That night, Daddy made up for it in a huge way. He had gone to the grocery and found my Frosty Paws Ice Cream. Yey for Daddies! I immediately recognized the box and tried to open it. Mommie let me have just a few licks. She said we should save it for when my tummy is all better.
Yesterday, we got bad news from the doctor. My platelets are down to 12,000 and they are enlarged. Sigh! Doc is upping my medicine again to twice a day. Yuk!!! Now I have to stay in my room coz the orders are no moving. I am no longer allowed kibble or treats that are hard or abrasive as I have had spontaneous bleeding in my mouth, tongue and gums. Before my nose and eyes would bleed, too. Doc says I risk getting a cut if I take in anything abrasive coz I am not clotting due to the low platelets. Also Mommie has to look out for any signs of internal bleeding so poop patrol needs to be more up close. No fun for Mommie.
Frosty Paws are great!
ReplyDeleteWe're sorry your platelets dropped. We hope the medicines bring them back up so you can get back to regular activity.
The Florida Furkids and Lexi
Oh Casper we are so sorry to hear you are not good again. Paws crossed the medicine makes you better again. Thinking of you.
ReplyDeleteBest wishes Molly
Paws crossed the medicine makes you better again well said!
ReplyDeleteDear Casper and Casper Fur Parents:
ReplyDeleteWe have been following your blog since we got our two toy lovable eskie nutbars, Sparky and Ollie. We are saddened to learn that you have not been well and may be getting sicker. Our hearts go out to you and your fur parents. We hope you will feel better soon so that you can continue to share your stories with us.
May I suggest you start a FB page to raise awareness for Evans syndrome and support for you and your parents? Just a thought.
We are thinking of you and are sending you lots of love.
Be well,
ocm, sparky & ollie
We are sending the strongest White Dog healing energies and positive thoughts and will not stop until you are back to full health. Take your neds, try to rest as much as possible, don't panic, and be strong.
ReplyDeleteThanks all! I have been doing my best to beat this. I'm sleeping most of the time but my gums are still pale. Hopefully the drugs will start working soon.
ReplyDeleteThere are FB pages called Evans Syndrome Community Network and IMHA Awareness and Support Group that we joined a while back. So sad to read all the stories on those pages.