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Eye Catching Results in Thalassemia Major

Images of Silver jubilee Event of Seyal Medical Cdentre

History with Imagaes of Seyal Medical

 

OUR MEDICINE

CASEMIA

Herbal Product derived from the whole flowering plant of Fagonia Cretica
A thirty five years of Dr Seyal’s Research
An Alternate Treatment in
Thalassemia Major, Moderate and Minor
Hepatitis C and supportive therapy in different malignancies
As adjunct with Chemotherapy in different Malignant Diseases.

Caution: Thalassemia is a genetic disorder and the only treatment so far is the bone marrow transplant that’s not free of its own complications; whereas Casemia has shown fascinating results in a group of patients and in others there was lot of improvement in the quality of life in a couple of months with marked improvement in the blood transfusion requirements.  Genetic mutation might take quite a bit of time (even two years) but the compliance in the treatment is very essential to have the best outcome.

It takes care of the major side effects of the cytotoxic drugs, without compromising the cytotoxic efficacy of the chemotherapy.
In chemotherapy it reduces: Need of Blood transfusion after each cytotoxic dose, Falling of hair, Loss of appetite, Discoloration of skin, Stomatitis, Glositis etc,etc.
In connective tissue disorders when the dose of Methotrexate is used this herbal product has an adjuvant effect.
When the patient is immuno-compromised after transplant surgery this drug has shown excellent results with rapid recovery of the heamopoetic system.


Caution:

Keep in dry cool place


Side effects:

it is quite safe and can be given during pregnancy. The only side effect observed is mild gastrointestinal disturbance when the hemoglobin level is below 10Gm


Dosage:

Each tablet is 300 mg. 120 mg/Kg body weight
The dose above 30 Kg remains the same i.e. 3.600 Gm/per day in three divided doses after meals


Possible Mode of Action:

It possibly acts on the stem cells and also acts as an immuno- modulator and has immuno-supportive effect.

 

 

 

 

In 1977, 56 year old lady had stage IV intraductal fungating adenocarcinoma of Breast. She was on combination Chemotherapy along with crude Extract of Casemia

 

She died in 2004

More Eye Catching Results in Thalassemia Major

Case Report of A severe Homozygous or Compound Heterozygous β Thalassemia Patient

Thirteen years old boy was diagnosed Thalassemia major at the age of three months. Blood transfusions invariable caused severe blood reactions. His clinical condition gradually deteriorated. On the first visit his spleen was more than seven cm palpable the costal margin and liver around five Cm. He had lot of ascietis. The bony deformities are evident from the Fig: ‘1’. His blood picture on the first and subsequent visits is given in Table 1V His clinical improvement is quite evident from the photographic Fig: ‘2’ and ‘3’.
He is still using Fagonia Cretica in tablet form without any chelating agents or supportive medicines like folic acid or calcium supplements over and above he has not had any blood transfusion ever since he started this treatment.

1st October 2012
Before Treatment Fig 1
Hb 3.8 Gm:     Hb F 98.6

21st January2013
After 3 ½ months Fig 2
 Hb 7.1 Gm

15th April 2013
After 6 ½ months Fig 3
Hb 8.7 Gm:     Hb F 81.7

Progress report of a 13 years old boy:

Suffering from BETA THALLASEMIA MAJOR

Parameter

1st diagnosed
at the age of 3 months

1st Oct 2012

21st January 2013

15th April 2013

Normal Value

Hb

           4.9

        3.8

        7.1

         8.7

13.00     18.00

Total RBC

           2.1

        1.7

        3.8

         3.1

4.50       6.50

Hct

         16.0

        1.5

      24.0

       29.0

38.00     52.00

MCV

         74.0

       76

      52.0

       92.0

75.00     95.00

MCH

         22.0

       20

      22.0

       28.0

26.00     32.00

MCHC

        30.0

       22

      28.0

       30.0

30.00     35.00

Platelet Count

      199.0

     160

   174.0

     216.0

150.00   400.00

Nucleated RBCs

        10.0

-

-

-

 

RBC MORPHOLOGY

Hypochromia

       ++

       +++

           +++

        ++

 

Microcytosis

       ++

       +++

           +++

        ++

 

Macrocytosis

       ++

      +++

           +++

        ++

 

Anisocytosis

     +++

      +++

           +++

        +++

 

Poikilocytosis

       ++

      +++

           +++

        ++

 

Schistocytes

         +

        ++

             ++

        +

 

HEMOGLOBIN ELECTROPHORESIS:

HBF:

98.6 %

 

 

 

81.7%

HB A2:
HBA:   

1.4 %
----

 

 

 

HB A2 0.7
HBA 17.6

 Liver and Spleen:

 

Spleen was 7 cm below costal margin; liver was 5 Cm below costal margin with lot of ascietis

His liver and spleen were hardly palpable after three months and there was no ascietis

.

 

Casemia is the first medicine discovered that reduces the level of HB F a cause of THALSSEMIA. It initiates and then improves the level of HB A, the normal hemoglobin in the body, to normal level

 

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