Halli's Mom
New member
I'm posting here, because I'm not sure where else to post. I seem to not be able to catch a break with my two girls....I keep hoping that the latest malady will be the last, but then something else happens.
Here's my timeline:
November, 2010 - Penny (1yo at this time) has reaction to vaccination - has ITP, and in ICU for 5 days, recovery and meds the next 9 months. She's in remission by June 2011.
July, 2011 - Jasmine (1yo at this time) diagnosed with EPI. Start her on Enzymes and living a somewhat normal life as we adjust to the new way of feeding.
August, 2012 - Jasmine has Aspiration Pneumonia, multiple stays in ICU, regurgitating her food several times a day; diagnosed with Mega-Esophagus
January 2013 - Jasmine's Myasthenia Gravis test comes back positive (underlying cause for the ME) , so more drugs treating for MG, while still dealing with the ME hand feeding, and keeping vertical.
June 2013 - Jasmine in remission from MG (and thus ME) - spend next 3 or 4 months weaning her off the drugs
January 2014 - Penny diagnosed with "mineralization in shoulder tendon" - physical therapy for many months, finally have to do surgery in October.
October, 2014 - Penny has surgery for her shoulder - 3-5 week recovery
November 2014 - Penny tears her ACL. TPLO - 12 weeks recovery. Physical therapy still ongoing.
March, 2015 - Jasmine starts having trouble getting up (appt this Friday), occasionally hold back leg up, but doesn't seem like a torn ACL, and just last night, licking front paw, which is clearly tender (yelps a little when I feel between the pads) - appointment tomorrow hopefully.
Should I cry yet? Not sure how much more I can take....it just seems like constant heartbreak.
Here's my timeline:
November, 2010 - Penny (1yo at this time) has reaction to vaccination - has ITP, and in ICU for 5 days, recovery and meds the next 9 months. She's in remission by June 2011.
July, 2011 - Jasmine (1yo at this time) diagnosed with EPI. Start her on Enzymes and living a somewhat normal life as we adjust to the new way of feeding.
August, 2012 - Jasmine has Aspiration Pneumonia, multiple stays in ICU, regurgitating her food several times a day; diagnosed with Mega-Esophagus
January 2013 - Jasmine's Myasthenia Gravis test comes back positive (underlying cause for the ME) , so more drugs treating for MG, while still dealing with the ME hand feeding, and keeping vertical.
June 2013 - Jasmine in remission from MG (and thus ME) - spend next 3 or 4 months weaning her off the drugs
January 2014 - Penny diagnosed with "mineralization in shoulder tendon" - physical therapy for many months, finally have to do surgery in October.
October, 2014 - Penny has surgery for her shoulder - 3-5 week recovery
November 2014 - Penny tears her ACL. TPLO - 12 weeks recovery. Physical therapy still ongoing.
March, 2015 - Jasmine starts having trouble getting up (appt this Friday), occasionally hold back leg up, but doesn't seem like a torn ACL, and just last night, licking front paw, which is clearly tender (yelps a little when I feel between the pads) - appointment tomorrow hopefully.
Should I cry yet? Not sure how much more I can take....it just seems like constant heartbreak.