| 4 years ago :: Mar 15, 2009 - 10:25PM #1 | |
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I'v read about this treatment called the lightening process thats apparently cured many people with CFS within days! If what I'v read is accurate then the results are just simply amazing but of course im cynical, if it seems to good to be true it ususally is. Just wondering has heard of this process or used it? |
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| 4 years ago :: Mar 17, 2009 - 12:15AM #2 | |
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It's good to hear from you! I haven't heard about this process, but the one thing that I can be sure of is that our insurance won't cover it. I've had a new symptom starting this year that I am afraid signals rheumatoid arthritis because all of my joints are visibly swollen and red--even my toes! They've been taking me down off the Lyrica because they think that there is a medicine that I can take that will improve things without the fun mini-convulsions Lyrica gave me if I took a dose less than 12 hours apart. I was willing to put up with all the crap that came along as long as it kept improving my mobility. I was told that the Lyrica might be causing the trouble with my joints. I don't think so because it is getting worse instead of better--at my age needing to crawl upstairs to reach my bedroom or the bathroom isn't very amusing. I think the main reason we all end up with CFS is simply that the fibro makes us hurt too much to get a deep night's sleep. I tried to tell myself for a few years now that I didn't have CFS ...maybe because I thought I had enough going on with out adding everything else into the mix. I see the pain doctor on the 18th and I hope we can get some things straightened out. I just started moving our family to different doctors--these are in the same extended group my former doctors joined, so we won't have to pay new patient fees or switch our records since they can access them by computer. One doctor pulled a double whammy--told my husband things my son had told her in confidence and spent the visit making fun of our son instead of doing a damn thing to help my husband. When I had to send my son last Monday, she told him he should learn to suck things up and go back to work. He had bronchitis and works in food service at the college. She put him on an antibiotic at least; the new doctor gave him medication for the coughs and told him he had no business coughing on other peoples food. Let's put it this way...I had to bring up doing a stress test last year. She thought she'd done a sleep study on me and I had a machine and that she'd sent me to a rheumatologist for my rheumatoid arthritis. I've NEVER been in that deep a fibro fog. She actually told me she'd just written my health problems off to my being just very nervous. I went to a pain doctor myself; she had nothing to do with it except write on my chart back then not to give me anything for pain because I went through it too fast. 30 Tylenol 3"S per 60 day period and I wanted more. Spinal stenosis, arthritis, degenerative disc, scoliosis, and fibromyalgia. How greedy of me to want a pill every other day. It's hard switching after 20 years, but her group is pretty burnt out. My out of state family has been begging me for years to find someone else. It's hard enough for me when I look in the mirror and see what I've become; the idea of facing someone for the first time is hard for me. I hope that I don't get too much of a riot act for being so overweight or have someone think that my problems are something to gloss over. Maybe seeing someone who hasn't written me off will make a difference. I hope so. Sorry for the rant--I'm just tired of having no energy, no sleep, and too much pain. I find myself wondering what I was thinking if I actually signed up to come back here and go through this stuff. I had gotten out a scrapbook my mother had made us a few years ago so my daughter to be could see more of the family and more baby/toddler pictures of my son so that I could hear her giggle. Having her around through the week is wonderful for all of us. time to crawl back to bed!
"You are letting your opinion be colored by facts again."
'When I want your opinion, I'll give it to you." these are both from my father. |
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| 4 years ago :: Mar 26, 2009 - 11:01PM #3 | |
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Good to hear from you Karbie! I don't think insurance here would cover the process here either but from what I have heard medical care is very expensive in the states. When I was very ill over christmas I missed a letter about my medical card renewal so I no longer have it. With it I had my doc visits and medicines paid for by the government along with any medical costs I could incur. I am lost without it, I am reapplying for it but with the recession I worry the goverenment might want to curtail the amount of medical cards they dispense even though I should be more then eligible for it! Rant away :) Sorry to hear you have been having a rough time of it! I agree with your family and think you should find someone else,it could make a great difference! I know how you feel , not sleeping no energy and the pain, it wears down on us after a time and its hard to find the energy to deal with it when theres nothing left to give. The level of care and attention we get from doctors can make such a difference in our quality of living. I agree about not getting proper sleep being related to cfs, my family doctor thought my problems may have began in my mid teens when I suffered from very bad insomnia for a year, even though it was many many years later after a period of working too hard and not gettin much sleep when I developed the symptoms at the level I have now. Looking back I can see times in my teen years that I recognise having similar symptoms to now, and times when I didn't have any energy at all. Myabe my doctor was right and this was something I have had for much longer then i thought but just didn't recognise. I hope you feel better Karbie! If not be sure to come and rant :) Oh heres the address for the lighning process, http://www.lightningprocess.com (not sure how insert links in this new fangled format) for anyone whose interested or would like to share their opinion on it. I think its based in the uk but I think the seem to have practitioners in many countries around the world. On a lighter note I came across a case of sweet irony. I was talking with an ex of mine who at the time we went out wasn't very sympathetic about my illness,( to say the least!) and I made sure he knew that! He has since had people he knows be diagnosed with fibro and cfs and is now studing nursing and he told me he had to write an essay on the stigmatism of patients with m.e. , needless to say he felt highly guilty and probably will for a long time to come :) At least theres one less person who will judge someone with cfs and instead be sympathetic. Hopefully this little lesson will make him a better nurse, i think for that I have been able to forgive him his previous treatment of me. Funny how these things go :) |
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| 4 years ago :: Apr 27, 2009 - 10:45AM #4 | |
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You sound a lot like me. I hurt all the time now. Nothing helps, not the Rx, not too much asprin. I just sit home, it hurts to walk, even in the mall. The Dr shrugs it off, like I'm telling untruths. Even a walk to the mail box is unpleasant these days. Depression is the worst, I have no interst in anything, it all hurts.... No friends to speak of, they're out having fun, I don't want to go and do, it hurts. Is there any help out there? I don't want to sit in the house alone forever and cry 'cause it hurts. |
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