Tuesday, 2 August 2016

Update on arm, with MRI results interpreted


16 June 2016
went GP to ask where is letter that I requested was sent to my Neurologist re diagnosis.  She said the Neurologist reports should be ok,  plus I had surgery on my spine previously. Also she said the report from the Neurologist for my recent MRI scan should be available and that I could get from their PA to the Neurologist.

17 June 2016
I called the PA and she informed me that she had sent it to my GP surgery on the 19 May 2016, but they say they never recieved it so she faxed it to them.

23 June 2016 Went to my GP to get feedback on report, plus I showed her the OT report (see below) stating Housing will not accept me onto their list without a diagnosis.

Housing had previously written  'we would advise that you look to secure alternative accomadation in the private sector.



*********************************************


The MRI head scan report is written by a man but I don't know his position, but I assume he is the one who interpreted the results.
I don't have a copy of to upload at moment, but I will type here what was written, not that it means much yet to me.

MRI head
Comparison is made with the cranial MRI of 27/1/15

There is scattered patches of T2 high signal within the white matter of both cerebral hemispheres. These are predominantly frontal and subcortical. There are a few the right frontal deep white matter signal changes. There is however no periventricular signal changes. The posterior fossa appearances are normal. There has been no interval change relative to the previous study.

The cervical and Thoracic vertebrae are normal appearance. There is dehydration and narrowing of the C3 -4 to C6-7 discs. Their are shallow radial discal bars at C4-5 and C6-7. The canal dimensions at theses and other levels throughout the cervical and thoracic spine are adequate. Uncoverebral   osteophytes are resulting in moderate stenosis of the left C5, right C6 and C7 neural foramina bilaterally. The cervical cord is of normal appearance.
Conclusion :
Patchy T2 high signal within the white matter of both cerebral hemispheres is predominantly subcortical and likely to be on a vascular basis. There has been no interval change relative to the study of 27/1/2015. There are no cord lesions are identified,
The GP  took my blood pressure,as said it had not been taken for 5 years. was 128/85 she said 'that's fantastic'

Chart taken from
http://www.bloodpressureuk.org/BloodPressureandyou/Thebasics/Bloodpressurechart

24 June 2016

I attended physiotherapy for my hand and all was fine so I was discharged,

Later that day i was informed my Dad had passed away.
He was 92, R.I.P. Dad.



1 August 2016
Yesterday I send I letter to my MP regarding my Housing difficulties due to not having a diagnosis, even though my OT assessment showed I needed more suitable accomadation.

I await his response.

I am still to copy shots of my MRI scan,,but will include soon.






Tuesday, 7 June 2016

Hand doing great and eye's also

 Following on from the 10 May 2016,,,,

23 May 2016
I attended fracture clinic . The caste was removed and xrayed.
the consultant then said the bone was fine and that I needed to exercise my fingers, (they were very stiff and weak) and wave like the Queen for her birthday and also do the exercise where you hold your hands together as if to pray and flaten your elbows out. He said Pysio would contact me for an appointment.




My hand was swollen throughout the 2 weeks in the second caste,and renderd un-usuable due to stiffness and pain.

After the caste was removed much of my skin was coming off so I soaked it in the Cold hot cold rotine to help with the swelling.

The bruising of my wrist increased and the fingers tingled with like raw nerve endings.It was painful and weak.

Video I put on fb of my hand


I exercised it also as much as I could . The skin was sore to touch but I gently applyed cocoa butter.

Wednesday 25 May
I didn't recieve any appointment so called the psysio deptartment, they said they hadn't recieved the referal yet and to try again the next day, although they may not recieve until friday. So to call then, as the letter they would send would ask me to call to arrange an appointment.

I knowing I had to go and collect my car from Ireland, meaning I needed to drive back from Scotland decided I would do better to go there prio my next hospital appointment for my eyes on the 6 June, yesterday. So I flew to Belfast and exercised my hand the whole time there, with the execises instructed by the consultant, but also the ones I used last year that I learnt in the posted video from that time, I think around July 2015.

I also purchased a squeezy putty thing and did it each day until it hurt too much. Mostly the pain was nerves and tendon stiffness, the swelling remained for about a week before it started to reduce.

I called the Physio dept Friday 27 May and they said they hadn't recieved the referal yet. I had spoken with the same staff member previously and explained to her my predicament. She went away and spoke with others and said I could have an appointment for the following Friday , the 3 June.

I drove back last Thursday 2 and went to the physio appointment. She said I had done well.
She saw my fingers were weak and said to exercise them to build new neuro pathways. Also continue doing the praying exerecise plus bending my wrist over ledge at right angles and back.

She also gave me a stretchy peice of plastic material that I am to grip and twist and then pull.

she was going to give me another stretching thing but then said no , she had met people like me before, (meaning she saw how I do everything with gusto) so I am to do and return in 3 weeks for reassessment.


Monday 6 June

I attended my apointment with the Consultant for my eyes.

I waited like everyone else an hour, but I had a time limit on my parking so ask at the desk how much longer. They checked the pile of files waiting outside the consultants office and showed my I was next , on top of the pile. Impatiently I waited at the hallway and saw the Romanian consultant who saw me last time pick up the file take to her room, then return with it and take the next. The nurse then went along and seemingly spoke to her about it, but the Consultant took the other file to her room. Out came the Male consultant I had been seeing prior to her and he took my file and called my name.

Prior to going in to see him a nurse did a eye test for each eye, and  noticed how I could read so much better than normal with my right eye.

He looked at my notes whilst I told him how I felt the muscle in my left eye had become stronger since wearing the prism glass lense cover and using the string with beads.

He put yellow drops in my eyes and said they were fine and to keep going to the other eye specialist and come back in 6 months.

I said how I felt my right eye had done better than normal in my eye test and he checked the results and said yes its now 6/6 ...(or something like that),,,,,,,and had improved.


Today 7 June I attended the other eye consultants appointment to check of my muscle that the weakness in causes double vision.He did several tests and he said I had improved and to come back in 3 months.
He said they didn't think it was thyroid eye desease any more as seemed only the muscle weakness without pain. He said I was unusual as normally this occurs in teens and then improves but maybe the thyroid eye desease I had prior caused some weakness, he added this was only an idea as he hadn't seen before.

I recieved my MRI scans for my brain and spine but am yet to turn into photos so I will do them soon but post this update for now. I add there is no diagnosis or written report with the scan so I will chase up that aspect too.

Today my hand is doing very well, a little weak and stiff in parts but improving daily.

Be back with scans as soon as I can but my Housing benifit claim has been suspended due to my change in circumstances and they require info and my annual accounts so that first. Bye for now

Thursday, 12 May 2016

Update on my broken arm,,,,,


I attended my MRI scan for Head and Spine cervical on Friday 29 April.
I believe they scanned my head and whole spine(cord).

Monday 2 May I was given my website back, and made a video on Targeted Individuals TI's, which was well received but now the number count appears to be interfered with.



Tuesday 3 May I awoke to 2 bruises on my arm, looking like finger marks.
I have bruises that come in the night on my Instagram account. They note when they appear.
Instagramhigherinsight


ESA stated they hadn't received my sick cert and housing benefits wrote to say they have suspended my claim until
ESA is sorted.

Monday 9 May

Went to fracture clinic, new consultant, she had my arm xrayed and showed me how the fracture has displaced my bone alignment, she said it had moved a bit since I last came.
She had it plastered and xrayed again, but due to the difficulty in postioning my arm it was hard to discern if there had been further movement.

She said come back in 2 weeks to have caste off and xrayed, and may start physiotherapy then.

The caste is now fibre glass so lighter, and smaller too.
Since this change my wrist has continued to hurt.


I also called my GP surgery to request a duplicate sick cert as one has to allow 9 working days from sending it, as the process takes that long, they told me.
Then I was to take to job centre for scanning to ESA.

Tuesday 10 May

It was raining but I took buses to collect duplicate sick cert and took to job centre, who had me sign it and added they may not accept if they can't recognise my signature ...


Today hand swollen, so trying to rest.

Monday, 25 April 2016

Broke and displaced Radius borderline for op

Wednesday 13, April 16 I slipped on some mud, whilst holding a hiking pole in right hand. Broke arm, radius, displaced bone at wrist. Was told may need surgery.
Had morphine, so dr could try to pull my bone back in place, whilst a nurse plastered my arm.
After xray it showed it was back in line.
I was told i would need it seen after a week at the fracture clinic. I was in Ireland and needed sick cert. I asked a nurse regarding getting one from the Dr, she said no I was to get one from my GP. When I called my GP's practice I was told I needed evidence, as dr couldn't write without seeing.
Meanwhile sickness benefit, that one has to apply for sets deadlines, so I waited for fracture clinic appointment, chased it, only to be told on the following Wednesday my appointment wasn't until Monday the next week.
I therefore went back to the hospital and requested my notes be sent to a London, hospital after liasing with them asking I be transsfered, so I could return home to obtain sick cert.

I returned home via boat and coach as caste would need splitting to fly.

On return I had received an appointment for the fracture clinic in London, for today, Monday 25 April.
along with appointment for MR|I scans, this week.

Today I attended GP to obtain sick note, then attended fracture clinic, the consultant had my arm xrayed and said it was boarderline, for surgery, and to come back again in a week, but as it is a bank holiday come back in 2 weeks.

On my return I had received notification of the MRIscan appointment again, as a reminder.



Friday, 8 April 2016

Eye appointment account + Neurologist letter states she couldn't find my MRI results

Thursday 24 March -GP appointment
went to my GP, to ask that they request a letter from the Neurologist for my housing application, as without a diagnosis they refused to even have me on the waiting list. I was seen by a locum doctor who listened well.
I told her how the Neurologist had said to tell them to write to her and she would respond, but that I didn't feel they would write and therefore could a letter be sent from my GP to ask for some form of letter re my needs due to my disabilities. She wrote notes and said they would write once they received the report from the Neurologist ,but nothing had arrived yet, I was seen on the 14 March.


Tuesday 5 April - Eye specialist appointment
I had my appointment with the eye specialist, whom tested my eye movement. She was very thorough. She said she didn't think it was thyroid caused nor Neurological, but a physical defect I have that has got progressively worse so now I notice it.
She said the eye goes out to the side as it is weak, and so gave me eye exercises to do, which involves a string with beads on at different lengths to practice moving my eyes along the string, converging my eyes.



She also stuck a prism film over my reading glasses left lense that helps loads, but don't look too nice; but I don't have the double vision at distance , only close up to read etc.





No letter or appointment for MRI came so
Wednesday 6 April 2016
I had not received my appointment for my MRI scan so I went to the hospital radiology dept and asked in person. They said they hadn't received a request for yet.
I therefore then went to the Neurology dept and the woman on the desk phoned the consultants secretary, whom said she hadn't done my letter yet, they take 4-6 weeks, but was on to it.

Thursday 7 April
The next day I received letter written by the Neurologist. (dated 1 April, in an envelope frank stamped 5 April. )


The Neurologist states in it that she notes that in the past I have had MRI brain and lumber spine, and that she could not find the results.

I went to my GP for a repeat prescription, and whilst there asked had they received the letter also from the consultant Neurologist. They said no. I told them it had the wrong GP /address on it , so would it be sent on if they received it. She said No, as they would no longer have my files.
So I photo copied it for my current GP, gave it to the receptionist.



Much interference whilst I try to do this post, so I will add later the Neurologists letter.....

Saturday, 19 March 2016

Neurology and bone density update



Update since 15 December 2015

Soon after my appointment I received a report from the eye specialist, along with 2 new appointments, one for eye movement tests in April and a follow-up appointment in June with eye specialist.


****************************************************************************

I had my full blood tests via my new GP which came back normal for all things except slightly higher than normal for Cholesterol and Sugar.
She asked I attend a days training 'Walking away from Diabetic' , which i did and recognised I need to loose weight.
She provided them with my Cholesterol score which was,,,,,,,,,,
HbA1c   43mmol

I have tried to walk more by using my poles I am able to walk further and faster.
I also swim.



I also went for bone density scan which says :-


BONE DENSITOMETRY

Lumbar Spine L2-L4
Bone mineral density (g/cm2) = 1.342  +/- 0.01
T Score =1.0  Z Score = 0.9

Mean L & R Total Femur
Bone mineral density (g/cm2) = 0.998 +/- 0.01
T Score = 0.0  Z Score = -0.1

CONCLUSION

This patient is considered to have normal bone density
according to the World Health Organisation guidelines.
Please refer to full data set on PACS.




On Monday 14 March I attended my appointment with the Neurologist

The consultant I normally see was there, but I was asked into his senior consultants office,, whom is the named consultant on my files.

She asked questions on what was my problem. I said how I have difficulty walking as knees swollen and balance not good and back weak.

she noted I didn't walk straight so asked me to walk. Said I was OK. which I was I explained I feel robotic in walking and poles help. Because they help me to balance and I don't trip. and can also walk faster; as when I walk fast I become less coordinated and feel like my feet are going faster than my brain. And that I break when i fall. I told her i broke both wrists last year, just from falling but I had bone density test and they show to be normal.

She asked about my back problem in relation to walking. I told her it gives way can become like jelly, from like my ribs downwards and it becomes hard to hold myself up.
She asked was there pain, to which I said no, not really, only if i was to push myself when i collapse. People don't seem to understand no pain, but it is more like I'm paralysed.
she said she will arrange a MRI scan for the whole of my spine.

I said I see eye specialist, who now say my double vision is most likely neurologically caused, and not Thyroid eye disease as they had been saying for past couple of years; although the first eye specialist, 2 years ago,  had noted my left eye muscle was too tight, ( I didn't see him again)
Now they say not likely TED as no other symptom, like protruding eyes, redness of lids, puffy eyes, and pain. all of which I had previously in 2019,along with double vision but all symptoms went when I treated myself, so I was discharged in 2010.

I have now been given appointment for eye movement test, April.

I informed her I had changed my GP and they had given me a full blood test, which showed all to be normal, except my cholestral and sugar to be slightly higher than normal.
They arranged for me to go on day training, 'walking away from diabetic'. where I recognised I need to loose weight.

Throughout the appointment I was jolting, where my arms and legs move involuntary.
She asked what was this tick, I said I don't know.
She asked when it first began. I said after surgery in 1998, but not bad. becomes worse when tired and that I was tired now. (12 noon).

I added in 2009 it became more noticeable and has got worse in the last couple of years.
She asked when I last had a brain scan, I said I think 2 years ago (I see now it was 27 January 15)
She looked at her screen and said I will arrange for another brain MRI scan.

She asked did I have mood swings. I told her yes, I can be fine and then for no reason become tearful.

She said there are no more tests she can do.
I asked about diagnosis and explained I needed in order to gain appropriate housing, as I had an OT assessment, who said I needed but the housing services say I can't have until i have a diagnosis.
The Dr said she can't give a diagnosis yet, but they could write to her and she would explain.

I offered her what I had previously prepared, a list of all the MS symptoms and how I experienced each symptom.
She glanced at it and gave me back. But I asked did she not want to keep it. She said yes, she would read later if she could have the copy. So I left it with her.

Here it is


    Signs & symptoms(taken from website)   https://www.mssociety.org.uk/what-is-ms

        Early signs of MS
       1,  Balance, walking and dizziness  - yes
       2, Bladder  - yes
       3, Bowel    -yes (this last 2 weeks constipation)
       4, Eyes and sight   -yes
       5. Fatigue   - yes
       6, Memory and thinking   -yes
       7, Mental health   -yes
       8, Pain   - yes
       9, Sexual problems   -yes
      10, Spasms and stiffness   - yes
      11, Speech   -yes
      12, Swallowing   -no
      13, Tremor  - yes


updating all on my current situation.
 My Signs & symptoms of MS

1, Balance, walking and dizziness
yes I have poor balance, and don't tend to walk straight, and my movements can become quite robotic especially when tired.
I can't stand on right leg for more than a few seconds most of the time, I practice regularly but still sometimes harder than others, Sometimes my legs go faster than my brain and its uncoordinated.


If i try to look up I can be dizzy and laying down,sometimes.
Also as I walk i lack spacial awareness of where my feet are so knock into things.
I walk slow and muscles can tire fast and inclines of any type are a struggle and strain on my lower back; which I previously have had a discectomy on L5/S1.  I find I lean with my pelvis tilted forwards as I walk.
I therefore now often use a walking pole(s) as advised by my neurologist; which enable me to walk faster, with longer strides. They help with balance and support my back enabling me to walk further too.
They also help prevent me from tripping over, which without I can trip over a match stick, which last summer (2015) resulted in both my wrists being broken from 2 falls on the pavement.
Recent bone density scans showed my bone density to be normal.

 2, Bladder
Sometimes I need to urinate frequently, yet don't have a full bladder.  I often have small amounts of urine leakage even when I don't have a full bladder, which sometimes happens if I cough.
When my back collapses , I becoming semi- paralysed and don't pass any urine.

 3,  Bowel
Not a problem
.....in last 2 weeks become constipated
 4, Eyes and sight
Double vision, which I am told by eye specialist the muscle controlling my left eye is too tight, also my vision varies and changes throughout the day.I am due to have tests on my eye movements in April 2016.
Previously they diagnosed Thyroid eye disease, as had previously (2010) plus had unstable thyroid that resulted in me being prescribed Thyroxine 100mgs a day.

 5, Fatigue
I can become tired after doing very little, even wake up tired. Other times I don't experience tiredness, then tiredness hits and can last for days.
Sometimes the tiredness can just be in my brain, not in my body, then my head feels thick in like top and front and sides....and concentration is too hard to focus to work or think, I can plod and go with a slow flow, to read becomes extremely hard, and I struggle to have single vision,,,or other times I need to lay down and rest or fall to sleep for a few hours ranging from 1-3 in the day, even after sleeping 8 hours at night.
Other times my body tires very fast after minimal activity , like having a shower, and can have me exhausted for the rest of the day, other times a rest or sleep can restore me ,but not always.
It can be hard to sit up sometimes, like my torsal has no strength. My muscle can tire very fast.
body vibrates and jumps/jolts more, and after big tiredness days each end with feeling like soaring inside,,,as is something is going very fast,,,feels like sitting on a fridge. Otherwise rigidity ,like tight clenching , stiff. Have to tell myself to relax. Then body jolts.
Tested blood for thyroid cause of tiredness but was within normal range.

I often feel very hot,,and my head sweats, in a rush....

i see i get like a battery life,,and have to work with that in mind, that i will use up the energy and need rest before can do things,,i work slowly in most things i do.

 6, Memory and thinking
I get cloudiness in my head sometimes and find it hard to focus, concentrate on tasks. reading can be hard in these times, like the words don't go in , so I need to read a sentence several times.

Often someone may say something to do, but I forget what they have said and struggle to retrieve the information.

I also sometimes stutter to get a word out.

Regarding multi tasking, I find I start things and then forget to finish, e.g. making a drink, I may prepare for then go on to do another task whilst kettle boils and forget that I was making a drink. I have many tasks on the go, but need to go through things in a sort of systematic way to make sure I cover all tasks I am to do.
I have 2 diary's and use lists of things to do, Or I wouldn't know what I am doing, like my awareness of seems absent.

Sometimes I put off tasks until my brain is working better, as trying to do task that require concentration when my head feels scrambled or thick can become very frustrating and feel overwhelming to do what is otherwise a relatively simple thing, like reading some information.

7, Mental health
I can become frustrated about not being able to concentrate, so everything can take longer and this  sometimes has me feeling inadequate and inferior, or shameful.
I can be tearful for short periods throughout the day with no rational for.

restlessness
sometimes even though my body may feel physically tired, I have restlessness and have thoughts to do things, but then have to acknowledge that I can't and yet find it hard to rest and relax.


8,Pain
stiffness in knees , especially after activity like walking. Then also they feel tight when bend , and like tendons will tear if pushed to far.
no rarely but yes muscles ache after activity more than normal folk, like painful uncomfortable
9,  Sexual problems
single with no big desire to find a sexual partner
10, Spasms and stiffness
after activity can have leg jolt and jump and arm,usually one side,then the other,then both and arms at same time.
and body like exploding from my waist,or solar plexus
like I'm being winded
very fast velocity.
Jolting - body jolts and shakes more when tired physically.
stamping,extreme at times where my arms and legs are thrown very fast all over the place, in sporadic involuntary movements. On a couple of occasions this has lasted for about 1 hour.

Foot sometimes locks in a spasm in pointed position.
At times I feel so tense my jaw clenches and muscles tighten and i don't move, but have to use my mind to like instruct myself to move.
11,   Speech
stutter to give words,sometimes and other times say different word to which I'm thinking and wanting to say.
12,   Swallowing
no problems
13,  Tremor
can have very faint ones,like as if an electric charge is going through me,like there chair is vibrating or wherever my body makes contact ,it feels like its causing the tremor. Sometimes the vibration can be very strong and my body then becomes very tense, feels like a soaring energy inside.


  Treatments, therapies and ways I find to cope

*  i rest
*  approach things slowly

* if torsal weakens until i need to lay down.

*swimming
- swimming I find is calming but after I am left tired physically, but It can sometime improve the energy I have.
*dancing helps release tension in muscles

*stretching
*exercises for knees and balance
- my knees have improved with exercise , in that the swelling has reduced, but the strength in them has no really changed.
* Exercises I do to help my balance do not seem to bring any improvement, sometimes my balance is better than others, but not determined by what I do.

* walk with poles so go further and faster and more stable , to prevent trip and break
- I now use walking pole(s) and this has helped me greatly, in that I am able to walk faster, albeit I feel like my brain goes slower than my feet, and I feel like I'm walking really fast, but meanwhile everyone is walking faster than me and I try sometimes to walk as fast as them but my feet just won't go that fast.
but the use of the pole helps me have more range of movement, so exercises more muscle. without the pole even slight inclines are a struggle, but with poles I am able to walk steeper inclines without strain.
Consequently I am able to walk further and exercise more.

Plus my poor balance can easily have me fall over, but with the pole i am far more stable.
other times I feel lack of energy to do things and use my car to
drive instead of walking to achieve more with the little energy I have, which yes  is unpredictable so i don't plan ahead much but go with the flow of things, setting myself no deadlines with physical nor mental tasks.

************************************************************************

I would like to add here that back at the beginning (2013) when offered help with my back weakness through a physiotherapist she wrote this report

Please note she writes in the 3rd conclusive paragraph.
' My impression is that this is mechanical low back pain with no neurology and there is therefore no clinical need to scan her back, .......'










17 March 2016
I phoned my previously allocated OT and left a message on her answer machine, re my housing needs. although I am aware I am no longer her client so she may not help, but I thought to try first with her as she knows my case.



Tuesday, 15 December 2015

The eye specialist agrees problem is most likely Neurological




I wrote to my GP back in October requesting a bone density test due to my easy breaks I had had. I hand delivered the letter to the surgeries mailbox.


No appointment ever came


Last week I spoke on my phone with a friend who is an advisor on disabilities. She said my symptoms sound like classic MS and to change my GP and ask for second opinion, which I'm entitled too. She told me that when I attend my eye appointment this week to tell them this.
I told her how the consultant I see don't seem to listen and when I showed him my MRI scan of my eyes going in different directions he said they looked normal.

I registered with new GP the next day and this week, yesterday 
Went to Hospital appointment with eye specialist.

I was seen by a new Dr, she had my notes and as soon as I arrived she wanted to discuss things in terms of my neurological reports she was reading.
She said they say he was sending me for blood tests and scans at another hospital.

I informed her I had a test where something was attached near my eye to measure muscle timing in twitches; It showed to be normal.

I added my brain scan showed too much white scars and he wasn't sure if I was MS or high Cholestral or high blood pressure. My blood test showed cholesterol higher than normal and I had informed him I changed my diet since. He said he would ask my GP to test regularly.

I told her I had just changed my GP as yes the last ones didn't seem to care and when I asked for thyroid test; that hadn't  been done since last year, they asked why and I told them because I was tired. But they didn't add in test for cholesterol. The results for my thyroid came back normal.

I added I had spoken to a friend last week who advises disabled people, she said to change Dr and that I can ask for a second opinion. I see the neurologist may not want to make a diagnosis but I need one.
I explained without one I was unable to receive appropriate housing and that I live in a tiny room and have to climb to get things from boxes piled high. I told her I break easy and have poor co ordination and balance. The housing services need diagnosis to help me.
This Dr took notes. She said It wouldn't be he don't want to make a diagnosis but that he can't.

I said I was due to go to new GP for check, procedure and was thinking to ask that they requested a diagnosis from the Neurologist, then maybe something would be decided.

She examined my eyes and said the optic nerve was ok. She added she didn't think it was Thyroid eye disease, as I didn't have enough symptoms, and I agreed telling her how previously in 2009 when I had my eyes hurt and protruded and my lids were red and puffy, but this time I only had double vision and one of her colleges had said initially it was the muscle in my left eye being too tight.
She agreed and said she would send me for tests of my eye movement. I await the appointment. She believes it is Neurologically caused.