Pete

Pete has granulomatosis with polyangiitis (GPA), a type of ANCA associated vasculitis which has affected his hearing and kidneys. After being well for several years, Pete relapsed in March 2020 just before the first COVID-19 lockdown.

Pete describes himself as a normal chap who is just getting on with life in spite of having granulomatosis with polyangiitis (GPA), a type of ANCA associated vasculitis. He enjoys helping others through a patient support group and being involved in research as a participant and patient partner. From his experience, Pete recommends that people listen to their doctors rather than relying on information from the internet.

At the end of 2011, Pete was a fit 58-year-old who enjoyed hiking holidays with his wife, cycling and going to the gym. He developed a stuffy nose and, over the next few months, increasing problems with sinusitis, facial pain and hearing loss. Pete was referred to ENT (ear, nose and throat) and audiology, where he was fitted with the first of two hearing aids. He recalls the fantastic feeling of hearing the birds whistling and being able to communicate again.

Other treatment included a grommet (tube) implanted in one eardrum to see if it would release pressure. The next day he awoke to find he had Bell’s palsy, a temporary paralysis (droop) of the muscles on one side of his face. Pete says blood tests at that point led to the vasculitis diagnosis and that he was quickly referred to a rheumatologist. During a short hospital stay all his organs were tested and the vasculitis found to be limited to the ear, nose and throat areas.

Pete started taking methotrexate to suppress his immune system. Four months later, he was feeling run down. He developed pneumonia and was admitted to hospital, where it was found that the vasculitis had now affected his kidneys. Following 10 days of treatment – which included a few sessions of kidney dialysis – Pete was surprised but delighted to be told his kidneys had recovered sufficiently for him to go home and complete his course of cyclophosphamide (chemotherapy) as an outpatient.

In 2014 the ear, nose and throat symptoms and fatigue returned. This time Pete phoned his kidney consultant directly. Within a week he had started rituximab, which suppressed his immune system and brought his vasculitis into remission again. At the first signs of a further relapse in March 2020, Pete again contacted his consultant. He was immediately started on rituximab, just as health services were reorganising for the first time as a result of the COVID-19 pandemic. Pete, who is due a six-month rituximab top-up, is currently well and tapering his steroids.

As a retired quantity surveyor, Pete’s instinct is to count things. He reckons he has had over 300 medical appointments in eight years, sometimes including visits to consultants at two different hospitals in a single day. He feels indebted to the raft of people who look after him, including doctors from audiology (hearing), ENT (ear, nose and throat), ophthalmology (eyes), rheumatology (joints) and nephrology (kidneys). Pete notices how everyone seems to gravitat around the nephrologist, his main vasculitis contact, and finds it comforting to know that they all talk to each other.

Pete says that, for people who benefit from medication, “there is life after vasculitis.”

Age at interview 67

Gender Male

Age at diagnosis 59

Vasculitis affects Pete’s hearing. Audiologists regularly adjust the hearing aids that made him feel like a “real person” again.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete finds it “comforting” that the doctors responsible for his vasculitis care “all talk to each other.”

Age at interview 67

Gender Male

Age at diagnosis 59

Pete is reassured that advances in treatment mean life for people with vasculitis “can only get better.”

Age at interview 67

Gender Male

Age at diagnosis 59

Fatigue from vasculitis is like “wearing a suit of chain mail,” but Pete has learned to manage it.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete depended on his wife when he was ill with vasculitis. They now enjoy being “back out the other side.”

Age at interview 67

Gender Male

Age at diagnosis 59

Pete was treated for vasculitis affecting his ear, nose and throat, but it went on to attack his kidneys.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete hadn’t heard of vasculitis before he was diagnosed, but quickly realised it was very serious.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete says that, for people who benefit from medication, there is life after vasculitis.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete is reassured that advances in treatment mean life for people with vasculitis can only get better.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete finds it comforting that the doctors responsible for his vasculitis care all talk to each other.

Age at interview 67

Gender Male

Age at diagnosis 59

Vasculitis affects Pete’s hearing. Audiologists regularly adjust the hearing aids that made him feel like a real person again.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete hadn’t heard of vasculitis before he was diagnosed, but quickly realised it was very serious.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete was treated for vasculitis affecting his ear, nose and throat, but it went on to attack his kidneys.

Age at interview 67

Gender Male

Age at diagnosis 59

Fatigue from vasculitis is like wearing a suit of chain mail, but Pete has learned to manage it.

Age at interview 67

Gender Male

Age at diagnosis 59

Pete depended on his wife when he was ill with vasculitis. They now enjoy being back out the other side.

Age at interview 67

Gender Male

Age at diagnosis 59