Since early childhood, I have experienced significant exercise intolerance, with an inability to walk distances greater than 50 meters, climb stairs or inclines, ride a bicycle, participate in gymnastics, or lift heavy objects.
After 65 years, a final diagnosis from the UK: Post-Polio.

In addition, confirmed diagnoses:
1961 psoriasis diagnosis
1964 ectopic pregnancy / left salpingectomy
1964 Dermatological Clinic Augsburg Psoriasis
1967 Derma- Clinic Nuremberg mainly treated with cortisol ( Volon 40 and Volon 80)
1979 Uterine dysplasia 4/hysterectomy
1980 Diagnosis of low cortisol at the University of Erlangen
1983 extreme migraine - neurology no treatment
1993 PTSD diag-Kaiser Permanente South Sacramento
1998 Diverticulosis and C-Dif - Kaiser Permanente South Sacramento
2000 (US) low cortisol average 4.5 - treatment prednisone
2000 (US) progressive muscle weakness in legs, upper arms and back muscles
2007 (US) low cortisol 1.1 - Endo: treatment prednisone
2008 (US) MRI with contrast Chiari Malformation I
2009 (US) Chiari Malformation I with Decompression Surgery
2011 (US) Hemilaminectomies with posterolateral fusion with pedicle screws
2013 (US) Myalgia (myositis) diagnosis UNMH 2013/15/16 ICD G93.3 CSF
2013 (US) MRI - Stenosis and Tarlov Cyst Spondylitis
2016 (US) OP L4 – L5 (CD)
2016 (US) OP Lumbar spinal hardware infection, Data 4/7/16 Body fluid back lumbar spine superficial GS/CX: very rare growth: bacteremia: Staph epidermidis and Peptostreptococcus , Peptostreptococcus , one colony Staph caprae , Corynebacterium species,” treatment: IV 6 weeks antibiotics Vancomycin
2018 (US) Aortoiliac vascular calcifications are noted.
2020 Germany Scapula ganglion cyst - bilateral, 5 cm 2 Fibrosing /granulomatous processes in the apex of the scapula (MRI) Clinik DON MRI
2020 Germany Myasthenia Gravis / Eaton-Lambert Syndrome??? (Report UNI-Regensburg inconclusive)
2021 Germany COVID-19 and mRNA - BioNTech results: Stevens-Johnson syndrome (SJS)
2021 Germany Rheumatoid arthritis, Thrombosis, jaundice, herpes, urticaria, POTS, PEM, anaphylaxis (Onco: DON)
2021 Germany Corticotropic insufficiency (Endo: Dr. Vlotides Ingolstadt)
2022 UK Post-Polio diagnosis in the UK, Dr. Shaw.
2022 Germany: Antiphospholipid Syndrome, vWillebrand Factor 2 and 5, Lupus, Petechiae, Gene: ACADM

Current Symptoms - but I manage and keep going at the age of 76:

Fatigue: Persistent and profound fatigue with a constant sense of exhaustion, rarely alleviated by rest.
Muscle Weakness: Generalized muscle weakness, particularly in the upper and lower extremities, exacerbated by physical exertion such as lifting, stair climbing, or walking uphill.
Autonomic Symptoms: Diagnosed with Postural Orthostatic Tachycardia Syndrome (POTS), with symptoms including irregular palpitations and significant tachycardia upon standing.
Ocular and Oral: Xerostomia (dry mouth), dry eyes, and episodic visual disturbances in the left eye (described as fogging or blurred focus).
Auditory: Intermittent hearing disturbances with tinnitus affecting the left ear.
DNA: gs191 Impaired NSAID drug metabolism - ADAMTS13 deficiency.
rs12340895(C;G); four times higher odds of developing V617F-positive myelofibrosis (MPN)
Good: rs5848(G;G) lower dementia risk. Lower risk of frontotemporal dementia, alzheimer's disease and parkinson's disease.

Mother: Cushing-Syndrome, vision problems, rheumatoid arthritis - died at age 56
Father: psoriasis, vision problems, rheumatoid arthritis- died at age 80
Brother 1: ALS - died in 2014 age 64
Brother 2: heart attack 2022 age 71

My attitude: "Let battle commence".