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ISRRT_COVID-19_book

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My relief and improvement were short lived however as after only being at home for a week<br />

my symptoms worsened and GP blood tests revealed the onset of sepsis and Acute Kidney<br />

Injury. I was once again taken to A&E and admitted to the “<strong>COVID</strong>-<strong>19</strong> Ward” in isolation.<br />

Further rounds of I.V. antibiotics, anticoagulants, nebulizers and analgesia continued for over<br />

a week. The respiratory Consultant performed an ultrasound chest scan and said he could see<br />

Kerley B lines in both bases, a term I recalled from my student days but had never heard since.<br />

After cannulation for I. Vs became near on impossible due to collapsed veins it was decided<br />

to switch me to oral drugs at which point I seized my chance and asked to be discharged as<br />

the loneliness in isolation on the <strong>COVID</strong>-<strong>19</strong> ward was becoming very difficult. I was<br />

surrounded by patients with dementia, who were obviously confused and distressed and<br />

cried out during the night, sleep was impossible and it was very upsetting to hear. The food<br />

was very limited, there was a shortage of fruit that was attributed to the lockdown restrictions<br />

and the lack of healthy options was not conducive to a speedy recovery.<br />

I managed to convalesce at home for almost 3 weeks until my blood test on Christmas Eve<br />

morning revealed a very high potassium level and reduction in renal function. A call from the<br />

out of hours General Practitioner (GP) doctor insisted I attend the Medical Assessment Unit<br />

some 40 miles away. As Christmas day arrived, the staff hurriedly treated me so I could at<br />

least spend most of the day at home. I suffered many long-term effects, cardiac arrhythmia,<br />

tachycardia at rest, chest pain shortness of breath and dysphagia. I continued to try to build<br />

up my stamina by walking, gradually increasing the distance despite the ongoing fatigue.<br />

I was absent from work for a further three months, resulting in the feelings of isolation<br />

returning, before an Occupational Health assessment allowed me to trial a phased return to<br />

work. As happy as I was to be returning to some form of normality I continued to struggle<br />

with fatigue, chest pain and shortness of breath exacerbated by the fit tested masks and the<br />

visor I had to wear. Communication with patients and colleagues was very difficult and<br />

exhausting initially and still can be a challenge today.<br />

My Rheumatologist insisted my GP refer me to The Long <strong>COVID</strong>-<strong>19</strong> Clinic for support and<br />

treatment of my ongoing chest pain, cardiac arrhythmias and breathing issues. I had all the<br />

pre referral tests done back in February 2021 and received a letter to say there is a long<br />

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