Tha do thaic gar cuideachadh gus an sgeulachd innse
Bho chòraichean gintinn gu atharrachadh clìomaid gu Massive Tech, tha The Impartial air an talamh nuair a tha an sgeulachd a’ leasachadh. Co-dhiù a tha e a’ sgrùdadh ionmhas an pro-Trump PAC aig Elon Musk no a’ toirt a-mach am prògram aithriseach as ùire againn, ‘The A Phrase’, a tha a’ deàrrsadh air na boireannaich Ameireaganach a tha a’ strì airson còraichean gintinn, tha fios againn cho cudromach sa tha e na fìrinnean a sgrùdadh. teachdaireachdan.
Aig àm cho èiginneach ann an eachdraidh nan SA, tha feum againn air luchd-aithris air an talamh. Leigidh an tabhartas agad leinn cumail oirnn a’ cur luchd-naidheachd a bhruidhinn ri gach taobh den sgeulachd.
Tha earbsa aig Ameireaganaich thar an speactram poilitigeach gu lèir anns an Impartial. Agus eu-coltach ri mòran ionadan naidheachd càileachd eile, tha sinn a’ roghnachadh gun a bhith a’ glasadh Ameireaganaich a-mach às ar n-aithris agus mion-sgrùdadh le ballachan pàighidh. Tha sinn den bheachd gum bu chòir naidheachdas càileachd a bhith ri fhaighinn leis a h-uile duine, le pàigheadh air a shon leis an fheadhainn as urrainn a phàigheadh.
Bidh an taic agad a’ dèanamh diofar mòr.
neach-ciùil Julian Lennonmac an rionnag Beatles nach maireann Iain Lennon agus tha a chiad bhean, Cynthia Powell, air innse gun deach dèiligeadh ris aillse craicinn an dara uair.
Air oidhche Chiadain (18 Dùbhlachd), roinn an seinneadair 61-bliadhna teachdaireachd leis an luchd-leanmhainn aige ag innse dhaibh gun deach e tro obair-lannsa air dà raon air a chraiceann, a ghualainn agus a ghàirdean, agus b’ e aon dhiubh sin melanoma.
Mhìnich Lennon gun d’ fhuair e fios èiginneach bhon dotair aige, a dhèilig ris roimhe airson a’ chumha, goirid mus do sgèith e gu Los Angeles airson sealladh air Madainn mhath Ameireagaidh agus taisbeanaidhean eile mar thaic do leabhar ùr.
“An dermatologist àlainn agam [was] am worry a ghlac agus a dh’ obraich air aillse craiceann moile o chionn beagan bhliadhnaichean, agus a shàbhail mo bheatha gu litireil, ”sgrìobh an neach-ciùil agus an dealbhadair.
“Co-dhiù, às deidh dha a bhith dìreach deiseil GMAFhuair mi teachdaireachd bhon Dr Tess, le beagan èiginn tilleadh gu Los Angeles, leis gu robh dà àite agam air mo chraiceann, mo ghualainn agus mo ghàirdean, agus b’ e melanoma aon dhiubh, a bu chòir a bhith air obrachadh cho luath !!
“Mar sin an àite a bhith a’ dol dhachaigh gus mo chraobh Nollaige a chuir suas agus crìoch a chuir air a ’bhliadhna gu toilichte, a’ gabhail fois aig an taigh, chaidh mi air ais gu dìreach gu Los Angeles, às deidh dhomh m ’obair gu lèir ann an New York a dhèanamh, agus chaidh mi gu dìreach bho phort-adhair LAX, gu obair-lannsa. .”
Thuirt Lennon, a bha cuideachd a’ roinn ìomhaighean den aillse craiceann ro agus às deidh obair-lannsa, gun robh an obair-lannsa soirbheachail ach thuirt e nach d’ fhuair e toraidhean an biopsy fhathast agus gum faodadh e a bhith a’ feitheamh gus às deidh na Nollaige.
“An toiseach, tha mi glè thaingeil don Dr Tess agus don Dr Tim, airson a bhith comasach air an obair-lannsa search engine marketing a cho-òrdanachadh cho goirid, ach airson a-rithist, an dòchas mo bheatha a shàbhaladh,” thuirt e.
“Chan urrainn dha duine a bhith ro mhisneachail ann an suidheachadh mar search engine marketing, ach tha sinn uile den bheachd gu bheil an Dr Tim air an latha a shàbhaladh… Mar sin chaidh corragan thairis airson a-nis.”
Faigh tlachd bho ruigsinneachd gun chrìoch air 100 millean òran agus podcast gun shanasan le Amazon Music
Clàraich a-nis airson deuchainn 4 mìosan an-asgaidh (3 mìosan airson buill nach eil nam Prìomh)
Thuirt e gur e an deagh naidheachd mun biopsy aige “an tiodhlac Nollaige as fheàrr a-riamh” ach bha e cuideachd airson cur an cuimhne a luchd-leanmhainn “feuch an toir do dhotair sùil ort fhèin”.
“Cha toir e ach beagan ùine sin a dhèanamh, agus is dòcha gu bheil thu dìreach a’ sàbhaladh do bheatha fhèin, aig deireadh an latha,” thuirt e, “mar sin feuch, air do shon fhèin, do theaghlach is do charaidean dìreach falbh gu do chuid fhèin. [doctor] agus dèan na dh’fheumar a dhèanamh …
“Is toil leam beatha agus tha mi airson a bhith beò airson ùine mhòr agus is e search engine marketing aon dòigh, agus roghainn, a dh’ fhaodadh do àm ri teachd a dhearbhadh.”
Cho-dhùin e: “Tha mi a’ guidhe saor-làithean sona dhut uile agus beatha fhada fhallain… Gràdh dha na h-uile [sic].”
Sgaoil Lennon a’ chiad chlàr aige ann an còrr air deich bliadhna, Jude, ann an 2022.
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A dad who was given lower than two years to reside in March 2022 as a consequence of a uncommon well being phenomenon which slowly hardens his pores and skin has stated he has “lots” of life left.
Scott Nell, 47, from Houghton-le-Spring, County Durham, requires chemotherapy and 250 capsules per week to outlive.
Scott was a wholesome particular person when he skilled uncommon chilly sensations in his fingers in November 2017, describing his digits as white as paper, earlier than he later struggled to breathe and located his airwaves have been “shutting off” if he leant to 1 aspect.
After present process checks and seeing specialists, the backyard designer was identified with diffuse cutaneous systemic sclerosis, a sort of scleroderma, a uncommon autoimmune situation which causes the pores and skin to harden and thicken, can result in severe organ issues and might be life-threatening.
In March 2018, he underwent chemotherapy therapy each month for a yr – now lowered to as soon as each six months – as a approach to assist soften the pores and skin and tissue round his inside organs.
However Scott now faces points together with his lung operate and ache as a result of muscle-wasting nature of the situation.
He was given lower than two years to reside in March 2022 however has exceeded this time-frame and he now desires to lift consciousness of the illness and urge others to push for early diagnoses to allow them to reside longer and spend extra time with their households – which for Scott is his spouse, Charlotte, 48, his 15-year-old daughter Tiffany and his step-sons.
“I used to be initially given lower than two years to reside and I’ve exceeded that already, I nonetheless really feel like I’ve bought lots left,” Scott instructed PA Actual Life.
Scleroderma is a uncommon, progressive autoimmune situation brought on by the physique producing an excessive amount of collagen ensuing within the hardening of the pores and skin, in line with Scleroderma and Raynaud’s UK (SRUK), the main charity supporting folks with the illness.
Round 19,000 folks within the UK reside with the situation which might cease components of the physique from functioning correctly and, in extreme instances, trigger bodily incapacity and be life-threatening.
Additionally it is frequent to have one other situation referred to as Raynaud’s alongside scleroderma, which causes the small blood vessels within the extremities such because the fingers, ft, fingers or toes to be over-sensitive to modifications in temperature, chilly circumstances and emotional stress.
Scott stated he began to expertise uncommon sensations in his fingers in November 2017 – which was later identified as Raynaud’s.
“There was one thing occurring with my fingers and one event, I used to be working and laying a drive and it was snowing nevertheless it was so chilly, I couldn’t stand it,” he stated.
“I took my gloves off and my fingers have been white, like sheet-of-paper white.
“I used to be actually fairly shocked and I had to enter the automotive and warmth them.”
Scott stated he then seen fluid showing beneath the pores and skin of one among his fingers and he additionally felt “excessively drained”.
He added: “I awoke one morning and I couldn’t straighten my legs and arms out, it took me a couple of minutes.”
This prompted Scott to rearrange a GP appointment the place they took stool and blood samples.
The latter got here again with a marker referred to as SCL70, an antibody which is current in round 20 % of sufferers with scleroderma, in line with the NHS.
“My spouse and I googled it however we by no means thought (scleroderma) have to be what I’ve bought,” he stated.
Scott then had an appointment to see a rheumatologist who discovered indentations on his fingertips which have been producing calcium deposits.
“They have been pushing away out of my fingertips… the pores and skin was so tight you couldn’t seize something and he stated I had scleroderma,” Scott stated.
He was taken for an X-ray of his lungs, because the situation can impression these organs in some ways, however no points have been discovered on the time.
Months handed and Scott was given treatment to assist relieve his preliminary signs, however in March 2018, he discovered he was struggling to breathe.
“As quickly as I leaned over to 1 aspect, my airwaves simply shut off,” he stated.
“I used to be attempting to sleep sitting up and it simply bought to some extent the place I couldn’t breathe.”
Scott was given morphine and located this improved his capability to breathe.
He was urged to attend an appointment with a specialist in Newcastle who was capable of formally diagnose him with diffuse cutaneous systemic sclerosis, a sort of scleroderma.
He was suggested to endure chemotherapy therapy as he stated the chemical substances included might help soften the pores and skin and tissue across the inside organs.
“It’s not intensive, similar to for a most cancers affected person, and I misplaced little or no hair,” he defined.
“I had chemotherapy each month for a yr to start out with they usually lowered that to as soon as each six months, which is the place I’m now.”
Alongside this, Scott now takes round 250 tablets every week, saying it’s a “complete association”.
A few of this consists of morphine, which helps together with his respiratory and ache, paracetamol, of which he takes round eight tablets a day, and antibiotics.
“I just about reside in a specific amount of ache,” he stated.
“I’m on tablets to cease me from having diarrhoea, tablets to cease me from being sick, immuno-suppressing tablets.
“It’s quite a bit. I believe a few of my tablets are to fight the ill-feeling from different tablets.”
Scott additionally wants to make use of oxygen tanks when he’s awake to assist him breathe.
“It’s troublesome to sleep and I sleep on the couch, it’s very uncommon that I really sleep with my spouse, as a result of there I can place myself so I’m not tossing and turning,” he stated.
The illness has additionally brought on Scott’s pores and skin to tighten.
“Sclero means hardening and derma means pores and skin – so hardening of the pores and skin,” he defined.
“It could actually produce a number of calcium deposits, which might generally trigger scarring and disfigurement.
“I believe as a result of I used to be identified actually shortly it saved the most effective a part of my look – I believe really the tightening of my pores and skin most likely took a couple of years off me.”
Scott stated his spouse, his daughter, Tiffany, from a earlier relationship, and his step-sons discover the illness troublesome to course of.
“My line of thought is their struggling, not mine,” he added.
“It’s not going to be a fast course of for me, I do know I’m going to endure for a very long time and the top.”
Scott suggested those that might have obtained a analysis “to not panic”.
“In case you assume you might need scleroderma, don’t again off if a health care provider suggests it could possibly be one thing else,” he stated.
“Anybody who has a confirmed analysis, I might say to not panic and there are new therapies popping out on a regular basis.
“Early analysis is the important thing – the earlier you’re on therapy, the longer you need to reside, the longer you’ve bought with your loved ones.”
From reproductive rights to local weather change to Huge Tech, The Impartial is on the bottom when the story is creating. Whether or not it is investigating the financials of Elon Musk’s pro-Trump PAC or producing our newest documentary, ‘The A Phrase’, which shines a light-weight on the American girls combating for reproductive rights, we all know how essential it’s to parse out the info from the messaging.
At such a essential second in US historical past, we’d like reporters on the bottom. Your donation permits us to maintain sending journalists to talk to either side of the story.
The Impartial is trusted by Individuals throughout your complete political spectrum. And in contrast to many different high quality information shops, we select to not lock Individuals out of our reporting and evaluation with paywalls. We consider high quality journalism ought to be accessible to everybody, paid for by those that can afford it.
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“Strips of tofu coated in a satay-style batter, dipped right into a crunchy peanut and cornflake crumb for the last word crunch, then served with a zingy slaw to chop by way of the saltiness and produce the dish to life,” says Christina Kynigos – behind the favored account @veryhungrygreek.
1. Preheat the air fryer at 200C for five minutes.
2. Slice the tofu into 6 blocks and put aside. In a bowl, combine the crushed cornflakes and peanuts with the curry powder and a few salt and pepper. In one other bowl, mix the peanut butter with the recent water till creamy, then combine within the soy sauce and sweetener.
3. Dip the tofu blocks into the peanut sauce, then into the crushed cornflakes, saving any leftover peanut sauce for later. Spray the air fryer base with oil and place the tofu fingers in it. Air fry at 180C for 8-10 minutes, till golden and crispy.
4. In the meantime, combine all of the elements for the zingy slaw collectively, including a superb pinch of salt. Serve with the tofu fingers, with any remaining sauce for dunking.
‘Wholesome Air Fryer Feasts: Quick, Simple, Excessive-Protein Recipes in 30 Minutes or Much less’ by Christina Kynigos (HQ HarperCollins, £20).