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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
So how about creating a WMG as in 'World Mental Grid' to do mental-crunching by? Well, sending mine of those to Maggi as I crunch WCG WUs...
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
Thank you andzgrid
- yes, there are quite a few people that are in need of the benefits of Mental Crunching. Your idea is excellent. And I'm pleased if you have sent maggilove your prayers and/or thoughts - and a tangible - sort of - thing like an e-mail will be received as a gift in maggilove's end. Thank you for caring ♥ it is the first encouraging mail we have had from her ♥ |
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RCC_Survivor
Veteran Cruncher USA Joined: Apr 28, 2007 Post Count: 1337 Status: Offline Project Badges:
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Under ideal conditions cancer is difficult, but with a single parent and a child it can be overwhelming.
----------------------------------------Did I remember correctly that Maggi is a single parent with a child? If so, how is the child doing?
Be kinder than necessary, for everyone you meet is fighting some battle.
Please join the team The survivors ![]() Bilateral Renal, Melanoma, and Squamous Cell cancers |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
rcc, as far as I know, Maggi's son Tom is a teenager or young adult.
However, Tom, as I understand it is an autist, and that complicates matters under normal circumstances and certainly complicates matters more under these circumstances. Let us hope that the shrinkage of Maggi's tumor will continue. And, please, if any of you can spare a minute, Maggi will be pleased to hear from you: maggi@mbee.co.uk |
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RCC_Survivor
Veteran Cruncher USA Joined: Apr 28, 2007 Post Count: 1337 Status: Offline Project Badges:
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If Tom is entirely dependent on Maggi that is quite a burden.
----------------------------------------I'll throw in some extra prayer for Tom.
Be kinder than necessary, for everyone you meet is fighting some battle.
Please join the team The survivors ![]() Bilateral Renal, Melanoma, and Squamous Cell cancers |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
We heard from Maggi again, and as she writes as the subject for her e-mail:
No news is not always good news... Maggi tells: Hi All Many thanks again for your kind thoughts, prayers and messages... please keep 'em coming. Life has been something of a nightmare since I last wrote. I had my chemo session on 14th as planned, and sadly this allowed the cellulitis to once again tighten its grip. I developed a fever resulting in rigor a couple of nights after, and the Intermediate Care Team (ICT) nurses began monitoring me with daily home visits. The antibiotic course was extended again, and things didn't appear to be progressing too badly... until Sunday (19th). My friend arrived in the morning and, unusually, had great difficulty waking me. The slight tremor and twitch I had developed of late had escalated to the point where I could not swallow or hold anything... I picked up my coffee and promptly deposited the scalding contents down my front and the bedroom wall as I "twitched". I then had to be half carried to the bathroom to deal with the scald, as my legs would not support me, even with the aid of my walking frame. My friend rang the ICT and was advised to call 999 immediately. The operator wrongly thought I might be having an epileptic fit, and stayed on the line until the ambulance arrived. Rather than admit me to hospital at that point, the ambulance crew summoned a doctor to the house. After he had examined me, a nurse was instructed to take some blood tests. My kidney function was way off kilter, and my inflammatory markers sky high. After lots of to-ing and fro-ing by various professionals, it was decided initially that I should be admitted to the cancer hospice for investigations and observations, but my condition was determined to be too acute, so I was eventually hospitalised that evening. Most of that is a blur to me (I don't remember the first ambulance crew at all), and I recall virtually nothing of the next two days, when my brain was on the planet Zog. I was aware of faces looming, accompanied by voices shouting "Maggi, can you hear me?", but little else except for the hypo when they struggled to get my blood sugar out of the critical zone. However, with some IV fuids and antibiotics, things began to improve. By the weekend, I was able to wash and dress myself again, and use the bathroom rather than a commode. There was talk of my being allowed home on the Tuesday, except that I was suffering unexplained breathlessness. This was relieved by oxygen, yet my saturation levels were not low enough to warrant prescribing oxygen for me at home. The explanation manifested itself in the wee small hours of Tuesday morning, when I suddenly began vomiting copious amounts of blood. I bled out more than three pints overnight, so had to endure another transfusion. IV drugs were administered to stem the bleed, and a new IV antibiotic prescribed by the Microbiology department after they did some cultures (at last) re the cellulitis. I was finally allowed home on Saturday afternoon, with orders to take things very slowly, as my blood count is still very low. All medical appointments have been cancelled for the next two weeks to allow me to rest and be sure the infection is completely beaten before resuming chemo. Mags xoxox Maggi's e-mail is always open Please send your encouragement, thoughts, music, pictures, poetry, daily occurrences with your dog to maggi@mbee.co.uk |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
Maggi has sent us a status report Dear all Thanks once again for your messages, photos, video clips etc... they are a real help in keeping my spirits up, so do please keep them coming. Since I last wrote, I have had yet another mini-break, courtesy of the NHS. I retstarted my chemo a couple of weeks ago, and this time had a very nasty reaction, possibly because the weight loss means the dose is more concetrated. I called the treatment centre after throwing up continually for two days and developing a temperature and a rash on both legs. This time, I was ordered to report to the oncology department at the main county hospital 30 miles away. This meant no visitors, but at least it is a tad more civilised there, with pay-to-watch TV at each bed. I stayed for three days, whilst they pumped me full of IV antibiotics and anti-emetics, along with a few units of the red stuff, as my blood count had not recovered again and I was severely anaemic. For the blood transfusion, I had three cannulas in the space of half an hour as the first tissued and the nurse went through the vein with the second - my arm had a swollen mass the size of a tennis ball, and is still black and blue. Thankfully, the doc that put the third in did an expert job. I skipped chemo last week, as the rash had not gone completely. I am recovered now and due to have my next dose tomorrow. I am rather nervous, though I know the dose is to be reduced. Please pray for me or send positive vibes, whatever is your thing... the nausea and the inability to eat are the worst aspects, and I could really use all the help I can get with those. I am also experiencing some pain since they stopped one of the more effective painkillers, as it was thought to have contributed to the internal bleed I had. I am seeing my hospice doctor on Thursday, and praying that he will come up with an effective alternative. Good news re the broken metatarsals... went to the fracture clinic last week... x-rays show they are healing nicely, and I now have permission to drive. God bless Mags xoxox As Maggi writes, she appreciates our e-mails, videos, photos whatever distracts her and makes her feel that we think of her. Don't be shy even if you don't know Maggi. She doesn't mind a "cold call", so why should you? Please send your thoughts, prayers and words and greetings, anything to: Maggi Loveland maggi@mbee.co.uk ![]() |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
Maggie sent us an update:
Hi all Thanks, as always, for your emails, photos, links etc. A prompt from our dear friend in Denmark reminded me that it has been a while since I have written. I don't like to bombard you all with constant updates, but it has now been over a month... sorry. Chemo resumed, and a new anti-emetic tablet has eased the sicknes, but wipes me out with drowsiness... but then I would rather be tired than sick all the time. I have now reached crunch time, so I need prayers, good wishes etc more than ever. I am about to leave for the hospital for my CT Scan. Depending on the result, they will either continue with chemo or abandon treatment. Much as I hate the chemo, I need it to continue if I am to fight this demon. In preparation, I spent the day at Walsigham again yesterday. I couldn't stay long enough for the sprinkling, as I had to get home for Tom, but we prayed and drank the water from the healing spring. On Friday morning I have a meeting with various officials from school, Social Services etc. to try to make some decisions about Tom's future. I am going to need a great deal of strengh to get through that. Please spare a thought for me at that time. God bless you all. Maggi xoxox Maggi ♥ asks for all the support we can give her to help her on through each day, and she specifically asks for our thoughts on Friday, where she'll meet with authorities concerning her son Tom's future - and as always she'll appreciate your e-mails, pictures, music, jokes, links, anything, and her e-mail is:maggi@mbee.co.uk |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
We have a new e-mail from Maggi.
Things are not going very well at the moment, so she needs your encouragement more than ever. Hi all I'm a tad depressed at the moment, not least because my beloved uncle passed away after a long illness - funeral was yesterday. News from the hospital is not good - the tumour has grown back almost to its original size at diagnosis. My oncologist thinks this is due to the number of chemo sessions I have missed, and says we should treat it as a new baseline scan and start over. I am to begin a combined therapy on Tuesday (GemCap). They are going to try to insert a PICC line in my arm on Monday. Please pray that the line goes in ok, and that I am able to tolerate the GemCap, so I can knock this demon back into shape. Another complication - I was called in last week for what I thought was a routine ECG, but turned out to be an Echo - seems I have a longstanding pericardial effusion (fluid on the heart). Love and blessings Maggi xoxox May I ask you kindly to e-mail Maggi, enclose links, pictures, music, anything that you would liketo receive yourself, were you in Maggi's situation, please, using this address: maggi@mbee.co.uk |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
Not even the little creature's comforts is Maggi's to enjoy. Please read her e-mail ....
Hi all Thank you for all the lovely messages of support - much appreciated as always. I am especially concerned about Monday because with the repeated cannulas, my veins have all but collapsed, so it is touch and go whether they will be able to insert the permanent line. I need that line. The heat is making me miserable and uncomfortable at the moment. I had hoped to enjoy what is likely to be my last summer outside. However, after being ripped off by a gardener last year (he took a large sum of cash, then took off without finishing the job), my garden is not fit to sit out in. I cannot afford to stump up a similar amount again for another landscaper, and there is nobody I can ask for help with it. Now I cannot even use my pool, which is the one place I am free from pain, because a couple of weeks ago some lowlife broke in and stole my filter pump. It was clearly stolen to order, as more expensive equipment was left behind and, since it had 50kg of sand in it, plus the water, it would have needed two or three people and a vehicle to remove it. The local paper ran an article on it, but to no avail. Here's hoping things get better. God bless Mags xoxox And please keep those e-mails to Magg coming, enclose links, pictures, music, anything that you would like to receive yourself, were you in Maggi's situation, please, using this address: maggi@mbee.co.uk Last time I forgot to mention that "cold calls" are welcome, too |
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