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#hellomynameisclaireprince and I am launching this blog to document my journey as a mother of a daughter with Learning Difficulties, Autism and Bipolar Disorder. I want to raise awareness and give support to others by sharing my experience and to let you follow our pursuit for the next step – supported living. The launch of…
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Tonight 15/01/2025 I generally pass this bridge daily on my dog walk. I wouldn’t ordinarily share this, but tonight I was desperate to get to this bridge. This is why: No matter the weather, when at the bridge, I hold the railing tight; sometimes it’s frozen and wet, sometimes not. I have to hold it…
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If you want to fail, you must be inconsistent – period! I have that ‘deja vu’ feeling….. After an MDT on Thursday, 08.01.2026, the team around Molly made a decision to increase the mood stabilisor lamotrigine to support Molly’s low mood. The blood trough resulted in reading her level as 1.8; the target therapeutic level…
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It’s always hard for a special needs autistic person, routines tend to go out the window even though we try our hardest to keep them!! Molly is here at Chertsey Mount with me, she is tucked up in bed hoping for a Reborn baby and an Adidas jacket off Santa. She is very repetitive but…
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16/11/2025 Let me start with an update before I tell you about my small mercies…. On the 9th October we had a meeting on teams with both Dr Anderson from RADS and Dr Strong from Carleton Clinic, both are psychiatrists. Unfortunately the previous positives for Molly presentation have not been sustained. Molly’s appetite continues to…
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Yesterday we had a meeting with her psychiatrist, truth is Mollys hypomania is not responding to Orlanzapine, the increase has made some things worse, increased appetite, agitation and irritability, some slight improvements to her sleep and obsessively changing her clothes (PJ’s), this behaviour has reduced. A decision was made to increase the dosage, monitor for…
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17/08/2025 I can’t lie, I could say I am fine, Molly is fine, as we all often do…even if we are trying only to convince ourselves. In truth today, for whatever reason, I couldn’t hide my sorrow, my sadness, my worry or the fact I am not sure how much more I can take. Seeing…
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On the 31st July 2025, I called the crisis team with concerns about Molly. She is not sleeping, changed her PJ’s many times through the night, has oculogyric crisis, is very repetitive and has no spacial awareness plus agitation. The said they would call back, they did at 2am which I missed… called back later…
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We have received the date for the X Ray this Thursday 17/07/25. This will rule out a bowel blockage or identify one…………now let me see. Vomiting is still there but not so much, bowel movements are less but still type 7 on the Bristol Stool Chart. Due you hypomania Amilsulpride was increased on 11/07/2025 just…
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Where do I start… now let me see… The weight loss enabled to GP to feel a bowel blockage, Molly went on a huge increase of her medication to support this for two weeks with the hope that it would unblock her, then 2 more weeks on half the amount. Type 7 bowel movements remained…
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Hey I’ve been thinking, thinking I need to stop trying to fix things, fix Molly…. At the last meeting in Newcastle I was told Molly, may be without Symptoms for many years however, it will return at somepoint. That was actually very hard to swallow, I think I thought we were going to fix her.…