We went to see Dr Z on Friday.She is a really lovely Dr and great with children.While she was gathering all the family history from both sides and talking to her about my leg issues,she asked me to stand up.So I stood up and straightened my legs for her.She saw that from the side my knees were almost bowed.She then did the same with my elbow.She asked to look at any scars that I have and I showed her the one on my finger.I also told her that I had been dx with Fibromyalgia. Well after looking at me (never mind that the app was for Broc) she dx me with Ehlers -Danlos Syndrome Type 3 or Hypermobility. We then realised Mark has many of the same issues so he probably has it too as we had a 50% chance of passing it down to our children.
Then she turns to Broc and carries on with his examine.She noted hooded eyelids on him,reflux,a few other things she never said and many heart issues so she is testing him for 22q11.2 deletion syndrome.She is not definite about that but wants to rule it out.
She then took him into another room to examine his legs properly.She noted that his right leg muscles and bones are smaller over all.She thinks that it is due to the lack of profusion from the occlusion of the femoral and illiac artery. She is really not concerned about his leg bones per say.She did say that we should see a ped. orthopedist to get a second opinion.
For now we are waiting to see what the blood test says.
Broc had a big event happen this weekend.He had his first sleepover at Grandma and Grandpa's house.I am thinking about him all the time and missing hearing his voice in the house.It is really quiet in the house without him.We miss you Buddy.
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