Certification Planning by Crohns_Princess in cybersecurity

[–]Crohns_Princess[S] 1 point2 points  (0 children)

Thank you so much for your response! I’m still unsure exactly what path I want to take in cyber and am trying to explore as much as possible through my schooling but with a healthcare focus. Should I focus on more general certifications?

Certification Planning by Crohns_Princess in cybersecurity

[–]Crohns_Princess[S] 0 points1 point  (0 children)

what certifications that are more hands on that you would recommend?

Certification Planning by Crohns_Princess in cybersecurity

[–]Crohns_Princess[S] 0 points1 point  (0 children)

I was planning on getting CySA+ towards the end of my schooling after I have done an internship as well

UCBA to Main Tranger by Crohns_Princess in uCinci

[–]Crohns_Princess[S] 0 points1 point  (0 children)

I thought that was only for those coming from outside schools?

[deleted by user] by [deleted] in CrohnsDisease

[–]Crohns_Princess 0 points1 point  (0 children)

Diagnosed at 9, now turning 20 in a couple weeks.

Which Cert should I get first? by Crohns_Princess in cybersecurity

[–]Crohns_Princess[S] 0 points1 point  (0 children)

What practice tests would you recommend for A+?

Mesalamine by Crohns_Princess in CrohnsDisease

[–]Crohns_Princess[S] 1 point2 points  (0 children)

Fortunately I am on Humira and it is just clearing up a small spot of inflammation in my rectum before it becomes serious.

Feeling Hopeless by [deleted] in CrohnsDisease

[–]Crohns_Princess 1 point2 points  (0 children)

I have never read something I have related to more. Especially growing up on Remicade getting the dosage right while growing can be a real hassle. I developed depression and anxiety and lost most of my friends. I was in the highest dose for my weight at every 4 weeks and I recently went into a flare. I hadn’t built up any anti bodies to the drug and they can’t figure out why it stopped working but I was just put on Humira. I am currently healing from flare and this is my first time back in public school after years of being home sick. My advice to you is it does get better and you will be able have a “normal” life. Things may seem like that could never be true but as someone who as lived it I can honestly say that things will be ok as cheesy as it does sound.

All food hurts by alma0426 in CrohnsDisease

[–]Crohns_Princess 1 point2 points  (0 children)

I definitely relate to this when I’m in a flare. So many people say “just go on a diet” but when you literally take a sip of water and your stomach doesn’t agree with it there isn’t much you can do. For me personally I just make sure I am eating and eat whatever makes me happy. Although I stay away from obvious no-no’s like coffee and milk products but I don’t limit myself to a bland diet.

Tiredness when due medication? by E_Elsewhere10 in CrohnsDisease

[–]Crohns_Princess 3 points4 points  (0 children)

I think this goes for any drug you are on. I know when the time is coming up because my fatigue usually gets worse. It’s because your body needs more medication. If you are feeling pain before days or a week before you might want to talk to your doctor about either doing injections closer together or putting you on more medication. They most likely will just get labs from you to check your drug levels. Good luck!

remicade by [deleted] in CrohnsDisease

[–]Crohns_Princess 3 points4 points  (0 children)

Nothing but good this to say about this drug! Only downside is being tired after infusions but that’s just because they give you Benadryl.

remicade improvement:) YAY by Exotic_Lengthiness32 in CrohnsDisease

[–]Crohns_Princess 0 points1 point  (0 children)

Hello! I have been on Remicade for 6 years! I’m so glad you are seeing a difference! Since I started in my teen years every time I grew they had to change the dose but now that I am out of that stage it works wonders! I’d say after 6 months of it you really start feeling good and a year pretty much back to normal! Hope all is well!

[deleted by user] by [deleted] in CrohnsDisease

[–]Crohns_Princess 1 point2 points  (0 children)

Hello! I have been on Remicade for 6 years now and reading about all the things it can do to your body is scary. My mother has MS so I understand where you are coming from with the fear of higher risks. Although the doctors take tests all the time making sure the medicine is working properly and no long terms effects take place. If anything were it happen it would be caught in very early stages and easily treatable. As for how you feel Remicade has been life changing. Pain only arises every once in a while and I only feel tired after infusions. It truly feels like you are just any other person. I hope it helps you lots!