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Everything posted by summer

  1. I also have low blood pressure, it has times dropped to 85/60 or thereabouts, my Cardiologist who I see for Tachycardia, wants me to eat more salt. Since having my Ileostomy, I have been told to add salt and also a banana into my diet, for pottasium. I constantly feel light headed and sometimes shaky, so I also drink plenty of fluids, which helps sometimes.
  2. I have swallowed a nasal gastric tube recently, or I should say forced to swallow, the tube went through the nose, into the back of the throat into the stomach. I had complications following a Loop Ileostomy, had an obstruction, and it wasn't very pleasant. I was awake during the procedure, wasn't sedated, due to the urgency there was no time for sedation or anything. I'm not too sure though, whether this is similar to what you are going to have. Summer
  3. Thank you all so much for all the good wishes, it is much appreciated. I am starting to get nervous now, only 5 more days to go :emoticon-insomnia: . I think waiting is the hardest, so much to think about, I shall be glad when it is over. I start the bowel prep on Tuesday and again Wednesday, nothing to eat only fluids, so I shall be well and truly exhausted for Thursday operation. I shall let you all know how I get on. Best wishes Summer
  4. Hello everyone, I haven't posted on here for sometime, but do pop in and read the posts from time to time. Next Thursday, I will be having an Ileostomy, hopefully that will resolve some of my bowel issues. I just got back from seeing the stoma nurse, and she has marked the site for the stoma. I wish next week would come sooner, I am getting nervous now, and know I am in for a horrendous week. I have to take bowel prep. for 2 whole days, fluids only, before the Ileostomy. I keep telling myself, this will be the last time, I have to take it. So goodbye toilet, goodbye nausea/v
  5. I am due to have a loop ileostomy in a couple of months time due to slow transit and Colonic Inertia. Does anyone know how we can find out about how this patient is going?, I have tried to email a contact person at the bottom of the report, without success. It certainly would be good if there was a trial on this. Many thanks Summer
  6. Hi, has there been any follow up on this, or has anyone had the oxygen therapy?. It seems a shame that there was no follow up. Many thanks Summer
  7. I am on a waiting list to have a loop ileostomy, hopefully within the next 3 months, and am just wondering how many people on this forum that have had to go down this path?. And also their experiences, pros and cons. I have Limited/crest scleroderma diagnosed in 2007. Many thanks Summer :emoticon-dont-know:
  8. I also forgot to add that I do have a nodule on my lung, but it hasn't changed in size or appearance.
  9. I have never heard of Valley Fever, I live in Australia, and have had Q fever over the last few years. I had a blood test which tested positive for that, but never had any symptoms. I have just looked on the internet to see what Valley fever is, it sounds like the Australian version of Q Fever. I had the health department call me when I tested positive for it a few years ago, asked me whether I had been around livestock and goats. At that time, we were living in an rural area with a lot of acreage, and I do know that goats were living on the land at the time. Strangely enough the doct
  10. Hi Sweet, I have it on my forehead, it comes and goes, weird. When I do have it, the skin on my forehead feels a bit bumpy and thick, and a touch oily. It doesn't peel though. Summer :happy-dance:
  11. Hi Andrea, the rheumatologist is Dr S, who we both go and see. Should be interesting. Summer
  12. I also have a nodule in the lung, they scanned it every so often, for my sake really, but it hasn't changed in size or anything. My PFT DLCO has also been declining, due to have another PFT next weeks after around 15 months of not having one. Summer
  13. I am applying for disability, and getting my rheumatologist to fill out the necessary paperwork in a couple of weeks. Apparently I will also need to have an interview with Centrelink about all the issues that I am having. Does anyone have any advice for me, and also what to expect? Thanking you all in advance, Summer
  14. Thank you all who responded to my post. I am seeing a surgeon today, about having a possible Ileostomy, so I am hoping today I will know what is happening. I shall let you all know how I get on. Take care Summer
  15. I haven't posted for some time, but I have CREST/Limited Scleroderma, with bowel involvement. I take it that there is a lot of bowel problems with people on this forum, and am wondering, what treatment you have had, and whether you have had to resort to having an ileostomy? Thanking you in advance. Summer
  16. Thank you for letting us know Robyn, it is much appreciated. Celia
  17. I watched the documentary last night on SBS. I was disappointed that they didn't go into more depth about the lady with scleroderma. They barely touched the surface. I don't know whether it was me, but I found that there was more coverage on the other two cancer patients, then the lady with Diffuse Scleroderma. I'm interested to know, what others thought of it. Summer :VeryHappy:
  18. Thanks for telling us the end Amanda, there is no need for me to watch it now. It's like, picking up a novel to read, but someone tells you the end of the story, before you read it. :temper-tantrum: Summer
  19. I'm not too sure, whether I am allowed to post this. Next Tuesday on an SBS one channel on television at 8.30pm, Melbourne time, there is a documentary on TV. It is about 3 terminally ill people, who have basically, been diagnosed with different diseases. One of them is a young lady, with children, who is diagnosed with Diffused Systemic Sclerosis, (Scleroderma). That is basically all I know about this program, but what I can gather by the adverts on tv, it is a sad story, so It may not be suitable for some people, who have just been diagnosed. If anyone requires anymore inform
  20. Thanks for all of the replies; sorry it has taken some time to answer. The good news is, that I only had the jaw pain stiffness for 3 days, now it has disappeared. My cracked lips have also healed. How do our mouths get smaller, with scleroderma? Does it shrink inside or outside or both? Many thanks Summer :emoticon-hug:
  21. Hello everyone, I haven't posted here for some time, but do check in and read posts on a daily basis. For the last couple of weeks, I have been waking up in the morning, with cracked lips, on the sides of the mouth. I do put lanolin on my lips every night, especially the corner areas, but it still doesn't stop them from cracking. I have also noticed that my mouth is getting much smaller these days. This morning I woke up to a stiff jaw, on one side of the face, near the ear. It doesn't hurt if I open my mouth, but does hurt, when I close my mouth, or clench my teeth. It is a weird feel
  22. Thanking you all for your advice and comments. I am still awaiting to receive an appointment, to see a surgeon. I will update you when I have seen the surgeon, about possible surgery. Best wishes Summer
  23. I finally made it down to the hospital to see my Gastro doctor. My bowels and digestive areas, have been terrible for the last 2 years. Numerous times in the toilet, every few days, with nausea, vomiting, cramps, constipation with diarrhea, and also hemorrhoids. I have experimenting with my diet, low fat, high fat, low fibre, high fibre, and also many other diets. I have had Colonoscopy/gastroscopy, last year, all was normal, biopsies and Celiac testing, all fine. So I told my gastro, I had had enough, I have no quality of life left. When I go out, I'm always searching for the toilets, sometim
  24. Finally made it to the dentist, I had an xray taken, decay in the centre of the tooth right down to the roots :temper-tantrum: . I was asked whether I was in any pain, so I said no, only slightly if I eat on that side of the mouth. So, I had it filled, the dentist put a child's block into my mouth, so I could relax my jaw, and even that block was too big :( . The dentist mentioned that I hardly had any saliva in my mouth, which I suspected anyway, so It looks like I have Sjrogren's, I also have dry itchy eyes. Later on in the day, my tooth started to really throb, so I called the dentist
  25. Hi Joelf, It is morning here in Australia, I hope to go to the dentist in one more hour. That is if I can get there. I know I am going to have bowel problems today as well, so I am hoping I don't need to go to the toilet :temper-tantrum: . Also, I need to see my Gastro doctor today, in the afternoon, and have to take my son with me. It is no fun for him, with me stuck in the toilet :emoticon-bang-head: . I'll let you know how I get on. Many thanks Summer
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