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Amanda Thorpe

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About Amanda Thorpe

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  1. That's great Dimarzio! When we find something that works we should really take that victory. Once upon a time, I was taking a massive dose of pregabalin but after I cut down another medication, I realised that pregabalin was exacerbating neuropathy. One of its side effects is actually neuropathy, ironic given that's what it's often prescribed for and that's why I take it. If I stick to a low dose I'm fine but if I increase it...woe betide me! Like Jo said, what works for one doesn't work for another but then we're all so marvellously different, aren't we? Alas, if you were all like me.
  2. Hey there MAT54 Welcome and you can't post too much but you can ask questions we can't answer, don't worry, though, when that happens we ratchet up the support. I have found the approach to bloodwork very different here in the UK to that in the US and ultimately it's not the most important issue. I'm a patient at the Royal Free, under Prof Denton's team and they're the experts for sure but my ANA SCL-70 status has never been discussed and they have been the only hospital to test my antibodies. I only know what it is because I have asked. I was diagnosed in 2007, my ANA only became posi
  3. Hey there Dimarzio After I read I had to comment, yeah I totally have to get in on this! Just a suggestion but have you thought that maybe your wife is scared witless at the thought of you being seriously ill? Fear makes us angry and when she exploded at the prospect of reading in detail what your lives could look like if you were, fear of loss may have been fuelling her anger. She seems in real denial and we've all been there. Who discovers one morning that they can't straighten their elbows, shows their husband and then both goes to work... me and my husband who were both in la la l
  4. Hello Mando I had LVBBB too...do I still have one...I dunno! Anyways, you're right it can be caused by connective tissue issues. I began with LVBBB in 2009, at that time my ejection fraction was 50%. Come 2010 and I also had myocardial fibrosis, ejection fraction of 32%, global disfunction (both sides of the heart affected) and serious heart failure with a 2 year life expectancy. Well lookit that...it's 2017! I had a bi ventricular ICD implanted and here I am today. I did the heart monitor and it was a waste of time for me, the right & left heart catheterisation and hear
  5. Hello Simon I hope that you continue to improve and you certainly seem to have a good attitude to your situation. Take care and keep posting.
  6. Hello Stace38 Welcome to the forums. I was 39 when I was diagnosed after rapidly progressing symptoms. Within 6 months I went from working to sitting on my couch, just about able to wipe my own butt and I am not saying that as an expression but as a literal statement of fact. You'll be pleased to know that I now have no problem attending to my own derriere but I can no longer work or walk. Swings and roundabouts, as they say. Anyways, Prof Denton is an immensely likable chap, very patient centered which is so important. Scleroderma is an odd disease because it affects everyone so
  7. Hey, there everybody with Raynaud's, which is most of you, could you please detail an attack for me? I'm interested in what it feels like, how painful is it, what is the pain like, is it a burning sensation or pins and needles etc, how long does it last and anything else relevant to how it feels. I'm not interested in what sparks it off, I know all that but what I don't know (I think) is what it feels like. If you're wondering why I'm asking, I'm trying to determine whether the pins and needles (think of the sensation being inflicted with knitting needles rather than little needles!) I am
  8. Hey Trena, just popping in to add my experience. My ANA only because positive around 2014 but my SCL-70 has always been negative, however, I was diagnosed in 2007 with diffuse scleroderma. It's all about the symptoms and test results (ECHO, lung function) so you see blood work isn't even a secondary issue. Hope this helps and take care.
  9. Hey Khohu welcome and shout out to your mum! Scleroderma is a tailor made disease, every one gets a different version of it. I have diffuse systemic scleroderma and although there are a bunch of symptoms I could have, what I do have will be very different from someone else with the same variant. My disease took 6 months to move my from my work desk to my couch and I never went back. I can't say things have got better, they've got a little bit worse every year since but I'm still here. Your mum could already have been living with scleroderma for years so she's doing well and it's
  10. Hey Bek, welcome and you're right, you are a ticking time bomb, we all are if you think about, one day we all go BOOM...GAME OVER! CREST aka limited scleroderma is generally slower in onset, slower in progression with a better outcome than the ugly sister, diffuse scleroderma. Nevertheless, you should be under the care of a scleroderma expert, however amiable your scleroderma may be now it has potential to be a wily critter which is why you should have tests (ECHO, lung function) to ensure nothing is going on and if it is, that treatment is swift. You will always live life normal
  11. Hey Mando, this is the first time I have heard of cardiotoxicity from hydroxycloroquine and you're right, the articles are scarey...sudden death, biventricular cardiomyopathy...oh my! Of course it's serious, I get that. For different reasons, I had my own stomach dropping moment back in 2010 when the damage had been done by the time it was found and I was looking at 2yrs without successful treatment. Where you are now is all uncertainty and fear but you're doing what you can for yourself by ensuring your medical team is on the ball. Until the ECHO results you won't know where you stan
  12. Hey Simon, even if your function never improved you can still live. I had a friend who lived with 50% function for years! I say "had" because we lost touch. However, I've no doubt that your experience will be one of improvement that you'll be able to share with us. I missed out on cyclophasphamide because by the time the fibrosis was found I was past the inflammation stage and into the oh, dear, too late stage. Mine is myocardial fibrosis, treated with implantation of a bi ventricular ICD. The wonders of modern medicine. Take care.
  13. Hello Debs I am late to this... Prednisone is a steroid, methotrexate is a DMARD disease modifying anti rheumatic drug, what has one got to do with the other? I don't get holding off on anything to slow down the immune system and therefore the scleroderma, like a DMARD or an immunosuppressant such as mycophenolate. Maybe see a scleroderma expect? Of course I am not a doctor and I know nothing about your disease, I just don't get holding off on a disease modifyer waiting to see if a steroid works. What happens if it doesn't do you get sent home untreated? Take care and keep po
  14. Dear Janet was here before me, I remember reading her posts and marvelling at her struggle which she was determined to overcome. Janet never gave up and was searing honest throughout. If anyone, particularly a newbie, wants to know how to manage scleroderma successfully, they want to read her story that unfolded through her posts. Janet was so very unique and never will the gap she has left be filled. Miocean, thank you and rest easy, friend.
  15. Hello Quiltfairy I want this! I have a similar thing on my smartphone which starts out great and then crashes and burns! All of a sudden "How are you doing" becomes "Have a tomato", my laptop is even worse, I don't think it understands English, it certainly doesn't speak it. I certainly do! Take care and have fun with it.
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