Hi Agi64,
I have been diagnosed also with foveoschisis and I have been postponing the operation, had 3 opinions, one proposing an immediate operation the other 2 wait and have the operation only if things get unbearable as the vision in my other eye is quite poor and cannot risk my "good eye" having any complications.
What do you mena funny vision? I see pixelated almost everything, smudged fonts in computer and something like the wavy things you see in the asphalt when it is too hot -like evaporating water.I see 6/9 currently in my last visit, improved from 6/12 in the previous (although my feeling is that things got worse)
I would suggest looking into low level laser therapy (LLLT). There are people experimenting with it for multiple uses (memory, vision). LLLT energizes mitochondria through complex IV of the electron transport chain. One user reports halting his vision degeneration due to Leber's Hereditory Optic Neuropathy, which is a mitochondrial disease. More info can be found here:
http://www.********.org/forum/topic/63228-lostfalcos-extensive-nootropic-experiments/page__st__1800
Thanks for the input, Agi64. I'm really sorry to hear about your myopic foveoschisis - that's a really dramatic development that's very hard to treat surgically. In case you are interested, I came across a recent article from mid-this year concerning surgical approaches to treating this entity:
http://www.retinalphysician.com/articleviewer.aspx?articleID=108627
I was interested in the recommendations of possibly including a buckle to help resolve the schisis, although of course it would depend on whether the locations of the retinal layer separation/schisis was in a section of the eyeball that COULD be 'buckled.' And on what other treatments have preceded any such further procedures, of course.
I'm still having distortion and blurring after 2+ months in the eye with the slightly steeper macular staphyloma, but even Dr Ward was unable to see a bleed or fluid leak on a macular OCT causing the problem. I'm praying it isn't a hidden lacquer crack or something worse. It will be interesting to see if the PPB surgery results in any difference in that eye's visual acuity, once the surgical trauma has resolved. I think Dukey mentioned that one of his eyes had a change in acuity (a bit better) post-surgery, although I am not expecting that in my case.
I'll check the Delphi forums too - thx for the tip! Good luck w/ your foveoschisis - I hope you and your doctor can find an additional treatment that might improve your vision from its subnormal state.
PS we were rooting for NZ to take the Cup! You all are our heroes - great competitors and gracious in defeat. Go Team NZ!
I really appreciate your updates.I too have DM...axial lengths 29mm right and 30mm left.I had 'funny' vision and went to see an opthomologist this time last year.I was dx with myopic foveaschisis in my left eye.After two vitrectomies and a cataract op in that eye, I still see 'funny' ...meaning my vision is subnormal.If its any consolation...I think you're on the right path,having the buckling with Dr Ward.Have you looked at Delphi forums? A couple of folks there have had the pole buckling done.Good Luck flossy93 and do update us
Hello ValveJob,
Just wanted to let you know I have seen Dr. Brian Ward and asked him about the 7-MX but he said he does not know of any patients who are on it. I asked him about Dukey (his patient from the University of Texas, whose name I do not know) and Dr. Ward said he did not know if Dukey had obtained the 7-MX or what results he was getting (if any). I also PM'd Dukey through MedHelp but never received a reply. Hopefully Dukey's sight is so good he's off living life rather than spending time on the Eye Care forum. :-)
I've done lots of Internet trolling but cannot find ANY source of 7-MX for patients in the US. I can only find industrial suppliers of powdered 7-MX, which I doubt is the same as medical grade material. I'm not planning to consume industrial chemicals from a drum.
BTW I am scheduled for posterior pole buckle surgery early next year in the symptomatic eye, and I will report back afterward. If it goes well, I'll likely try it in the other eye as well.
I'm already very, very nervous, but on balance if I do lose my vision later in life, I'd like to be able to look back and feel as though I did everything I could to preserve central vision as long as possible. Of course, if I end up with a disease or rejection from the donor sclera material, it will have been a poor choice, but there are no guarantees either way I guess.
I also have degenerative myopia and an axial length of over 30!! I even had a CNV (choroidal neovascularization) in the left eye in January 2012, had 2 injections of Avastin which definitely did what it was supposed to, but I was left with distorted vision in that eye.
In any case, at the beginning of 2012 I e-mailed an ophthalmologist in Copenhagen named Klaus Trier, mentioned by Dukey, who has done research on myopic children to see if 7-MX would slow down the progression. He actually e-mailed me back saying that it was too early to know if it worked in adults and that he should have more information in about a year. So, at the beginning of this year, I e-mailed him again, but he never wrote back! I am so frustrated.
Anyhow, if you ever find anything out about the use of this drug in adults, I would love to know!
Has anyone other than Dukey been able to obtain this drug to help strengthen the collagen in the sclera to inhibit future eyeball expansion/lengthening? Even if not approved in US yet I would really like to know more.
I'm going to try PMing Dukey through MedHelp although I don't know if the message will go through. Haven't seen recent posts from Dukey but would so love to know how the drug might be working - and also how the performance of the Posterior Pole Buckles have been over the past 2-4 years.
I was just diagnosed (finally!) with Degenerative Myopia w/ axial length in both eyes over 30mm; I am devastated. Surprisingly, aside from stable severe myopia, I haven't had many symptoms yet. What sent me to multiple retinal specialists was a recent distortion/blurring episode in my LE diagnosed as a Fuch's Spot. The first doctor said 'Your retina doesn't look that bad, wait 2 years and come back unless things change first.' No axial length measurement or fluorescein angiography. Luckily the second doctor was more thorough and already suspected what might be happening due to my history.
I am already trying to learn about the PPBuckle option as well as any chemical/supplement/medication options to help slow down progression of the DM in the future.
My refractive error has been stable for over 10 years at -14.0D, but w/ an axial length of over 30mm it sounds like the writing is on the wall for me. If anyone has thoughts about the meds or the PPB, please speak up. Thanks!
HiAre there any updates on the drug? And. How do I get my hands on tthem?
I have recently been experiencing the ravages of pathological myopia. I would really like to know what your experience has been using this drug. I will probably send you a PM to get all the details, but I would just like to know if the progression of your myopia has slowed down.
I am very interested how I can obtain the drug in England
I'm excited to come to this site and learned new treatment you are taking. I'm suffering from this hell disease for a long time. I wonder if it's effective for an adult. Can you tell us if it works for you after having taken it for one year now? thanks
Frank
Wow. It gives me so much hope to hear of this new drug. I have suffered greatly from high myopia (posterior vitreous detachments caused traction tears in my retina, now have scleral buckles and IOLs in both eyes). Doctor has suggested I take AREDS and Fish Oil. Im in the U.S. My night vision is terrible and currently am seeing 20/40. I would like to applaud you for your tenacity. I will inquire via PM about 7-methylxanthine.
Best, Emo_8a
Hi Dukey - I sent you a PM a few days ago. Please respond as time permits. Thanks much, NP
Hey yeh so I am now taking the drug (800 mg/day). I am also now taking AREDS with Lutein (2 x day) and fish oil (3 x day). Obviously there are no immediate changes with the drug. We are trying this mainly to try and reduce any future elongation associated with pathological myopia so we dont expect to see any improvement per se, but we really do not know what to expect. I have not noticed any side effects of anything that I am taking, including the 7-MX. I would say that out of everything, the fish oil seems to be having the most notable effects on my vision and lots of other things too. This could be the infamous palcebo effect though so don't take my word for it. We will be monitoring my axial lengths every year.
If anybody is interested in this drug, please contact me via private message as I am not sure it is appropriate for me to be posting instructions on how to obtain a non-FDA approved drug on a US website!!!!
Hey dukey, just wondering if you'd made any progress with the new medication...?
I still do not have the pills in hand yet so I wont view this as a success until then. When I do get them, I will write a summary or something to explain how I did it. Technically, it is illegal to import non-FDA approved drugs into the USA, but there are some loopholes which I may need to exploit if I get trouble from the CBP. Fingers crossed though. Will post back ASAP.
Thanks berrywoo. I wish it was a "cure" but I'm hoping it may prevent the very serious degeneration which may occur in the coming years. If I had "simple" myopia, I would not be doing this that is for sure. One can dream!
I'm quite impressed by the lengths you've gone to try and cure your myopia. Best of luck!
Would you mind explaining exactly how you acquired your script from Dr. Trier? I would like to do the same.
OK so I am now awaiting delivery of my drug after everything else was finalised. I was asked to get an axial length measurement done (surprisingly I hadn't had one) so that we can measure it as I go through the treatment. My length was not actually that bad (28.3mm) so it cheered me up a little bit as I was expecting 30mm or above. I am also now taking fish oil and AREDS to try and combat this thing or at least reduce it's progression.
How are you acquiring your script - are you directly meeting with one of them when you return to England?
Excellent, congrats. Please do check back. I'm eager to see any benefits, as I'm sure many of us are.
Well after much effort, I will be getting a prescription written by the lead scientist on this work in Europe and will then get the pills shipped to me here in the USA. The cost is $1/day bascially, which is fortunate. Will confirm back when I have received them and started taking them.