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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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07-01-2009, 12:44 AM | #11 | ||
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Hi Dew,
I have had blurry vision since RSD. There all people who have RSD in their eyes. You would know-the burning. I really don't know why our eyes are affected.I'm going to get a eye check up soon. I've had the laser surgery about 12 years ago. I've been using readers from the drug store. But, maybe it's time to get a perscription for eye glasses. I think there is a question on the rsdrx.com website about our eyes. It just seems it never ends=our getting some new symptom. I think we are going to put our home on the market. I love it, but it's too big. We bought it knowing the area was going to be special and value would increase. We met with realtors yesterday. I don't like the idea of people coming and going so will show by appointment. It is 4 bedroom 4 bath with an office. Hope it doesn't take forever to sell. We have never lived in a house for sale before. A new adventure. We are beating ourselves up for not buying a lot about 10 years ago we had a chance to buy. We used to build homes for a living. This house was in frame stage, so we got to pick out everything, which is nice. I think it's about 3700 sq.ft. Some days, I can barely walk up the stairs. Our neighbor built after us, and they put in an elevator. Just in case, they never want to move again. I dread that, but I know my daughter and son=in=law will be a big help and we always get a moving van with a couple of big guys. My husband has had two back surgeries and we don't need a third. Today is a good day for me. I feel like I could get on an airplane and go somewhere. Yesterday was terrible. I think it was the storm coming in. I sure hope Pete gets to keep in home! That would make his life so much better, especially since it's all set up for RSD. I can't imagine the stress he is under. It's wonderful all the support he is getting. Sleep well my friend. How are you doing in that area? Sorry about your head getting warm. I think I get overly warm too, I'm all broke out on my scalp, those little red dots. And in my ears too. Honestly, I hope the disorder get the exposure that it deserves, and we deserve. Take care, your dessert buddy, loretta |
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"Thanks for this!" says: | Dew58 (07-01-2009) |
07-01-2009, 09:38 AM | #12 | |||
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The blurriness and burning,itching eyes is what I have experienced concerning my eyes. I purchased Optive Lubricant Drops;Moisturizing Dry Eye Solution. It has helped me. I see the PM doc on 7/7/09.
I will inquire about my eyes, and the increased sweating of my head,neck, and face. It is not only sweat, it feels hot...actual cool washcloths bring relief. I don't think it is the Cymbalta. I have been on Cymbalta for 5 yrs,now. This started with the new meds are OpanaER and Tramadol IR. Thank you for your replies..love you, my buddies!
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. A Positive Attitude Will Assist Me Toward An Active Life, Once Again . WC Injury 03/24/07;Two Right Knee Surgeries on 5/22/07 and 01/16/08. Surgeons and Physical Therapists ignored my concerns of burning pain, swelling, and no improvement and getting worse. Diagnosed RSD/CRPS I/Sympathetically Mediated Pain Syndrome/Chronic Pain on 06/2008 by family doc;on 08/2008 and 12/2008 diagnosis confirmed by two WC PM Doctors: Both legs;hips; hands; and spine effected by this culprit. SSDI granted 01/2009. |
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