Comprehensive medical history through June 2026, combining clinical conclusions,
longitudinal lab data, source reports, and raw tables from the Health archive.
7 Bank House, Cornmarket, Christchurch, Dublin 8, D08DX28
GP
Dr Nada Yasir, Dame Medical Centre
TUH MRN
1300993
Cardiology
Dr Breda Hennessey, Blackrock Private Clinic
Rheumatology
Prof Richard Conway, Blackrock Private Clinic
Current clinical picture
Doctor Brief
Established coronary artery disease
Moderate multi-vessel CAD with coronary ectasia, calcium score 1207.2 AU
(99th percentile), and documented transmural inferior wall MI. LV systolic
function preserved, EF around 65-66%.
Inflammatory arthritis / autoimmune overlap
Relapsing flares since June 2025 with tenosynovitis, effusions, enthesitis,
dactylitis symptoms, heat/stress triggers, and seronegative profile. June 2026
CRP and ESR show no biochemical inflammatory activity.
June 2026 metabolic and biochemical flags
HbA1c 50 mmol/mol (~6.7%), ferritin 618.4 µg/L with normal transferrin
saturation, calcium 2.64 mmol/L and adjusted calcium 2.57 mmol/L with normal
PTH, triglycerides 1.80 mmol/L, bilirubin 28 µmol/L, ALT 56 IU/L, GGT 81 IU/L.
Repleted nutrition markers
Vitamin D 139 nmol/L, B12 511 ng/L, serum iron 24 µmol/L, transferrin
saturation 38%, total protein 76 g/L, and PTH 2.5 pmol/L on 28 June 2026.
Medication reconciliation items to verify
Source documents conflict on two doses: ezetimibe appears as 20 mg in summary
sections and 10 mg in the current medication list; bimekizumab appears as monthly
in the therapy section and weekly in the medication list.
Latest flagged laboratory values
Extracted from the 28 June 2026 blood report source tables.
Diagnosis / medical condition register
Medical Conditions
1
Coronary artery disease
Established CAD + prior MI
Moderate multi-vessel coronary artery disease with extensive atherosclerotic burden,
coronary ectasia, and established transmural inferior wall myocardial infarction.
Left ventricular systolic function is preserved.
Key evidence
Coronary calcium / Agatston score 1207.2 AU, 99th percentile for age and gender.
Possible dermatomyositis + psoriatic arthritis overlap
Onset June 2025 with near-daily, brief relapsing inflammatory flares. The pattern is
atypical: rapid onset around 10 minutes, 1-4 hour duration, heat/stress triggers, and
resolution faster with cold.
Clinical pattern
Episodic hot swollen joints: knees symmetrical L>R; hands/wrists, shoulders, and neck sometimes asymmetrical.
Minimal tenderness and no axial involvement reported in the source summary.
Associated enthesitis, recurrent right forearm tendonitis, intermittent plantar fasciitis, costochondral pain, and episodic dactylitis.
Heat-related non-pitting oedema of hands and feet since December 2025; mild morning stiffness.
Evolving picture includes worsened pain, fatigue and nausea with flares, more muscle pain/inflammation, and more persistent low-grade fevers.
Imaging and ultrasound evidence
Informal ultrasound by Dr Adsurada: right hand extensor tendon tenosynovitis; bilateral knee effusions in subcutaneous tissue; loss of trilaminar plate on right middle fingernail suggesting nail involvement.
Cervical MRI: diffuse disc dehydration; C5-C6 and C6-C7 disc bulging with dural compression but no myelopathy; foraminal cysts contacting/near nerve roots.
SI joint MRI normal with no inflammation or erosions.
Right shoulder MRI: rotator cuff tendinopathy, subacromial bursitis/impingement, and glenohumeral chondral thinning.
Wrists/hands and knees normal; feet/ankles show posterior calcaneal enthesophyte only.
Serology and monitoring
Seronegative profile: HLA-B27 absent; RF and anti-CCP negative; ANA and ENA/dsDNA markers negative; antiphospholipid tests negative.
Coeliac serology negative; C3 normal and C4 borderline low in December 2025.
June 2026: CRP <1.00 mg/L and ESR 2 mm/hr, with no biochemical inflammatory activity.
June 2026 RF <10.0 IU/mL, CTD screen 0.20 ratio, C3 1.330 g/L, C4 0.181 g/L, CK 119 U/L.
June 2026 FBC overall normal, with mildly elevated MCH 33.9 pg and MCHC 36.4 g/dL.
Current and previous therapy
Current: methotrexate 25 mg subcutaneous weekly, started 22 May 2026.
Current: Bimikizumab 160 mg subcutaneous monthly, started 27 May 2026, as written in the source summary.
Previous: methotrexate dose changes between 15 mg and 20 mg weekly; decrease appeared to worsen flares; previous transient neutropenia and thrombocytopenia.
Previous: adalimumab/Hulio escalated from every 2 weeks to weekly with minimal effect.
Colchicine 0.5 mg twice daily was poorly tolerated and did not convincingly help; secukinumab was started April 2026 before change to Bimikizumab.
3
?Avoidant/restrictive food intake disorder
Not formally diagnosed
The source notes that the clinical presentation meets diagnostic criteria for ARFID,
but this has not been formally diagnosed and is not yet integrated into multidisciplinary care.
Dietary pattern
High carbohydrate, low fibre pattern.
Diet described as carbohydrates, cheese, and nuts, with no fruits, vegetables, or meat.
Associated consideration
Possible autism spectrum disorder, not formally assessed.
4
Nutritional deficiencies and metabolic findings
Repleted vitamins; active HbA1c, ferritin, calcium flags
Previous iron, vitamin D, vitamin B12, protein, and PTH issues have been treated or
repleted, but the June 2026 bloods show HbA1c in the diabetic range, elevated ferritin,
and elevated calcium with normal PTH.
Current micronutrient panel
Iron 24 µmol/L with normal transferrin saturation after IV iron replacement.
Ferritin 618.4 µg/L, elevated despite normal transferrin saturation.
Vitamin D 139 nmol/L and B12 511 ng/L after replacement.
Total protein 76 g/L and PTH 2.5 pmol/L on the most recent testing.
HbA1c 50 mmol/mol, approximately 6.7%, on 28 June 2026.
HbA1c increased from 45 mmol/mol / 6.3% in December 2025.
Source clinical note: likely multifactorial, including poor diet quality, weight distribution, and metabolic inflammation.
Iron and calcium/PTH
Serum iron 24 µmol/L; iron saturation 38%; TIBC 63 µmol/L.
Total calcium 2.64 mmol/L and adjusted calcium 2.57 mmol/L, elevated against source range 2.15-2.50 mmol/L.
PTH 2.5 pmol/L within source range 1.6-6.9 pmol/L; phosphate 1.13 mmol/L normal.
5
Gilbert's syndrome
Intermittent jaundice and bilirubin elevation
Pattern
Elevated total and direct bilirubin with intermittent episodes of jaundice.
June 2026 bloods
Total bilirubin 28 µmol/L.
Mild ALT elevation 56 IU/L and GGT elevation 81 IU/L.
AST, ALP, albumin, and total protein normal in the source summary.
6
Attention-deficit/hyperactivity disorder
Formally diagnosed
Diagnosis and constraint
Formally diagnosed at ADHD Doc.
Stimulant medications contraindicated due to cardiac history and cardiologist concern.
Current management
Atomoxetine initiated.
7
Androgenetic alopecia
Maintenance treatment
Current management
Maintained on finasteride 1 mg daily.
8
Structural, urological, and reproductive conditions
Multiple structural findings; no Irish specialist follow-up noted
Left inguinal hernia
Incidental ultrasound finding in January 2024.
2.2 cm protrusion of abdominal contents.
No intervention to date; not yet linked with Irish specialist for management planning.
Left varicocoele
Identified on scrotal ultrasound in January 2024.
Associated with abnormal semen parameters.
No intervention to date; no specialist follow-up arranged in Ireland.
Prostatomegaly
Mild prostatomegaly on ultrasound, approximately 30 g.
PSA 0.37-0.44 µg/L, normal; most recent source note says November 2025.
Family history: father had prostate cancer despite normal PSA.
Erectile dysfunction
Good response to tadalafil 5 mg daily.
Semen analysis, March 2024
Total sperm concentration 0.30 × 10⁶/mL, low against normal >15 × 10⁶/mL.
Total sperm count 0.6 × 10⁶ sperm, low.
Overall motility 25%, low against normal >40%.
Source interpretation: severe oligozoospermia with reduced motility, likely secondary to varicocoele.
Visual summary
Diagrams
Cardiovascular Map
Inflammatory Disease Pattern
Unit Provenance
Chronology
Medical Timeline
Current list from main source
Medication
Longitudinal graphs
Lab Trends
Graphs use the canonical longitudinal tables in the June 2026 medical history file,
then display values in the selected Irish, Brazilian, or South African unit profile.
Extracted from all Markdown files
Raw Tables
Full Health archive
Source Documents
Selected source
Select a source document
Safety notes
Units and Source Integrity
Canonical comparison
The June 2026 longitudinal tables remain the underlying comparison source.
The visible site converts recognized measurements into the selected country
unit profile without changing the source files.
Raw source values
Brazilian reports commonly use mg/dL and /mm³. Irish reports commonly use
mmol/L, µmol/L, 10⁹/L, g/L, and IFCC HbA1c mmol/mol. South African display uses
SI-style chemistry units with local defaults configured in the unit switcher.
Clinical verification
This is a patient-prepared website. Clinical decisions should use the original
reports. Values without an explicit unit in the raw source are left as written
rather than guessed.