Hey Any advice on tics in school

Merry Christmas hope everyone has a lovely time

(My native language is not English, I'm sorry in advance for any mistakes if there are any) It would be interesting to hear the stories of people who have OCD and tics combined. My tics, when they get worse, are very similar to Tourette's syndrome, and a couple of doctors even suspected this syndrome in me (I just have mixed tics, but no tourette‘s). God, on the one hand, it's not easy when there are very strong tics for several months, and at other times obsessions and compulsions are exhausting. And they are constantly replacing each other. In addition, I have very big problems in the social sphere (I even took tests for autism, high results everywhere. Besides, it's much easier for me to communicate with such people than with those who are called "normal"). Is anyone familiar with this? How do you make your life easier? 😄 P.S. My OCD and tics were diagnosed by a doctor

hi! i was wondering, what kind of things qualify you for a mobility aid? i have pots and a whole plethora of diagnosed physical+mental conditions, and lately flare ups have been much more severe and frequent. i often have trouble getting out of bed because of fainting after standing, and throughout the day will have lots of difficulty sinply existing; standing, walking up/down stairs, etc., and its gotten to the point where i've began to consider using a mobility aid. however, there's a few questions/setbacks. 1. i'm not sure how to pick the mobility aid i need. how do i go about figuring out whats best for my disability/life style? 2. unfortunately, i am under 18 so i'm still living with my parents, and they don't like the idea of a mobility aid. i've been diagnosed with a number of conditions, and all they seem to do is tell me to drink more water. how would i convince them that this is a worthwhile alternative to days of pain, especially if that pain isn't cared for or acknowledged by them? 3. many of the places i go often are not very accessible/disability friendly, any tips for getting around more smoothly? 4. and 4, how do i get over the anxiety surrounding using a mobility aid? i fear that showing up to school with a mobility aid would attract a lot of unwanted attention, especially considering the fact that i would be thr only person with one in the ~2000 kid school. especially with my social anxiety, i worry about being a burden for others and i often put my own health at risk for social comfort, and i'm not sure how to stop that.

Telling your friends that you need a therapist versus telling your parents/guardians it’s so much harder.

Does anyone here also have ME/CFS or Long Covid and if so, what has helped you the most? (physically or mentally)