Beth

Beth’s primary school age daughter was “quite poorly” with Covid in March 2021, experiencing fatigue, breathlessness, and persistent coughing. She developed a secondary infection in her lungs and spent six months going back and forwards to the GP with repeated chest infections, being treated with antibiotics, and being told it takes time to recover from Covid. After six months, Beth requested a referral to a paediatrician, where an X-ray showed a deep-rooted infection in her lungs and inflammation. She now has a treatment plan with three-monthly appointments with the paediatrician. Taking montelukast and using a Ventolin inhaler is helping Beth’s daughter to participate more in activities, both in school and outside school. Managing her fatigue takes planning and affects what they can do as a family. Beth says it’s a relief to have a treatment plan and they “can start to move forwards.” Beth was interviewed in April 2022.

Beth’s daughter was “quite poorly” with Covid in March 2021; she had persistent coughing, shortness of breath, and fatigue. After a month she was continuing to cough and not recovering.  She was back and forwards to the GP where they examined her and told her “It takes time to recover, give it a bit longer.” This continued for six months. Beth was worried about how often her daughter was needing antibiotics, so she started searching for some information about Long Covid in children on social media. Through a Long Covid Facebook group she found information and support which led her to request a referral to a paediatrician. At that point, her GP referred for a chest X-ray which showed there was still a deep-rooted infection in her lungs. She had another course of antibiotics, and a second X-ray a few weeks later showed there was a lot of inflammation in her lungs. She was referred to a local paediatrician.

When they saw the paediatrician, it was explained that Beth’s daughter had inflammation in her lungs, and they were going to try ways to control it to help her cough and shortness of breath. She is now taking montelukast and using a Ventolin inhaler. She has three monthly appointments with the paediatrician to see how the medication is working and repeat X-rays. She also has a paediatric care plan for school. Beth says it’s a relief to have a treatment plan and they can “start to move forwards” and for her daughter to get “the help and support she needs.”

Since starting on the Ventolin inhaler and montelukast, Beth’s daughter has been able to participate in activities more but still finds P.E. lessons, school swimming lessons, and playing with her friends at the park difficult. When she needs to have a break during school P.E. or swimming lessons, she is allowed to take a break to rest. At the beginning, there were times when she would not feel well enough to re-join the classes but more recently, she is able to participate more. Beth says that school has been very supportive and flexible. She uses her inhaler a lot during sports to help her join in because she doesn’t want to feel different from her friends.

Beth’s daughter’s friends at primary school find it difficult to understand why she can’t join in with activities so much and needs to rest. Being an invisible illness, it is hard to explain to young children.

Beth has experienced mixed responses and understanding about her daughter having Long Covid; some people have questioned that Long Covid exists, and she felt at times people thought she was making it up. Since seeing the paediatrician and having her daughter’s symptoms confirmed and an X-ray taken, attitudes towards her have changed. Beth thinks there should have been a quicker referral to the paediatrician and that her GPs were insinuating Long Covid didn’t exist, and she was jumping on the ‘Long Covid train,’ that this was not what her daughter was experiencing.

Beth and her husband have needed to use their annual leave when their daughter has been off school ill. Her husband has no annual leave left to spend time with their older daughter during the school holidays. They know there may be times in the future when they will need to take unpaid leave which would be tricky, so they are thankful there is a treatment plan in place now.

Beth attended a workshop with others in her community about support services for Long Covid patients and was amazed to see how many people attended and had similar experiences to her. Shared experience helped her to know “you’re not going crazy.” She says to others not to give up on their fight to be heard as you know your child and often a mother’s gut instincts about their child are right.

Beth’s eldest daughter is understanding of the impact her sister’s Long Covid symptoms have on family activities and tries to take care of her and reminds her about taking her medication and having her inhaler with her. Beth and her husband work as a team; through needing to plan things more as a family and talk about it “openly and honestly” together, her daughter’s Long Covid has brought them all together more.

Beth’s daughter is slowly able to do more. Beth says she is very resilient, has a “can-do attitude,” and wants to try to do more. Having her inhaler to support her when she has shortness of breath helps her to feel confident. They often don’t know how much she can do with some things – for example, her Christmas dance show which she really wanted to take part in – so they just give it a go. Currently, Beth’s daughter has to miss out on a lot of things outside school; playdates after school are too exhausting for her and for birthday parties, like roller skating, she can only manage for ten minutes. As a family they are constantly managing activities to reduce her level of fatigue so that it has less impact on school.

Since having Covid, Beth’s daughter’s struggles with some aspects of schoolwork like reading or taking longer to write stories.

Beth would like to see support for mental health and wellbeing as well as the physical aspects of Long Covid. She has noticed a change in her daughter’s mental wellbeing and as it continues it is becoming more of a worry. Beth thinks mental health support should be an integral part of the Long Covid services that are offered to people.

Beth wanted other parents to know that they are not alone, and they shouldn’t give up fighting for what they believe in.

Age at interview 36

Beth thinks that a specialist in mental health should be part of the team providing support for young people at Long Covid clinics.

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Beth has seen some improvements in her daughter, who uses Ventolin and montelukast, but is keeping an eye on her for potential side effects including behaviour changes.

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Beth is hoping that vaccinating her 8-year-old daughter will result in less severe symptoms should she catch Covid again (interviewed April 2022).

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Beth says her relationship with her husband has not been affected by their daughter’s Long Covid. They’ve been through tough times previously and this has brought them closer together.

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Beth’s older daughter has been very understanding about her younger sister’s Long Covid, but Beth suspects “there will always be that underlying frustration.”

Age at interview 36

Beth described how her daughter was determined to take part in her drama club’s Christmas show. She has to miss out on playdates and birthday parties sometimes.

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Beth’s annual leave could only be taken at fixed times. Her husband was using his leave to cover days when their daughter was too unwell for school.

Age at interview 36

Beth’s family either live abroad or work full-time so are unable to provide help.

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Beth’s young daughter’s friends think it’s a “made-up thing” and find it difficult to understand why she needs to rest, can’t go swimming or might be feeling grumpy at times.

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Beth and her family worked together to support her daughter by including the children in decisions and adapting their plans to support her daughter’s needs.

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Beth says her daughter’s mental health is suffering as she is not able to do the things she used to do. She says it’s caused anxiety and is frustrated that no one is helping.

Age at interview 36

It was hard for Beth to pinpoint when her daughter’s Long Covid symptoms started.

Age at interview 36