Vision blurry
 

The last few days my vision is blurry at times then goes away.
Is this normal for CRPS or should I worry?:confused:

Hey Russell,

I don't know if this is normal or not for CRPS but, I can tell you that I have the same issues with blurry vision off/on and for me it seems to be a side effect from medications; could this be possible for you?

Hi Zoo,
Thanks for the reply.
If it was a side effect how come this is happening now and not when I started my new dose two months ago??

As I understand it from the information given to me by my doctor is that not all side effects present them selves immediately. It takes a while for some medications to build up in the system an thus can cause side effects as the serum levels increase. What I did to determine what was causing my blurry vision was to note when it was occurring in my daily journal, also noting when I took my meds and then it was obvious that within 2 hours of taking the meds or using my bolus dose the vision was impaired. Sometimes I also notice it more in the mornings or if I have been while laying down. My doctor said that this happens because of meds pooling in the body and once we start moving the medications are actually better utilized as our muscles move it throughout the body through compression.

If blurry vision is your only symptom I would note it and discuss it with your doctor at your next appointment. If however, you have slurred speech, increase in headaches, clumsiness, blood pressure issues etc., then I would contact your doctor right away. If it is a side effect, then it may improve over the next few weeks as your body continues to adjust to dosing or new meds. As long as it is not a life threatening or psychotic type side effect then it might be beneficial to allow enough time for the body to adjust. All to often we stop medications because of transient effects before we reach the therapeutic dosage.

I do hope this resolves quickly.. it is so annoying!!

I just got off the phone with my neurologist and she is scheduling me for a CT scan.
She said in my case of an ongoing atrophy of the cerebellum this might be related to that. I'll give you an update afterwards... :(

Good luck Russell. You may also want to consider an eye exam. Hope Zoo is right and this turns out to be a transient side effect of a med. Wishing you wellness ~Lottie

I will add as many might or already did,medications causes so many side effects and obviously ,sight is one of the most affected but I got a recommendation from my ophthalmologist on my last visit ,hope helps you.
During my exam I mentioned had rsd and also explained what it was and also mentioned is neurological condition as well, well he recommended me a 3d picture of the Inside of the eyes and follow the changes if any so I can related in the future ,if anything got worse with my sight,there is already pictures showing those changes and if you are under wc process ,which is my case unfortunately,sight can be added to be part of the claim but also track any change that can indicate damage inside by the many neuro changes ,is not cover by the insurances but is peace of mind to invest no ore than 7o bucks here in California for those pictures which are priceless when you are dealing with rsd ,so please consider that option as well ,get it in your own record folder and hope nothing else get worse ,but is real good to know ,dr can listen and care ,some drs but few still existed ,good luck and hope the what ,take care from Jesika .:grouphug:

blurry vision
 

I have had blurry vision with my CRPS type2. I have full body RSD CRPS mine started with a severely broken right leg. An eye doctor specialist said it was difficult to treat because RSD can transcient nature. Whether my face is flaring or which side is hurting. One visit he would see issues with my right eye and left was good the next it was reversed. Also some medications can have blurry vision as a side effect...Lyrica caused my vision to blur. Also some medications can cause your blood sugar to rise...esp. some anti-depression drugs or if you are prescribed steroids for flares. All this being said I would check with your doctor and eye doctor. I hope that you are having a low pain day. prayers & gentle hugs
:eek::hug:
Leonice

Welcome cooltea. :Tip-Hat:

Just got back from doc. had a CT done to see if my brain shrunk anymore. Sad to report it has. My neurologist said the average size of the cerebellum is about the size of a half dollar. Mine is the size of a dime. Thought you should know...Major bummer....

Hey Russ! I have had some eye issues, including blurriness, and the drs have concluded that it is RSD related. It is good that you contacted the dr and are ruling out anything else. Medications can always be a factor too, but not for me since I wasn't taking anything.

Good luck to you!!
Nanc

Russell - so sorry about the scan results. What can cause the cerebellum to shrink???
Sounds scary, how are you coping? We are all here for you. Gentle hugs ~ Lottie

I'm so sorry Russell - what if anything can be done? Is this caused by CRPS or something different entirely? Just curious.

Wishing you better days,
Tessa

Honesty I wasn't expect those result but sure your neurologist might find a way to treat the damages cause sure by the rsd ,I hope soon you have some options and as always ,hope you and wish you the best ,gentle hugs and lots of love,Jesika .take care :grouphug:

Hi Russell,
I am so sorry to hear your news. Please let us know how we can help. Sending hugs and prayers your way!

Hi Jesika, (Love the spelling!)
I hate to be the bearer of bad news, especially about myself, but there's really nothing that can be done. Except for experimental surgery so that's out!
Noboby's cutting into my head while I am able to stop it!
I just hope it stops by itself before any further damage.
I've already lost some of my motor skills. Hard to talk, walk, and stand. Now I cant sleep on my back for fear of choking on my own tongue.
Sorry for the bad update...
Love all you guys... :grouphug:

Man I'm sorry Russman. We're all here pulling for you. Much love.

I'm really sorry to hear this news.

There's literature out there to suggest that gray matter shrinks in RSD. Is this a problem we all have but just may not be aware of? I mean, I have blurry vision, brain fog and all the other symptoms they claim go along with this shrinking gray matter. Just wondering.

Russell,
I'm sure in disappointing diagnosis but they are now some new medical trials and hope you fit on one of than,one thing ,you have to keep the strong positive attitude as you do.
I'm sure you are scare and feeling confuse for all things going on but you can do it !!! Have hope and faith ! We love you and sure wouldn't think twice to trade places with you and keep going even as hard as this can be ,keeping good attitude helps and I'm sure a solutions will appear soon.
I heard from rsds is going to launch several trials for rsd suffers starting November ,I'm desperate and anxious waiting for those FDA new medications and trials .
We are all here ,full,of faith each believing in our on way of belief but sure no matter what religions we belief or maybe many don't believe on any,I'm sure we all thinking and wishing the best for you,we are your brothers and sisters in pain and we might not share same options of belief ,but sure we share same Lives and only want the best .:grouphug:
I'm open to any corrections on my spellings ,I'm still learning and not get offended ,plus my iPad make it worse !!!!
But is fine ,I do need help in many areas and grammar not my mayor .
Loving soft gentle hugs from Jesika .
:grouphug: I'm truly touch by your strength and hope only the best .