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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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Getting ready to go into Flare mode and I need your prayers. The snowstorm, and all the excitement of having a birthday and finding out that I am going to be a grandma has just started me into a flare....I am worried about getting my refills this week because there is another snow storm on the way AND we are in the single digits...I hardly ever whine on here, but I know you all understand...Love to you all and thank you for all the support..
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SO sorry.. hang in there!! Love, KS.. ![]() |
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Cindi
I will cer tainly lift you up in prayer,,Im sorry to hear about your flare,,im in a deep one too,as well as quite a few others who are on this site that i've talked to lately,,,May the lord bless us all and bring healing and peace to us,,,,,bobber,,,,,,,p.s ,,,,,my mom lives in W.Va,,and they are getting hammered with snow for the last couple of days,,,,Stay warm,stress free,and in prayer,,,,your buddy,bobber |
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I am so sorry. We all feel your pain. I pray the Lord comforts you during this time. Drink a cup of warm (decaf) tea, and listen to some music soothing to you. I found this website... lastfm.com if you put in 'sleep music' it comes up a sleep channel and it has earth sounds.. it is very very calming. I was very suprised. And you can type in any other artists you like. Music has always been calming to my ears, but make sure your body responds in a calming way, not all 'calming' sounds or cds are calming for everyone!!!
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#5 | ||
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rent some funny movies for the kids. turn the fireplace on and have a little Dom, we don't have RSD so we can have it. I would like some of our vacations that I don't have in an album yet, and finish that project-it would be so much fun. Have Michael bluble on and other favorite CD's. Now reality,could you call in for refill and it would be ready when someone is able to get out? Does the Pharmacy have a delivery service to patients. Are you presently taking an anti-anxiety med? They work well on the sympathetic nervous system thus lowering pain level. The anti-depressant med like cymbalta does the same-lower anxiety thus lowers pain meds. Some towns have Pick Up and Delivery Service. That would be in the yellow pages. Take care, I'm staying in, I'm in a flare too Cindi. I have a lesion on the back of my leg, last year I had two and they got infected, bad news. I'm also have hot spots. I am totally mobile, except left hand got delayed in treatment so have 50% range of motion. But I can type, cut my own food. I'm grateful. I have terrible headaches. My plan is to have HBOT this summer. My Dr. just opened two clinics that each have a HBOT. So saving up for it now. Hope you get thru this mixed up weather with as little pain as possible.Take care, loretta with soft hugs ![]() ![]() |
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luv, Kathy ![]() |
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#8 | ||
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I am sorry for your pain and I hope today you don't suffer any flares..or for a very long time for that matter!!!! Hugz, k ![]() |
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#9 | ||
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Senior Member
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Kathy - it sounds like you live in a flare - I'm so, so sorry.
What is the date of your appt with Dr. S? Hopefully it is less than one month away, so you are counting the days. Is this your first appt with him? Or are you already lined up for treatment? Do you know that you are going in for a certain ketamine treatment when you go to Drexel in March? Have you tried any other treatments so far - like blocks or lidocaine infusions? How did they work? How about PT or OT to keep things moving? There is a lot of evidence that suggests that aggressive PT can help RSD. My RSD spread to my right leg last year, but I have never stopped moving (I walk as many miles a day as the cold weather permits) and it remains mobile (but really painful). Of course, my original injury wasn't to one of my feet, so I am not walking on a neuroma like some other RSDers would have to do in order to stay mobile - I wouldn't want to say that I could do something as incredibly painful as that might be...however, the motto is "use it or lose it." One thing that I have a real problem with because of the chronic pain is my blood pressure. Have you had yours checked? In the absence of meds yours could be out of control because of your pain - just be careful. Have a good day - the sun is finally shining..hopefully my head will stop throbbing soon..hopefully... Peace, Sandy |
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#10 | ||
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Are you on any anti-anxiety meds? I take Lorazepam 4 1mg a day. they help a lot. You know hot tubs are not good for us. too hot. How long have you had this? How did it get started etc? I used to have the jolts,jerks, electric shocks go thru the body thru my brain. Would scare me to death. During sleep my head would jump right off the pillow. He put me on 3200 mg of neurotin. I hated it but they stopped. If you are on that watch your weight gain. I did change to Lyrica 400 mg. it seem to work better with the pain. I slowly went off and don't have the jerks any more. Do you have a foot tub with jets? that with warm water and epson salts helps the bones! So does the Warm Waxing of the hands and feet. you put the plastic sacks over the hand and feet and then in the soft towel gloves and when it cools it peels right off. That helps the bones too. You can get both at Wallmart or Discount cosmetic stores. I forgot to look where you live. I'm in Arizona, so the winters are nice, but the summers are terrible, especially since I went internal pelvic region. That's why they changed the name from RSD to CRPS. The word Regional applys to the burning pelvic region. Well, I hope you are knee deep in snow. My son in low left this morning for Chicago for his 4 day shift of flying in the north northeast or Dallas. He had a lot of flights he couldn't do last week. Really cold in Chicago. Take care, your AZ buddy, loretta with soft hugs ![]() |
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"Thanks for this!" says: | cindi1965 (02-12-2010) |
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