Guest guest Posted May 20, 2004 Report Share Posted May 20, 2004 In a message dated 5/20/2004 1:21:53 PM Eastern Standard Time, hanna5918@... writes: My doctor didn't understand why it worked but I know it did. I'm really desparate for some relief. I called the neuro yesterday who ordered the test and he prescribed antivert which isn't doing anything but making me more tired. Any ideas? Hi Hanna, I have actually heard this before. People with Chronic fatigue sydrome who have the tilt test done often feel worse for a few days afterwards. I would imagine it would be similar with any patient who has a positive test. They are basically stressing your body when you have the tilt test and since any type of stressor can bring on symptoms in a mito patient, it would make sense that you could feel worse afterwards. I didn't feel well for the rest of the evening after I had my test last year, but I think I felt ok the next day. I hope you feel better! REST until things get better. Malisa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 20, 2004 Report Share Posted May 20, 2004 Has anyone here had a tilt table test? I had the test Tuesday and since then I feel like every symptom I've ever had is back. I am extremely weak and fatigued, my heart races when I move, I have trembling, chills, my skin is itching and tingling all over, nausea and retching, eye pain, and the list goes on. I didn't feel well before the test but nothing like this. I'm tempted to take some leftover prednisone, as I took this in the past when I had bad symptoms. My doctor didn't understand why it worked but I know it did. I'm really desparate for some relief. I called the neuro yesterday who ordered the test and he prescribed antivert which isn't doing anything but making me more tired. Any ideas? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 20, 2004 Report Share Posted May 20, 2004 Hanna You might have been coming down with a virus when you went for the test and now you are battling both. I usually take some extra CoQ10 before or after any test that is stressful. Prednisone worked for me a couple of times and then didn't anymore. I just took a week long burst. You should probably check with the doctor before taking it. I hope you get to feeling better. laurie > > Reply-To: > Date: Thu, 20 May 2004 17:18:17 -0000 > To: > Subject: Feeling terrible since tilt table test > > Has anyone here had a tilt table test? I had the test Tuesday and > since then I feel like every symptom I've ever had is back. I am > extremely weak and fatigued, my heart races when I move, I have > trembling, chills, my skin is itching and tingling all over, nausea > and retching, eye pain, and the list goes on. I didn't feel well > before the test but nothing like this. I'm tempted to take some > leftover prednisone, as I took this in the past when I had bad > symptoms. My doctor didn't understand why it worked but I know it > did. I'm really desparate for some relief. I called the neuro > yesterday who ordered the test and he prescribed antivert which isn't > doing anything but making me more tired. Any ideas? > > > > Medical advice, information, opinions, data and statements contained herein > are not necessarily those of the list moderators. The author of this e mail is > entirely responsible for its content. List members are reminded of their > responsibility to evaluate the content of the postings and consult with their > physicians regarding changes in their own treatment. > > Personal attacks are not permitted on the list and anyone who sends one is > automatically moderated or removed depending on the severity of the attack. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 21, 2004 Report Share Posted May 21, 2004 ---Hi Hanna, I am sorry you are having such a hard time. Your symptoms sound to familiar. I am dx with POTS too. I strongly recommend you drink lots of fluid and increase your salt intake, you really need to keep yourself hydrated. Propel is a good electrolyte drink, which really helps me. They have found that people with POTS have low volume and we need lots of extra fluids esp during a crisis. I also recommend that when you are laying down to have your head propped up on something so you are not always flat. Try and sit up as much as possible. Laying a lot makes your symptoms worse. For POTS I presently take a beta-bloker..nadolol ( this has kept my heartrate down and has kept me from hyperventilating which I did a lot of) Many POTS patients benifit from a low dose SSRI. I take effexor which many can not tolerate. It really helps raise my blood pressure and helps with fatique. Plus I have some depression issues. I take florinif which helps the body retain more sodium and keeps the fluid levels up. I am very dizzy and symtomatic without it. I have also increased my salt and fluid intake. I wear compression hose if I need to stand a lot. It took a while and a lot of trial and error to find the right combination of meds for me. I finally feel like my symptoms are under control most of the time. THe tilt test is a stressor to your body which really affects mito symptoms. I hope you are feeling better soon. I know how awful those symptoms can feel. Hang in there. Dawn In , " hanna5918 " wrote: > Has anyone here had a tilt table test? I had the test Tuesday and > since then I feel like every symptom I've ever had is back. I am > extremely weak and fatigued, my heart races when I move, I have > trembling, chills, my skin is itching and tingling all over, nausea > and retching, eye pain, and the list goes on. I didn't feel well > before the test but nothing like this. I'm tempted to take some > leftover prednisone, as I took this in the past when I had bad > symptoms. My doctor didn't understand why it worked but I know it > did. I'm really desparate for some relief. I called the neuro > yesterday who ordered the test and he prescribed antivert which isn't > doing anything but making me more tired. Any ideas? Quote Link to comment Share on other sites More sharing options...
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