Help With Analee's Medical Bills

In 2020, we welcomed Analee into this world 3 months ahead of time at 27 weeks. After a 74 day stay in NICU, we were able to bring her home. Since that day in November 2020, she has been through a series of challenges including the diagnoses of:

 

Mast cell activation syndrome

Growth hormone deficiency

Von Willebrand disease

Galactosemia

Polycystic kidney disease

Autoimmune deficiency

Hypoglycemia

Asthma

GERD

FPIES

Gastroparesis

Low IgG

Underterminded pain

 

We are in the process of getting genetic testing to confirm the diagnoses of:

 

Galactosemia

Polycystic kidney disease

Carnitine palmitoyltransferase 2 deficiency

Cohen syndrome 

We received the initial genetic testing at no cost but we are fundraising for the expanded testing and the upcoming referrals to the M.A.G.I.C. Clinic in Calgary, as well as a further referral to the Children's Hospital of Philadelphia and all the associated costs.

 

Any donations are more than welcome.

 

Thank you so much!!