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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Crps


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Old 04-04-2014, 06:21 PM   #1
Vicsls
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Crps

Looking for any information on CRPS and blurred vision. Wondering where to find others who are dealing with CRPS. My daughter is 13 and has had CRPS for one year. They have not found a way to decrease her pain or frequency of flare ups yet. Would love to hear how others are dealing with their CRPS. Yesterday, she started complaining of blurred vision and painful and dry eyes. Any help would be appreciated.

 
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Old 04-05-2014, 06:53 PM   #2
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Re: Crps

I have only been diagnosed 3/21/14. I've done a lot of research and read that it does affect your eyes. I wish I could remember where I read that so you could go look for yourself. Unfortunately I don't think this board is very active. I have a lot of questions myself.
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Old 04-06-2014, 03:01 AM   #3
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Re: Crps

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Originally Posted by Vicsls View Post
Looking for any information on CRPS and blurred vision. Wondering where to find others who are dealing with CRPS. My daughter is 13 and has had CRPS for one year. They have not found a way to decrease her pain or frequency of flare ups yet. Would love to hear how others are dealing with their CRPS. Yesterday, she started complaining of blurred vision and painful and dry eyes. Any help would be appreciated.
Thank you. I did find out a little more about it. I am sorry that you are going through this, too. Finding others who are dealing with CRPS is helpful in living with this disease. Is there a support group you could contact in Florida?

I took my daughter to the eye dr. and the dr. said she thinks it is all related to the CRPS. Her optic nerve is affected. She will see a specialist in the next couple weeks.

Are you finding something that helps with your pain?

 
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Old 04-06-2014, 12:59 PM   #4
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Wink Re: Crps

Thank you.

 
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Old 04-06-2014, 05:22 PM   #5
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Re: Crps

Thank you. sorry your daughter has this awful ailment. Thanks for the new info too.
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