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Stem Cells Cure Blindness
The Controversy
Earlier this November, scientists from the University College London Institutes of Ophthalmology and Child Health and Moorfields Eye Hospital were able to restore vision to blind lab mice. This scientific breakthrough signifies that millions of people with optical conditions such as macular degeneration (loss of sight experienced by the elderly), diabetic retinopathy, and a variety of other forms of blindness could be able to regain sight through a remarkably simple procedure. However, the fact that the procedure requires stem cells from foetuses—currently viewed as a highly controversial method by many politicians—has prevented this procedure from becoming more publicized in the U.S. (1).
The Breakthrough
Researchers have identified certain cells on the margin of adult retinas that are similar to stem cells. Additionally, retinal cell replacement may be the most effective method of "cell transplant therapy because photoreceptor loss initially leaves the rest of the wiring to the brain intact” (1). In other words, major surgical reconstruction is not necessary. Any surgical procedure would only involve the superficial layer of the retina and not the particularly sensitive optic nerve wiring at the back of the eye. However, in order to attain human retinal cells at the necessary stage of development, stem cells would need to be extracted from a foetus during the second trimester of pregnancy (1). Because stem cells are able to proliferate and develop into many other types of cells within the human body, they can be extracted from any part of the foetus. However, the timing is imperative if the procedure is to work.
Three Blind Mice… See How the Procedure Works...
1. Early stage retinal stem cells were extracted from a 3 to 5 day old newborn mouse (1).
2. The retinal cells were transplanted onto the retinal surface of a blind mouse whose condition was genetically programmed to resemble the gradual loss of sight characteristic to the human disease retinitis pigmentosa or age-related macular degeneration (1).
3. The cells embed themselves and connected with other cells on the retina of blind mouse. Within 30 minutes the photoreceptors from the retinal stem cells implanted themselves and fused electrical connections with the animals' existing retinal nerve cells (3). As a result, the formerly blind mice's pupils began to respond to light and there was activity in the optic nerve (indicating that the eye was transmitting signals to the brain) (1).
Anatomy & Physiology of the Eye: Photoreceptors
The retina (around 0.5 mm thick) lines the back of the eye. It is lined with a network vascular blood vessels and neurons that gradually channel towards the optic nerve which contains the ganglion cell axons that connect the ganglion cells to the brain. The ganglion cells—the neurons of the retina that transmit images to the brain—are located in the innermost region of the retina and extend toward the lens, or anterior portion of the eye (2). The photoreceptors—the rod and cone shaped cells—are situated toward the outermost portion of the retina and are closer to the back of the eye (5). As a result, light must penetrate the nerve cells within the retina before reaching and activating the rods and cones. Once reached, the rods and cones absorb photons through their visual pigments and translate the photons into a biochemical message and then into an electrical message that stimulates all of the succeeding neurons of the retina. Consequently, “the retinal message concerning the photic input and some preliminary organization of the visual image into several forms of sensation are transmitted to the brain [by] the spiking discharge pattern of the ganglion cells” (2). From then on the brain is responsible for identifying, processing and interpreting the visual image (2).
Candidates for retinal cell replacement surgery must have some retinal cone and rod photoreceptors intact (1) . The retinal cell replacement surgery primarily serves to repair the nerve synapses in the retina, the macula lutea, and the fovea. The surgery cannot generate new photoreceptors.
The surgery mainly repairs the macula and the fovea. The macula functions as a short wavelength filter while the fovea, characterized by a dark circular area towards the back of the eye, is considered to be the most vital portion of the retina. Like the lens, it functions as “a protective mechanisms for avoiding bright light and especially ultraviolet irradiation damage” (2). The fovea is entirely composed of a mosaic cone photoreceptors that are arranged in a hexagonal structure. Outside of the foveal pit, the density of cone photoreceptors becomes increasingly more balanced with that of rod photoreceptors. There is a peak in the density of rod photoreceptors at about 4.5mm (or 18 degrees) from the foveal pit where the rod photoreceptors arrange themselves in a ring around the fovea (5). (Naturally, the optic nerve (the blindspot) is entirely free of photoreceptors) (5). If the macula or fovea cones are damaged (as happens gradually over many years), instant blindness results (2). However, macular degeneration could be easily remedied since stem cells take only about half an hour to develop into photoreceptors.
Repairing the Cornea
In August of 2003, Mike May, a Californian man who had been left blind for 40 years as the result of an accident that happened when he was three years old had his vision restored. Though the vision in his left eye was permanently lost, he could still sense light with his right eye. Researchers implanted corneal and limbal stem cells into his right eye. Five months after the surgery, May was able to sense movements and recognize simple shapes. After two years, he was able to see forms, color, and motion nearly accurately. His 3D perception and face and object recognition remained impaired, though his ability to sense motion was the best restored visual faculty (4).
Like photoreceptors, the cornea is responsible for channelling light through the eye's surface. The corneal surface refracts to provide 2/3 of the eye's focusing power. he corneal surface is entirely transparent and not lined with blood vessels, so the uniformity of cells may contribute to its ability to regenerate more rapidly than other cells in the human body. On the other hand, it is extremely sensitive. There are more nerve endings on the cornea than anywhere else on the human body (6). The cells that compose the layers of the cornea are found to regenerate at a rapid pace, though less rapid than photoreceptor cells. Again, a simple surgical procedure, most of which is processed by human mechanisms, could restore sight to millions of people if only the procedure were to be legalized.
courtesy of U.S. National Library of Medicine
(1) "Cell transplants 'restore sight.'" BBC International News Online. (http://news.bbc.co.uk/2/hi/health/6120664.stm)
(2) Simple Anatomy of the Retina. (http://webvision.med.utah.edu/sretina.html)
(3) "Cell Transplants Restore Vision in Mice." Live Science. (http://www.livescience.com/healthday/535968.html)
(4) "Cell Transplant Restores Vision." BBC International News Online. (http://news.bbc.co.uk/2/hi/health/3171993.stm)
(5) Photoreceptors. (http://webvision.med.utah.edu/photo1.html)
(6) "Cornea." Eye Anatomy. (http://www.stlukeseye.com/anatomy/Cornea.asp)
Comments
stem cells in cnina
I have the exact same condition Daniel and I have contacted the same clinic in china. Dr Zang has been my contact. Have you heard anything about them or have you gone for treatment?
I am interested in exploring
I am interested in exploring this too, if only it wasn't so expensive. Please keep me posted Daniel.
Spinal cord injuiry
After c4 and c5 repair my brother lost his vision. Can you help to repair his vision or suggest a Doctor to help?
albinism
hello, my name is nathanael yebgui, i am a 17yr old from london, i have albinism and suffer from nystagmus, im greatly pleased to see that some research is being conducted, during my own research i have found that stem cell resaerch is greatly promicing for my situation, i have read that a man who lost his vision in one eye due to an accident where he had damaged his retina and optic nerves has had his vision restored by stem cell treatment, is there any hope to cure my nystagmus and repair my retina and optic nerves with stem cell treatment? as you may know albinism results in low vision due to an underdevoped retina mainly in the fovea (which is greatly believed to be linked to nystagmus as it is responcible for the fine detail and focusing of the eyes) and misrouting/misshapement of the optic nerves. but could the same be done for an underdevoloped retina?
now that stem cells can be derived from the adult body in fat, muscle and bone marrow, it is almost certain that the stem cells will not be rejected by the body, therefore would it be possible derive stem cells from anyone of those places, then geneticaly engeneer them to repair the albino/nystagmus gene and place the repaired cells where necessary?
thankyou for your time
nathanael yebgui
Legally Blind
My name is Nicolette, I am a 25 year old woman who developed Pre-eclampsia 3 year's ago while pregnant with twin's. When I awoke the next morning after giving birth the night before, I was blind. The doctor explained that my high blood pressure caused a minor stroke behind my eye's leaving my nerve's damaged.
I am looking for treatment and/or any information that could help me. Please reply.
Thank you,
Nicolette
Ruptured brain anuerysm followed by stroke
Hello -
A yr. ago I had a ruptured brain anuerysm. Following the clipping surgery I suffered a stroke while in the hospital. The stroke has taken away 3/4 vision in each eye. Would this type of surgery work for me?
Thank-you!
seven year old son
hello,
my seven year old son was diagnosed with stargardts about a years ago , his doc says that we do not have to worry about it yet,but in yhe last year he has almost completely lost his vision , he has a terrible time in school and has been having several accidents i.e. running into to pole son the playground, tripping over things and running into other pupils .our doctors did some genetic testing and are now saying it is not stargardts but rod cone dystrophy, they also state that there is nothing that can be done and that it will not get any worse, they do not want to see him agaian for a year.His vision is deteriorating very quickly though and no one will give us any answerers , this is very scary to his , it is so sad to see him not being able to recognize his mother or brothers anymore or doing all the kid stuff he used to enjoy.Does any one have any advice for us ,I would give him my eyes if I could .
Stargardts
I am so sorry to hear about your son as my 35yr. old daughter was diagnosed at the age of 10. Two years before that she was stricken with diabetes. It has been a very hard, long road and her vision is getting worse. We were told the Stargadts would only get to a certain level and not worsen. We were told not to bother with braille. We went to Boston last month & was told she may have another eye disease!! It's too much to take sometimes. We are going for all the testing next month & pray whatever is happening will progress slowly. As I'm sure you are aware the stem cell & gene therapy experimentation is very hopeful and we all must pray for the cure. We need to also vote for a government who will allow stem cell research. If possible, I strongly suggest getting to the Mass eye & ear hospital as they are one of the best in the country. They will not let you leave without answers good or bad. God bless, feel free to e-mail me as I know only the parents of children stricken with these horrible diseases understand the pain.
Stargardts
Hi,
In responce to your sons suspected stargardts condition, my husband is one of 2 siblings with the condition, his older sister was diagnoesed at the age of 4 now 30, and my husband at the age of 17 now 28. At that time they didn't even know what it was, so there were no preventative measures, but now they have seeked treatment from multiple doctors throughout North America. He has seen a Dr. in Farmington CT. Dr. Gerard Nolan of the Nolan Eye institute, where he administers a low-dose eye drop twice a week, and has noticed minimal repair, but a significant amount of prevention. The condition seems to be at a stand still!! The only advice that I can give you as a wife, which too is followed from his mom, is to make him keep as much independance as much as he can, wear protective eye wear, sun is the worst, as well as take Lutein/amino acid rich vegetables (green leafy veggies). My husband can no longer drive, which sadly is his only passion in life!! But keeping your chin up is so hard, but try to remember there is always someone who has things worse!!
Take Care
retinal dysthropy
i am a single man at 49, diagnosed with retinal dysthropy, almost ten years ago. it is very hard on my part as i am working in IT. thank God, our software now can be resized to its maximum length to be able to read by the afflicted person. Moreover, with new discoveries, like stem cell, i am optimistic that soon our scientists will make our conditions be normal again. but for the meantime, since there is no cure yet, i have to gain/train myself to be independent
Presumed Histo
I am a forty eight women who has presumed Histo. There has been damage to my retina and the fovea. As a result I am unable to see much from the center of my vision. I understand there are many detila undisclosed, but will this new discovery allow for the repair of tissue, thus the ability to regain some vision.
Restoration of central vision due to detachment of macula?
Hello I read this very exciting article and was wondering. I had an accident a
few years back and suffered a retinal detachment with the macula being detached
for a few weeks. My vision is somewhat restored after the 2 surgeries one
including lens replacement. I still can't make out things sharply, clearly, or
more than 10 or 12 ft away. I was wondering if this process could improve my
vision if it is ever allowed to where I could atleast read an eye chart
Thank You
My son is 24 years old who
My son is 24 years old who had optic nerve damage from a fall, he can see light and dark. Is accident was in 2005 we have been reseaching stem cell in Mexico, Costa Rica and China and we are so confused. Can you tell me is one facilty better than the other. We have been ready to go for the past 2 months and just have so many unanswered questions from each of the facilities, can you give us any feed back on where you feel is the best of the 3. China wants to do 6 injections, Costa Rica 3 injections and Mexico 1 injection why such a diffence and the money is not much different between them all?
Hope you can help us resolve this issue.
SIncerely Eric Hurttgam
I have a daughter who lost
I have a daughter who lost her eyesight in 1996. she suffered optic nerve damage in a car accident. Where can these procedures be performed? What are the track
records? Where can the stemm cells be harvested from? What are the costs???
Injections in China, Mexico, Costa Rica
My name is Ola Pacyna and I am researching options for treatment for my friend who has optical nerve damaged after a brain tumor growth. I saw that you contacted the facilities in the countries above and had some knowledge about the injections and treatment options. I am at the begining of finding out about this new "hope" and would be very grateful if you could send some info, contact names and numbers of these facilities and your advice based on what you and your son went through. I hope everything went well and he is going to see soon.
Sincerely,
Ola Pacyna
31 year old with underdeveloped optic nerve
I've been blind in my right eye since birth. I was told that my optic nerve never fully developed. My right eye never fully grew beyond its infant size. My question is, will or can stem cells be used to correct this problem? If it treats the nerve underdevelopment will it also treat the underdeveloped eye?
I am sorry i don't have any
I am sorry i don't have any help for you however did you get a reply as i am 17 and have the same condition with my optic nerve but not my eye please forward me any infomation you recieve
Thank you
rod cone distrophy
My 9 year old son has been diagnosed with rod cone distrophy
he had sight, then about 2 years ago suddenly lost it, he has had many tests and they really dont know what caused this.
I am wanting to know what can be done to maybe restore his sight, i have just had a child and kept the blood cord from this child in the hope that it could help my 9 year old son.
where can i go to see what can be done for him, as the doctors say there is nothing they can do
we live in Albury, australia
homonomous hemianopsia left side
On 11/23/2003 I had a stroke due to a 100% blocked internal right carotid artery. Can stem cell therapy offer me any hope for the future? I'm 58 yrs. old and had the stroke at 53. Until the moment of the stroke I had no symptoms of impending doom.
Sincerly Bob Gerace Phila. Pa.
pls do help me
hi..
My best friend has cone cell dystrophy..pls people out there tel me what are the new steps that has been taken in this field.and also as much as possible details about cone cell dystrophy.Is it possible to cure it?
pls kindly help me details.
Describe the process of learning to see again
I am writing a book where a character is blinded by a gunshot in the head. Twenty years later, he regains sight through surgery and stem cell implants to repair the damaged optic nerve. Can someone describe the process of learning to see again to make my story evocative and plausible.
Thank you very much
Maybe you can focus on
Maybe you can focus on philosophic part of this process. Something like this for inspiration: ("The Blind Learning To See") http://www.ralphmag.org/CO/blind.html
Good luck with your book!
Hemianopsia
I suffered a TBI in a car accident and have homonymous hemianopsia to my right side. Will stem cell research be able to regenerate the optic nerve to cure this condition?
Central retinal arterial occlusion
I suffer from blindness in my right eye due to a Central Retinal Arterial Occlusion which occurred in 2004. Are there any techniques available (or possible) to rectify this damage?
We hear of stem cell research but no-one - that I have seen - mentions if it is possible in this sort of case.
I also have a cataract forming in my 'good' eye so this is very worrying...
Thank you for any comments.
central retinal artery oclusion
I went blind in right eye OCT 12 2008 20/200 in left also was told cataract in left eye. I was told that a flap in my upper chambers in my heart caused a mini stroke that caused a clot before this I helped orphans in COSTA RICA where we say PURA VIDA. FOR 10 Years I called myself a TICO Some People in the US
I say PURA COCA OR IN ENGLISH PURE CRAP THEY JUST DON'T CARE COLOR COUNTRY CULTURE it doesn't matter
damaged retina and nerves
My partner became blind in his right eye at the age of 9 years due to an accident with a toy bow and arrow. He is now 36years old. He was told many years ago that the damage was irrepairable due to the fact that it was his Retina that was damaged and also the nerve which attaches it to the brain I beleive. Would the Stem Cell procedure work for him? Are there any other advances that might help him? Thank you
Artery Replacement
My Grandfather lost his vision recently. We have gone dotor to doctor, we were told it was due to the arteries behind his eyes. If they could be regrown he would be able to get his vision back. Is there anything that could be done for this to happen????
Cone Rod Dystrophy
My friend has cone rod dystrophy. I would like to know as much as possible about this disease. More specifically, I would like to stay current on all the treatment and possible cures. Can you put me on a mailing list? Thank you Dr. Ken James, you gave us hope.
hi i have cone rod dystrophy
hi i have cone rod dystrophy if you have heard anything on possibles cures and such i would really appreciate it since you may know alot more than i do due to your research on the matter thanks for your time
cone rod dystrophy
HI!
My son just got diagnosted with CRD. He's 5 years old. Have you found any therapies or vitamins or herbs or anything I may be able to do for him before he goes blind?
Thanks!
ONH
Hello, I have a 11 month old who has ONH a disorder in whic the optical nerve did not develop properly in utero. Please if anyone has any information as to how I can access the stem cell transplant surgery I would be very greatful. Her father and I are even willing to give up sight in one of our eyes if it would help my baby, we say one eye bcause we still need sught to care for our other child who is perfectly fine.
We are in Columbus, Ohio where we are supposed to have a high tech childrens hospital who told me when she was four months old " she's blind there is nothing you can do about it, no glasses or contacts will help, bring her back in one year for a check up" in those exact words, I reported the physician because I didn't care for his lack of interest and empathy.
Any info please post
Sincerely,
Sad, depressed mom
ONH
Hi i was wandering if you ever recieved any info on curing your daughter's ONH! My son was just diagnosed with the same. The doctor's are telling my husband and I that there is nothing we can do to change this were not ready to accept that answer. If you have any information please let us know!!!!
RE: ONH
Hi, I saw your posting. I would love to talk regarding ONH. My son is 6 years old and he was diagnosed at 3 months. It has been challenging these last few years. I would love to give you some insight into what you are up against. Plus, I have been checking into the stem cell therapy in China. My son has taken all the necessary tests to pre-register. Feel free to email me.
Best Regards,
Lori
I see several postings here
I see several postings here that I think the following information may help. I have ONA and am exploring the Stem Cell treatments in China after reading an article 2 weeks ago in the local paper about a young girl with ONH. They have been extremely successful with ONH and SOD in younger people. You may find the following resources helpful:
stemcellchina_onh_sod Yahoo! group where people can exchange information and questions about the stem cell process. Both those who have gone and those who are considering it participate in this group. The url for the group is http://groups.yahoo.com/group/stemcellchina_onh_sod.
www.stemcellschina is a site with many blogs and personal stories of people who have had the treatment for a variety of conditions.
www.stemcellsforhope.org is a site that contains more technical information about the process as well as some other stories.
Feel free to e-mail me if I can be of more help. I'm just beginning the exploration myself and have found a ton of information.
I hope this helps,
Karey
I have a child with o.n.h.
I have a child with o.n.h. and would just like to talk with someone going through the same thing.
ONH
Lori,
I would like to get your E-Mail so I can get some information about the stem cell in China. I've been looking into it a little bit and I think you are 10 steps ahead of me. Please E-mail me back so I can gain some of your knowledge.
Thanks a lot.
Optic Nerve Atrophy
Hello Lori-
My dad and I both have ONA. Please email me with any updates with regards to stem cell research. Thank you so very much for your time and God bless you and your's.
Jared Price
Nerves Atrophy
My husband was operate by an craniopharingioma and now has optical nerves atrophy.
Please if somebody can tell me if exist the transplant with cell stem for him.
I'm from Romania
Thank you
Hi there My husband also has
Hi there
My husband also has a craniophrayngioma and optic nerve atrophy - did you get any useful answers to your question?
Thanks
Blindness caused by optical nerve damage
Hi Sir/Mme,
I am a Mother of a 3 yr old little girl that lost her eye vision, due to a growth of a tumor that put pressure on her optical nerve and caused
damage to it. So my question is, in this research found is it possible to repair an optical nerve, after such damaged caused by such
circumstances? If so may I have more information as to how this can work and why? Please get back to me.
Thank you.
Have you got any more information
My brother had head injury back in sept 2005 and he was losing vision gradually but we found out in 2008 that he had brain tumor which was removed. We have been informed by the doctors that his optic nerve was damaged and nothing can be done about it. He has been declared legally blind. His right eye vision is almost zero but left eye has very limited vision. He is my youngest brother 45 years age. His profession was a driver and now he can not drive. I would like to find out if any one can provide any resources in US India or China for this kind of condition?
Any Success
Hi There,
I have recently began working with a lady who is blind due to a tumour damging the optical nerve.
I have started reseaching the topic and came across your question on the serendip webpage.
I am wondering did you have any replies and is there a chance of future success for restoring sight.
It would be much appreciated if you could let me have some information on this subject.
Kind Regards
Peter Taylor.
Hello, my 2 yr old daughter
Hello, my 2 yr old daughter is goin through the same thing. Did u get any help or anything. Cause im looking for some help. She lost her eyes site when she was 17 months old a week before she turned 18 months. She has neuroblastoma which is a rare childhood cancer. She had 2 tumors one by her abdomen and the other putting a lot of pressure on her optic nerves. They tired all the could to get the pressure off fast like radiation but i dont think it really helped. they couldnt get it out because it would be to complicated. Right now she is doin fine, i juss wish she could see again. I have been looking for some answers for ever and nobody can do nothing. and when i seen that you have the same problem i had to reach out to yea. please help.
whom it may concern
HEllo,
My name is cecilia castleberry my daughter was diagonosed with GBS menegitious, when she was a month and three days old. It caused her to have brain damage, diebeties insipidous,optic nerve atrophy, and etc. This happened in August 2002 she stayed in the hospital until october 2002. The next year we started niticing her eye sight was going away now she is what they called legally blind with optic nerve atrophy and i knowthatshe can shee a little.
My question to you is there a surgury for this, a medicine that she can take to help correct it. could she have a eye replacement for this. What is it that i can do about this please let me know
thanks, cecilia castleberry
Optic Nerve regeneration
There are a couple of things, but first, Have her take the suppliment Idebedone along with vitamin B12 and C. Take Idebedone at 400 to 650mg daily. Then there are the studies at Harvard with Dr. Banowitz, Ph.D with Oncomodulin and elevated levels of cAMP inhibitors. Lastly, genetic treatments are right around the corner, where the doctors will genetically encode a viral cell and introduce this cell into the body. This code will be a refreshing DNA command from your own personal genome and you will have a brand new Nerve again. This has already been accomplished in both mice and dogs in America this last year.
QUESTIONS ANSWERED
Greetings,
I saw all of your questions, and first I would like to extend my sympathies and blessings. I'm a doctor as well, and have been a patient as well in the past, so I speak from experience on both sides of the "looking glass."
In regards to stem cell therapies, you will hear alot of negative reactions, mostly from idiots who have no scientific background training, or from those who fail to read and learn. The bottom line is, stem cell therapies work. We just need to refine them. And we will, and quickly. Unfortunately, because certain gov't officials in the developed world have less brain cells than the average individual, and attempt to hinder the development of this "blessing" in therapy, we will have to rely on "relocated" clinics that operate in countries who tolerate this. The doctor in China who helped develop the stem cell treatment for Parkinson's did a wonderful job with fabulous results. There are treatments already for damaged heart tissue, autism, Parkinsons, stroke, type II diabetes, etc.. see www.cellmedicine.com for some of the newer treatments you can have in Costa Rica and Mexico.
Stem cells have the capability of repairing the damage from glaucoma, optic nerve damage, tissue removal due to tumour surgery, etc. Keep in touch, and I will let you know as soon as I find out about any stem cell therapy related to your query.
Keep an optimistic outlook, because this is a field that NO gov't can stop forever.. Why? Because another gov't somewhere else will allow it, and scientists and their investors will relocate there, so that some progress can be made and money as well. These motivations as strange as may sound, advance medicine.. they always have and always will..
For the affected and afflicted, let us thank God there is finally hope. For the pessimistic: well, if you are so against stem cell therapy, fine...WHEN YOU NEED SOME BODY PART OR TISSUE REPLACEMENT AND YOU OR YOUR LOVED ONE ARE ON THEIR DEATHBED AND A STEM CELL CURE IS AVAILABLE, JUST SAY NO SINCE YOU'RE SUCH A BEING OF PRINCIPLE. BUT LEAVE US OUT OF IT... THANK YOU
Dr Ken James
is stem cell for LCA(Leber)
Hello Dr James,
Will the stem cell work for Leber patients too?
how does teh treatment work? Where do they give teh stem cell injection, in the retina?
Please advise. Thanks.
compound myopic agtigmatism in both eyes and cone rod in RE
Hi Doc,
Read your wonderful comment about stem cell therapy.
I've my nephew 5 years old with opthalmic history of BE-Nystagmus and presenting complaint of dimness of vision and Final Dx of compound myopic agtigmatism in both eyes and cone rod in RE.
If you can help me in finding something regarding therapies anywhere or ongoing research, I'll really appreciate.
Thanks
Dr. Sangwan
Optic Nerve treatment/regeneration
I am writing on behalf of my niece.
She is 16yrs old who recently lost her vision. She seems to have suffered what is called Cavernous Sinus Thrombosis (CST). The more specific conclusion in London now is that she has what is called " Posterior Ischemic Optic Neuropathy".
I can send all her medical reports in order to please have a look at them and advise if she could benefit from any farther current investigation/research regarding Optic Nerve treatment/regeneration?. Or if you could direct us to any other option/s?
Best regards,
Nuri
I was in a construction
I was in a construction accident and i'll spare you the details. I had a bunch of facial trauma and because of the swelling and the force i was hit in the face with my optic nerve in my left eye was damaged "beyond repair". My question is, are there any new developments in the optic nerve repair area that could help someone in my prediciment. If there are any details you could give me i would greatly appreciate. Thanks