocuk kardiyolojik doktoru genislenme cok iyi olduguna oyledi v eve o membrane, elektonk olculen kapatilmis( delik bir gozenek boyutu kadar oldu) ve bu mukemmelbir haberi oldu. Cocuk iyilesi demektir.

Maria, her hani bir engel olmadan, okul arkadaslri ile beraber bedel egitimi saatleri katilabilir.
Yuzlerce ve binlerce insan, degisik hastaliklari ile sizin kabine kapini gectigine biliyorum ( tiroid bezi hastaliklariile, ulser, sinir sistemin hastaliklari, karaciger, losemi, prostat ve omurga s.a.).

Sizin uygulanan tedavileri, bizim cocugu tedavisi dahil, enerji gecerler ile, bitkili caylari kombinasyonlari, bitkili sikistirir ve badijonarileri, gizli recetelerine gore, bazen uzun zaman alir, cok yetenikli olduguna ve biz her zaman hekeze size tavsi ediyoruz.

Tesekur ediyoruz,
ANCA VE OCTAVIAN POPESCU

26.07.2004

Sayin Zenaida Stoenescu,
Biz, Popescu Maria-Laura kizi ebeveyler, sistolik ufurum yerinde kalbin agir bir hastaligi olan DVS (ventrikuler septal defekt perimembranos), biz hasta ile ilgili bir gunluk defteri turmaya dusunduk ve bana tutmaya normal geliyor ve sonuclar ilgili bir sey oldugun zaman hemen size iletilmek icin cok iyi olacaktir. Ve siz, yazili olarak bir ifadenizi olacak.

Duzgun bir sekilde, tedavi devam etmek icin 17.05.2004 tarihinden randevu aldik ve o tarihte seve seve bizi muayene aldiginiz ( son aylar sizin ve Maria-Laura araniza yaklasik daha belirli oldugu)ve kizin kalbinde aurikul ve vetrikul arasi olan bosluk 2mm olacak, ve ameliyat gerekmeden olacak, ve bu durum, uzun bir zaman icinde olacak ve cok citti alinacak.

Ayrica, bosluk, belki tam olarak kapanabilir, ama yeniden sabirli olmak bize onerdiniz ve gelecek zamani rahatlanici bir tedavi olacagina soylediniz bize, cunku cocuk cok kucuk olduguna.

Ama bu tedavi ile en dogrusu daha rahat, yaklasik 2 ½ ay bizi bir ekokardiyogram yapmaya gonderdiniz , ve kiz 23.07.2004 tarihinde bunu yapmis ve sonuclar anlamli olduguna ve sizede gonderiyoruz. Bosluk capi 2004 subat tedavi baslangicindan 8 mm iken 4,7mm a kadar azalti.

Bunu ile ilgili 23.07.2004 tarihinden tibbi sertifikasi ekliyoruz.
Yeniden sie tesekur ediyorum, ve tedavi devam etmek icin yeni bir randevu istiyoruz.

Ayrica, 2003 araliktan sizing ile ilgili yazilan bir kose yazi oldugunuza Libertatea gazetesine almiyorsa, belki sizin mucize tedavilerin faydalanmicaktik.

Keske daha fazla insane, her yaslarda cesitli hastaliklard size duymak isterdim . Saygilariyla.
ANCA VE OCTAVIAN POPESCU

12.05.2004

Sayin Zenaida Stoenescu,
1 yil ve 8 ay – Maria Laura- bi kizi ebeveyleriz oluyoruz, hala yaptiginiz mucize etkisi altindaiz.

Ama olaylari size anlatalim:
Kizi dogumundan, cocuk hakimi , stetoskop yardimi ile vurgulayan sistolik ufurum saptandi ve bu durum hastaneden cikistan kac gun sonra aile doktoru tarafindan konfirme edildi.

Bize Bukresten “M.S.Curie” hastanede bir ekokardiyografi yapmasina onerildi, ama hemen degil, dogumdan kac ay sonra demisler, cunku zaten simdilik hic bir seye yaramicak, yani durumu duzeltmeyecek( yani sistolik ufurum eliminasyonu).

Maria’nin , 9 ay doldurduktan sonra, bu ekokardiyografi , onemli bir cocuk kalp doktorun tarfindan yapildi ve basit sistolik ufurum yerinde kalbin agir bir hastaligi olduguna yani DVS olduguna saptandi(ventrikuler septal defekt perimembranos)- yani kalbin sol atrium ve ventrikul arasi 8 mm capidan bir delik oluyor.

Bu saptanmakatn sonra, doktor, normal bir basit sistolik ufurum drumundan, olan delik buyuklugu 1-2 mm arasinda olmalidir ve 1 yil a kadar kapaniyor ve eger kapanmiyorsa, 1 mm kaldigin zaman olan cocuk veya insane tum hayat boyu buyuk problemler yasamadan devam edebilir ve bizim durumda, kizin deligi cok buyuk oldugun icin kapatilmaz.

Boylece, 4 yasi a kadar, eger buyuk komplikasyonlar cikmiyorsa, ve onun hizlendirmasi olmuyorsa, bir ameliyat yapilacak, ve bu ameliyat anlatmasini; 8 mm bir duar yapilacak, cigerlerine asagi nufuz kan akisini engellemek icin , ve 4 yasi olduktan sonra, cocuk buyutugunzaman ve kalp gucu artildigin zaman bu ameliyat yapilmadigin zaman olum tehlikesi olur.

Bu yasi a kadar, 6 aydi biri kontrole gelmemis bize onerildi ve kan incelemesi icin ekokardiyografi sonuclarina gore ilac tedavizi onerildi.
Cagresiz durum olduguna icin, cunku tanilri ogrenmesi bize yildirim gibi carpti, o doktoru iyi bir uzman olduguna ragmen, bska bir doctor ve baska bir hastane danismaya krar verdik.

Yapilmis muayenesinde, yeni doctor, ilk tani konfirme edilmis ve basla bir yolu olmadigina bize soyledi, ve kucuk olduguna ragmen riskileri var ve vucut ustunden bir kesim lacak ve goguzu kesileck bize anlatmis.

Onerilen ilaclari ile tedavi basladik, ama bir ameliyat duncesi kabul etmedik- bizim bebegimiz kalbin uzerinde ameliyat.
6 ay sonra kontrole gittik( yani 31.10.2003 tarihinden) ilk doktore, ve durum ayne parametrede oluyor ve 6 ay sonra bizi tekrar cagirmis.
Ayne zamanda, tesadufen, aralik 2003 te sin biotherapit oldugunuza ve olumlusonuclari oldugunuza ogrendik.
Sizin kabinede irtibata gectik ve 16 subat 2004 randevu aldik.

Ilk basinda, sicaklik ile bizi kabul edildiginiz, ve bizin sasirmaniza Maria nin hastaligi ameliyat olmadan iyilestirebilir, zun br zaman bir tedavi il, yaklasin 2 ½ ay boyunca( 2004 nisan ayin sonun a kadar) ve bariz bir iyilesme hissediyorsunuz soylediniz ve bir ekokardiyografi yeniden yapilmasi istedi ve biz gelinen asamada ventrikuler septal gormek icin.

11 mayis 2004 Maia-Laura yeni bir muayene oldu ( bu tarih 6 ay bir donemde aine olduguna)ve yeniden sasirdik cunku kardiolojik hakim bakan kiza nadir bir sey olduguna soylemis yani o bolgeden olan dokulari calismaya basladi yani bozuk olan valve ypistirmasi olabilir , yanisol atrium ve ventrikul arasi olan yer yapistirabilir, v bu durumda yeni bir tani koymus: Dikis anevrizma olusumu ile tricuspicle septal defekt vanasini egilimi SIV.

Bize bu durum cok azolduguna anlatiyor ve boyle oldugun zaman 8-12 ay arasinda oluyor bize anlatmis. Yani 11/2 ayda degil, ozelikle 8 mm olan capi ile.
Ayrica, delik capi 6mm olduguna anlatmis ve gelecek zamaninda eger 2 mm a kadar kucukliyorsa , o zaman ameliyat gerekmez.

Bizim kizimiz gecmisine gore, hastaligin muhtesem evrimine gore , biz size cok tesekurediyoruz ve tedavi devam etmek icin sizden en yakin, aci ile zamanda bize yeniden randevu ermekte sizde rica ediyoruz
.
Buna gore, yukardaki yazilan tibbi evraklari size gonderiyoruz.
Allh size cok saglik ve enerji versin cok ailede mutluluk getirmek icin.
ANCA VE OCTAVIAN POPESCU