Biliary Tract Health Feed

Dear it is genetic disorder
we have to adjust in life.
Learn how to live happily.
We have two such friends living near my residence doing well. Contact genetic counceller.

AS YOU KNOW IT IS GENETIC DISORDER.
THERE IS NO TREATMENT.
WE HAVE TO ADJUST LIFE STYLE.
COUNCELLING IS REQUIRED

It is a cancer of vocal cord.
But still in initial phase and outcome of the treatment can be favourable.

Yes vitamin a is very essential for vision but in normal condon.
In case if a disease proper treatment is required with that.

Hi, Lybrate user, exact valve affected be pointed out inorder to begine homoeo medication, properly.
Related report be needed, privetly in this regard, please, till then, tk, homoeopathic medicine, underlying:
@ crategus oxq -10 drops with little water ,thrice.
Tk, care.

Retinitis pigmentosa is a rare, inherited degenerative eye disease that causes severe vision impairment.
Symptoms often begin in childhood. They include decreased vision at night or in low light and loss of side vision (tunnel vision).
There's no effective treatment for this condition. Wearing sunglasses may help protect the remaining vision.

It could be either atypical facial pain or trigeminal neuralgia. Consult neurologist for clinical diagnosis and further treatment.

Hello lybrate-user.
It can be trigeminal neuralgia.
And it will not go by allopathic treatment. The pain killers will give effects for few hours only.
You can consult me at Lybrate for homoeopathic treatment.
Till then take spigelia 30.

Are you losing your sight day by day? Does it make difficult to see you at night? Is this the onset of Blindness? Get to know about Retinitis Pigmentosa with these tips.

What actually is Retinitis Pigmentosa?

Retinitis Pigmentosa (RP) refers to a group of diseases, which causes a slow, but progressive vision loss. It is a genetic disorder that affects the ability to respond to light.This inherited disease causes a slow loss of vision, beginning with decreased night vision and l...more

Tetralogy of Fallot (TOF) is a commonest congenital cyanotic heart disease.
TOF is having a combination of large VSD with severe obstruction of blood flow to the lungs that result in bluish-black discoloration of lips and fingers due to flow of oxygen-deficit blood to the body parts.
The four defects that commonly associated with Tetralogy of Fallot (TOF) are

Ventricular Septal Defect (VSD) a hole formed in ventricular septum that is situated between two lower chambers of hea...more