Welcome @Doggie28, you’ve found a wonderful group for support, we are so very glad you joined us!
I say “Bully for you”! It’s fantastic to read when members have little or no side effects. Let me see if I can answer most of your questions…
First, I’d personally take the three weeks off, your doctor is giving you this time to get your strength back. It also may give you some time to get your iron back up. Eat a lot of vegetables that provide iron. Though you may also be on a supplement if it’s too low. There’s a fairly long list of vegetables that give us iron, I think it’s on WebMD but you can do an Internet search if you’re interested.
Bruising is quite normal, arterial lines can do that. But couple that with iron deficiency and Brilinta it’s no wonder you’re bruised. I couldn’t say for certainty it’s just the arterial lines because you have a cocktail of things that cause bruising.
I didn’t have the WEB device and I ruptured but have had four procedures to stabilize the little bugger which #4 did and it was with the Neuroform Atlas Stent. It seems to me the majority of those who ruptured get migraines and there are many members who see an aneurysm repair as the cause of their migraines. Hopefully those with a WEB will reply to how they did after a procedure. Since you’ve already been a recipient of the blasted headaches, I would think the reason you get them may be the same, but one can hope your WEB has taken care of that issue. I wouldn’t see why you would get any worse from the procedure, but I’m not a doctor, not even in the medical field.
I do tend to be on the more positive side of things which I believe has helped my recovery and survival. It can be a bit irritating to some for me to always see the positive side, I wonder if it’s just encoded in my DNA sometimes. Nevertheless, I urge you to stay on the positive side of things as well, it helps life as a whole.
Recovery for any cerebral procedure is as different as we are, we may have some similarities, but nothing concrete. I believe you can look at your own lupus and those you know that have it for a better understanding. Dad had SLE, a co-worker had SLE. The co-worker once screamed and yelled at me about my father doing better than she and demanded I tell her why. I really didn’t have an answer but I did ask her how her Vit B-12 was as Dad used to get in tithers and had to have a monthly shot.
So be grateful you’re doing so well! I’m doing a happy dance for you, that’s for sure. Again welcome and we look forward to hearing from you and sharing your experience.
By the way, did you know Ben’s Friends has a lupus support group? If not, you may want to check them out…
All the best
Moltroub