As the title says really. I am so incredibly overwhelmed and stressed. I just have so much on my plate, all the time.
I have ADHD, and my therapist suspects um autistic. DD10 has ADHD, moderate learning difficulties, developmental language disorder, a heart defect and is on the ASD waiting list. She needs constant supervision and support with her daily needs. She's very full on. She's not badly behaved she's just a lot at times, and our needs clash because she's a sensory seeker, I'm a sensory avoider. I can tolerate touch, but not to the extent DD needs it. I'm here safe space and she just wants to be on and around me All. The. Time. DH intercepts her and entertains her if I need space, but I'll only get 10-30 minutes because then she gets anxious I'm not there and needs a cuddle.
DH has a physical disability and needs support with some aspects of his care (although this is generally short and easy). I have to provide a low level of care to him including rubbing his legs to restore circulation, cutting his toenails because he physically can't. Without going into too much detail he has nerve damage to his bowel and I sometimes have to support him with the consequences of that, even if it's just cleaning his clothes while he sorts himself out.
I'm also chronically ill at the moment. I get hemiplegic migraines that leave my hand and eye twitching, and can sometimes mimic a stroke by causing weakness down one side, or mimic a partial seizure (EEGs have shown no epilepsy). I also ended up in hospital a couple of weeks ago in intense pain, prolonged nausea and unexpected loss of appetite and weight loss. I had investigative procedures that showed I have a stomach deformity (Cascade stomach), that is uncommon enough that nobody knows how to treat it as there's very little information out there. I've been referred to Gastroenterology, to see if I'm a candidate for a type of gastric sleeve, as my deformity is quite severe, and a gastric sleeve would change the shape of my stomach, and mean that eating would stop causing pain and nausea. However the wait is 34 weeks. I'm also waiting for the results of biopsies as hospital suspect crohns disease as well, and I'm on another long waiting list for an Ehlers Danlos diagnosis from rheumatology, and a spinal MRI to check for scoliosis because during my hospital admission the registrar had concerns about how symptomatic my hypermobility is, and noticed that my chest wall is asymmetrical.
We're moving nearly 200 miles away on Saturday so I'm trying to desperately catch up on packing, after spending a good couple of weeks being unable to do anything due to being ill and in extreme pain. DH works full time so he was either WFH or balancing commuting with being home on time to pick DD up from school, and sort her out.
DDs anxieties, clinginess, repetitive questions, signs of dysregulation are naturally ramping up due to the anxiety created by moving away from a familiar place. There are strategies in place but as DDs primary carer, I'm spending half my time using the strategies and half the time just firefighting because DD is dysregulated. I know things will soon go back to their baseline, I'm just exhausted.
Then to add the icing on the cake DD got given a lower than usual rate of DLA after a stressful renewal where the DWP lost her forms initially and then rushed a decision through in 24 hours. So now I also have to sit on hold for god knows how long to request a statement of reasons so that I can request a mandatory reconsideration to try and get DD a DLA award that reflects her needs.
How can I stop feeling so overwhelmed and stressed all the time? I know I have a lot going on, and I've been searching online for stress management advice, but everything just talks about removing the stress from your life. but I can't get rid of the main sources of stress, because it happens to be my daughter. I just want to find healthy coping mechanisms.
I'm sorry for the length of this rant. It was like opening floodgates.