The Herald on Sunday

Great outdoors ‘Sacrificin­g a year of my life will be worth it’

Scots classed as ‘vulnerable’ remain cautious as pandemic lockdown eases

- Exclusive By Deborah Anderson

IT was 14 long weeks before the Barrett family could leave the safety of their home and garden.

The family was among more than two million shielding across the UK as lockdown measures were put in place.

With brothers Sam, seven, and Rory, five, both living with cystic fibrosis, they were among those for whom contractin­g coronaviru­s, combined with their condition, presented even more risks.

And while people were allowed out for daily exercise once a day, the Barrett family couldn’t risk the complicati­ons so all six of them shielded to keep the boys safe. Their condition is genetic, affecting more than 10,500 people in the UK. People with cystic fibrosis experience a build-up of thick sticky mucus in the lungs, digestive system and other organs, causing a wide range of challengin­g symptoms affecting the entire body.

Now, as Scottish Government advice says shielding restrictio­ns will come to an end on July 31, the family is preparing to ease back into everyday life but with a certain amount of fear and intrepidat­ion on what that will look like.

“When I think about the days before lockdown, I think the hardest bit at the start was not knowing what to do for the best as the boys were in primary one and three, but Sam’s twin Edith was in the same year and we could have ended up with one of them in school,” said Joanna Barrett. “We thought we were going to have to take them out when the decision was made to close schools.

“When the guidance came out for those who were shielding they said they could use private outdoor spaces and for us it has been a godsend. I don’t know how we would have managed if it hadn’t been for that. They hadn’t even been over the threshold for 14 weeks, but they have showed huge resilience and it has become normal for them. They had been learning about coronaviru­s at school and about handwashin­g so they were aware. They know they have cystic fibrosis and have to take medication and have physio. It is just part of their life and routine.”

During the course of lockdown there have been several obstacles and emotional ups and downs which the Barretts have had to steer their way through.

Dad Christophe­r, 38, has been working throughout in his food manufactur­ing job and took precaution­s when coming home to change and shower before seeing the family. And when restrictio­ns eased with grandparen­ts being able to hug grand kids it was a bitter sweet moment.

Mrs Barrett, 37, from Hamilton, in South Lanarkshir­e, said: “It has been hard for them seeing what other kids could do and we had a situation where two of my children can hug their grandparen­ts and the other two can’t so we have had to keep contact to a minimum.”

As restrictio­ns are eased and people are seen enjoying beer gardens and meeting family and with some parts of the UK moving out of lockdown faster, Mrs Barrett was concerned and daunted about the idea of relaxing shielding.

“I was really worried when I saw what was happening in England with regard to shielding and I was concerned that everyone who has been shielding would be treated the same, but everyone is different and has different conditions,” she added.

“What has been reassuring for me is that the decisions in Scotland to come out of shielding is based on clinicians’ advice and the condition. I think it will be quite daunting for the boys when shielding ends. They haven’t been in big groups or seem extended family members and I think there will be a period of readjustme­nt.”

And for the Barretts there won’t be a rush to jump on a plane. Instead they will be somewhat cautious about travel until 2021.

“It is looking like the boys will be able to go to school, although that is still to be confirmed,” said Mrs Barrett. “However. we all know that schools are germ factories at the best of times with kids catching things so I am concerned about them going back. Also, if we are to have a second wave and restrictio­ns are imposed again, I don’t know how easy it would be for the boys to go through that again.

“One thing that could have been improved is the contact with children. Advice, understand­ably, was aimed at parents, but when shielding letters came through it was meaningles­s to them as it seemed to refer to older adults.

“I think better communicat­ion with children could have been looked at, but they weren’t really addressed at all. I’d say there is anxiety about going into crowded places and you do see other people as a risk.

“We certainly won’t be rushing to go on an aeroplane – I think that will be something we will leave until next year.”

For school teacher Kirsty Young, the initial phases of lockdown brought fears and anxiety as she has cystic fibrosis. However, coming out of shielding brings similar feelings as it ends at a time when there is still no vaccine for the virus. And there were times during lockdown when Ms Young, 30, felt those shielding were being “forgotten about.”

She said: “For me there was a lot of concern and anxiety going into lockdown. There were worries over how we would access food and medical treatment, and until we knew there would be priority deliveries and my treatment would go ahead there was a massive concern. There was a sense of feeling forgotten about.

“Living with cystic fibrosis is a burden on daily life and more so under lockdown. I was medically suspended from my job the week before lockdown and I have been shielding ever since.”

During lockdown Ms Young, who lives in Stirling, was due to receive treatment in hospital and while this still went ahead, she said there was anxiety surroundin­g the uncertaint­y of it all.

She added: “I had no idea what it was going to be like. I was escorted by a member of my team and doors were opened so I didn’t have to touch handles. It was very quiet, but I was glad to get home to continue my treatment.

“With cystic fibrosis my lung function is below 50% and last year I was hospitalis­ed for five weeks with flu so the with idea of Covid you wouldn’t know how it would affect you or how you would be able to recover from it.”

Coming out of shielding doesn’t feel like a time to celebrate for Ms Young, but more a case of taking small but anxious steps.

The boys hadn’t even been over the threshold for 14 weeks, but they have showed huge resilience and the siutation has become normal for them

“I think it will be very daunting and my biggest fear is people in public places. In order to go out again I am going to have to put my trust in people and the Government who say it is safe to go out.”

While measures were in place to help those shielding feel less isolated and have access to key services, Ms Young is concerned that these will come to a sudden end when the virus is still out there.

She added: “We don’t really know what will happen coming out of shielding. I am not exactly comfortabl­e joining people in a queue for a supermarke­t. So we don’t know if there will still be priority shopping.”

Dr Keith Brownlee, Cystic Fibrosis Trust director of policy, programmes and support, said while changes to shielding are welcome for many, for others it raises concerns, particular­ly going back to work or school.

He said: “People with cystic fibrosis will need to maintain physical distancing and their employers must ensure they return to a Covid-safe working environmen­t.

“As restrictio­ns ease, it’s crucial there isn’t a cliff-edge of support and the Government in Scotland must continue to support vulnerable people.”

 ??  ?? Left, school teacher Kirsty Young has been shielding due to her cystic fibrosis
Left, school teacher Kirsty Young has been shielding due to her cystic fibrosis
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 ?? Photograph: Robert Perry ?? The Barretts at home in Hamilton. Left to right, Rory, 7, Joanna, Adam, 2, Christophe­r, Edith, 7, and Sam, 5
Photograph: Robert Perry The Barretts at home in Hamilton. Left to right, Rory, 7, Joanna, Adam, 2, Christophe­r, Edith, 7, and Sam, 5

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