thursday i spoke to a lady dr ive been seeing about a trial of buspirone, she said she needed to look into it and would get back to me
friday a dr who does not know me at all called and refused to give it me and said i needed to go back on mirtazipine which made me evil and said he would contact mental health again for me to go see them
friday afternoon i called to talk to my reg dr who was not in so called this morning and left a message for him to look into buspirone
well hes just called me back and has agreed to a months trial and im to collect it tomorrow
Written by
mandy72
To view profiles and participate in discussions please or .
I bet you are relieved Mandy72 - I don't see why an alternative cannot be prescribed if the patient feels worse on a particular one. Sometimes the doctors seem cruel but the one whose prescribed an alternative deserves praise for listening to the patient and understanding a little.
I hope you feel much better on the new prescription.
i feel better knowing that there may actually be a light at the end of the tunnel
the dr i spoke to friday joined my surgery in june of this year as a trainee
he knows nothing about me only what he can see on the screen
the dr i spoke to today is lovely, he used to collect and deliver my mums meds when she was ill and helped me lots when we lost her, id sooner see him than any other dr as he never rushes you, hes very sympathetic and will listen and is open to other options
only thing is my pulse is all over the place lately still trying to get my T3 adjusted so im feeling ok
i just want to see an improvement in the anxiety side
but anxiety has been a long term thing so maybe my pulse will settle as the meds kick in and i wont need to take the beta blockers (only take when needed)
the two main side effects that have been on nearly all the meds ive tried is shortness of breath and rapid pulse and i suffer those anyway and it normally made them worse
buspirone dont have any of them listed so fingers crossed
I've been fortunate to be able to control mine (with a bit of difficulty at first as I hadn't a clue what was going on (160+ at times). Thankfully since I've been on T3 only it's remained around 60's. I've had lots of heart checks and it's fine so it had to be the medication.
my heart rate started increasing towards bedtime but i was a bit worried on taking another dose, ill try the 3 doses today and see how i go
i wake up every morning and anxiety is through the roof for some unknown reason, but no real side effects just yet so fingers crossed these will help
i was awake most the night really thirsty though but thats one of the side effects, ill try and find a cheap humidifier for bedroom as that helped when i was on trazadone (kids pulled mine apart for some strange reasonesone of them things where no one knows what happened to it)
way to go mandy , you - like me - need to nurture that doc , he/she seems to be just like ours ,,,,, one that actually listens outside of the box of the mainstream for the benefit of themselves AND their patients [ for themselves because the less time taken up by appointments , prescriptions , drugs issued, and associated costs drain the funds from other areas of the trust fund ].....[ for the patient it allows a shorter tunnel to a reasonable level of tolerable health for the individual patient ---- we all need different regimes of meds ---] .....therefor it can only be a win/win/win scenario .....you will get there with the help of this doc , even if it does take some time keep going girl ......alan xx
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.