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YFChoice

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About YFChoice

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  1. It's been awhile since I've been on so I thought I'd pop in and see what's going on. Some interesting topics. I can personally say I have no bra problems but then I am a guy, so that's a huge relief. Just a quick note....I've had systemic sd...is that what it's called now?...for 28 years and my wife has had it for about 16. We just celebrated 10 years of marriage. People think I'm strange when I say I'm glad I have scleroderma, but If it hadn't been for this roller coaster disease, I never would have met the love of my life. We're celebrating now by being grandpa and grandma to 3 and
  2. This is one of those questions that I don't like to entertain. It is a very thought provoking one and sure makes you think. But in my 27 years with this illness (and lupus) I have never done the "what if" game. SD is such an unpredictable disease and there is no set pattern as to the way it progresses, or not. It has worked, for me, to have the attitude that I will be able to handle EVERYTHING scleroderma throws at me. It has worked. Of course I have done plenty to prepare myself for whatever happens -- eat right, take my meds, workout (body, mind and soul), laugh, enjoy life. And I kno
  3. Hey Razz........I'm sorry for your loss. Hang in there.
  4. Sarah.......I've had SD for 26 years and my wife has had it for 15 years. I still hike in the mountains and ski and snowshoe. Sometimes I'm a cyclist. My wife also plays golf. We still work and play. I am 52. I know more about SD than it knows about me. I refuse to give in, give up or give anything to this disease. So, learn all you can. Take what works for you. And, by all means, run that marathon in February.
  5. Amanda, you are so right. Having had SD for 26 years, I have learned so much about myself. I have learned that I am much stronger, mentally, physically, spiritually than I could ever have imagined. I have learned to live each day to the fullest, to not sweat the small stuff, and to embrace family and friends. My joy in life is to have Sunday dinners with my sons and wives/girlfriends. My "job" in life is to be "Papa" to my 2 and 4 yr old grandsons. But my love in life is my wife of 10 years, who also has had SD for 15 years. There is something special when you don't have to explain all
  6. Hi lotokids. I live just down the street from you in Sandy. My wife and I both have SD. She's had it for approx 15 years and I've had it for 26 years. The pft test is an absolute must. We both have lung issues and get tested every 6 months. I have been on celebrex and prednisone a long time. The 5 mg of prednisone I take is something I've done for years. The celebrex is a lifesafer for me. I've also added lyrica to my med cabinet. Also prilosec. To me, it's about quality of life. Yes, some meds can cause problems (ALL meds can cause problems) but SD can cause problems too. So if I
  7. Razz, you must be lurking in my house and watching me. I have brain fog all of the time. But my wife doesn't. Must be payback for something I've done. I found that if I slow down a little and take a moment to think before I talk, I can sometimes come out of the fog. Now if we could only get our politicians to quit misthinking AND quit misspeaking!!!!!
  8. Hi Sweet.....I have SD (26 years) and lupus. My doctor put me on 225mgs of Lyrica for pain and I love it. I take it about 9:30pm (I don't go to sleep til midnight). I sleep much better now, and, even if I get up in the nite (to take the dog out) I'm able to drift back to sleep. Before, if I woke up, the odds were pretty good I wouldn't get back to sleep. Plus the pain has for the most part been kept at bay. I have had no side effects at all. When I was first put on it, I took it in the morn and was a zombie all day. So I switched to at nite where being a zombie is not such a bad thing.
  9. Razz......my exercise routine prob won't work for you, but I'll tell you anyway. By the way, you're right.....it is amazing the way you feel once you start a routine and stick to it. It becomes a part of your day and it's sorely missed when you have to pass on it once in awhile. Anyway, I do weight training. Even with my rebuilt arm, I find that weights make me feel good and make me look good (at least that's what my wife tells me, but she could be pulling my leg). I also like to hike in our Utah mountains. I can't wait for winter cause then I get to snowshoe and ski. I have given up cy
  10. Congrats Razz.........Now I have a big question. When I buy my copy (and I will) can I send it to you and have you autograph it so that, years later, when you become another James Patterson, I can say to my friends, "Ah, I knew her when she was just one of us."? Seriously, you deserve all of the platitudes for a job well done.
  11. So I called my pulm.doc and left a message voicing my concerns. I've been on pred forever....usu. in the 5-10mg range....and I've been on 70 before for months. So I'm well versed in this good/bad drug. I've also done the cyclophosphamide thing, tho only in IV form and not pill. Anyway, he called me back and we talked for 10 minutes. He decided on no action now, we'll do the PFT test again at the end of the month. Then, we would look at the results and decide what action to take. He even suggested that if need be, we can do the cyclophosphamide without the pred or maybe a lower dose. He said he
  12. Karen......I could make housecalls to Long Island, but since I live in Salt Lake City, I'd have to charge you a bunch for the outcall.
  13. Well, I went back to pulmonary doctor, got my prescription for the cyclophosphamide, prednisone and some antibiotic. They're sitting on my kitchen counter, staring at me. I'm getting over a chest cold (ignited by my bronchoscopy done 2 weeks ago) and so I'm supposed to call back on Monday. If I'm better, I will then start. Interesting. The last 3 times I did this, I had no reservations. But then I wasn't taking the drug combo I'm going to take this time. Honestly, I'm more bothered (not worried) about taking 60mg of pred every day for 3 weeks. I know what it's going to do. Not looking forward
  14. First of all, Karen, think about changing your pillows. My wife (who also has scleroderma) and I went to a local bed and bath store and bought the Therapedic pillows. They're a bit pricey, around $100, but well worth it. They conform to you head and neck. We were able to get rid of all of the other pillows and use just the one. She got the small one and I got the large. Also, look for one of the many different herbal bags that you can find (like the rice bags).....probably also at this store. They come in different shapes so as to conform to your shoulders or neck or both. They can
  15. After 26 years of having SD and lupus, I can now say that I am in a better place than ever before. Having a potentially debilitating and/or fatal disease forces you to change. It forces you to look inward and find out what kind of a person you are. That can be scary. Many people won't or can't do it. I think they change for the worse. They don't deal with the disease either well or at all. That decision decides how others look at and treat them. It's a decision only you can make. Only you can decide how you're going to live your life. And you do have to consider influences of daily l
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