I’m making every effort to take care of my health, have been involving advocates and have shown up to the ER repeatedly.
Unfortunately medical care for rare or chronic illnesses involves a lot of barriers, jumping through hoops and waiting. I have been seeking help and answers for a very long time.
I have been seeing specialists and have recently had to change hospitals because I wasn’t getting anywhere with the previous ones and they don’t perform the procedure I now need.
I’m currently being handballed between a private specialist and a public system that is dragging its feet. Even if I convince this doctor and pay out of pocket the earliest I could see him is September. I will also continue to attend the ER to build a relationship with the new hospital and try to expedite things further. (I have an existing referral to their specialists that has already been expedited but I could still be waiting a while.)
I will continue to do my best to get the treatment but it’s likely to be an ongoing struggle and I’m not 100% sure that I will get it soon enough.
Horrible subject. Normally I don’t talk about it. The only reason I even posted is that things are getting serious so I wanted to warn you guys and give you ample time to adjust to the idea if by some chance I don’t make it.
Thanks for the update - I think we were all a bit concerned. If this eases your mind, I'm fairly sure someone here (might even be me) will take care of Melbcat if needed in a hurry and you don't have time to set up a preferred option. I don't have a cat at present, so can offer no charge care in my home which is cat proofed in anticipation of getting a cat in the near future.
I’m stressed about it but if worst comes to worst I’m speaking with a support worker about taking Melbcat. With luck it won’t need to happen but I’ll get my ducks in a row.