Medical Alert Info
Melissa Ellen Milton. DOB: 3/23/1960.
Primary care physician: Dr. Joeseph O’Connell
MANA Clinic, Fayetteville, Arkansas
His office: 479-443-3536
MANA has the medical records for the past 25 years on this patient.
Emergency Contacts: Michael Milton (husband) 479-459-8997. Daughters Liz Krauft 479-200-1913 and Helen Smith 479-595-3413.
Ehlers Danlos Syndrome
Body manufactures faulty collagen.
Fragile blood vessels and other tissue (vascular EDS).
Hypermobile cartilege and ligaments (hypermobility EDS).
Diagnosed by genetic testing (vascular) and clinical exam by rheumatologist.
Has caused repeated tearing in eye retina tissue. Six repair surgeries.
Has caused sensorineural hearing loss. 45% loss in right ear. 35% loss in left ear. Face patient and be close up when speaking.
Has caused a hiatal hernia (from vomiting).
Causes mystery bruising and mystery sprains.
Dysautonomia (Autonomic Nervous System malfunction)
Tachycardia and bradycardia.
Hypertension and Hypotension. (Highs over 200/180. Lows as low as 6/30), Cycles up and down. NO BLOOD PRESSURE MEDS!)
Patient on oxygen 24/7 to prevent passing out daily (for 30-90 minutes) from hypoxia during random blood pressure crashes.
Hypotension easily resolved with oral caffeine (coffee works fine). Being upright raises bp too.
Hypertension easily resolved by lying patient down and warming skin with warming blankets, heating pads, warm bath, etc.
Body position and room temperature are triggers.
Upright = hypertension. Lying down = hypotension.
Cold = hypertension. Hot = hypotension.
Probably caused by the EDS.
Diagnosed by two Tilt Table Tests (patient fainted from bp crash each time).
Ankylosing Spondylitis
Patient is immunocompromised, per Dr. O’Connell.
Prone to runaway infections from minor injuries, minor insect bites, minor burns, etc.
Doxycycline is primary care physician’s go to oral antibiotic.
Diagnosed by genetic testing and having two siblings also with AS.
DRUG INTERACTIONS
No blood pressure meds (up or down)!
No NSAIDS (caused fluid in lungs)
No Fluroquinolone antibiotics (No Cipro. No Levaquin. etc.)
Due to Ehlers Danlos Syndrom puts at risk for aortic dissection
No nitrous oxide (genetic testing indicates dangersous interactions)
Local anesthesia does NOT work on this patient. Due to Ehlers Danlos Syndrome (local anesthesia dissipates too quickly through the tissue).
CURRENT PRESCRIPTIONS:
Oral: Furosemide, 40 mg, 1 or 2 twice daily for edema.
Oxygen 24/7. Two Liters. For Dysautonomia. Buoys blood oxygen levels so the patient won’t pass out during blood pressure drops. Without oxygen patient passes out daily from hypoxia for 30-90 minutes.
Inhaler: Albuterol (as needed)*
Eye Drops: Flurometholone steriod eye drops (as needed)*
Occasional Doxycycline or amoxicillin as “go to” antibiotics for minor injuries (minor bug bites, minor burns, minor chest congestion, etc.) that otherwise turn into runaway infections.
*For pain control & breathing during bi-monthly autoimmune flares (from Ankylosing Spondylitis). Use Inhaler 4 times daily for breathing with lung inflammation. Use Eye drops times daily for eye inflammation pain. Also Ibuprofin + Tylenol 4 times daily for joint inflammation pain. No use of these during the 4-6 weeks between autoimmune flares.
FAMILY HISTORY
Both Parents, 3 siblings, deceased.
1 living sibling.
Two siblings also inherited the Ankylosing Spondylitis autoimmune issues.
Married, husband. Two adult children. Two grandchildren, one with suspected Ehlers Danlos Syndrome.
1 Niece deceased at age 29 from Vascular Ehlers Danlos Syndrome and Dysautonomia, non-repairable aortic dissection.
A grandmother and brother died of kidney failure. Two other grandparents and mother died of cancer. A brother died of liver failure. A grandparent died of stroke. Mother had severe stroke leaving her brain damaged for final ten years of life.
PRIOR SURGERIES:
Gall bladder removed
Thyroid surgery to remove lump (was benign)
Breast surgery to remove lump (was benign).
Breast reduction surgery and implants.
Many oral surgeries (jaws too small for teeth, a common EDS trait).