Autopsy Options

Jennifer J

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Ouuu, so many questions I have. Thank you for this thread and for any information you have found and can share. :hug:

I know I am not alone in wanting my body to be donated to ME/CFS research, with a full autopsy so that fellow patients and my children might have better answers for their own futures.

Does anyone have suggestions on the logistics of this? Is there any organization or research institute interested in our sorry bodies and brains? Do we need to do some leg work to find an entity who will work with those of us who wish to donate our bodies? (I am in the US)
Has anyone come up with some more information regarding this? I really want to put something in place especially if it can help with ME/CFS research.


The body needs to be collected quickly and it may be too late by the time someone finds a written will. There may also be problems if one commits suicide depending on the method used (toxicology and contamination etc).
She strongly recommended that we donate to the NIH Brain Bank, specifying ME. She is going to email me more information. I'll pass that on as soon as I get it.
I looked at the NIH Brain donation site. They need the brain within 24 hours.
Did anyone figure out the logistics of making this happen especially since it has to happen quickly?

I emailed the Solve ME/CFS Initiative to ask about body donations and also requested a paper consent form for their tissue biobank. I didn't even know this existed! Thank you, @SpecialK82 I'm going to fill one out for me and my (healthy) husband and mother. http://solvecfs.org/solvecfs-biobank/eligibility/
Is Solve ME/CFS the way to go? Or are there other ME/CFS research places, we should consider also? Can it be combined with the NIH Brain donation specified for ME/CFS?

My blood has finally been donated to research, but if anything were to happen, I would want the rest donated to research also.
Curious, the blood can be donated separately to one place and the rest donated elsewhere? @Strawberry if you don't mind saying, where did you donate your blood and was it marked as research for ME/CFS?

Thank you everyone, for your contributions to this thread. :)
 

Strawberry

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@Strawberry if you don't mind saying, where did you donate your blood and was it marked as research for ME/CFS?
:)
I agreed to donating blood for OMF research when I visited Dr Kaufman at the OMI. I didn't ask how many vials were for blood tests, and how many were for research donation, but all in all it was 20+ vials. I think the research part was 5 or 6 vials.

Glad you resuscitated (haha pun intended) this thread. I've been meaning to make a "MCAS alert" card for my wallet, and should add "if deceased please donate any or all tissue to MCAS and ME/CFS research."

There. Reminded myself. Now lets see if I remember. :rolleyes:
 

Strawberry

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Did it. I used the pictures on this website for a template:
http://www.theemptynesthousewife.com/allergies-safety-travel/

This is what I came up with so far:

MEDICAL ALERT

I have Mast Cell Activaton Syndrome

I am allergic to anesthetics

I take Ketitofen, Zyrtec (H1 blocker) and Zantac (H2 blocker)

I also have reactions to medications, food dyes, and fillers

I have orthostatic intolerance and may need saline

If deceased, please donate any tissues to MCAS and ME/CFS research. Please donate to the NIH Brain Bank, specifying ME
I left off some of the cautions because I have no idea if I have issues to those or not. Actually, I don't even know that I have issues with anesthetics. My dad and brother nearly died under anesthesia (and my dad's brother is deceased from anesthesia), so my mom has always made sure the doctors and anesthesiologists know there is a family allergy. I have always had the "safer" anesthetics. But probably safe to assume that I would as I am the only one that has obvious symptoms/reactions of MCAS.

I will make sure to email the solvecfs biobank for the eligibility letter, and add any pertinent information to the card when I print it.

Anyone have any suggestions that I should add?
 
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I am a member of the UK post-mortem research group and the results on some of the post mortems that have been carried out so far here in the UK have been published - see below

However, none of the post-mortems carried out so far have found the sort of widespread and significant neuroinflammation that would be consistent with an encephalomyelitis (ie inflammation of brain and spinal cord)

The dorsal root ganglion (where inflammation has been found) forms part of the peripheral nervous system

We are continuing to carry out post-mortems when the opportunity arises

If you live in the UK you can use our 'Statement of Intent' form on the MEA website to register your permission for body parts and tissues to be used for post mortem research into ME/CFS:

http://www.meassociation.org.uk/wp-content/uploads/MEA-RRF-Statement-of-Intent-2015.pdf

I am not aware of any ME/CFs charities outside the UK who are doing this kind of research

This work is not yet directly linked to the work of the ME/CFS Biobank that we fund at the Royal Free Hospital in London. The ME/CFS Biobank is currently only dealing with collection, storage and distribution of blood samples with the anonymised clinical data attached

Dr Charles Shepherd
Hon Medical Adviser, MEA

Pathology of Chronic Fatigue Syndrome: Pilot Study of Four Autopsy Cases
DG O’Donovan1, 2, T Harrower3, S Cader2, LJ Findley2, C Shepherd4, A Chaudhuri2
1Addenbrooke’s Hospital Cambridge UK
2Queen’s Hospital Romford Essex UK
3Royal Devon & Exeter Hospitals UK
4Honorary Medical Advisor to ME Association UK

Chronic Fatigue Syndrome / Myalgic Encephalomyelitis is a disorder characterised by chronic exercise induced fatigue, cognitive dysfunction, sensory disturbances and often pain. The aetiology and pathogenesis are not understood.

We report the post mortem pathology of four cases of CFS diagnosed by specialists.

The causes of death were all unnatural and included: suicidal overdose, renal failure due to lack of food and water, assisted suicide and probable poisoning.

Selected portions of tissue were made available by the various Coroners in the UK and with the assent of the persons in a qualifying relationship.

The cases were 1 male, and 3 female. Ages (years) M32, F32, F43 & F31.

One case showed a vast excess of corpora amylacea in spinal cord and brain of unknown significance but Polyglucosan Body Disease was not supported by clinicopathologial review. No ganglionitis was identified.
One case showed a marked dorsal root ganglionitis and two other cases showed mild excess of lymphocytes with nodules of nageotte in the dorsal root ganglia.

This raises the hypothesis that dysfunction of the sensory and probably also the autonomic nervous system may lead to abnormal neural activity eg hyperalgesia & allodynia rather than anaesthesia and may explain some of the symptoms of CFS / ME such as pain, hypotension, hyperacusis and photophobia. However, the syndrome may be heterogeneous.

Nevertheless, the precise relationship of fatigue, which may be either peripheral or central, to abnormalities in the peripheral nervous system (PNS) needs to be studied.

The differential diagnosis of ganglionitis should be investigated in CFS / ME patients hence Varicella Zoster, Lyme disease, HIV, Sjogren’s disease, paraneoplastic sensory ganglionopathy should be excluded by appropriate history and tests.

Thorough histopathological study of cases coming to autopsy may help to confirm or refute the hypothesis, that CFS is a disease process, and whether the symptomatology may be explained by inflammation of the sensory and autonomic divisions of the PNS.

A specific CFS / ME brain and tissue bank in the UK is proposed.

Dorsal root ganglion anatomy:



 

Pyrrhus

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Another option might be to contact a researcher who has expressed an interest in post-mortem tissue analysis and set up some personal arrangement with them.

(e.g. Maureen Hanson, PolyBio Research Initiative, Avi Nath at NIH, etc.)
 

Rvanson

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I don't know of anyone in the USA sorry. We have had a few autopsies in the UK. Dr Shepherd from the MEA , I think has organised these in conjunction with Dr Chaudhuri.

The body needs to be collected quickly and it may be too late by the time someone finds a written will. There may also be problems if one commits suicide depending on the method used (toxicology and contamination etc).

In death we are often treated as badly as in life. "Just" because we die there is no automatic interest in our cause of death in terms of ME. I don't think that we can assume that an adequate autopsy will always be carried out for that reason even if we want one.
So true. It will be many weeks before my body is found. No matter, I will be with my master, God, finally.

Before I caught ME/CFS. I used to donate blood. Lots of blood, every two weeks and platelets as well. But once I saw that no one cared about us, after I fell ill with ME/CFS, I stopped donating blood. I can't imagine giving this disease to anyone at all. It has totally ruined my life and lead to a life of extreme loneliness, and no one to touch and talk too at all.

That said, I won't donate my body to the idiots who don't believe in ME/CFS and even make fun of it. All this while Americans and the FDA will not allow us to try to get better with Ampligen, proven to help 70 percent of ME/CFS sufferers in most studies.