regeneration of eye sight, retinal deattachment(ROP)-6 years old

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Dear Marileete,

Aditi,Is a premature baby born at 26 wk gestation

period her birth weight was only 640gms.Immediately

after her birth in a month or so she had retinal

deattachment(ROP).She was operated for retinal

deattachment,but unfortunately no sucess so,she has no

vision in her lt eye.since her birth now she is 6yrs &

4 month.This was a cosmetic surgery only to bring her

eye in the centre so that her eyelooks in the centre.

At this moment since the surgery is done her eye is

red.If i can heal her so that she is ok with that eye.

 

Also if i can do the renegeration of her retina which

is possible to do.Pls guide me with the protocol for

renegration of her retina.

 

Thanks

 

==============================================================

 

 

Dear Prakash,

 

Namaste.

 

Thank you for the additional information.

 

 

Medical Background:

 

alternative name: retrolental fibroplasia

 

Retinopathy of prematurity (ROP) is a potentially

blinding eye disorder that primarily affects premature

infants weighing about 2¾ pounds (1250 grams) or less

that are born before 31 weeks of gestation (A

full-term pregnancy has a gestation of 38–42 weeks).

The smaller a baby is at birth, the more likely that

baby is to develop ROP. This disorder—which usually

develops in both eyes—is one of the most common causes

of visual loss in childhood and can lead to lifelong

vision impairment and blindness. ROP was first

diagnosed in 1942.

 

Today, with advances in neonatal care, smaller and

more premature infants are being saved. These infants

are at a much higher risk for ROP. Not all babies who

are premature develop ROP. There are approximately 3.9

million infants born in the U.S. each year; of those,

about 28,000 weigh 2¾ pounds or less. About

14,000–16,000 of these infants are affected by some

degree of ROP. The disease improves and leaves no

permanent damage in milder cases of ROP. About 90

percent of all infants with ROP are in the milder

category and do not need treatment. However, infants

with more severe disease can develop impaired vision

or even blindness. About 1,100–1,500 infants annually

develop ROP that is severe enough to require medical

treatment. About 400–600 infants each year in the US

become legally blind from ROP.

 

In addition to birth weight and how early a baby is

born, other factors contributing to the risk of ROP

include anemia, blood transfusions, respiratory

distress, breathing difficulties, and the overall

health of the infant.

 

An ROP epidemic occurred in the 1940s and early 1950s

when hospital nurseries began using excessively high

levels of oxygen in incubators to save the lives of

premature infants. During this time, ROP was the

leading cause of blindness in children in the US. In

1954, scientists funded by the National Institutes of

Health determined that the relatively high levels of

oxygen routinely given to premature infants at that

time were an important risk factor, and that reducing

the level of oxygen given to premature babies reduced

the incidence of ROP. With newer technology and

methods to monitor the oxygen levels of infants,

oxygen use as a risk factor has diminished in

importance.

 

Although it had been suggested as a factor in the

development of ROP, researchers supported by the

National Eye Institute determined that lighting levels

in hospital nurseries has no effect on the development

of ROP.

 

ROP occurs when abnormal blood vessels grow and spread

throughout the retina, the tissue that lines the back

of the eye. These abnormal blood vessels are fragile

and can leak, scarring the retina and pulling it out

of position. This causes a retinal detachment. Retinal

detachment is the main cause of visual impairment and

blindness in ROP.

 

Several complex factors may be responsible for the

development of ROP. The eye starts to develop at about

16 weeks of pregnancy, when the blood vessels of the

retina begin to form at the optic nerve in the back of

the eye. The blood vessels grow gradually toward the

edges of the developing retina, supplying oxygen and

nutrients. During the last 12 weeks of a pregnancy,

the eye develops rapidly. When a baby is born

full-term, the retinal blood vessel growth is mostly

complete (The retina usually finishes growing a few

weeks to a month after birth). But if a baby is born

prematurely, before these blood vessels have reached

the edges of the retina, normal vessel growth may

stop. The edges of the retina—the periphery—may not

get enough oxygen and nutrients.

 

Scientists believe that the periphery of the retina

then sends out signals to other areas of the retina

for nourishment. As a result, new abnormal vessels

begin to grow. These new blood vessels are fragile and

weak and can bleed, leading to retinal scarring. When

these scars shrink, they pull on the retina, causing

it to detach from the back of the eye.

 

ROP is classified in five stages, ranging from mild

(stage I) to severe (stage V):

 

Stage I — Mildly abnormal blood vessel growth. Many

children who develop stage I improve with no treatment

and eventually develop normal vision. The disease

resolves on its own without further progression.

 

Stage II — Moderately abnormal blood vessel growth.

Many children who develop stage II improve with no

treatment and eventually develop normal vision. The

disease resolves on its own without further

progression.

 

Stage III — Severely abnormal blood vessel growth. The

abnormal blood vessels grow toward the center of the

eye instead of following their normal growth pattern

along the surface of the retina. Some infants who

develop stage III improve with no treatment and

eventually develop normal vision. However, when

infants have a certain degree of Stage III and " plus

disease " develops, treatment is considered. " Plus

disease " means that the blood vessels of the retina

have become enlarged and twisted, indicating a

worsening of the disease. Treatment at this point has

a good chance of preventing retinal detachment.

 

Stage IV — Partially detached retina. Traction from

the scar produced by bleeding, abnormal vessels pulls

the retina away from the wall of the eye.

 

Stage V — Completely detached retina and the end stage

of the disease. If the eye is left alone at this

stage, the baby can have severe visual impairment and

even blindness.

 

Most babies who develop ROP have stages I or II.

However, in a small number of babies, ROP worsens,

sometimes very rapidly. Untreated ROP threatens to

destroy vision.

 

Medically, the most effective proven treatments for

ROP are laser therapy or cryotherapy. Laser therapy

" burns away " the periphery of the retina, which has no

normal blood vessels. With cryotherapy, physicians use

an instrument that generates freezing temperatures to

briefly touch spots on the surface of the eye that

overlie the periphery of the retina. Both laser

treatment and cryotherapy destroy the peripheral areas

of the retina, slowing or reversing the abnormal

growth of blood vessels. Unfortunately, the treatments

also destroy some side vision. This is done to save

the most important part of our sight—the sharp,

central vision we need for " straight ahead " activities

such as reading, sewing, and driving.

 

Both laser treatments and cryotherapy are performed

only on infants with advanced ROP, particularly stage

III with " plus disease. " Both treatments are

considered invasive surgeries on the eye, and doctors

don't know the long-term side effects of each.

 

In the later stages of ROP, other treatment options

include:

 

* Scleral buckle. This involves placing a silicone

band around the eye and tightening it. This keeps the

vitreous gel from pulling on the scar tissue and

allows the retina to flatten back down onto the wall

of the eye. Infants who have had a sclera buckle need

to have the band removed months or years later, since

the eye continues to grow; otherwise they will become

nearsighted. Sclera buckles are usually performed on

infants with stage IV or V.

* Vitrectomy. Vitrectomy involves removing the

vitreous and replacing it with a saline solution.

After the vitreous has been removed, the scar tissue

on the retina can be peeled back or cut away, allowing

the retina to relax and lay back down against the eye

wall. Vitrectomy is performed only at stage V.

 

While ROP treatment decreases the chances for vision

loss, it does not always prevent it. Not all babies

respond to ROP treatment, and the disease may get

worse. If treatment for ROP does not work, a retinal

detachment may develop. Often, only part of the retina

detaches (stage IV). When this happens, no further

treatments may be needed, since a partial detachment

may remain the same or go away without treatment.

However, in some instances, physicians may recommend

treatment to try to prevent further advancement of the

retinal detachment (stage V). If the center of the

retina or the entire retina detaches, central vision

is threatened, and surgery may be recommended to

reattach the retina.

 

Infants with ROP are considered to be at higher risk

for developing certain eye problems later in life,

such as retinal detachment, myopia (nearsightedness),

strabismus (crossed eyes), amblyopia (lazy eye), and

glaucoma. In many cases, these eye problems can be

treated or controlled.

 

Source: National Eye Institute, National Institutes

of Health.

 

Pranic Healing:

 

1. Invoke and scan before, during and after

treatment.

 

2. Touch your heart with the pads of the fingers of

your passive hand. Smila. Project loving kindness

towards the patient for a several minutes.

 

Maintain this attitude and posture throughout the

treatment.

 

3. General sweeping.

 

4. Localized thorough sweeping on the front and back

solar plexus chakra and the liver. Energize the solar

plexus with LWG, LWB then with ordinary LWV.

 

5. Localized thorough sweeping on both eyes, with

more emphasis on the affected eye, alternately with

LWG and ordinary LWV.

 

6. Localized thorough sweeping on the ajna chakra.

Energize the eyes through the ajna chakra with LWG.

Wait for a few sedconds. Then, energize with LWY

(crown-hand), ordinary LWV, then LWB. Visualize the

energy going into the eyes while energizing.

 

7. Localized thorough sweeping on the brain, forehead

chakra, crown chakra, backhead minor, temple minor and

jaw minor chakras.

 

8. Energize the backhead minor chakra with a little

LWG then with more of ordinary LWV then with gold.

Visualize the energy going into the eyes.

 

9. Energize the forehead, crown, temple minor and jaw

minor chakras with LWG then with more of ordinary LWV.

 

10. If the patient is middle aged or older, apply

localized thorough sweeping also on the throat, heart,

navel and basic chakras. Energize them with W. The

heart is energized through the back heart chakra.

 

11. Stabilize and release projected pranic energy.

 

12. Repeat treatment 3 times per week.

 

Avoid unecessary stress and over using the eyes.

 

Source - Advanced Pranic Healing by Master Choa Kok

Sui.

 

Love,

 

Marilette

 

1. Pranic Healing is not intended to replace orthodox medicine, but rather to

complement it. If symptoms persist or the ailment is severe, please consult

immediately a medical doctor and a Certified Pranic Healer.

 

2. Pranic Healers who are are not medical doctors should not prescribe nor

interfere with prescribed medications and/or medical treatments. ~ Master Choa

Kok Sui

 

Miracles do not happen in contradiction to nature, but only to that which is

known to us in nature. ~ St. Augustine

 

Reference material for Pranic Healing protocols are the following books

written by Master Choa Kok Sui:

Science and Art of Modern Pranic Healing, Advanced Pranic Healing, Pranic

Psychotherapy, Pranic Crystal Healing.

 

Ask or read the up to date Pranic Healing protocols by joining the group through

http://health./

 

MCKS Pranic Healing gateway website: http://www.pranichealing.org.